When thinking about Aeromonas, the first thing that comes to our minds might be “water” or “fish.” Indeed, bacteria from this genus naturally inhabit aquatic environments and are known as a threat for aquaculture systems (Barger et al., 2021). The hazardousness of Aeromonads for several fish species as well as other waterborne animals has been strongly discussed (Beaz-Hidalgo and Figueras, 2013; Dallaire-Dufresne et al., 2014; Fernández-Bravo and Figueras, 2020). However, the potential of these microorganisms to cause human health disorders must be highlighted.

Worldwide distributed, Aeromonas were already isolated from a broad range of sources like fresh water, sewage, soil, fruits, vegetables, and processed food (McMahon and Wilson, 2001; Gonçalves Pessoa et al., 2019; Barger et al., 2021). Thus, contact between these bacteria and human beings can be easily established. Aeromonads are considered emergent pathogens and its detection in various diarrheal stool samples clearly shows they are not as far from clinical routine as other enteric microorganisms (Li et al., 2015; Mohan et al., 2017; Mbuthia et al., 2018). Consequently, interest about the genus Aeromonas, which embraces 36 recognized species, has risen over the past years (Fernández-Bravo and Figueras, 2020; Ahmed et al., 2021; Conte et al., 2021).

Several case reports involving Aeromonads infections brought up the diversity of clinical manifestations that these bacteria can provoke to human health. Symptoms range from acute self-limiting diarrhea to lethal sepsis; however, wounds, skin, bones, heart, lungs, eyes, and other organs can be potentially affected (Parker and Shaw, 2011; Ahmed et al., 2021; Meng et al., 2021). Most reports classify Aeromonas’s human infections as events caused by “rare” or “uncommon” microorganisms (Lai et al., 2007; Khalil et al., 2013; Hasan et al., 2018; Salehi et al., 2019). Indeed, other bacterial genus causing the same clinical symptoms are more frequent at hospital level. For example, Campylobacter spp., Salmonella spp., Shigella spp., and Escherichia coli are listed as the main pathogens in clinical cases of acute gastroenteritis (Fleckenstein et al., 2021). Moreover, Staphylococcus aureus and Streptococcus pyogenes are frequently detected in skin and wound infections reports (Cefalu et al., 2017; Clebak and Malone, 2018).

Noteworthy, one of the peculiar characteristics of the Aeromonas genus is the unreliable phenotypical identification by conventional biochemical tests or commercial systems, like Vitek, API20, and Microscan, which are commonly used in the quotidian of most hospital laboratories (Lamy et al., 2010; Jin et al., 2011; Gonçalves Pessoa et al., 2019; Meng et al., 2021). It is known that Aeromonas strains show similarities to other bacterial genera, and accurate data still lies on molecular biology techniques aiming amplification of housekeeping genes for phylogenetic differentiation (Yáñez et al., 2003; Beaz-Hidalgo and Figueras, 2013; Hoel et al., 2017).

The Aeromonas possess wide spectra of antibiotic resistance profile and occurrence of multi-resistant strains have already been reported (Galler et al., 2018; Conte et al., 2021). As inhabitants of aquatic environments, these microorganisms can be used as ecological indicators of water pollution since they harbor antibiotic resistance genes obtained from wastewater effluents (Baron et al., 2017; Grilo et al., 2020). Furthermore, the global indiscriminate use of antimicrobials has changed the perspective of medicine regarding bacterial infections for the next years. The incidence of multidrug-resistant microorganisms has increased and it is expected to be the main public health problem in the future (Dimopoulos et al., 2016). Aeromonads are prone to be susceptible to fluoroquinolones but usually resistant to ampicillin and other beta-lactams (Parker and Shaw, 2011; Fernández-Bravo and Figueras, 2020). In a clinical scenario, however, the execution of an antibiogram test must not be dispensed so as to ensure suitable antibiotic prescriptions (Abbott et al., 2003).

