Front. Microbiol. Frontiers in Microbiology Front. Microbiol. 1664-302X Frontiers Media S.A. 10.3389/fmicb.2018.00942 Microbiology Original Research Distribution of Major Pilin Subunit Genes Among Atypical Enteropathogenic Escherichia coli and Influence of Growth Media on Expression of the ecp Operon Munhoz Danielle D. 1 Nara Júlia M. 1 † Freitas Natália C. 1 Moraes Claudia T. P. 1 Nunes Kamila O. 1 Yamamoto Bruno B. 1 Vasconcellos Francielli M. 1 Martínez-Laguna Ygnacio 2 Girón Jorge A. 2 Martins Fernando H. 1 Abe Cecilia M. 1 Elias Waldir P. 1 * Piazza Roxane M. F. 1 * 1Laboratório de Bacteriologia, Instituto Butantan, São Paulo, Brazil 2Centro de Detección Biomolecular, Benemérita Universidad Autónoma de Puebla, Puebla, Mexico

Edited by: Lorenza Putignani, Bambino Gesù Ospedale Pediatrico (IRCCS), Italy

Reviewed by: Elena Mazzolini, Istituto Zooprofilattico Sperimentale delle Venezie, Italy; Abigail Clements, Imperial College London, United Kingdom

 *Correspondence: Waldir P. Elias, waldir.elias@butantan.gov.br Roxane M. F. Piazza, roxane.piazza@butantan.gov.br

†Present address: Júlia M. Nara, Laboratório de Doenças de Suínos “Washington Sugay", Instituto Biológico, São Paulo, Brazil

This article was submitted to Infectious Diseases, a section of the journal Frontiers in Microbiology

 15 05 2018 2018 9 942 17 07 2017 23 04 2018 Copyright © 2018 Munhoz, Nara, Freitas, Moraes, Nunes, Yamamoto, Vasconcellos, Martínez-Laguna, Girón, Martins, Abe, Elias and Piazza. 2018 Munhoz, Nara, Freitas, Moraes, Nunes, Yamamoto, Vasconcellos, Martínez-Laguna, Girón, Martins, Abe, Elias and Piazza

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Atypical enteropathogenic Escherichia coli (aEPEC) strains are unable to produce the bundle-forming pilus (BFP), which is responsible for the localized adherence pattern, a characteristic of the pathogenicity of typical EPEC strains. The lack of BFP in aEPEC strains suggests that other fimbrial or non-fimbrial adhesins are involved in their adhesion to the host cells. The aim of this study was to investigate the distribution of major subunit fimbrial genes known to be important adherence factors produced by several E. coli pathotypes in a collection of 72 aEPEC strains. Our results demonstrate that a high percentage (94–100%) of aEPEC strains harbored ecpA, fimA, hcpA, and lpfA fimbrial genes. Other fimbrial genes including pilS, pilV, sfpA, daaC, papA, and sfa were detected at lower frequencies (1–8%). Genes encoding fimbrial subunits, which are characteristic of enteroaggregative E. coli or enterotoxigenic E. coli were not found. No correlation was found between fimbrial gene profiles and adherence phenotypes. Since all aEPEC strains contained ecpA, the major pilin gene of the E. coli common pilus (ECP), a subset of ecpA+ strains was analyzed for transcription of ecpRABCDE and production of ECP upon growth in three different culture conditions at 37°C. Transcription of ecpRABCDE occurred in all conditions; however, ECP production was medium dependent. In all, the data suggest that aEPEC strains are highly heterogeneous in terms of their fimbrial gene profiles. Despite lacking BFP production, other mechanisms of cell adherence exist in aEPEC strains to ensure host colonization, e.g., mediated by other prevalent pili such as ECP. Moreover, the production of ECP by aEPEC strains might be influenced by yet unknown post-transcriptional factors.

 diarrhea atypical EPEC adhesion fimbriae ECP 2004/12136-5 2009/14845-7 2013/06589-6 301302/2013-8 Fundação de Amparo à Pesquisa do Estado de São Paulo10.13039/501100001807 Conselho Nacional de Desenvolvimento Científico e Tecnológico10.13039/501100003593 Introduction

