Front. Cell. Infect. Microbiol. Frontiers in Cellular and Infection Microbiology Front. Cell. Infect. Microbiol. 2235-2988 Frontiers Media S.A. 10.3389/fcimb.2024.1358270 Cellular and Infection Microbiology Original Research Antifungal and antibiofilm effects of probiotic Lactobacillus salivarius, zinc nanoparticles, and zinc nanocomposites against Candida albicans from Nile tilapia (Oreochromis niloticus), water and humans El-Gazzar Nashwa 1 † Elez Rasha M. M. Abou 2 * † Attia Amira S. A. 3 Abdel-Warith Abdel-Wahab A. 4 Darwish Manal M. 5 6 Younis Elsayed M. 4 Eltahlawi Rehab A. 7 Mohamed Kawthar Ibraheem 5 Davies Simon J. 8 Elsohaby Ibrahim 9 10 11 * † 1 Department of Botany and Microbiology, Faculty of Science, Zagazig University, Zagazig, Egypt 2 Department of Zoonoses, Faculty of Veterinary Medicine, Zagazig University, Zagazig, Egypt 3 Department of Veterinary Public Health, Faculty of Veterinary Medicine, Zagazig University, Zagazig, Egypt 4 Department of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia 5 Medical Microbiology Department, Faculty of Medicine, Ain Shams University, Cairo, Egypt 6 Microbiology and Immunology Department, Faculty of Pharmacy, October University for Modern Sciences and Arts, Giza, Egypt 7 Microbiology and Immunology Department, Faculty of Medicine, Zagazig University, Zagazig, Egypt 8 Aquaculture Nutrition Research Unit ANRU, Carna Research Station, Ryan Institute, College of Science and Engineering, University of Galway, Galway, Ireland 9 Department of Infectious Diseases and Public Health, Jockey Club College of Veterinary Medicine and Life Sciences, City University of Hong Kong, Hong Kong, Hong Kong SAR, China 10 Centre for Applied One Health Research and Policy Advice (OHRP), City University of Hong Kong, Hong Kong, Hong Kong SAR, China 11 Department of Animal Medicine, Faculty of Veterinary Medicine, Zagazig University, Zagazig, Egypt

Edited by: Mohamed S. Hasanin, National Research Centre, Egypt

Reviewed by: Payal Gupta, Graphic Era University, India

Atamjit Singh, Guru Nanak Dev University, India

*Correspondence: Ibrahim Elsohaby, ielsohab@cityu.edu.hk; Rasha M. M. Abou Elez, rmmohamed@zu.edu.eg

†These authors have contributed equally to this work

 04 06 2024 2024 14 1358270 19 12 2023 29 04 2024 Copyright © 2024 El-Gazzar, Elez, Attia, Abdel-Warith, Darwish, Younis, Eltahlawi, Mohamed, Davies and Elsohaby 2024 El-Gazzar, Elez, Attia, Abdel-Warith, Darwish, Younis, Eltahlawi, Mohamed, Davies and Elsohaby

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 Introduction

Candida albicans (C. albicans) can form biofilms; a critical virulence factor that provides effective protection from commercial antifungals and contributes to public health issues. The development of new antifungal therapies, particularly those targeting biofilms, is imperative. Thus, this study was conducted to investigate the antifungal and antibiofilm effects of Lactobacillus salivarius (L. salivarius), zinc nanoparticles (ZnNPs) and nanocomposites (ZnNCs) on C. albicans isolates from Nile tilapia, fish wash water and human fish sellers in Sharkia Governorate, Egypt.

 Methods

A cross-sectional study collected 300 samples from tilapia, fish wash water, and fish sellers (100 each). Probiotic L. salivarius was immobilized with ZnNPs to synthesize ZnNCs. The study assessed the antifungal and antibiofilm activities of ZnNPs, L. salivarius, and ZnNCs compared to amphotericin (AMB).

 Results

Candida spp. were detected in 38 samples, which included C. albicans (42.1%), C. glabrata (26.3%), C. krusei (21.1%), and C. parapsilosis (10.5%). A total of 62.5% of the isolates were resistant to at least one antifungal agent, with the highest resistance to nystatin (62.5%). However, 75% of the isolates were highly susceptible to AMB. All C. albicans isolates exhibited biofilm-forming capabilities, with 4 (25%) isolates showing strong biofilm formation. At least one virulence-associated gene (RAS1, HWP1, ALS3, or SAP4) was identified among the C. albicans isolates. Probiotics L. salivarius, ZnNPs, and ZnNCs displayed antibiofilm and antifungal effects against C. albicans, with ZnNCs showing significantly higher inhibitory activity. ZnNCs, with a minimum inhibitory concentration (MIC) of 10 µg/mL, completely reduced C. albicans biofilm gene expression. Additionally, scanning electron microscopy images of C. albicans biofilms treated with ZnNCs revealed asymmetric, wrinkled surfaces, cell deformations, and reduced cell numbers.

 Conclusion

This study identified virulent, resistant C. albicans isolates with strong biofilm-forming abilities in tilapia, water, and humans, that pose significant risks to public health and food safety.

 Candida albicans virulence genes zinc nanoparticles probiotic nanocomposite antibiofilm activity section-in-acceptance Veterinary and Zoonotic Infection Introduction

Candida albicans (C. albicans) is a dimorphic fungus that causes a significant portion (50–90%) of candidiasis cases in humans (Romaní et al., 2006; Kadosh and Lopez-Ribot, 2013; Sardi et al., 2013; Salvatori et al., 2016; Tsui et al., 2016). It colonizes the mucosal surfaces and skin of healthy humans, animals, and fish (Cannon et al., 1995; Koh et al., 2008; Gow et al., 2011). Clinical manifestations of candidiasis range from localized to invasive and systemic disease, depending on individual’s immune status (Papon et al., 2013). C. albicans can cause life-threatening infections, especially infections caused by drug-resistant strains, in immunocompromised patients (Pfaller et al., 2010), resulting in significant morbidity, high mortality, and increased healthcare costs (Sherry et al., 2017). Other Candida spp., such as C. tropicalis, C. glabrata and C. parapsilosis, cause 30 to 54% of candidiasis cases (Silva et al., 2009; Donadu et al., 2021). Candida spp. can also cause acute diseases when contaminating potable water and are increasingly recognized as an emerging cause of chronic water quality problems (Montagna et al., 2012; Montagna et al., 2013; Mhlongo et al., 2019) as they are natural inhabitants of water and can thrive in low circulation areas of water systems (Caggiano et al., 2020).

Several factors, including the host’s immune status, virulence-associated genes, and biofilm formation ability, contribute to the transition of Candida spp. from commensal to pathogenic form (Spellberg, 2008; Galocha et al., 2019). The pathogenicity of Candida spp. is primarily linked to specific virulence genes, such as agglutinin-like sequence genes (ALS3), secretory aspartate protease (SAP4), hyphal wall protein 1 (HWP1), and a hyphal-regulated gene (HYR1), which facilitate the invasion of host tissues (Dwivedi et al., 2011; Mayer et al., 2013; de Oliveira et al., 2017; Bu et al., 2022). These genes are essential for mycelial formation, adhesion, and the development of C. albicans biofilm (Schild et al., 2011; de Oliveira et al., 2017; Bu et al., 2022).

C. albicans biofilm consist of diverse three-dimensional combinations of hyphae and yeast embedded extracellularly by large numbers of matrix units (Douglas, 2002; Lohse et al., 2018). C. albicans can form biofilms on the surfaces of implantable medical instruments and is associated with device-related nosocomial infections. These Candida biofilms exhibit resistance levels 30 to 2000 times higher than those of planktonic cells to various antifungal agents, such as fluconazole, ketoconazole, itraconazole and amphotericin (Seneviratne et al., 2008), as well as reduced susceptibility to host immune reactions (da Costa et al., 2009; Berman and Krysan, 2020). The widespread and prolonged use of conventional antimicrobial agents has led to the emergence of fungal drug fights (Abdel-Shafi et al., 2020; Enan et al., 2020; Judan Cruz et al., 2021). Researchers are now exploring innovative strategies to combat multidrug-resistant microbial strains, including the use of nanomaterials (El-Gazzar and Ismail, 2020; Ismail et al., 2020a; Sitohy et al., 2021) and probiotics (Osman and El-Gazzar, 2021), as the development of new antibiotics is challenging.

Nanomaterials composed of various substances, including lipids, metals, and natural or synthetic polymers, serve as efficient drug carriers (El-Gazzar and Enan, 2020). Their rapid and effective biological absorption compared to larger macromolecules makes them excellent materials for delivery systems (El-Bahr et al., 2021; El-Gazzar et al., 2021). In recent years, zinc nanoparticles (ZnNPs) have garnered significant attention as one of the most extensively studied nanostructures produced through nanotechnology, known for their antimicrobial properties against bacteria and fungi. ZnNPs disrupt fungal membranes, leading to cell death by compromising cell structure and function (Hosseini et al., 2019). On the other hand, probiotics, which are diverse antimicrobial substances produced by lactic acid bacteria (LAB) strains, can inhibit C. albicans proliferation, adhesion, and biofilm formation (Matsubara et al., 2016; Osman and El-Gazzar, 2021).

Several studies have shown that Lactobacillus rhamnosus, Lactobacillus reuteri, and Lactobacillus salivarius (L. salivarius) possess potent antifungal activity against C. albicans infection (De Gregorio et al., 2019; Vazquez-Munoz and Dongari-Bagtzoglou, 2021; El-Ashmony et al., 2023). Supernatants of L. salivarius demonstrate antifungal effects against Candida spp., with lactic acid accumulation in the medium (Zangl et al., 2019). Additionally, organic acids produced by Lactobacillus spp. enhance the efficacy of antifungal agents by increasing fungal plasma membrane permeability, facilitating azole uptake. However, lactic acid, low pH, and other secreted metabolites are environmental signals sensed by C. albicans, triggering changes in gene expression and the transition to hyphal growth. Another potential mechanism for the probiotic effect could involve competition for available niches and reduced adhesion (Krzyściak et al., 2017). Therefore, the present study aimed to (i) detect the occurrence of Candida spp. in tilapia fish, fish wash water, and fish sellers in Sharkia Governorate, Egypt, (ii) identify the virotypes and genotypes of the isolated C. albicans, (iii) assess the susceptibility to antifungal drugs and biofilm forming abilities of the identified C. albicans, and (iv) investigate the antifungal and antibiofilm effects of L. salivarius and ZnNPs and nanocomposites (ZnNCs) on isolates of C. albicans.