In this review, information about the main clinical features of Aeromonas infections will be provided to highlight how dangerous these bacteria can be for human beings. The knowledge about epidemiology, differential diagnosis, and strategies for antibiotic therapy are also explored.

Aeromonas species generally associated with human infections include A. caviae, A. schubertii, A. hydrophila, A. veronii (biovars veronii and sobria), and A. jandaei (Lamy et al., 2010). These microorganisms have been isolated in hospitals worldwide, and different types of clinical samples, especially fecal, have been used for this investigation. Moreover, the frequency of the species may differ according to the region where they were isolated.

A study performed with diarrheal stool from 1,595 patients identified Aeromonas in 50 samples in India; the biochemical speciation was made on 35 strains showing that the most common species were A. caviae (34%), A. veronii biovar veronii (29%), A. veronii biovar sobria (26%), and A. hydrophila (9%; Mohan et al., 2017). In Kenya, 188 fecal samples were studied to determine the etiological agents of diarrhea, of which only five were caused by A. hydrophila and three by A. caviae (Mbuthia et al., 2018). In 16 hospitals in the city of Shanghai, China, 4,529 specimens from diarrheal patients were collected, in which 193 cases were related to Aeromonas infection: A. veronii (42.5%), A. caviae (25.3%), A. aquariorum (14.5%), A. hydrophila (5.7%), A. enteropelogenes (4.7%), A. media (3.1%), unknown (1.6%), A. salmonicide (2.1%), and A. allosaccharophila (0.5%; Li et al., 2015). While a study at a hospital in Beijing city, China, 1,286 stool samples were analyzed from people with acute diarrhea, and 17 strains of Aeromonas causing extra-intestinal infections were identified in blood or bile. The distribution of Aeromonas species in these isolates obtained from intestinal and extra-intestinal samples followed A. veronii (31.3%), A. caviae (41.7%), A. dhakensis (13.9%), A. media (1.7%), A. hydrophila (5.2%), A. sanarellii (1.7%), A. enteropelogenes (1.7%), A. bivalvium (0.9%), and unknown (1.7%; Zhou et al., 2019).

During the period from January 2015 to December 2017 at Hospital Galdakao-Usansolo, Spain, 98 patients (having a median age of 62 years, and 51% of the cases were women) with positive stool cultures for Aeromonas were counted, being 85 cases of A. caviae, 12 of A. veronii, and 1 of A. hydrophila; estimating an occurrence of 32 cases for every 10⁵ inhabitants per year (Elorza et al., 2020).

Different biological samples, such as stool, eye, sputum, and blood, were tested in microbiological laboratories in Australia for Aeromonas search. From 100 isolates, 39 were A. dhakensis, 21 A. veronii, 20 A. hydrophila, 14 A. caviae, 4 A. jandaei, 1 A. bestiarum, and 1 A. sanarellii (Sinclair et al., 2016). A study of 109 Aeromonas clinical isolates from diarrhea patients was conducted in Mexico and Spain, and the most common species in both countries were A. caviae, A. hydrophila, and A. veronii (Aguilera-Arreola et al., 2007). A retrospective analysis from January 2006 to December 2012, carried out at the Hospital del Mar in Barcelona, Spain, detected 221 clinical samples positive for Aeromonas spp. in 204 patients. Gastroenteritis was the most common form of infection, comprising of 78.4% from patients. It was found that age above 80 years, admission to the intensive care unit, and malignancy were associated with increased mortality rate during the 1-year follow-up of infected patients (Nolla-Salas et al., 2017).

Regarding extra-intestinal infections caused by Aeromonas, there are varieties of sites that can be affected. A range of non-gastrointestinal infections can involve Aeromonas species, some have been associated with contaminated water, for example, soft tissue infection due to injury to an aquatic environment (Lujan-Hernandez et al., 2020), and wound infection after medical leech therapy that may have occurred due to contamination of the water where the leeches were bred (Masters et al., 2020).