Bacterial adherence to host tissues is a multifactorial process involving distinct fimbrial and non-fimbrial adhesins that act in concert at different stages during infection. So far, a variety of fimbrial types has been identified and characterized in bacteria (Ofek et al., 2003; Jonson et al., 2005). The chromosomes of commensal and pathogenic Escherichia coli typically harbor between 12 and 16 different pili operons but the function of the majority of these pili systems and whether they are expressed or not remain uncharacterized (Brunder et al., 2001; Doughty et al., 2002; Torres et al., 2002, 2004; Rendón et al., 2007; Xicohtencatl-Cortes et al., 2007; Saldaña et al., 2009b; Samadder et al., 2009; Ross et al., 2015). Epidemiological data gathered around the world indicate that some pili types define some of the different classes of pathogenic E. coli and are associated with their adhesive potential and virulence. For example, the plasmid-encoded bundle-forming pilus (BFP), colonization factors (CFs), and aggregative adherence fimbriae (AAF) are found in enteropathogenic (EPEC), enterotoxigenic (ETEC), and enteroaggregative (EAEC) E. coli strains, respectively (Girón et al., 1991; Nataro et al., 1992; Czeczulin et al., 1997; Bernier et al., 2002; Qadri et al., 2005; Boisen et al., 2008; Jønsson et al., 2015). Type 1 pili, the long polar fimbriae (LPF), and the E. coli common pilus (ECP) are among the ubiquitous fimbrial adhesins of E. coli pathotypes. The ECP that has been detected in enterohemorrhagic E. coli (EHEC), EPEC, EAEC, ETEC, uropathogenic and avian pathogenic E. coli (Rendón et al., 2007; Blackburn et al., 2009; Saldaña et al., 2009a, 2014; Avelino et al., 2010; Hernandes et al., 2011; Stacy et al., 2014). In typical EPEC (tEPEC) strains, ECP appears to act synergistically with BFP during formation of the localized adhesion (LA) pattern (Saldaña et al., 2009a).

A subclass of EPEC strains lacking BFP genes has emerged in several regions of the world as an important cause of childhood diarrhea (reviewed in Gomes et al., 2016). This subclass is referred to as atypical EPEC (aEPEC) and does not produce the typical LA on cultured epithelial cells associated with BFP production (Scaletsky et al., 1984). Instead, aEPEC strains adhere poorly to cultured cells forming loose clusters, a pattern called localized-adherence like (LAL) (Rodrigues et al., 1996; Scaletsky et al., 1999). Some studies have demonstrated that aEPEC strains harbor a wide range of fimbrial genes in different combinations (Gomes et al., 2004; Afset et al., 2006; Tennant et al., 2009; Scaletsky et al., 2010; Hernandes et al., 2011; Piazza et al., 2013). However, only a few studies have characterized the expression of fimbrial genes in aEPEC strains (Hernandes et al., 2011; Nascimento et al., 2014). Thus, it is important to search for highly prevalent virulence markers in this pathotype in order to better understand their adherence mechanisms aiming to identify targets for diagnosis and/or prevention of aEPEC infections.

Therefore, the aim of the present study was to investigate the distribution of known pathogenic E. coli fimbrial adhesins genes in aEPEC strains displaying different adherence phenotypes. Since the ecpA gene was present in all the aEPEC strains tested, we also investigated the influence of growth media in the differential expression and production of ECP among these strains to gain knowledge on the regulation of ECP.

 Materials and Methods Bacterial Strains

We studied all 72 aEPEC strains isolated from children with diarrhea in a case-control survey conducted between 2003 and 2004 in the city of Salvador, Brazil (Bueris et al., 2007). These strains were previously characterized as aEPEC showing the following features: eae+/EAF-/stx-/BFP- (Abe et al., 2009; Nara et al., 2010). They belong to a wide range of serotypes, and exhibit distinct patterns of adherence: LAL, diffuse adherence (DA), aggregative adherence (AA), non-characteristic, and non-adherent (Abe et al., 2009). Strains used as controls in different assays are listed in Supplementary Table S1.