 Materials and methods Study design and sampling

A cross-sectional study collected 300 samples from Nile tilapia (Oreochromis niloticus), fish wash water, and human fish sellers (100 from each) at various retail fish markets in Sharkia Governorate, Egypt, between April 2022 and January 2023. Sterile cotton swabs were used to collect samples from fish and sellers. The swabs gently rubbed the fish surface and the human seller’s hand before being immersed in tubes containing buffered peptone water (BPW). Additionally, 100 mL of fish wash water was collected in sterile screw-capped glass bottles. The specimens were labeled with the sample identifier, sample type, and date of sampling, and then transported to the laboratory for later testing.

 Isolation and biochemical identification

All samples were cultured on Sabouraud Dextrose Agar (SDA; CONDA, Spain) slopes supplemented with 0.05 µg/mL of chloramphenicol and incubated for 24-72 h at 37°C (Amin et al., 2014). Any visible growth on the SDA slopes was further identified through microscopic examination, Gram staining, germ tube testing, and urea hydrolysis testing (Deorukhkar and Roushani, 2018). Pasty and creamy colonies displaying Gram-positive staining and a negative urea hydrolysis test were purified and inoculated into CHROM agar for 48 h at 37°C (Nadeem et al., 2010). Colonies exhibiting a light green color were presumptively identified as C. albicans and preserved on SDA slopes at 4°C for further characterization.

 Molecular characterization of <italic>C. albicans</italic>

Suspected C. albicans colonies were confirmed using PCR targeting the ITS1 region of the C. albicans genome. DNA was isolated with a QIAamp DNA Mini Kit (QIAGEN GmbH, Hilden, Germany) following the manufacturer’s guidelines. The PCR master mix (25 μL) included 12.5 μL of 2X Dream Taq Green master mix kit, 5.5 μL of PCR grade water, 1 μL of both forward and reverse primers (20 pmoL, each), and 5 μL of DNA template. The primers used were obtained from Metabion (Germany) and the PCR conditions are described in Supplementary Table S1 . Molecularly confirmed C. albicans isolates were subjected to virotyping by targeting the ALS3 gene (Tsang et al., 2012), HWP1 gene (Inci et al., 2013), RAS1 gene (Tsang et al., 2012) and SAP4 gene (Sikora et al., 2011). Positive controls (C. albicans ATCC 90028) were included in the PCR assay with the tested strains.

Genotyping of C. albicans was performed using RAPD-PCR fingerprinting with the primer OPA-18 following a previously described method (Bautista-Muñoz et al., 2003). The RAPD-PCR fingerprinting information was presented as a binary code based on the absence or presence of every band. The discriminatory power of RAPD-PCR was assessed using Simpson’s index of diversity (D), as previously described (Hunter and Gaston, 1988).

 Antifungal susceptibility test

The antifungal susceptibility of C. albicans strains was assessed through Kirby-Bauer Disc Diffusion procedure with Mueller Hinton agar. Inhibition zones were determined and interpreted using the Clinical and Laboratory Standards Institute instructions (CLSI, 2008). Eight antifungal agents, including amphotericin (AMB; 20 μg), nystatin (NYS; 100 I.U.); fluconazole (FLZ; 25 μg), itraconazole (ITR; 10 μg), flucytosine (FUS; 1 μg), caspofungin (CAS; 5 μg), micafungin (MIC; 1 μg) and terbinafine (TER; 30 μg), were tested. C. albicans ATCC 90028 was used as a quality control. The multiple antifungal resistance (MAR) index was calculated (Cavalcanti Filho et al., 2017). Multidrug resistance (MDR) was also determined (Sanglard, 2016).

 Biofilm formation and quantification

Biofilm production of the C. albicans strains was assessed using the microtiter plate method (Pierce et al., 2008; Dhanasekaran et al., 2014). A loopful of colonies from fresh agar plates was cultured in SDB media (Oxoid Ltd., Cambridge, UK), overnight at 30°C at 150 rpm in an orbital shaker (Lab-line Incubator Shaker; Elliott Bay Laboratory Services Inc., Seattle, WA, USA). The yeast cells were harvested by centrifugation at 3,000 rpm for 10 min, washed twice in sterile phosphate-buffered saline (PBS, Sigma-Aldrich, St. Louis, MO., USA), resuspended in RPMI 1640, counted using a hemocytometer, and concentration-adjusted to 1 × 106 cells/mL. A 100 μL aliquot of cell suspension (C. albicans + SDB) was inoculated into individual well of the 96 well-flat bottom microtiter plates in triplicate. Wells of every plate are containing SDB that were recognized as negative controls. The plates were incubated for a day at 37°C, before being washed three times with sterile 200 µL PBS. The plates were inverted, and PBS was removed. The biofilms were subsequently fixed with 150 μL of 95% ethanol for 20 min. Finally, the biofilm was stained with 0.1% (w/v) crystal violet and left at room temperature for 15 min, then washed twice with PBS and left for 1 h to dry.

The optical density (OD) of stained adherent C. albicans biofilm was measured at wavelength of 590 nm by an ELISA reader subsequent to the negative control (ODNC) at zero. The means and standard deviations of OD values were recorded for all C. albicans isolates, positive (C. albicans, ATCC 90028) and negative controls. The isolates were then considered to be non-biofilm formers (OD590 ≤ ODNC), weak (ODNC< OD590 ≤ 2 x ODNC), moderate (2 × ODNC< OD590 ≤ 4 × ODNC), or strong (4 × ODNC< OD590) biofilm formers.

 DNA sequencing and phylogenetic analysis

The DNA products amplified from two MDR and strong biofilm-forming C. albicans strains were isolated with a QIAquick PCR Kit (QIAGEN, Valencia, CA, USA), following the manufacturer’s guidelines. ITS gene sequencing was carried out with primers ( Supplementary Table S1 ) and an automated sequencer, as previously described (Tarini et al., 2010).

The obtained sequences were resolved with the Basic Local Alignment Search Tool (BLAST® analysis) of Informative Biotechnology website on the National Center. Gene sequences of the C. albicans isolates were submitted to the GenBank sequence database under accession numbers OQ150021 and OQ150022. Initial BLAST® analysis was performed to establish sequence identity with GenBank accessions (Altschul et al., 1990). These sequences were then aligned with others available in the GenBank sequence database. A phylogenetic tree was constructed using MEGA 6 (Tamura et al., 2013).

 Effects of probiotic <italic>L. salivarius</italic>, ZnNPs and ZnNCs on <italic>C. albicans</italic> Biosynthesis of ZnNPs and ZnNCs

ZnNPs biosynthesis followed the protocol previously described by El-Gazzar and Ismail (2020). It involved using a 1 mM salt of ZnO2 metal (Nanotech for Photo-Electronic Co., Dreamland, 6-October, Egypt) with enzyme extract from Aspergillus fumigatus. The mixture was then incubated at 28°C until ZnNPs biosynthesis was complete.

The probiotic strain L. salivarius DSM 20555 from the Belgian Co-ordinated Collection of Microorganisms (BCCM) was cultivated in Mane Rogosae Sharp (MRS) broth (Oxoid, Roskilde, Denmark). Probiotic solution (1 mL) was applied to MRS broth (9 mL) and incubated for 24 h at 37°C. Probiotic cultures were centrifuged after incubation for 10 min at 4000 rpm, and the supernatant was collected and purify-sterilized by a 0.2 mm membrane syringe filter.

The synthesis of ZnNCs was carried out through a sono-chemical method, in which 1 g of ZnNPs mixed in 200 mL of deionized distilled water was added to a 250 mL beaker with 1 mL of probiotic L. salivarius and subjected to sonication under conditions of 0.5 cycle and 50% amplitude for 2 h until a homogeneous mixture was obtained (Ismail et al., 2020b).

 Characterization of ZnNPs and ZnNCs

ZnNPs and ZnNCs were characterized using dynamic light scattering (DLS) to determine the particle diameter (El-Gazzar and Ismail, 2020). Additionally, transmission electron microscopy (TEM) was performed on both ZnNPs and ZnNCs. In a solution of double-deionized water, ZnNPs and ZnNCs were added and then sonicated for 50 min at a frequency of 50 kHz with a cycle length of 0.65 and amplitude of 85% (UP400S, Hielscher, Germany). The resulting slurry was aliquoted (5 µL) and applied to a copper grid with carbon coating. TEM analysis was conducted using a TEM-2100 (JEOL, Tokyo 196-8558, Japan) (Sitohy et al., 2021).

X-ray diffraction (XRD) test was performed using a Bruker D8 Discovers Set (Billerica, MA, USA) to determine the colloidal nature and evaluate the homogeneity and reunify of the synthesis methods for ZnNPs, probiotic L. salivarius, and ZnNCs. The probiotic L. salivarius and ZnNCs were subjected to assessment via Energy Dispersive-X-ray Spectroscopy (EDS) (Sitohy et al., 2021).

 Antibiofilm effect

A suspension (100 μL) of C. albicans (1 × 106 cells/mL) was plated in 96-well microtiter dishes as described earlier and incubated with agitation. The effects of ZnNPs, probiotic L. salivarius, ZnNCs, and antifungal (AMB) on hyphal development and the early phases of biofilm consistence (preventative) were assessed. Free floating cells were removed 1.5 h after adhesion by thoroughly washing each well with 200 μL of PBS. Subsequently, after another 24 h at 37°C with agitation, adhesive cells were exposed to 200 μL of various doses of the test drugs that had been diluted on a separate microtiter dish.