Aeromonas wound or pus isolates were collected from a medical center in southern Taiwan, and 76 species were reported, A. dhakensis (37), A. veronii (14), A. hydrophila (13), A. caviae (11), and A. media (1; Chen et al., 2014b). Another study was conducted at this same medical center, in which among 514 stools from adults with diarrhea, 13 had Aeromonas detected, and of the 167 asymptomatic persons, only six were isolated. The most common species in these isolates were A. veronii, A. caviae, A. sanarelli, and A. dhakensis (Chen et al., 2014b). These data show that, although Aeromonas infections may occur in the same region, the difference in anatomical sites may reflect a distinct distribution among their isolate species.

Bacteria belonging to the Aeromonas genus are known as the main pathogens of fish and other marine animals, being responsible for deleterious outbreaks in aquaculture systems due to their wide distribution in various aquatic environments (Beaz-Hidalgo and Figueras, 2013; Liu, 2015; Figueras and Ashbolt, 2019). Moreover, they were already detected in bugs, reptiles, amphibians, birds, and other vertebrates (Percival and Williams, 2014; Praveen et al., 2016; Gonçalves Pessoa et al., 2019). Despite being firstly reported in 1891, the Aeromonas were only recognized as potential human pathogens about 60 years later, in 1954, when these microorganisms were detected in clinical samples obtained from an immunosuppressed woman who died due to a fulminant metastatic myositis (Parker and Shaw, 2011; Liu, 2015; Fernández-Bravo and Figueras, 2020). Currently, it is known that these bacteria can cause predominantly gastrointestinal tract disorders as well as infections in wounds, soft tissues, muscles, lungs, bones, and septicemia, to name a few (Parker and Shaw, 2011; Bhowmick and Bhattacharjee, 2018; Fernández-Bravo and Figueras, 2020). The main illnesses provoked by Aeromonads are shown in Figure 1.

Aeromonas species are classified into two main groups: (i) psychrophilic, usually non-motile strains which grow well between 22°C and 28°C, and (ii) mesophilic, motile with desirable growth temperature into 35°C–37°C or higher (Parker and Shaw, 2011; Percival and Williams, 2014; Liu, 2015; Fernández-Bravo and Figueras, 2020). The psychrophilic group is represented by the Aeromonas salmonicida, which is described as an important cold-water fish pathogen (Fernández-Bravo and Figueras, 2020; Pérez-García et al., 2021). However, this bacterium has already been detected from blood samples of an infected 20-year-old man diagnosed with endocarditis (Salehi et al., 2019). On the other hand, the mesophilic group is often related to both fish and human infections and is mainly represented by A. hydrophila, A. caviae, and A. veronii, but it embraces the other Aeromonas’s species excepting the psychrophilic A. salmonicida (Percival and Williams, 2014; Pérez-García et al., 2021).

Broadly described as opportunistic bacteria, pathological processes generated by these microorganisms are frequently reported in immunosuppressed patients. However, even healthy persons, from any age, can be potential hosts to illnesses caused by Aeromonas (Chuang et al., 2011; Silva et al., 2017). The wide range of diseases generated by Aeromonads is characterized as a joint action of several virulence factors, such as lipases, proteases, hemolysins, aerolysins, cytotoxins, and enterotoxins, that contribute both to its survival and environmental adaptation as well as to the multifactorial and complexity of its pathogenesis, whose mechanisms and processes are usually not evident (Pemberton et al., 1997; Zhou et al., 2013; Rasmussen-Ivey et al., 2016; Hoel et al., 2017).