 Detection of Fimbrial Genes

The following fimbriae-encoding genes were searched among the 72 aEPEC strains by PCR: fimA, fimH, papA, sfaD-E, bfpA, ecpA, espA, ldaH, aggA, aafA, agg3A, agg4A, pilS, pilV, lngA, cfaB, cooA, cotA, cstA, cofA, csaA, csfA, cssA, daaC, sfpA, hcpA, lpfAO113, lpfA1-1, lpfA1-2, lpfA1-3, lpfA1-5, lpfA2-1. Primer sequences, annealing temperatures and sizes of amplified fragments are listed in Supplementary Table S1. Amplification was performed in a total volume of 50 μL containing: dATP, dTTP, dCTP, and dGTP (0.1 mM each), 1.5 U Taq DNA polymerase, 5.0 μL 10x PCR buffer and 2 mM MgCl2 (Invitrogen, Boston, MA, United States), 40 pmol of each primer, and 2.0 μL of DNA template, obtained from a colony from culture on Luria-Bertani (LB) agar boiled in 300 μL of water for 10 min. The PCR was carried out at 94°C for 5 min, 30 cycles of 94°C for 1 min, annealing temperature (see Supplementary Table S1 for specific temperatures and incubation times), 72°C for 1 min, followed by a final extension for 5 min at 72°C. The PCR products were analyzed by agarose gel (0.7–1%) electrophoresis after GelRed staining (Uniscience, Miami, FL, United States), and the images captured by the AlphaImageTM 2200 program (Alpha Innotech, San Leandro, CA, United States). Twenty-two LAL aEPEC strains were selected for PCR analysis of ecpRABCDE genes as described above.

 Growth Conditions for Analysis of ECP Production

Among the 72 aEPEC strains tested, four LAL-producing aEPEC (BA2103, BA3378, BA4132, and BA4147) were selected for ECP production. For analysis of ecpRABCDE transcription and ECP production the strains were initially grown in LB at 37°C for 18 h. The bacterial cultures were then transferred to LB, Dulbecco’s modified Eagle Medium (DMEM) or preconditioned DMEM (PC-DMEM) (1:100) followed by static incubation at 37°C until a final absorbance of 0.6 at 600 nm (A600). PC-DMEM was prepared by incubating DMEM (without antibiotics and fetal bovine serum) in the presence of monolayers of HeLa cells for 48 h at 37°C. The supernatant referred to as “preconditioned medium” was collected, adjusted to pH 7.4, and filtered through a 0.2 μm pore membrane (Girón et al., 2002). tEPEC E2348/69 and E. albertii 1551-2 strains (Levine et al., 1985; Yamamoto et al., 2017) were used as positive and negative controls of ECP production, respectively.

 Transcription of <italic>ecp</italic> Operon

Strains BA2103, BA3378, BA4132 and BA4147, as well as appropriate control strains were grown in LB, DMEM and PC–DMEM and centrifuged at 4,000 × g for 5 min. Pellets were resuspended in 1 mL of the respective culture media and subsequently used for RNA extraction using RNA Protect and RNeasy Mini kit (Qiagen, Hilden, Germany), according to the manufacturer’s recommendations. cDNAs were synthesized using 1 μg of RNA for each strain, by Superscript III First-Strand Synthesis Systems kit for RT-PCR (Invitrogen, Boston, MA, United States), following the manufacturer’s recommendations. The presence of ecpRABCDE genes in the cDNAs obtained were assessed by PCR as described in Table 1. PCR for the constitutive gene rpoA was included as control of cDNA integrity. All reactions were performed in triplicates in three independent experiments.

Primer sequences of ecp operon and PCR conditions used to study ecp operon.

Gene Sequence Annealing temperature (°C) Mg (mM) Fragment (bp) Reference
ecpA (F) ACCTCGGGAAGAAAAGCAA 56 2 640 This study∗
(R) CAATTCCGTCCAGGAATAAA
ecpB (F) TCTGATGTACCAGCAGGG 47 1.5 780 This study∗
(R) CTTTCAGTCCTGGGGAGA
ecpC (F) ACGACAATGCCTTTACGAG 57 1 1,130 This study∗
(R) CGATCCATATGAAAGCTACG
ecpD (F) AGTTTGTGTTTGTCGAAAAC 56 1 760 This study∗
(R) GCCGAGGCTAACGACGA
ecpE (F) CGGTGGATGGTGAACTACTT 60 2 458 This study∗
(R) CGGACAGGAATCCGTTAATCT
ecpR (F) CTGTAAAAATTATAGGTTTG 57 2 683 This study∗
(R) ACCAGAGCTATTGCCAGA
∗Primers designed using ecp operon sequence of tEPEC E2348/69 (GenBank accession number: NC_011601). Production of ECP