The produced biofilm biomass was quantified for ZnNPs, probiotic L. salivarius, ZnNCs, and AMB in comparison to untreated controls. The crystal violet assay was used to quantify the resulting biofilm biomass compared with untreated controls. An ELISA reader (Sunrise R4, Tecan) calculated the OD of the biofilm at 590 nm after the negative control (ODNC) was set at zero. The negative and positive controls used were sanitized medium only and the working solution, respectively (Pierce et al., 2008; Abou Elez et al., 2023). The rate (%) of biofilm inhibition was measured through the subsequent equation:

B i o f i l m   i n h i b i t i o n   r a t e   ( % )   = 1 −   O D 590   o f   t r e a t e d   c e l l s   O D 590   o f   n o n t r e a t e d   c o n t r o l   × 100 Antifungal effect

The antifungal efficacy of ZnNPs, probiotic L. salivarius, and ZnNCs was assessed against C. albicans isolates using the agar well diffusion method (CLSI, 2008). In brief, 25 mL of SDA agar was individually inoculated with 100 µL (0.5 × 10^3 CFU/mL) of C. albicans isolates. The mixture was then added into a Petri dish and allowed to settle at room temperature for 30 min. Subsequently, a 10 mm diameter well was created in the agar using a sterile corkborer. The wells were supplied with 100 µg of each ZnNPs, probiotic L. salivarius, and ZnNCs. Wells filled with (20 µg) and broth media served as positive and negative controls, respectively. The plates were adjusted for 48 h at 37°C, and the diameters of the inhibition zones were measured using a ruler.

The minimum inhibitory concentration (MIC) values of ZnNPs, probiotic L. salivarius, and ZnNCs against C. albicans were calculated by agar well diffusion technique as mentioned above. Different concentrations ranging from 5 to 100 µg/mL of each ZnNPs, probiotic L. salivarius, and ZnNCs were applied to the wells, and the plates were adjusted for 2 days at 37°C. The lowest agent concentration that inhibited germination parallels to the positive control after 48 h of incubation at 37°C was considered the MIC. The test was conducted in triplicate.

 Quantitative analysis of biofilm gene expression

Transcript expression was used to assess the effect of the tested factors on C. albicans adhesion (ALS3), filamentation (HWP1), the hyphal regulator (RAS1), and hyphal formation and virulence (SAP4), as previously described (Tsang et al., 2012). A 1 mL suspension of each C. albicans strain, OQ150021 and OQ150022, was transferred to the wells of pre-sterilized 24-well microtiter plates with a flat bottom and incubated at 37°C for 1.5 h under agitation. The wells were washed with PBS. Fresh RPMI 1640 medium (1 mL) containing MIC-50 of ZnNPs, probiotic L. salivarius, ZnNCs, and AMB was added to each well, and the plate was further incubated for 24 h at 37°C. The control wells were used for comparison. The wells were washed twice with PBS and 600 mL of RLT buffer was added to the wells. The plate was incubated for 10 min, and then transferred to 1.5 mL microcentrifuge tubes. For sample homogenization, a 2-min high-speed (30-Hz) tissue lyser was used.

For each harvested fungal culture, including untreated fungal culture (control) and the treated fungal culture (ZnNPs, probiotic L. salivarius, ZnNCs, and AMB-treated C. albicans), one volume was added to one volume of RNA protection reagent at each sampling time (Qiagen, Hilden, Germany) following the manufacturer’s instructions. RNA isolation was carried out using the QIAamp RNeasy Mini Kit (Qiagen, Hilden, Germany) following the manufacturer’s guidelines. SYBR Green I-based real-time PCR with specific primers for ALS3, HWP1, RAS1, and SAP4 virulence genes was used as previously described (Tsang et al., 2012). The ITS gene was employed as a housekeeping gene (Tarini et al., 2010). The PCR reaction contained 12.5 µL of SYBR Green PCR Master Mix (QIAGEN), 0.25 µL of reverse transcriptase (200 U/µL), 0.5 µL of each primer (20 pmoL), 8.25 µL of nuclease-free water, and 3 µL of RNA template. The amplification curves and cycle threshold (Ct) values were determined by Stratagene MX3005P software. The ΔΔCt method was performed, according to Yuan et al. (2006).

 Scanning electron microscopy analysis

The impact of ZnNCs on the morphology and structural integrity of C. albicans biofilm was examined using scanning electron microscopy (SEM) (Jeol 2100, Tokyo, Japan), following established protocols (Ramage et al., 2002). Initially, 2 mL suspension of C. albicans OQ150021 cells at a concentration of 1 × 106 cells/mL in RPMI 1640 was incubated at 37°C for 24 h. Subsequently, the resulting biofilm was formed on sterile plastic coverslips (Nalge Nunc International) placed in 24-well tissue culture plates (Costar, Corning Inc., USA). The biofilm was treated with ZnNCs, washed with PBS, and then fixed in a solution of 0.1 M cacodylate buffer and 2.5% (vol/vol) glutaraldehyde (pH 7.2) overnight. After fixation, the cells were subjected to a series of ethanol washes for dehydration and air-dried in a desiccator. SEM analysis was conducted on the gold-coated samples using a Baltec SDC 050 sputter coater.

 Data analysis

All statistical tests and data visualization were performed with R software (version 4.2.0). A dendrogram was generated with the “hclust” function from the stats package. One-way analysis of variance compared the effects of AMB, ZnNPs, probiotic L. salivarius, and ZnNCs on C. albicans biofilm formation and biofilm gene expression. P-values <0.05 were considered statistically significant.

 Results <italic>Candida</italic> spp. isolation and identification

Candida spp. were detected in 38 (12.7%) of the specimens, comprising 18 (18%) from Nile tilapia, 7 (7%) from fish wash water, and 13 (13%) from human sellers ( Table 1 ). Four Candida spp. were isolated as C. krusei, C. glabrata, C. parapsilosis and with C. albicans (42.1%) being the most frequently recovered. Notably, when focusing on hand swabs from human sellers, C. albicans accounted for a high percentage, specifically 42.9%.

Occurrence of Candida spp. in Nile tilapia, fish wash water and fish sellers.

Sample type No. of samples No. Candida spp. positive samples (%) No. (%) of samples positive to
C. albicans C. krusei C. parapsilosis C. glabrata
Nile tilapia 100 18 (18) 8 (44.4) 3 (17.6) 2 (11.8) 5 (29.4)
Fish wash water 100 7 (7) 3 (42.9) 2 (28.6) 1(14.3) 1(14.3)
Fish sellers 100 13 (13) 5 (38.5) 3 (21.4) 1 (7.1) 4 (28.6)
Total 300 38 (12.7) 16 (42.1) 8 (21.1) 4 (10.5) 10 (26.3)
Molecular characterization of <italic>C. albicans</italic> isolates

Biochemically identified C. albicans were molecularly confirmed by detecting the ITS1 gene. C. albicans virulence-associated genes, including RAS1, HWP1, ALS3, and SAP4, were identified ( Table 2 ). The most frequently identified gene was ALS3 (81.3%), followed by HWP1 (56.3%), RAS1 (50%), and SAP4 (31.3%).

Virulotypes, antifungal resistance patterns and biofilm degree of C. albicans isolates recovered from Nile tilapia, fish wash water and fish sellers.

ID Source Virulence genes1 Genotyping Antifungal resistance2 Biofilm degree3
RAS1 HWP1 ALS3 SAP4 Profile Cluster Patterns MAR index
F1 Tilapia − + + + R5 III NYS, ITR, MIC 0.37 M
F2 Tilapia + + + − R10 IV FLZ, CAS 0.25 S
F3 Tilapia − − + − R9 Single NYS, FLZ 0.25 M
F4 Tilapia + − − − R7 Single ITR, TER 0.25 M
F5 Tilapia − + + − R2 I FLZ, ITR, FUS, MIC 0.50 M
F6 Tilapia + + + − R5 III NYS, CAS 0.25 M
F7 Tilapia + − − − R1 I FLZ, CAS 0.25 M
F8 Tilapia + + + + R10 IV AMB, NYS, FLZ, FUS, CAS, MIC, TER 0.87 S
W9 Water − − + + R2 I NYS, ITR, TER 0.33 M
W10 Water − + + – R2 I NYS, ITR, MIC 0.33 M
W11 Water + – – + R3 II ITR, FUS 0.25 M
H12 Sellers + + + − R3 II AMB, FLZ 0.25 S
H13 Sellers − − + − R4 II NYS, FLZ, MIC 0.37 M
H14 Sellers + + + + R8 Single AMB, NYS, FLZ, ITR, FUS, CAS, TER 0.87 S
H15 Sellers − − + − R6 Single NYS, ITR, FUS 0.37 M
H16 Sellers − + + − R1 I AMB, NYS, CAS 0.37 M

1 +: virulence genes positive, −: virulence genes negative.

2 AMB, amphotericin B; NYS, nystatin; FLZ, fluconazole; ITR, itraconazole; FUS, flucytosine; CAS, caspofungin; MIC, micafungin; TER, terbinafine; MAR, multiple antibiotic index.

3 M, moderate biofilm forming; S, strong biofilm forming.

RAPD-PCR analysis of the 16 C. albicans isolates revealed 10 distinct profiles, denoted as R1 to R10 ( Table 2 ). The power of RAPD-PCR was high, with a D value equal to 0.95. Cluster I included isolates obtained from tilapia, fish wash water, and human sellers ( Figure 1 ). The similarity between the isolates from sellers and those from tilapia and water in clusters I and II was 100%, as determined by the Jaccard coefficient.

RAPD-PCR dendrogram for C. albicans isolates recovered from Nile tilapia, fish wash water, and fish sellers.

The ITS region of two representative virulent biofilm-forming C. albicans, obtained from tilapia and human sellers, was sequenced and subsequently listed under accession numbers OQ150021 to OQ150022. Phylogenetic tree analysis revealed that the ITS sequences of C. albicans strains of fish and human sellers were associated with the lineage of other C. albicans from GenBank and were distinctly separated from other Candida spp. ( Figure 2 ).

Phylogenetic tree of C. albicans isolated from Nile tilapia and fish seller (red dot) based on ITS gene sequences. A phylogenetic tree was generated using the neighbor-joining approach and 1000 bootstrap values.

 Antifungal susceptibility of <italic>C. albicans</italic>

The antifungal resistance patterns of C. albicans isolates to the 8 antifungal drugs are presented in Tables 2 and 3 . Among the isolates, 62.5% exhibited resistance to at least one antifungal agent. Notably, the isolates demonstrated an increase in the degree of resistance to NYS (62.5%), followed by FLZ and ITR (50% each). Conversely, the isolates displayed a high level of susceptibility to AMB (75%). The MAR index ranged from 0.25 to 0.87, with an average of 0.56 ( Table 2 ).