Aforementioned, Aeromonas are natural habitants from aquatic environments and could be detected in samples obtained from different sources (Praveen et al., 2016; Harnisz and Korzeniewska, 2018). Furthermore, these bacteria can resist potable water treatment processes for human consumption, representing a potential contamination route (Janda and Abbott, 2010). Phylogenetic studies previously performed suggest feasible relations between Aeromonas strains isolated from both municipal water and clinical samples within the same geographic region (Pablos et al., 2009, 2011). The intake of contaminated food like animal-derived proteins (meat, chicken, and, mainly, fisheries), vegetables, and, additionally, the preparation methods of some culinary recipes are reported as the main cause for Aeromonads infections (Castro-Escarpulli et al., 2003; Pablos et al., 2009; Hoel et al., 2017). Environmental factors can influence outbreaks caused by these microorganisms. Studies have shown that temperatures over 22°C might provoke loss of virulence factors in A. salmonicida strains (Fernández-Bravo and Figueras, 2020). On the other hand, it has been reported that different temperatures modulate the expression of virulence genes in distinct isolates of A. hydrophila; most of the assessed genes were expressed by culturing the strains at 28°C (Pattanayak et al., 2020). Moreover, it was demonstrated that an A. hydrophila strain endured under low temperatures and starvation by shaping its virulence factors content (Bruscolini et al., 2014). Other Aeromonas species related to human health disorders grow well in higher temperatures and, consequently, lead to an increase in the number of infections under warm seasons due to the high bacterial cell count in the environment, especially in water (Bhowmick and Bhattacharjee, 2018).

Herein, based on case reports, the main clinical manifestations developed during infectious processes generated by Aeromonas will be discussed; reinforcing its relevance in public health and the importance of researches involving this bacterial genus in the field of medical microbiology.

Although Aeromonas species can cause extraintestinal infections, such as skin and soft-tissue infections, one of the main consequences of Aeromonas infection is gastroenteritis, as observed according to the epidemiological data presented. Microbiology laboratories do not usually investigate Aeromonas spp. in diarrheal stools. The most commonly searched bacteria are Salmonella, Shigella, Campylobacter, and Escherichia coli (Schuetz, 2019).

Gastroenteritis may be caused by viral, bacterial, and parasitic pathogens whose clinical symptoms may be similar, so analysis with the patients’ stool becomes indispensable to promote differential diagnosis. Aeromonas spp. can grow in routine culture media commonly used in clinical laboratories, such as sheep blood agar (SBA) and chocolate agar. In addition, these microorganisms also grow in specific culture media for the isolation of enteropathogenic bacteria, for example, hektoen enteric agar, xylose deoxycholate agar (XLD) agar, and MacConkey agar (Carr, 2016). Moreover, Aeromonas recovery has been facilitated using enrichment broths, for example, alkaline peptone water under overnight incubation and subcultured onto blood ampicillin and cefsulodin irgasan novobiocin (CIN) agars (Igbinosa et al., 2012).

In addition to growth in culture medium, it is important to perform other phenotypic tests, such as different biochemical tests, for more accurate identification. For example, the fact that most Aeromonas organisms have a positive oxidase reaction, resistance to the vibriostatic compound O/129, absence of ornithine decarboxylase activity, and no growth in 6% NaCl allows their differentiation with the genera Vibrio and Plesiomonas (Batra et al., 2016). Aeromonas can grow on selective and differential enteric agars; however, the carbohydrate contained in these agars can influence the growth of these microorganisms and is therefore not ideal for primary isolation in fecal samples of Aeromonas. For example, the ability to ferment carbohydrates can depend on the species, carbohydrates, such as xylose and lactose, can inhibit the growth of some Aeromonas, and a false-negative oxidase reaction can occur due to an acidification process in the medium (Oliveira et al., 2020).

However, the laboratory screening using phenotypic tests can still generate doubts about the correct diagnosis of the bacteria causing the infection; for example, the distinction between V. cholera and Aeromonas spp. in stool samples from patients with diarrheal episodes can only be achieved with genome sequencing analysis (Van Zwetselaar et al., 2018). The molecular identification of Aeromonas species can be performed through 16S rRNA gene analysis, housekeeping genes, genotyping techniques, the latter includes different methods, such as multilocus sequence typing (MLST) and enterobacterial repetitive intergenic consensus-PCR (ERIC-PCR; Fernández-Bravo and Figueras, 2020). Aeromonas specification is not commonly performed clinically, although its species can be identified quickly, for example by employing matrix-assisted laser desorption–ionization time-of-flight mass spectrometry (MALDI-TOF; Benagli et al., 2012; Akyar and Can, 2013; Chen et al., 2014a).