The production of ECP was studied by immunofluorescence microscopy (IFM) in LAL aEPEC strains BA2103, BA3378, BA4132, and BA4147 growing in the three different media described above. Briefly, the 18 h bacterial cultures were centrifuged for 5 min at 900 × g and the pellets were resuspended in 10 μL of the respective medium and fixed on glass slides with 4% p-formaldehyde at 4°C for 18 h. The slides were washed twice with 0.01 M phosphate buffer saline pH 7.4 (PBS), blocked with 10% goat serum in PBS (GS–PBS) for 1 h at room temperature, followed by incubation at 4°C for 18 h with rabbit anti-EcpA antibody (diluted 1:1,000 in GS–PBS). The slides were washed twice with PBS and incubated with goat anti-rabbit IgG conjugated with FITC (Sigma-Aldrich, St. Louis, MO, United States) diluted 1:500 in GS–PBS at room temperature for 1 h. After incubation, the slides were washed twice with PBS and mounted with Vectashield antifade mounting medium (Vector Laboratories, Burlingame, CA, United States) and covered with glass coverslips. The preparations were visualized under laser scanning confocal (LSM 510 META, Zeiss, Oberkochen, Germany) microscopes with original magnification of 1,000×. Triplicates of three independent experiments were performed.

We also determined ECP production in cultures of strain BA2103 obtained in LB, DMEM or PC–DMEM by transmission electron microscopy (TEM) using immunogold-labeling method. Strains E2348/69 and 1551-2 were used as controls. Briefly, preparations were blocked with a solution of 0.2% BSA in PBS and then incubated with rabbit anti-EcpA at 1:100 dilution for 2 h at room temperature. Following this period, the preparations were incubated with goat anti-rabbit antibody labeled with 10 nm colloidal gold particles (Sigma-Aldrich, St. Louis, MO, United States) at 1:50 dilution for 2 h at room temperature. Preparations were negatively stained with 2% uranyl acetate in water, applied onto formvar-coated nickel grids and observed under TEM (LEO 906E – Zeiss, Oberkochen, Germany) at 80 kV. Triplicates of three independent experiments were performed.

 Results <italic>E. coli</italic> Fimbrial Genes Are Found in aEPEC Strains in Different Combinations

Fifteen fimbrial genes were detected in our collection: ecpA (100%), fimH and hcpA (97.2%), fimA (94.4%), lpfA1-2 (68%), lpfA2-1 (50%), lpfA1-1 (19.4%), lpfAO113 (13.8%), lpfA1-3 (11.1%), pilS and ldaH (8.3%), pilV (4.2%), papA and daaC (2.7%) and sfpA (1.4%) (Figure 1). This large repertoire of fimbrial genes was distributed in different combinations among the 72 strains, demonstrating no correlation between fimbrial gene profiles and adherence pattern (Table 2). None of the aEPEC strains contained the following fimbrial genes: aggA, aafA, agg3A, agg4A, cooA, cotA, cstA, cofA, csaA, csfA, cssA, lngA, lpfA1-5, and sfa (Table 2).

Distribution of the frequency of fimbrial genes among 72 aEPEC strains studied.

Genetic fimbrial profile of aEPEC strains.