Antifungal susceptibility results of 16 C. albicans isolates recovered from Nile tilapia, fish wash water, and fish sellers.

Antifungal class Antifungals (µg/mL)1 Number (%) of C. albicans
Resistant Intermediate Susceptible
Polyenes AMB (20 μg) 4 (25.0) 0 (0.0) 12 (75.0)
NYS (100 U) 10 (62.5) 0 (0.0) 6 (37.5)
Azoles FLZ (25 μg) 8 (50.0) 3 (18.8) 5 (31.2)
ITR (10 μg) 8 (50.0) 6 (37.5) 2 (12.5)
Flucytosine FUS (1 μg) 5(31.2) 4 (25.0) 7 (43.8)
Echinocandins CAS (5 μg) 6 (37.5) 2 (12.5) 8 (50.0)
MIC (1 µg) 5 (31.2) 3 (18.8) 8 (50.0)
Allylamines TER (30 μg) 4 (25.0) 2 (12.5) 10 (62.5)

1 AMB, amphotericin B; NYS, nystatin; FLZ, fluconazole; ITR, itraconazole; FUS, flucytosine; CAS, caspofungin; MIC, micafungin; TER, terbinafine.

 <italic>C. albicans</italic> biofilm formation ability

All C. albicans isolates exhibited biofilm-forming capabilities, with 4 (25%) isolates displaying strong biofilm formation ( Table 2 ). However, the remaining 12 (75%) isolates showed moderate biofilm formation abilities.

 Effects of probiotic <italic>L. salivarius</italic>, ZnNPs and ZnNCs on <italic>C. albicans</italic> Characterization of ZnNPs and ZnNCs

ZnNPs were biosynthesized by Aspergillus fumigatus and have a characteristic peak at 45.82 nm ( Figure 3A ), however, ZnNCs had a characteristic peak at 85 nm ( Figure 3B ). Under TEM, ZnNPs exhibited spherical and cubic shapes ( Figure 3C ), while the ZnCNs have sub-rectangular shapes ( Figure 3D ). X-ray diffraction patterns for ZnNPs, probiotic L. salivarius, and ZnNCs are presented in Figure 4 . ZnNPs displayed characteristic peaks at 2θ angles of 35.862°, 39.044°, 43.176°, 54.659°, 69.507°, and 76.012° ( Figure 4A ). Probiotic L. salivarius exhibited characteristic peaks at 2θ angles of 9.145°, 18.398°, 28.305°, 41.484°, 49.805°, 58.560°, 60.231°, 68.803°, and 79.697° ( Figure 4B ). On the other hand, ZnNCs displayed sharp characteristic peaks at 2θ angles of 9.124°, 14.558°, 18.734°, 20.637°, 28.284°, 33.442°, 40.194°, 40.662°, 54.659°, 59.291°, and 68.802°, indicating a cubic lattice of nanocomposites ( Figure 4C ). The elemental composition of the surface of the probiotic L. salivarius and ZnNCs was analyzed using EDS. In the spectrum of probiotic L. salivarius, carbon (55.10%), nitrogen (1.8%), oxygen (31.9%), calcium (9.4%), and silicon (1.79%) were found ( Figure 4D ). In the spectrum of ZnNCs, carbon (49.10%), nitrogen (1.75%), oxygen (27.79%), calcium (9.3%), silicon (1.89%), and zinc (9.35%) were identified ( Figure 4E ).

Characterization of ZnNPs and ZnNCs. DLS diameter of ZnNPs (A) and ZnNCs (B); transmission electron microscopy of ZnNPs (C) and ZnNCs (D).

Powder X-ray diffraction (XRD) pattern for ZnNPs (A), probiotic L. salivarius (B), and ZnNCs (C), and energy-dispersive X-ray spectroscopy (EDX) pattern for probiotic L. salivarius (D) and ZnNCs (E).

 Antibiofilm effect

Figure 5 displays the biofilm inhibition rates of AMB, ZnNPs, probiotic L. salivarius, and ZnNCs on C. albicans isolates recovered from tilapia, fish wash water, and fish sellers at 37°C. ZnNCs exhibited the highest biofilm inhibition rate at 84.4%, followed by ZnNPs. C. albicans treated with AMB displayed a significantly lower biofilm inhibition rate compared to those treated with ZnNPs, probiotic L. salivarius, and ZnNCs. Moreover, a significant difference in biofilm inhibition rate was observed when C. albicans was treated with probiotic L. salivarius and ZnNPs (P = 0.012) and ZnNCs (P = 0.0003). On the other hand, no significant variation was found within ZnNPs and ZnNCs (P = 0.685).

Biofilm inhibition rate of amphotericin B (AMB), ZnNPs, probiotic L. salivarius and ZnNCs against C. albicans isolates recovered from Nile tilapia, fish wash water, and fish sellers.

 Antifungal effect

The antifungal effects of ZnNPs, probiotic L. salivarius, and ZnNCs against C. albicans isolates recovered from tilapia and fish sellers were assessed using the disc diffusion method ( Table 4 ). AMB, which was sensitive to most of the isolates (75%), was used as a positive control. ZnNPs, probiotic L. salivarius, and ZnNCs exhibited significantly larger inhibition zones than AMB (20 μg) for all C. albicans isolates. Furthermore, the MIC for inhibition of C. albicans growth was 10 µg/mL for ZnNCs and 20 µg/mL for both ZnNPs and probiotic L. salivarius ( Supplementary Table S2 ).

Antifungal activity of amphotericin B (AMB), ZnNPs, probiotic L. salivarius and ZnNCs against C. albicans isolates recovered from Nile tilapia, fish wash water, and fish sellers.

C. albicans Inhibition zone diameter (mm) of 100 µg/mL concentration of
Source ID AMB ZnNPs L. salivarius ZnNCs
Tilapia F1 19.1 ± 0.2 35.5 ± 0.5 36.3 ± 0.3 38.1 ± 0.7
F2 21.3 ± 0.3 31.1 ± 0.8 38.8 ± 0.2 41.8 ± 0.5
F3 21.2 ± 0.3 31.2 ± 1.0 40.3 ± 1.3 43.4 ± 0.2
F4 18.2 ± 0.2 27.6 ± 0.4 39.0 ± 0.5 43.0 ± 0.6
F5 19.2 ± 0.3 29.0 ± 0.5 40.2 ± 0.4 44.2 ± 0.2
F6 19.3 ± 0.3 33.6 ± 0.8 40.7 ± 0.3 43.1 ± 0.5
F7 18.8 ± 0.8 30.3 ± 0.7 41.8 ± 0.7 46.4 ± 0.4
F8 18.3 ± 0.3 39.1 ± 0.2 44.2 ± 0.2 50.2 ± 0.2
Wash water W9 18.1 ± 0.2 30.3 ± 1.8 38.0 ± 0.7 48.2 ± 0.2
W10 20.1 ± 0.2 36.3 ± 0.3 37.7 ± 0.6 47.2 ± 0.2
W11 20.3 ± 0.6 31.2 ± 0.3 38.3 ± 0.4 44.6 ± 0.5
Sellers H12 20.2 ± 0.3 33.4 ± 0.4 39.4 ± 1.1 45.6 ± 0.5
H13 20.3 ± 0.6 34.8 ± 0.3 38.3 ± 1.2 46.7 ± 0.6
H14 18.0 ± 0.0 36.8 ± 0.1 42.4 ± 0.1 48.1 ± 0.2
H15 18.3 ± 0.4 35.3 ± 0.3 39.4 ± 0.4 47.1 ± 0.3
H16 21.2 ± 0.3 37.1 ± 0.3 34.6 ± 0.6 48.3 ± 0.3
Effect on biofilm gene expression

Figure 6 displays the particular gene expression patterns of four biofilm-forming genes (ALS3, HWP1, RAS1, and SAP4) in two C. albicans resistant isolates with strong biofilm-forming abilities that were subsequent tested with AMB, ZnNPs, probiotic L. salivarius, and ZnNCs. Treatment with ZnNPs significantly decreased the expression of the four biofilm genes compared to non-tested control isolates. However, ZnNCs showed a complete reduction in biofilm gene expression.

The relative mRNA expression levels of C. albicans adhesion (ALS3), filamentation (HWP1), hyphal regulator (RAS1), and hyphal formation and virulence (SAP4), before and after treatment with amphotericin B (AMB), ZnNPs, probiotic L. salivarius and ZnNCs.

 SEM analysis

SEM images of biofilm formation by C. albicans (control) and those treated with ZnNCs ( Figure 7 ). Untreated cells displayed a typical mature biofilm with multiple layers of pseudohyphae, blastoconidia and an extracellular matrix forming a dense and heterogeneous polysaccharide network in which cells, pseudohyphae, and hyphae were embedded. Yeast germ tubes, hyphae, bud scars and pseudohyphae are encased in matrix material. The yeast layer and hyphal conglomerate development embedded in the matrix material are not visible and upper layer mainly the hyphal layer is indicated.

Scanning electron micrographs of biofilm formation by C. albicans. C. albicans (Control): showing mature biofilm with (M): multilayer of extracellular matrix, (Y): Yeast cells, (T): True hyphae, (B): Bud scars, (P): pseudohyphae. Yeast cells, hyphae and bud scars are seen encased, conglomerate and embedded in matrix material (M). Treated C. albicans with ZnNCs: showing (S): small shrinkage blastoconidia and the cell wall presented a rugged surface (A): absence of pseudohyphae, (D): Destruction, swollen and rupture of cell membranes of yeast cells, the outer layer seemed to detach from the cell and masses of cellular debris were seen with release of cell contents., (R): reduction of matrix layer.

Conversely, C. albicans treated with 10 µg/mL ZnNCs exhibited the biofilm structure and prevented the formation of matrix material, resulting in an unusual biofilm architecture consisting of a single layer of loosely arranged yeast cells with noticeable morphological alterations, including small shrinkage of blastoconidia, absence of pseudohyphae, and reduction of the matrix layer.