Prescribing antibiotics in clinical practice was undoubtedly a revolutionary milestone in medicine regarding therapy against bacterial infections (Baron et al., 2017). The antibiotics era, which began around 1930 until the current days, has saved countless lives throughout the story. However, it brought one of the major and unavoidable public health problems of the modern world: the generation of multi-resistant bacteria (Dimopoulos et al., 2016; Baron et al., 2017; Dodds, 2017; Sánchez and Demain, 2017). The uncontrolled usage and irregular disposal of antibiotics, among other chemical compounds, that is, several drugs and personal use products, promote a propitious environment for the development of hard-to-treat microorganisms that become a threat to human health by sharing and acquiring resistance mechanisms which they naturally might not have (Chaturvedi et al., 2021). Although there has been great concern in recent years about environmental contamination by chemical and antimicrobial compounds, with a consequent increase in resistant microorganisms (Figueira et al., 2011), the history of humanity’s relationship with antibiotics has established a cycle of dependence that—apparently—will no sooner end. These medicines are still our front line in the fight against bacterial infections, and their consumption is estimated to globally increase approximately 200% by 2030 (Klein et al., 2018; Zheng et al., 2021).

Wastewater effluents derived from hospitals, veterinary clinics, industries, and aquaculture farms make aquatic environments great spreaders of multi-resistant pathogens (Baquero et al., 2008; Baron et al., 2017). Thus, Aeromonas, as natural inhabitants of these ecosystems, have a wide antibiotic resistance profile and are constantly isolated from several species of fish and other animals (Beaz-Hidalgo and Figueras, 2013). Aeromonads acquire and share antibiotic resistance genes by transmitting mobile elements like plasmids, integrons, insertion sequences, and transposons (Piotrowska and Popowska, 2015; Stratev and Odeyemi, 2016). These genetic compounds are known as the “mobilome” and are permanently subjected to evolution according to changes in the environment (Piotrowska and Popowska, 2015).

It has been described the production of 4 main groups of beta-lactamases, divided from Class A to Class D, which confer to the Aeromonas a potential defense against the action of beta-lactam drugs (Stratev and Odeyemi, 2016; Fernández-Bravo and Figueras, 2020). The antimicrobial resistance of 24 strains of Aeromonas isolated from Nile tilapia and domestic fowl was evaluated. The strains showed to be invulnerable to the beta-lactams amoxicillin and ampicillin/sulbactam, as well as to streptomycin, from aminoglycoside’s class (Abu-Elala et al., 2015). Aeromonads isolates from cow fecal samples from different farms also showed complete resistance to a large group of beta-lactam antibiotics and susceptibility to cephamycin, tetracycline, ciprofloxacin, and gentamicin (Igbinosa et al., 2015). In addition, sensitivity to cefepime was also observed in strains obtained from commercialized/farmed shellfish as well as aquatic environment samples (Chen et al., 2021). Aeromonads from cultured freshwater fishes showed main resistance to ampicillin and amoxicillin and absolute sensitivity to levofloxacin (Azzam-Sayuti et al., 2021). Besides beta-lactams, resistance against colistin can also be chromosomally mediated or transferred by the mobilome. This antibiotic can disrupt the membrane of gram-negative bacteria by interacting with surface LPS and is used as last resort for infections cause by multi-drug resistant microorganisms (MDR). Reports showed the existence of colistin-resistant Aeromonads, especially among the isolates obtained from clinical samples (Gonzalez-Avila et al., 2021).

Aeromonas are also capable of colonizing water treatment plants and, consequently, contaminate both the content intended for human consumption and the environment in which effluents are disposed (Figueira et al., 2011). Strains obtained from a domestic and hospital treatment system have been shown to resist three or more classes of antibiotics, including tigecycline, another drug used as a last line in cases involving MDR (Harnisz and Korzeniewska, 2018). The hazardousness of the dissemination of these microorganisms in the environment, arising from the addition of hospital waste to domestic effluents in municipal water treatment systems, has already been reported (Varela et al., 2016).