Strains Fimbrial adhesins profile Adherence pattern Serotype
BA558 pilS, pilV, lpfA1-2, lpfA1-3, ecpA, hcpA LA O111:H40
BA1652 fimA, fimH, ecpA, hcpA LAL O131:H4
BA2853 fimA, fimH, ecpA, hcpA LAL ONT:H10
BA487 fimA, lpfA1-3, ecpA, hcpA LAL O55:H7
BA714 fimH, lpfA1-2, ecpA, hcpA LAL O111:H-
BA2034 fimA, fimH, lpfA1-2, ecpA, hcpA LAL ONT:H10
BA3733 fimA, fimH, lpfA1-2, ecpA, hcpA LAL O119:H19
BA4095 fimA, fimH, lpfA1-1, ecpA, hcpA LAL O4:H45
BA1649 fimA, fimH, lpfA2-1, ecpA, hcpA LAL O111:H38
BA3378 fimA, fimH, pilS, ecpA, hcpA LAL O104:H2
BA1250 fimA, fimH, lpfA1-2, ecpA, hcpA LAL ONT:H6
BA1324 fimA, fimH, lpfA1-1, lpfA2-1, ecpA, hcpA LAL O34:H45
BA3157 fimA, fimH, lpfA1-2, lpfA2-1, ecpA, hcpA LAL O119:H2
BA3574 fimA, fimH, lpfA1-2, lpfA2-1, ecpA, hcpA LAL ONT:H38
BA4047 fimA, fimH, lpfA1-3, lpfA2-1, ecpA, hcpA LAL O1:H16
BA4077 fimA, fimH, lpfA1-2, lpfA2-1, ecpA, hcpA LAL O64:H23
BA4147 fimA, fimH, papA, lpfA1-3, ecpA, hcpA LAL O55:H7
BA320 fimA, fimH, lpfA1-2, lpfA1-3, ecpA, hcpA LAL O55:H7
BA589 fimA, fimH, pilS, lpfA1-2, lpfA2-1, ecpA, hcpA LAL O5:H2
BA3851 fimA, fimH, lpfA1-1, lpfA1-2, lpfA2-1, ecpA, hcpA LAL ONT:H38
BA4132 fimA, fimH, lpfA1-1, lpfA1-2, lpfA2-1, ecpA, hcpA LAL O51:H48
BA3977 fimA, fimH, lpfA1-1, lpfA1-2, sfpA, ecpA, hcpA LAL ONT:H45
BA2103 fimA, fimH, lpfAO113, lpfA1-2, lpfA2-1, ecpA, hcpA LAL O26:H11
BA92 fimA, fimH, ecpA, hcpA AA O2:H16
BA4157 fimA, fimH, ecpA, hcpA AA ONT:H25
BA2482 fimA, fimH, lpfA1-2, ecpA, hcpA AA O119:H11
BA585 fimA, fimH, lpfA1-2, lpfA1-3, ecpA, hcpA AA O157:H16
BA3690 fimA, fimH, lpfA1-2, lpfA2-1, ecpA, hcpA AA O111:H38
BA2145 fimA, fimH, lpfAO113, lpfA1-2, lpfA2-1, ecpA, hcpA AA O105:H7
BA2297 fimA, fimH, lpfAO113, lpfA2-1, ecpA DA O153:H11
BA2073 fimA, fimH, lpfA1-1, lpfA1-2, ecpA DA ONT:H5
BA4009 fimA, fimH, lpfAO113, lpfA1-1, lpfA2-1, ecpA DA O114:H25
BA3170 fimA, fimH, ecpA, hcpA UND O145:H2
BA4182 fimA, fimH, ecpA UND O125:H6
BA462 fimA, fimH, ldaH, ecpA, hcpA UND O51:H40
BA2964 fimA, fimH, lpfA1-2, ecpA, hcpA UND O51:H40
BA4192 fimA, fimH, lpfA1-2, ecpA, hcpA UND O111:H25
BA1768 fimA, fimH, lpfA2-1, ecpA, hcpA UND O51:H40
BA1887 fimA, fimH, lpfA2-1, ecpA, hcpA UND O111:H38