 Discussion

Candida spp. are commensal yeasts found on the gastrointestinal tract, skin, and other mucosal surfaces in healthy humans. These opportunistic pathogens are generally harmless to healthy individuals but can potentially lead to invasive diseases in immunocompromised individuals (Pappas et al., 2018). C. albicans is typically present in the human microbiota and is commonly associated with organic matter. However, this opportunistic disease is known to increase the prevalence of pathogenicity in immunocompromised persons (Asadzadeh et al., 2022). In our study, Candida spp. were identified in 12.7% of the samples, with 18% originating from tilapia, which aligns with the finding of a previous Egyptian study in which Candida spp. were isolated from tilapia, catfish, and gray mullet (Tartor et al., 2018). Among the identified Candida spp., C. albicans was the prevalent strain, consistent with findings in previous studies (Delgado et al., 2009; Hise et al., 2009; Junqueira et al., 2012; Li et al., 2013; Terças et al., 2017). The high isolation rate of C. albicans can be attributed to its remarkable adaptability, as C. albicans can thrive in vastly different environments characterized by varying nutrient availability, temperature fluctuations, pH levels, osmolarity, and oxygen concentrations (Paramythiotou et al., 2014).

In the current study, at least one of the virulence-associated genes (ALS3, HWP1, RAS1, and SAP4) was identified in all C. albicans isolates. Previous studies in Egypt have reported a higher prevalence of HWP1 and ALS1 genes in C. albicans isolates from patients (Shrief et al., 2019; Hamady and Marei, 2021). Additionally, another study revealed that RAS1 and ALS1 were present in all Candida isolates, while HWP1 and SAP4 were found in half of the isolates (Soliman et al., 2020). In addition, Inci et al. (2013) reported that 53.9% of recognized C. albicans strains had the ALS1 gene and only 5.3% of recognized strains had the HWP1 gene. The variation in the frequency of virulence genes among these studies may be attributed to differences in sample size, source of C. albicans isolates, the host, geographic location, the number of isolates studied, the site from which C. albicans was isolated, sample types, and diagnostic technique used (Vijayalakshmi et al., 2016).

Antifungal susceptibility testing is a crucial tool for determining clinical responses, facilitating the selection of appropriate antifungal agents, predicting treatment outcomes and studying the epidemiology of drug-resistant C. albicans. Monitoring the emergence of resistant isolates is essential for providing valuable information to clinicians for effective therapeutic decisions (Khan et al., 2018). In our current study, AMB is the preferred drug for treating candidiasis in animals, poultry, and humans in Egypt. However, most of the isolates in our study exhibited resistance to NYS, FLZ, and ITR, which consistent with the findings of previous studies (Costa-de-Oliveira and Rodrigues, 2020; Dhasarathan et al., 2021). In contrast, Sonmez and Erbas (2017) reported an increase in resistance (100%) to FLZ, AMB, and FUS, with high susceptibility to ketoconazole. Lyon et al. (2010) observed a significant increase in FLZ susceptibility in 2005 from 87.5% to 97.4% in 2007. Monroy-Pérez et al. (2016) found that all C. albicans isolates were susceptible to NYS, while 94.9% and 97.4% were resistant to FLZ and ketoconazole, respectively. Shrief et al. (2019) noted that resistance to antifungal agents, ITR, FLZ, and CAS, was 8% for each and 9% for AMB. Furthermore, Dos Santos Abrantes et al. (2014) reported that more than 50% of C. albicans isolates from South Africa and Cameroon exhibited resistance to FLZ. On the other hand, an earlier South African investigation revealed 100% susceptibility of C. albicans to FLZ.

Biofilm formation is essential for long-range colonization in host tissues and resistance to external stressors, such as oxidative stress and antifungal factors (Douglas, 2003; Sherry et al., 2017). Once a biofilm forms, candidal cells are encased in an extracellular matrix that confers resistance to fungicides and various sanitizing techniques (Ramage et al., 2009; Sherry et al., 2017). Innovative antibiofilm therapies are urgently needed to address these challenging conditions.

In our study, all C. albicans isolates demonstrated biofilm-forming abilities, consistent with the presence of biofilm-associated genes. Biofilm associated genes such as ALS3, ALS1, and HWP1 within the ALS family are integral to the adhesion and biofilm formation processes of Candida spp. (Khan et al., 2010). These genes encode proteins that are essential for cell wall integrity and play a role in the initiation of hyphal development. ALS3 and HWP1 are cell wall proteins that play roles in intercellular adherence and cell-substrate interactions for proper formation of three-dimensional biofilm architectures (Nobile et al., 2006; Nobile et al., 2008). Previous studies in Egypt have reported that 84.6% of C. albicans isolates are capable of forming biofilms (Ismail et al., 2020a), while 58% of C. albicans isolated from intensive care unit patients with nosocomial infections exhibit biofilm-forming abilities (Shrief et al., 2019). The ability of C. albicans to form biofilms is a major part of most C. albicans infections (Nett and Andes, 2006), necessitating the development of alternative treatment strategies to combat biofilm-associated candidiasis.

Recently, there has been an interest in the use of nanoparticles and probiotics to counteract microbial pathogenicity, particularly related to biofilm formation (Lara et al., 2015; Hosseini et al., 2019; Sitohy et al., 2021). Various studies have shown the broad-spectrum actions of different probiotics, which can inhibit C. albicans proliferation, adhesion, and biofilm formation, making them valuable antimicrobial agents (Matsubara et al., 2016; Osman and El-Gazzar, 2021). L. salivarius exhibits an antifungal effect against Candida spp. through the production of lactic acid and organic acids that positively influence the efficacy of antifungal agents by increasing the permeability of the fungal plasma membrane structure followed by changes in gene expression and the transition to hyphal growth (Krzyściak et al., 2017; Zangl et al., 2019). In addition, L. salivarius showed a decrease in both the number of colonies and the biofilm biomass, as did the cross-linking of the biofilm structure (Zangl et al., 2019). Therefore, the development of safe antimicrobial probiotics with nanoparticle drug delivery capabilities is essential. Where, we investigated the inhibitory roles of ZnNPs, probiotic L. salivarius, and ZnNCs against C. albicans biofilm formation.

Zn-NPs have a long history of use in treating various ailments and have garnered significant interest from the scientific community (Hosseini et al., 2019). These agents have already demonstrated their potency as antiseptic and antimicrobial agents, making them particularly attractive for developing a new class of antimicrobial agents based on nanomaterials (Hosseini et al., 2019).

The DLS data showed a single peak at 45.82 nm for ZnNPs. TEM revealed an even distribution without agglomeration and a variety of shapes of ZnNPs in solution. This information may help explain the diversity of molecules involved in ZnNPs production, as these compounds can act as capping and agglomeration-preventing agents (El-Gazzar et al., 2021). X-ray analysis confirmed the appearance of a distinctive cubic lattice and peaks corresponding to the ZnNPs in a novel probiotic nanocomposite. The nanocomposite of probiotics with ZnNPs was further investigated by EDS surface area analysis, which supported previous findings (Sitohy et al., 2021).

The inhibitory effects of nanoparticles can vary depending on their size and concentration (Sitohy et al., 2021). In the present study, ZnNCs demonstrated significantly higher antifungal activity than ZnNPs, probiotics, or AMB. This finding aligns with Mare et al. (2021), who demonstrated a synergistic interaction when two agents are combined, resulting in an inhibitory effect greater than the sum of their individual effects. Another previous study revealed that the combination of FLZ or voriconazole with silver nanoparticles effectively treated drug-resistant C. albicans. The relationship between nanoparticle concentration and fungicidal action depends on the type of fungus (Li et al., 2018).

Biofilms are microbial colonization of tightly adherent cells to a surface that is embedded in a polymeric extracellular matrix. ZnNCs disrupted the ultrastructure of C. albicans biofilms due to their strong antifungal activity. Prior research has shown that nanoparticles alter fungal cell walls and membranes (Bonilla et al., 2017; Lee and Jun, 2019). In this study, ZnNCs prevented C. albicans from budding and forming germ tubes, similar to findings with silver nanocomposites (Guisbiers et al., 2017).

ZnNPs easily bind to biofilms and improve probiotic penetration, disrupting the lipidome. The antibiofilm activity of ZnNPs included inhibiting blastospores and hyphae and preventing Candida biofilm formation (Lara et al., 2015; Różalska et al., 2018). The inhibitory efficacy of probiotics is attributed to bacteriocins and organic acids. Bacteriocins’ positive charged sediment of amino acids creates pores and electrostatic difference in cell membranes, combined with cell lysis. Organic acids in probiotics reduce pH, creating an acidic environment where pathogenic Candida spp. cannot thrive (Osman and El-Gazzar, 2021).

C. albicans’ virulence depends on the ability of C. albicans to transition from yeast to hyphae, promoting adherence and biofilm formation. Inhibiting this transition can prevent infection (Modrzewska and Kurnatowski, 2015; Saibabu et al., 2020). A gene expression experiment showed that ZnNCs significantly decreased the expression of C. albicans genes, which are implicated in the yeast-to-hypha transition. This downregulation was observed in previous studies, and was associated with delayed or halted infection (Maubon et al., 2014; AJenull et al., 2017). In addition, previous studies have shown that the saturation of adhesion sites and coaggregation of Lactobacillus spp. prevent adherence of C. albicans. Gene expression in C. albicans changes due to the presence of Lactobacillus. The expression of genes responsible for adherence and yeast hyphal formation is reduced. The presence of Lactobacillus can alter the host immune response during Candida colonization to attract granulocytes and promote immune defense (Zangl et al., 2019). Thus, ZnNCs have the potential to target C. albicans’ virulence factors, suggesting that ZnNCs could be a novel therapeutic approach for treating candidiasis.

 Conclusion

This study isolated Candida spp. from Nile tilapia, fish wash water, and human fish sellers in retail markets in Sharika Government, Egypt. C. albicans was the most frequently isolated Candida spp., with all isolates having at least one virulence gene, resistance to one antifungal agent, and moderate to strong biofilm-forming abilities, thus posing a significant risk to food safety and public health. The findings demonstrated that ZnNPs, probiotic L. salivarius, and ZnNCs have potential antifungal and antibiofilm activities against C. albicans. Our results suggested that ZnNCs could be promising, cost-effective antifungal drugs for inhibiting key virulence factors and preventing pathogenesis in C. albicans. In addition, ZnNCs demonstrated significantly higher antifungal activity than ZnNPs, probiotics, or AMB. However, further research is essential to determine the full potential of ZnNCs as robust antifungal and antibiofilm agents for managing critical C. albicans infections.