Although the wide antibiotic resistance and susceptibility profiles within the Aeromonas genus, it is believed that the therapeutic administration of these drugs should not be restricted to specific species (Janda and Abbott, 2010). Strains of A. trota obtained from clinical samples were susceptible to ampicillin, an antibiotic generally not recommended for the treatment of infections caused by this genus (Carnahan et al., 1991; Janda and Abbott, 2010; Bhowmick and Bhattacharjee, 2018). In addition, (Hughes et al., 2016) isolated A. veronii from a stool culture and found that this strain was resistant to ertapenem and susceptible to imipenem and meropenem. These same authors also identified in perirectal isolates from two different patients the species A. veronii and A. hydrophila, which were resistant to all carbapenems previously cited. Carbapenems are widely used for therapy against MDR infections and resistance to this antibiotic is a global concern (Nordmann and Poirel, 2019; Kaluba et al., 2021). Previous detection of carbapenem-resistant bacteria is extremely important to improve the patient’s prognosis and thus reduce mortality. Noteworthy, the execution of the antibiogram test in clinical practice is crucial in prescribing antibiotics able to contribute to the therapeutic process (Hughes et al., 2016; Nordmann and Poirel, 2019).

Symptoms of acute gastroenteritis present commonly as self-limiting within approximately 5 days (Graves, 2013). Dehydration, caused by successive diarrheal episodes, is reversed by oral or intravenous rehydration techniques to balance body fluids and electrolytes (Graves, 2013; Mosegui et al., 2019). In these cases, antibiotics have been prescribed to quickly reduce the frequency of diarrhea, shorten the recovery time, and control the contagion, since it reduces the release of the pathogen in stools (Graves, 2013; Cohen et al., 2017). When dealing with antibiotics, the appropriate choice of empirical treatment before antibiogram results is very important, especially for reducing bacterial resistance (Zhu et al., 2021). Aeromonas spp. isolates from stool samples from children in a diarrheal outbreak demonstrated susceptibility to gentamicin, amicin, and cefepime (Soltan Dallal et al., 2016). Ciprofloxacin was used empirically in association with rehydration therapy in cases of gastroenteritis by A. hydrophila (Van Zwetselaar et al., 2018). Oral prescription of the same antibiotic was reported according to the results of the antibiogram performed with an A. hydrophila strain detected by stool culture from a patient experiencing gastroenteritis (Ahishali et al., 2007). Empirical infusion of sulbactam/ampicillin was used to treat enteritis by Aeromonas, with subsequent change of therapy by oral levofloxacin (Kishimoto and Watari, 2018).

Considering the therapy against peritonitis associated with PD, it is recommended by the International Society for Peritoneal Dialysis that antibiotics should be prescribed even if the infection is only a suspect; being administrated preferably by intraperitoneal route (Al Sahlawi et al., 2020). Vancomycin and ceftazidime were used empirically in a case of peritonitis involving a PD patient. Based on susceptibility testing, only ceftazidime was continued in the course of treatment of A. hydrophila infection (Kim et al., 2018). In a similar case involving A. sobria, the PD patient was treated with empirical teicoplanin and cefotiam. According to the antibiogram, therapy was replaced by intraperitoneal and intravenous infusion of amikacin and levofloxacin, respectively (Song et al., 2019).