BA1444 fimA, fimH, lpfA1-2, lpfA2-1, ecpA, hcpA UND O115:H8
BA2062 fimA, fimH, lpfA1-2, lpfA2-1, ecpA, hcpA UND O171:H48
BA2459 fimA, fimH, lpfAO113, lpfA1-2, lpfA2-1, ldaH, ecpA, hcpA UND O26:H11
BA1244 fimA, fimH, papA, pilS, pilV, lpfA1-2, lpfA1-3, lpfA2-1, daaC, ecpA, hcpA UND O55:H7
BA4058 fimH, lpfA1-1, ecpA, hcpA NA O20:H-
BA179 fimA, fimH, ecpA, hcpA NA O23:H16
BA442 fimA, fimH, lpfA1-2, ecpA, hcpA NA O35:H19
BA580 fimA, fimH, lpfA1-2, ecpA, hcpA NA O119:H2
BA2294 fimA, fimH, lpfA1-1, ecpA, hcpA NA O9:H33
BA2613 fimA, fimH, lpfA1-2, ecpA, hcpA NA O101:H33
BA3392 fimA, fimH, lpfA1-2, ldaH, ecpA, hcpA NA O124:H11
BA3800 fimA, fimH, lpfA1-2, ecpA, hcpA NA ONT:H19
BA852 fimH, lpfA1-2, lpfA2-1, ecpA, hcpA NA O88:H25
BA356 fimA, fimH, pilS, lpfA1-1, ecpA, hcpA NA O333:H7
BA365 fimA, fimH, lpfA1-2, lpfA2-1, ecpA, hcpA NA ONT:H19
BA655 fimA, fimH, lpfA1-2, lpfA2-1, ecpA, hcpA NA O88:H25
BA2065 fimA, fimH, lpfA1-1, lpfA1-2, ecpA, hcpA NA ONT:H5
BA2117 fimA, fimH, lpfA1-1, lpfA1-2, ecpA, hcpA NA ONT:H5
BA2975 fimA, fimH, lpfA1-2, lpfA2-1, ecpA, hcpA NA O88:H25
BA2991 fimA, fimH, lpfA1-2, lpfA2-1, ldaH, ecpA, hcpA NA O34:H-
BA3443 fimA, fimH, lpfA1-2, lpfA2-1, ecpA, hcpA NA O88:H25
BA3836 fimA, fimH, lpfA1-2, lpfA2-1, ecpA, hcpA NA ONT:H19
BA3148 fimA, fimH, lpfAO113, lpfA1-2, ecpA, hcpA NA O35:H19
BA956 fimA, fimH, pilS, pilV, lpfA1-1, ecpA, hcpA NA O111:H15
BA86 fimA, fimH, lpfA1-2, lpfA2-1, daaC, ecpA NA O76:H19
BA151 fimA, fimH, lpfA1-2, lpfA2-1, ecpA, hcpA NA ONT:H9
BA3160 fimA, fimH, lpfA1-2, lpfA2-1, ldaH, ecpA, hcpA NA O110:H-
BA2468 fimA, fimH, lpfAO113, lpfA1-2, lpfA2-1, ecpA, hcpA NA ONT:H19
BA2775 fimA, fimH, lpfAO113, lpfA1-2, lpfA2-1, ecpA, hcpA NA O113:H19
BA4013 fimA, fimH, lpfAO113, lpfA1-2, lpfA2-1, ecpA, hcpA NA O88:H-
BA1738 fimA, fimH, lpfA1-2, lpfA2-1, ecpA, hcpA NA O80:H26
BA4135 fimA, fimH, lpfA1-1, lpfA1-2, lpfA2-1, ecpA, hcpA NA O108:H25
BA2923 fimA, fimH, lpfAO113, lpfA1-2, lpfA1-3, lpfA2-1, ldaH, ecpA, hcpA NA O34:H6
LA, localized adherence; LAL, localized-adherence like; AA, aggregative adherence; DA, diffuse adherence; UND, undetermined; NA, non-adherent. ECP Is Differentially Produced by aEPEC That Harbor a Functional <italic>ecp</italic> Operon