 Data availability statement

The original contributions presented in the study are included in the article/ Supplementary Material . Further inquiries can be directed to the corresponding authors.

 Ethics statement

The studies involving humans were approved by Institutional Review Board under the number ZU-IRB #11274 -29/11-2023. The studies were conducted in accordance with the local legislation and institutional requirements. Written informed consent for participation in this study was provided by the participants’ legal guardians/next of kin. The animal study was approved by Institutional Animal Care and Use Committee (IACUC) of Zagazig University (Ref. No.: IACUC/2/F/234/2023). The study was conducted in accordance with the local legislation and institutional requirements.

 Author contributions

NE: Conceptualization, Data curation, Investigation, Methodology, Validation, Visualization, Writing – original draft, Writing – review & editing. RA: Conceptualization, Data curation, Investigation, Methodology, Resources, Validation, Writing – original draft, Writing – review & editing. AA: Conceptualization, Investigation, Methodology, Resources, Writing – review & editing. AA: Data curation, Funding acquisition, Resources, Validation, Writing – review & editing. MD: Methodology, Data curation, Investigation, Resources, Software, Validation, Visualization, Writing – review & editing. EY: Funding acquisition, Resources, Validation, Writing – review & editing. RE: Data curation, Investigation, Methodology, Resources, Validation, Visualization, Writing – review & editing. KM: Investigation, Methodology, Resources, Validation, Writing – review & editing. SD: Funding acquisition, Resources, Validation, Writing – review & editing. IE: Data curation, Formal analysis, Software, Validation, Visualization, Writing – original draft, Writing – review & editing.

 Funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. Finical support for article publishing charges (APCs) was provided by the Researchers Supporting Project (RSP2024R36), King Saud University, Riyadh, Saudi Arabia.

 Acknowledgments

This work was supported by the Researchers Supporting Project (RSP2024R36), King Saud University, Riyadh, Saudi Arabia. Also, the authors express gratitude to Zagazig University for its research facilities and support during the work.

 Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

 Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

 Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fcimb.2024.1358270/full#supplementary-material