Skin infections are classified according to the location of the lesion, analysis of its extension, and degree of involvement of the adjacent superficial and deep tissues (Ramakrishnan et al., 2015; Jabbour and Kanj, 2021). Thus, the therapeutic strategy can range from topical treatment to administrate antibiotics and surgical procedures to remove necrotic tissues (Jabbour and Kanj, 2021). Due to the multiple causes and origins of lesions and skin contamination, emergencies usually require rapid administration of empirical antibiotics, before susceptibility testing, to preserve the patient’s life and eventually reduce the need for invasive approaches (Abrahamian et al., 2008). Aeromonas hydrophila has been frequently reported in several cases of skin infection with previous trauma. Gentamicin and carbenicillin were used empirically to treat an infection in a puncture wound. Culture of purulent material and subsequent susceptibility testing isolated a strain of A. hydrophila sensitive to the aminoglycoside class, tetracycline, and chloramphenicol (Katz and Smith, 1980). The same species was detected in a case of postoperative sepsis due to a hand injury. Antibiogram revealed strain sensitivity to different classes of antibiotics, but resistance to amoxicillin/clavulanic acid, erythromycin, and clindamycin (Yang et al., 2004). Aeromonas hydrophila was also detected in purulent samples collected during surgical incision at sites of foot trauma infection. Levofloxacin and ampicillin/sulbactam were used empirically for adult and pediatric patients, respectively. After test results, the strains obtained from the cultures demonstrated susceptibility to levofloxacin and trimethoprim/sulfamethoxazole (Larka et al., 2003). Aeromonas species were detected in a study involving 129 cancer patients who experienced polymicrobial skin and soft tissue infections without previous exposure to water. Therapeutic administration of ceftazidime, ciprofloxacin, and ceftriaxone was reported (Chao et al., 2013a).

The management of other skin and soft tissue infections has also been reported. Aforementioned, A. hydrophila has been the underlying cause of folliculitis (Mulholland and Yong-Gee, 2008; Manresa et al., 2009; Olszewski et al., 2017). In these cases, the main therapeutical strategy has been using topical drugs and oral antibiotics have been chosen as a second-line treatment if there is no improvement in the infectious scenario (Clebak and Malone, 2018). Topical administration of gentamicin was prescribed to treat pediatric patients experiencing Aeromonas folliculitis (Manresa et al., 2009). The isolated strain of A. hydrophila has also been shown to be susceptible to other antibiotics. In the case of spa bath folliculitis, oral dicloxacillin was used empirically, being later replaced by oral ciprofloxacin according to antibiogram (Mulholland and Yong-Gee, 2008). Empirical use of ampicillin/sulbactam did not contain the progression of infection in a patient suffering from NF by A. sobria. Therapy was initially changed to ceftriaxone and levofloxacin and then to meropenem and linezolid. Susceptibility testing revealed resistance of the strain to meropenem, which was discontinued and replaced by ceftazidime (Spadaro et al., 2014). On the other hand, the prescription of meropenem was crucial in the prognosis of a patient diagnosed with NF by A. caviae, whose infection was also not controlled by empirical administration of antibiotics (Park et al., 2010). In these cases, in addition to drug therapy, surgical procedures of debridement and fasciotomies are also critical in the treatment and survival of the affected patient (Clebak and Malone, 2018). Other therapeutical strategies for uncommon Aeromonas human infections are summarized in Table 1.

For a long time, the genus Aeromonas was erroneously dissociated from the group of bacterial pathogens that have caused infections in humans. Some signs, like several diarrheal outbreaks around the world and widespread distribution of the Aeromonas in the environment reveal that these microorganisms were present in the medical routine for a very long time. Moreover, a great number of lives were taken under the consequences of its infectious processes. Given the diversity of clinical manifestations that Aeromonads can cause in both immunocompromised and immunocompetent patients, physicians should not underestimate this bacterial genus. As emergent pathogens, Aeromonas species are as common as other bacterial pathogens and are more prone to acquire multi-drug resistance, representing a severe threat to human health in the future. Therefore, progress in scientific studies aiming at new methods for Aeromonas identification as well as appropriate antimicrobial strategies will be a potential help for clinical approaches.

RBGP and LCBBC designed the structure of the manuscript. RBGP and WFdO wrote the review. MTdSC, AF, and LCBBC reviewed and approved the final version of the manuscript. All authors contributed to the article and approved the submitted version.

Conselho Nacional de Desenvolvimento Científico e Tecnológico, Fundação de Amparo à Ciência e Tecnologia do Estado de Pernambuco, and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior were responsible for fellowship.

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.

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