The 22 LAL ecpA+ aEPEC strains contained also the ecpR, ecpB, ecpC, ecpD, and ecpE, suggesting that the ECP operon is highly conserved among aEPEC (data not shown). To better understand the correlation between the expression of ecpA and production of ECP in different culture conditions we selected four representative LAL aEPEC strains (BA2103, BA3378, BA4132, and BA4147), all of which display different fimbrial profiles (Table 2). All the six-ecp genes were expressed in the four strains regardless of the growth medium (Supplementary Figure S1). However, among the LB-grown bacteria only BA2103 produced ECP. When cultivated in DMEM and PC-DMEM three (BA2103, BA4132, and BA4147) of the four strains produced ECP. Despite the fact that the entire ecp operon was expressed in BA3378, this strain did not produce ECP in any of the growth conditions tested (Figure 2). In general, a noteworthy increase in ECP production is apparent when the strains were grown in PC-DMEM in comparison to DMEM (Figure 2). Confirmation of ECP production by strain BA2103 was demonstrated by TEM and immunogold labeling (Figure 3).

Growth medium-dependent production of ECP visualized by confocal microscopy. aEPEC strains BA2103, BA3378, BA4132, BA4147 grown in LB, DMEM, and PC-DMEM were reacted with rabbit anti-EcpA antibody and goat anti-rabbit IgG antibody conjugated with FITC. E2348/69 and 1551-2 were used as positive and negative controls of ECP production, respectively. Images were originally taken at 1,000× magnification.

Growth medium-dependent production of ECP visualized by TEM. aEPEC strain BA2103 grown in PC-DMEM, DMEM and LB was reacted with rabbit anti-EcpA antibody and goat anti-rabbit IgG antibody conjugated with 10 nm colloidal gold particles. E2348/69 and 1551-2 were used as positive and negative controls of ECP production, respectively. Bars: 0.2 μm.

 Discussion

tEPEC adherence to enterocytes is multifactorial involving the formation of localized microcolonies on host epithelial cells, which is mediated by BFP, promoting bacterium-cell and bacterium–bacterium interactions (Girón et al., 1991; Tobe and Sasakawa, 2001); followed by the interaction of the intimin adhesin with its receptor Tir triggering the attaching and effacing (A/E) lesion (Jerse et al., 1990; Kenny et al., 1997). On the other hand, the initial interaction of aEPEC with host epithelial cells is instead mediated by distinct cell surface appendages (Hernandes et al., 2006, 2011; Scaletsky et al., 2010; Gomes et al., 2011; Hu and Torres, 2015).

Here, we evaluated a collection of 72 aEPEC for the presence and distribution of several E. coli major fimbrial subunit genes known to be involved in bacterial adhesion processes. In agreement with previous reports, none of the genes encoding EAEC fimbriae or the CFs of ETEC were present in the aEPEC strains studied (Vieira et al., 2001; Gomes et al., 2004; Afset et al., 2006). On the other hand, ecpA, fimA, fimH, hcpA, lpfAO113 and polymorphic variants of lpf (A1-1, A1-2, A1-3, and A2-1) genes were present in the majority (94–100%) of the strains, while pilS, pilV, sfpA, daaC, papA, and sfa genes were detected at lower frequency (1–8%) regardless of their adherence pattern. Since each strain studied displayed a specific genetic fimbrial profile, these data indicated that there was no correlation between fimbrial gene profile and adherence pattern phenotypes, as similarly elsewhere described (Afset et al., 2006; Hernandes et al., 2009; Gomes et al., 2016).

The high frequency of ecpA, hcpA, lpf, fimH, and fimA genes among aEPEC strains indicates that they have likely been conserved to play a role in aEPEC adhesion. It is possible that the acquisition of different gene combinations in specific lineages of E. coli may contribute to the emergence of virulent strains (Afset et al., 2006; Bando et al., 2009; Scaletsky et al., 2009). It remains to be determined if recent aEPEC clinical strains are also heterogeneous in terms of their fimbrial adhesins profile. The presence of papA, sfa, pilS, pilV, ldaH, and/or daaC genes in certain strains deserves further investigation regarding their role as adhesins in host colonization.

Amongst the genes studied, ecpA was detected in 100% of our aEPEC collection. The ECP mediates host cell adherence and colonization by both pathogenic and commensal E. coli strains (Rendón et al., 2007). While the role of the ECP in adherence to epithelial cells has been demonstrated for several E. coli pathotypes, its involvement in the LAL phenotype by aEPEC has not been investigated. The high prevalence of this gene among aEPEC strains and other E. coli pathotypes isolated from several studies was previously described (Pouttu et al., 2001; Rendón et al., 2007; Blackburn et al., 2009; Scaletsky et al., 2010). The presence of all the genes responsible for ECP biogenesis in aEPEC has not yet been investigated. Here, we found that all the six-ecp genes were present in the 22 LAL-aEPEC strains studied suggesting that the ecp operon is highly conserved.

The expression of the ecpRABCDE operon and production of ECP was investigated in four aEPEC growing in rich and minimal culture media. The production of virulence markers is still necessary to be evaluated in order to elect an antigen for diagnosis and/or prevention of aEPEC infection. We found that all the strains transcribed the ecp genes when cultured in the three growth conditions tested. In terms of ECP production, only BA2103 produced ECP when the strains were grown in LB rich medium. These data are in agreement with previous reports that showed that some ETEC and EHEC strains do not produce ECP in CF antigen agar and LB, respectively (Rendón et al., 2007; Blackburn et al., 2009). Three strains produced ECP when cultivated in DMEM and PC-DMEM. Interestingly, an apparent increase in the number of bacteria producing ECP was noted when the strains were cultured in PC-DMEM in comparison with DMEM, as the reactivity of the anti-EcpA antibody was remarkably more intense in PC-DMEM grown bacteria. This data suggest that eukaryotic cell-derived molecules present in PC-DMEM might trigger expression of the ecp operon and synthesis of ECP by aEPEC.