References Abdel-Shafi S. Al-Mohammadi A. R. Almanaa T. N. Moustafa A. H. Saad T. M. Ghonemey . (2020). Identification and testing of antidermatophytic oxaborole-6-benzene sulphonamide derivative (OXBS) from Streptomyces atrovirens KM192347 isolated from soil. Antibiotics 9, 176. doi: 10.3390/antibiotics9040176 Abou Elez R. M. M. Elsohaby I. Al-Mohammadi A. R. Seliem M. Tahoun A. B. Abousaty A. I. . (2023). Antibacterial and anti-biofilm activities of probiotic Lactobacillus plantarum against Listeria monocytogenes isolated from milk, chicken and pregnant women. Front. Microbiol. 14. doi: 10.3389/fmicb.2023.1201201 Altschul S. F. Gish W. Miller W. Myers E. W. Lipman D. J. (1990). Basic local alignment search tool. J. Mol. Biol. 215, 403–410. doi: 10.1016/S0022-2836(05)80360-2 Amin H. Zali M. H. S. Seyedgholizadeh S. Malekan M. Yahyapour H. (2014). Prevalence of subclinical Candidiasis in broiler flocks Urmia, Iran. Scholars. J. Agric. Vet. Sci. 1, 153–155. doi: 10.36347/sjavs.2014.v01i04.001 Asadzadeh M. Mokaddas E. Ahmad S. Abdullah A. A. De Groot T. Meis J. F. . (2022). Molecular characterisation of Candida auris isolates from immunocompromised patients in a tertiary care hospital in Kuwait reveals a novel mutation in FKS1 conferring reduced susceptibility to echinocandins. Mycoses 65, 331–343. doi: 10.1111/myc.13419 Bautista-Muñoz C. Boldo X. M. Villa-Tanaca L. Hernández-Rodríguez C. (2003). Identification of Candida spp. by randomly amplified polymorphic DNA analysis and differentiation between Candida albicans and Candida dubliniensis by direct PCR methods. J. Clin. Microbiol. 41, 414–420. doi: 10.1128/JCM.41.1.414-420.2003 Berman J. Krysan D. J. (2020). Drug resistance and tolerance in fungi. Nat. Rev. Microbiol. 18, 319–331. doi: 10.1038/s41579-019-0322-2 Bonilla J. J. A. Guerrero D. J. P. Sáez R. G. T. Ishida K. Fonseca B. B. Rozental S. . (2017). Green synthesis of silver nanoparticles using maltose and cysteine and their effect on cell wall envelope shapes and microbial growth of Candida spp. J. Nanosci. Nanotechnol 17, 1729–1739. doi: 10.1166/jnn.2017.12822 Bu Q. R. Bao M. Y. Yang Y. Wang T. M. Wang C. Z. (2022). Targeting virulence factors of Candida albicans with natural products. Foods 11, 2951. doi: 10.3390/foods11192951 Caggiano G. Diella G. Triggiano F. Bartolomeo N. (2020). Occurrence of fungi in the potable water of hospitals: A public health threat. Pathogens 9, 783. doi: 10.3390/pathogens9100783 Cannon R. D. Holmes A. R. Mason A. B. Monk B. C. (1995). Oral Candida: clearance, colonization, or candidiasis? J. Dent. Res. 74, 1152–1161. doi: 10.1177/00220345950740050301 Cavalcanti Filho J. R. N. Silva T. F. Nobre W. Q. Oliveira De Souza L. I. Silva E. Silva Figueiredo C. S. . (2017). Antimicrobial activity of Buchenavia tetraphylla against Candida albicans strains isolated from vaginal secretions. Pharm. Biol. 55, 1521–1527. doi: 10.1080/13880209.2017.1304427 Clinical and Laboratory Standards Institute (CLSI) (2008) Reference method for broth dilution. Ref. method broth dilution antifungal susceptibility testing. Yeasts . Available online at: https://clsi.org/media/1461/m27a3. Costa-de-Oliveira S. Rodrigues A. G. (2020). Candida albicans antifungal resistance and tolerance in bloodstream infections: The triad yeast-host-antifungal. Microorganisms 8, 154. doi: 10.3390/microorganisms8020154 da Costa K. R. Ferreira J. C. Komesu M. C. Candido R. C. (2009). Candida albicans and Candida tropicalis in oral candidosis: quantitative analysis, exoenzyme activity, and antifungal drug sensitivity. Mycopathologia 167, 73–79. doi: 10.1007/s11046-008-9154-8 De Gregorio P. R. Silva J. A. Marchesi A. Nader-Macías M. E. (2019). Anti-Candida activity of beneficial vaginal lactobacilli in in vitro assays and in a murine experimental model. FEMS Yeast Res. 19, foz008. doi: 10.1093/femsyr/foz008 Delgado A. C. De Jesus Pedro R. Aoki F. H. Resende M. R. Trabasso P. Colombo A. L. . (2009). Clinical and microbiological assessment of patients with a long-term diagnosis of human immunodeficiency virus infection and Candida oral colonization. Clin. Microbiol. Infect. 15, 364–371. doi: 10.1111/j.1469-0691.2009.02707.x de Oliveira J. R. Figueira L. W. Sper F. L. Meccatti V. M. Camargo S. E. A. De Oliveira L. D. (2017). Thymus vulgaris L. and thymol assist murine macrophages (RAW 264.7) in the control of in vitro infections by Staphylococcus aureus, Pseudomonas aeruginosa, and Candida albicans . Immunol. Res. 65, 932–943. doi: 10.1007/s12026-017-8933-z Deorukhkar S. C. Roushani S. (2018). Identification of Candida species: conventional methods in the era of molecular diagnosis. Ann. Microbiol. Immunol. 1, 1002. Dhanasekaran D. Vinothini K. Latha S. Thajuddin N. Panneerselvam A. (2014). Human dental biofilm: Screening, characterization, in vitro biofilm formation and antifungal resistance of Candida spp. Saudi J. Dent. Res. 5, 55–70. doi: 10.1016/j.ksujds.2013.10.001 Dhasarathan P. Alsalhi M. S. Devanesan S. Subbiah J. Ranjitsingh A. Binsalah M. . (2021). Drug resistance in Candida albicans isolates and related changes in the structural domain of Mdr1 protein. J. Infect. Public Health 14, 1848–1853. doi: 10.1016/j.jiph.2021.11.002 Donadu M. G. Peralta-Ruiz Y. Usai D. Maggio F. Molina-Hernandez J. B. Rizzo D. . (2021). Colombian essential oil of ruta graveolens against nosocomial antifungal resistant Candida strains. J. fungi (Basel) 7, 383. doi: 10.3390/jof7050383 Dos Santos Abrantes P. M. Mcarthur C. P. Africa C. W. (2014). Multi-drug resistant oral Candida species isolated from HIV-positive patients in South Africa and Cameroon. Diagn. Microbiol. Infect. Dis. 79, 222–227. doi: 10.1016/j.diagmicrobio.2013.09.016 Douglas L. J. (2002). Medical importance of biofilms in Candida infections. Rev. Iberoam Micol 19, 139–143. Douglas L. J. (2003). Candida biofilms and their role in infection. Trends Microbiol. 11, 30–36. doi: 10.1016/S0966-842X(02)00002-1 Dwivedi P. Thompson A. Xie Z. Kashleva H. Ganguly S. Mitchell A. P. . (2011). Role of Bcr1-activated genes, Hwp1 and Hyr1 in Candida albicans oral mucosal biofilms and neutrophil evasion. PloS One 6, e16218. doi: 10.1371/journal.pone.0016218 El-Ashmony M. Rasslan F. Abdelhamid D. Hafez H. Abd El-Rahman O. (2023). Potential anti-fungal activity of Lactobacilli Probiotic against Fluconazole Resistant Candida albicans clinical isolates. Azhar. Inter. J. Pharma. Med. Sci. 3, 120–131. doi: 10.21608/AIJPMS.2022.131769.112 El-Bahr S. M. Elbakery A. M. El-Gazzar N. Amin A. A. Al-Sultan S. Alfattah M. A. . (2021). Biosynthesized Iron Oxide nanoparticles from petroselinum crispum leaf extract mitigate lead-acetate-induced anemia in male albino rats: hematological, biochemical and histopathological teatures. Toxics 9, 123. doi: 10.3390/toxics9060123 El-Gazzar N. Almanaa T. N. Reda R. M. El Gaafary M. N. Rashwan A. A. Mahsoub F. (2021). Assessment the using of silica nanoparticles (SiO2NPs) biosynthesized from rice husks by Trichoderma harzianum MF780864 as water lead adsorbent for immune status of Nile tilapia (Oreochromis niloticus). Saudi J. Biol. Sci. 28, 5119–5130. doi: 10.1016/j.sjbs.2021.05.027 El-Gazzar N. S. Enan G. (2020). Advances in phage inspired nanoscience based therapy. In: Saxena S. Khurana S. (eds) Nano. Bio. Med. (Singapore:Springer) 237–257. doi: 10.1007/978-981-32-9898-9_10 El-Gazzar N. Ismail A. (2020). The potential use of titanium, silver and selenium nanoparticles in controlling leaf blight of tomato caused by Alternaria alternata . Biocatal. Agric. Biotechnol. 27, 101708. doi: 10.1016/j.bcab.2020.101708 Enan G. Al-Mohammadi A. R. Mahgoub S. (2020). Inhibition of Staphylococcus aureus LC554891 by moringa oleifera seed extract either singly or in combination with antibiotics. Molecules (Basel) 25, 4583. doi: 10.3390/molecules25194583 Galocha M. Pais P. Cavalheiro M. Pereira D. Viana R. Teixeira M. C. (2019). Divergent approaches to virulence in C. albicans and C. glabrata: Two sides of the same coin. Int. J. Mol. Sci. 20, 2345. doi: 10.3390/ijms20092345 Gow N. A. Van De Veerdonk F. L. Brown A. J. Netea M. G. (2011). Candida albicans morphogenesis and host defence: discriminating invasion from colonization. Nat. Rev. Microbiol. 10, 112–122. doi: 10.1038/nrmicro2711 Guisbiers G. Lara H. H. Mendoza-Cruz R. Naranjo G. Vincent B. A. Peralta X. G. . (2017). Inhibition of Candida albicans biofilm by pure selenium nanoparticles synthesized by pulsed laser ablation in liquids. Nanomedicine: NBM 13, 1095–1103. doi: 10.1016/j.nano.2016.10.011 Hamady A. Marei Y. (2021). Detection of ALS1 and HWP1 genes involved in biofilm formation in Candida albicans isolated from catheter associated candiduria. Microbes Infect. Dis. 2, 558–566. doi: 10.21608/mid.2021.76052.1153 Hise A. G. Tomalka J. Ganesan S. Patel K. Hall B. A. Brown G. D. . (2009). An essential role for the NLRP3 inflammasome in host defense against the human fungal pathogen Candida albicans . Cell Host Microbe 5, 487–497. doi: 10.1016/j.chom.2009.05.002 Hosseini S. S. Ghaemi E. Noroozi A. Niknejad F. (2019). Zinc Oxide nanoparticles inhibition of initial adhesion and ALS1 and ALS3 Gene expression in Candida albicans strains from urinary tract infections. Mycopathologia 184, 261–271. doi: 10.1007/s11046-019-00327-w Hunter P. R. Gaston M. A. (1988). Numerical index of the discriminatory ability of typing systems: an application of Simpson’s index of diversity. J. Clin. Microbiol. 26, 2465–2466. doi: 10.1128/jcm.26.11.2465-2466.1988 Inci M. Atalay M. A. Özer B. Evirgen Ö. Duran N. Motor V. K. . (2013). Investigations of ALS1 and HWP1 genes in clinical isolates of Candida albicans . Turk. J. Med. Sci. 43, 125–130. doi: 10.3906/sag-1205-90 Ismail M. G. Abd El-Haliem N. F. Aboelmagd E. K. (2020a). Assessment of virulence factors and antifungal susceptibility of Candida species isolated from catheter associated urinary tract infections. Al-Azhar Intern. Med. J. 1, 179–188. doi: 10.21608/aimj.2020.35322.1278 Ismail S. Mohamed G. Amer A. Amer M. (2020b). Comparative killing activity of different nanoparticles and nano-composites based on Dermanyssus gallinae. Nano. Biomed. Eng. 12, 338–350. doi: 10.5101/nbe.v12i4.p338-350 Jenull S. Tscherner M. Gulati M. Nobile C. J. Chauhan N. Kuchler K. (2017). The Candida albicans HIR histone chaperone regulates the yeast-to-hyphae transition by controlling the sensitivity to morphogenesis signals. Sci. Rep. 7, 8308. doi: 10.1038/s41598-017-08239-9 Judan Cruz K. G. Alfonso E. D. Fernando S. I. D. Watanabe K. (2021). Candida albicans biofilm inhibition by ethnobotanicals and ethnobotanically-synthesized gold nanoparticles. Front. Microbiol. 12. doi: 10.3389/fmicb.2021.665113 Junqueira J. C. Vilela S. F. Rossoni R. D. Barbosa J. O. Costa A. C. Rasteiro V. M. . (2012). Oral colonization by yeasts in HIV-positive patients in Brazil. Rev. Inst. Med. Trop. Sao Paulo 54, 17–24. doi: 10.1590/S0036-46652012000100004 Kadosh D. Lopez-Ribot J. L. (2013). Candida albicans: adapting to succeed. Cell Host Microbe 14, 483–485. doi: 10.1016/j.chom.2013.10.016 Khan M. S. A. Ahmad I. Aqil F. Owais M. Shahid M. Musarrat J. (2010). Virulence and pathogenicity of fungal pathogens with special reference to Candida albicans . Combating Fungal Infections: Problems Remedy Springer Berlin Heidelberg, 21–45. doi: 10.1007/978-3-642-12173-9_2 Khan M. Ahmed J. Gul A. Ikram A. Lalani F. K. (2018). Antifungal susceptibility testing of vulvovaginal Candida species among women attending antenatal clinic in tertiary care hospitals of Peshawar. Infect. Drug Resist. 11, 447–456. doi: 10.2147/IDR.S153116 Koh A. Y. Köhler J. R. Coggshall K. T. Van Rooijen N. Pier G. B. (2008). Mucosal damage and neutropenia are required for Candida albicans dissemination. PloS Pathog. 4, e35. doi: 10.1371/journal.ppat.0040035 Krzyściak W. Dorota K. Monika P. Palina V. Katarzyna Z. Iwona K. . (2017). Effect of a Lactobacillus salivarius probiotic on a double-species Streptococcus mutans and Candida albicans caries biofilm. Nutrients 9, 1242. doi: 10.3390/nu9111242 Lara H. H. Romero-Urbina D. G. Pierce C. Lopez-Ribot J. L. Arellano-Jiménez M. J. Jose-Yacaman M. (2015). Effect of silver nanoparticles on Candida albicans biofilms: an ultrastructural study. J. Nanobiotechnology 13, 91. doi: 10.1186/s12951-015-0147-8 Lee S. H. Jun B. H. (2019). Silver nanoparticles: synthesis and application for nanomedicine. Int. J. Mol. Sci. 20, 865. doi: 10.3390/ijms20040865 Li Y. Y. Chen W. Y. Li X. Li H. B. Li H. Q. Wang L. . (2013). Asymptomatic oral yeast carriage and antifungal susceptibility profile of HIV-infected patients in Kunming, Yunnan Province of China. BMC Infect. Dis. 13, 46. doi: 10.1186/1471-2334-13-46 Li H. Wang L. Chai Y. Cao Y. Lu F. (2018). Synergistic effect between silver nanoparticles and antifungal agents on Candida albicans revealed by dynamic surface-enhanced Raman spectroscopy. Nanotoxicology 12, 1230–1240. doi: 10.1080/17435390.2018.1540729 Lohse M. B. Gulati M. Johnson A. D. Nobile C. J. (2018). Development and regulation of single- and multi-species Candida albicans biofilms. Nat. Rev. Microbiol. 16, 19–31. doi: 10.1038/nrmicro.2017.107 Lyon G. M. Karatela S. Sunay S. Adiri Y. (2010). Antifungal susceptibility testing of Candida isolates from the Candida surveillance study. J. Clin. Microbiol. 48, 1270–1275. doi: 10.1128/JCM.02363-09 Mare A. D. Ciurea C. N. Man A. Mareş M. Toma F. Berţa L. . (2021). In vitro antifungal activity of silver nanoparticles biosynthesized with beech bark extract. Plants 10, 2153. doi: 10.3390/plants10102153 Matsubara V. H. Wang Y. Bandara H. Mayer M. P. A. Samaranayake L. P. (2016). Probiotic lactobacilli inhibit early stages of Candida albicans biofilm development by reducing their growth, cell adhesion, and filamentation. Appl. Microbiol. Biotechnol. 100, 6415–6426. doi: 10.1007/s00253-016-7527-3 Maubon D. Garnaud C. Calandra T. Sanglard D. Cornet M. (2014). Resistance of Candida spp. to antifungal drugs in the ICU: where are we now? Intensive Care Med. 40, 1241–1255. doi: 10.1007/s00134-014-3404-7 Mayer F. L. Wilson D. Hube B. (2013). Candida albicans pathogenicity mechanisms. Virulence 4, 119–128. doi: 10.4161/viru.22913 Mhlongo N. T. Tekere M. Sibanda T. (2019). Prevalence and public health implications of mycotoxigenic fungi in treated drinking water systems. J. Water Health 17, 517–531. doi: 10.2166/wh.2019.122 Modrzewska B. Kurnatowski P. (2015). Adherence of Candida spp. to host tissues and cells as one of its pathogenicity features. Ann. Parasitol. 61, 3–9. Monroy-Pérez E. Paniagua-Contreras G. L. Rodríguez-Purata P. Vaca-Paniagua F. Vázquez-Villaseñor M. Díaz-Velásquez C. . (2016). High virulence and antifungal sesistance in clinical strains of Candida albicans . Can. J. Infect. Dis. Med. Microbiol. 2016, 5930489. doi: 10.1155/2016/5930489 Montagna M. T. Caggiano G. Lovero G. De Giglio O. Coretti C. Cuna T. . (2013). Epidemiology of invasive fungal infections in the intensive care unit: results of a multicenter Italian survey (AURORA Project). Infection 41, 645–653. doi: 10.1007/s15010-013-0432-0 Montagna M. T. Giglio O. Napoli C. Lovero G. Caggiano G. Delia M. . (2012). Invasive fungal infections in patients with hematologic Malignancies (aurora project): lights and shadows during 18-months surveillance. Int. J. Mol. Sci. 13, 774–787. doi: 10.3390/ijms13010774 Nadeem S. G. Hakim S. T. Kazmi S. U. (2010). Use of CHROMagar Candida for the presumptive identification of Candida species directly from clinical specimens in resource-limited settings. Libyan J. Med. 5, 1–6. doi: 10.3402/ljm.v5i0.2144 Nett J. Andes D. (2006). Candida albicans biofilm development, modeling a host-pathogen interaction. Curr. Opin. Microbiol. 9, 340–345. doi: 10.1016/j.mib.2006.06.007 Nobile C. J. Nett J. E. Andes D. R. Mitchell A. P. (2006). Function of Candida albicans adhesion HWP1 in biofilms formation. Eukaryot. Cell 5, 1604–1610. doi: 10.1128/EC.00194-06 Nobile C. J. Schneider H. A. Nett J. E. Sheppard D. C. Filler S. G. Andes D. R. . (2008). Complementary adhesion function in C. albicans biofilm formation. Curr. Biol. 18, 1017–1024. doi: 10.1016/j.cub.2008.06.034 Osman A. El-Gazzar N. (2021). Lipolytic postbiotic from Lactobacillus paracasei manages metabolic syndrome in Albino Wistar Rats. Molecules (Basel) 26, 472. doi: 10.3390/molecules26020472 Papon N. Courdavault V. Clastre M. Bennett R. J. (2013). Emerging and emerged pathogenic Candida species: beyond the Candida albicans paradigm. PloS Pathog. 9, e1003550. doi: 10.1371/journal.ppat.1003550 Pappas P. G. Lionakis M. S. Arendrup M. C. Ostrosky-Zeichner L. Kullberg B. J. (2018). Invasive candidiasis. Nat. Rev. Dis. Primers 4, 1–20. doi: 10.1038/nrdp.2018.26 Paramythiotou E. Frantzeskaki F. Flevari A. Armaganidis A. Dimopoulos G. (2014). Invasive fungal infections in the ICU: how to approach, how to treat. Molecules 19, 1085–1119. doi: 10.3390/molecules19011085 Pfaller M. A. Castanheira M. Messer S. A. Moet G. J. Jones R. N. (2010). Variation in Candida spp. distribution and antifungal resistance rates among bloodstream infection isolates by patient age: report from the SENTRY Antimicrobial Surveillance Program, (2008-2009). Diagn. Microbiol. Infect. Dis. 68, 278–283. doi: 10.1016/j.diagmicrobio.2010.06.015 Pierce C. G. Uppuluri P. Tristan A. R. Wormley F. L. Mowat E. Ramage G. . (2008). A simple and reproducible 96-well plate-based method for the formation of fungal biofilms and its application to antifungal susceptibility testing. Nat. Protoc. 3, 1494–1500. doi: 10.1038/nprot.2008.141 Ramage G. Mowat E. Jones B. Williams C. Lopez-Ribot J. (2009). Our current understanding of fungal biofilms. Crit. Rev. Microbiol. 35, 340–355. doi: 10.3109/10408410903241436 Ramage G. Saville S. P. Wickes B. L. López-Ribot J. L. (2002). Inhibition of Candida albicans biofilm formation by farnesol, a quorum-sensing molecule. Appl. Environ. Microbiol. 68, 5459–5463. doi: 10.1128/AEM.68.11.5459-5463.2002 Różalska B. Sadowska B. Budzyńska A. Bernat P. Różalska S. (2018). Biogenic nanosilver synthesized in Metarhizium robertsii waste mycelium extract - As a modulator of Candida albicans morphogenesis, membrane lipidome and biofilm. PloS One 13, e0194254. doi: 10.1371/journal.pone.0194254 Romaní A. M. Fischer H. Mille-Lindblom C. Tranvik L. J. (2006). Interactions of bacteria and fungi on decomposing litter: differential extracellular enzyme activities. Ecology 87, 2559–2569. doi: 10.1890/0012-9658(2006)87[2559:IOBAFO]2.0.CO;2 Saibabu V. Fatima Z. Ahmad K. Khan L. A. Hameed S. (2020). Octyl gallate triggers dysfunctional mitochondria leading to ROS driven membrane damage and metabolic inflexibility along with attenuated virulence in Candida albicans . Med. Mycol. 58, 380–392. doi: 10.1093/mmy/myz054 Salvatori O. Puri S. Tati S. Edgerton M. (2016). Innate immunity and saliva in Candida albicans-mediated oral diseases. J. Dent. Res. 95, 365–371. doi: 10.1177/0022034515625222 Sanglard D. (2016). Emerging threats in antifungal-resistant fungal pathogens. Front. Med. (Lausanne) 3. doi: 10.3389/fmed.2016.00011 Sardi J. C. O. Gullo F. P. Pitangui N. S. Fusco-Almeida A. M. Mendes-Giannini M. J. S. (2013). In vitro antifungal susceptibility of Candida albicans isolates from patients with chronic periodontitis and diabetes. Clin. Microbial. 2, 103. doi: 10.4172/2327-5073.1000103 Schild L. Heyken A. De Groot P. W. Hiller E. Mock M. De Koster C. . (2011). Proteolytic cleavage of covalently linked cell wall proteins by Candida albicans Sap9 and Sap10. Eukaryot. Cell 10, 98–109. doi: 10.1128/EC.00210-10 Seneviratne C. J. Wang Y. Jin L. Abiko Y. Samaranayake L. P. (2008). Candida albicans biofilm formation is associated with increased anti-oxidative capacities. Proteomics 8, 2936–2947. doi: 10.1002/pmic.200701097 Sherry L. Ramage G. Kean R. Borman A. Johnson E. M. Richardson M. D. . (2017). Biofilm-forming capability of highly virulent, multidrug-resistant Candida auris . Emerg. Infect. Dis. 23, 328–331. doi: 10.3201/eid2302.161320 Shrief R. Zaki M. E. S. El-Sehsah E. M. Ghaleb S. Mofreh M. (2019). Study of antifungal susceptibility, virulence genes and biofilm formation in. Open Microbiol. J. 13, 241-248. doi: 10.2174/1874285801913010241 Sikora M. Dabkowska M. Swoboda-Kopec E. Jarzynka S. Netsvyetayeva I. Jaworska-Zaremba M. . (2011). Differences in proteolytic activity and gene profiles of fungal strains isolated from the total parenteral nutrition patients. Folia. Microbiol. (Praha) 56, 143–148. doi: 10.1007/s12223-011-0023-3 Silva S. Henriques M. Martins A. Oliveira R. Williams D. Azeredo J. (2009). Biofilms of non-Candida albicans Candida species: quantification, structure and matrix composition. Med. Mycol. 47, 681–689. doi: 10.3109/13693780802549594 Sitohy M. Al-Mohammadi A. R. Osman A. (2021). Silver-protein nanocomposites as antimicrobial agents. Nanomaterials (Basel) 11, 3006. doi: 10.3390/nano11113006 Soliman M. Kandil M. M. Sa E. Abuelnaga A. (2020). Prevalence of virulence genes and antifungal resistance in Candida albicans isolated from raw goat milk. World’s Vet. J. 10, 670–677. doi: 10.54203/scil.2020.wvj81 Sonmez M. Erbas G. (2017). Isolation and identification of Candida spp. from mastitis cattle milk and determination of antifungal susceptibilities. Int. J. Vet. Sci. 6, 104–107. Spellberg B. (2008). Novel insights into disseminated candidiasis: pathogenesis research and clinical experience converge. PloS Pathog. 4, e38. doi: 10.1371/journal.ppat.0040038 Tamura K. Stecher G. Peterson D. Filipski A. Kumar S. (2013). MEGA6: Molecular evolutionary genetics analysis version 6.0. Mol. Biol. Evol. 30, 2725–2729. doi: 10.1093/molbev/mst197 Tarini N. Wahid M. Ibrahim F. Yasmon A. Djauzi S. (2010). Development of multiplex-PCR assay for rapid detection of Candida spp. Med. J. Indones 19, 83–87. doi: 10.13181/mji.v19i2.387 Tartor Y. Taha M. Mahboub H. El Ghamery M. (2018). Yeast species associated with diseased fish: Occurrence, identification, experimental challenges and antifungal susceptibility testing. Aquaculture 488, 134–144. doi: 10.1016/j.aquaculture.2018.01.033 Terças A. L. Marques S. G. Moffa E. B. Alves M. B. De Azevedo C. M. Siqueira W. L. . (2017). Antifungal drug susceptibility of Candida species isolated from HIV-positive patients recruited at a public hospital in São Luís, Maranhão, Brazil. Front. Microbiol. 8. doi: 10.3389/fmicb.2017.00298 Tsang P. W. Bandara H. M. Fong W. P. (2012). Purpurin suppresses Candida albicans biofilm formation and hyphal development. PloS One 7, e50866. doi: 10.1371/journal.pone.0050866 Tsui C. Kong E. F. Jabra-Rizk M. A. (2016). Pathogenesis of Candida albicans biofilm. Pathog. Dis. 74, ftw018. doi: 10.1093/femspd/ftw018 Vazquez-Munoz R. Dongari-Bagtzoglou A. (2021). Anticandidal activities by Lactobacillus species: an update on mechanisms of action. Front. Oral. Health 16. doi: 10.3389/froh.2021.689382 Vijayalakshmi P. Thenmozhi S. Rajeswari P. (2016). The Evaluation of the virulence factors of clinical Candida isolates and the anti-biofilm activity of Elettaria cardamomum against multi-drug resistant Candida albicans . Curr. Med. Mycol. 2, 8–15. doi: 10.18869/acadpub.cmm.2.2.3 Yuan J. S. Reed A. Chen F. Stewart C. N. (2006). Statistical analysis of real-time PCR data. BMC Bioinform. 7, 85. doi: 10.1186/1471-2105-7-85 Zangl I. Pap I. J. Aspöck C. Schüller C. (2019). The role of Lactobacillus species in the control of Candida via biotrophic interactions. Microb. Cell 7, 1–14. doi: 10.15698/mic2020.01.702