As production of ECP was not detected in aEPEC BA3378 in any growth condition tested, it is possible that this strain produces a variant of EcpA, which is not recognized by the anti-ECP employed, or is under strict regulation. Thus, post-transcriptional factors possibly regulate ECP production in some strains, as in BA3378 of our study. In fact, the operon regulator EcpR/MatA was shown to have dual role in the control of operon expression in a neonatal meningitis Escherichia coli (NMEC) strain (IHE 3034) via mat promoter, either by a positive autoregulatory circuit or repressing the negative control exerted by H-NS (Lehti et al., 2013). EcpR/MatA is also able to increase the stability of the processed ecpA mRNA under some conditions as low growth temperature, acidic pH or elevated levels of acetate (Lehti et al., 2013). The disparity in stability may be due to temperature-dependent conformation of ecpA transcript as shown for mRNA of the major cold-shock protein CspA (Giuliodori et al., 2010). Small RNAs (sRNAs) could be another post-transcriptional system involved in ECP production, which generally demands the RNA chaperone Hfq and use different mechanisms, like binding to the ribosome-binding site (RBS) and blocking translation, binding to an anti-RBS hairpin and activating translation, or by the recruitment of RNases destabilizing transcripts (Waters and Storz, 2009). Also, Gruber and Sperandio (2015) recently reported that in EHEC, GlmY and GlmZ selectively destabilize parts of the LEE4 and LEE5 transcripts playing an important role in the post-transcriptional regulation of A/E lesion formation. Genes within the GlmY and GlmZ regulon include stress-related genes, virulence factors, genes involved in osmoregulation and adhesins, which is the case of ECP. The role of these post-transcriptional regulators in ECP production by our strains is currently under investigation by our group.

The reactivity of anti-EcpA antibody was remarkably more intense in bacterial cell grown in PC-DMEM than in DMEM. Similar to tEPEC strains, in which ECP and BFP act in combination to promote adherence, it is reasonable to suggest that ECP could act together with other adhesins of aEPEC to favor gut colonization and survival in and outside the host. Also, the high prevalence of ECP among aEPEC indicates that this adherence factor has been maintained during evolution to ensure intestinal colonization.

In summary, our data demonstrated that different E. coli fimbrial genes profiles are present in the aEPEC strains studied and that there is no correlation between these profiles and adherence patterns. The high prevalence of ECP, HCP, and type 1 fimbriae among aEPEC suggest that they are likely to contribute to cell adhesion. We also demonstrated that culture conditions influenced ECP production by aEPEC strains, likely attributed to post-transcriptional regulation.

 Author Contributions

DM, JN, KN, BY, FV, YM-L, FM, CA, WE, and RP: conception and design. DM, JN, NF, CM, KN, BY, FV, FM, and CA: acquisition and analysis. DM, JN, NF, CM, KN, BY, FV, YM-L, JG, FM, CA, WE, and RP: interpretation and substantial contributions. DM, CM, YM-L, JG, FM, CA, WE, and RP: drafting the work or revising it critically. DM, JG, CA, WE, and RP: final approval of the version to be published.

 Conflict of Interest Statement

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.

Funding. This work was supported by grants from São Paulo Research Foundation (2004/12136-5, 2009/14845-7, 2010/11624-5, and 2013/06589-6) and Conselho Nacional de Desenvolvimento Científico e Tecnológico (301302/2013-8). DM, JN, NF, FV, and FM were recipients of fellowships from the São Paulo Research Foundation.

The authors thank Beatriz E. C. Guth and Tania A. T. Gomes (UNIFESP, Brazil) for kindly providing some control strains for gene searching and ECP production and Henrique K. Rofatto and Alexsander S. de Souza for the confocal microscopy analysis.

 Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmicb.2018.00942/full#supplementary-material

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