Virulence profiling of Shiga toxin-producing Escherichia coli recovered from domestic farm animals in Northwestern Mexico

Abstract

Shiga toxin-producing Escherichia coli (STEC) is a zoonotic enteric pathogen that causes human gastrointestinal illnesses. The present study characterized the virulence profiles of O157 and non-O157 STEC strains, recovered from domestic animals in small rural farms within the agricultural Culiacan Valley in Mexico. Virulence genes coding for adhesins, cytotoxins, proteases, subtypes of Shiga toxin (Stx), and other effectors were identified in the STEC strains by PCR. The genotyping analysis revealed the presence of the effectors nleA, nleB, nleE, and nleH1-2, espK, and espN in the O157:H7 and O111:H8 STEC strains. Furthermore, the genes encoding the autoagglutinating adhesin (Saa) and subtilase (SubA) were exclusively identified in the O8:H19 eae-negative strains. The adhesin (iha) and the silent hemolysin (sheA) genes were detected in 79% of the O157 and non-O157 strains. To examine the relative toxicities of the STEC strains, a fluorescent Vero cell line, Vero-d2EGFPs, was employed to measure the inhibition of protein synthesis by Stx. Analysis of culture supernatants from serotype O8:H19 strains with the stx gene profile stx_1a, stx_2a, and stx_2c and serotypes O75:H8 and O146:H8 strains with the stx gene profile stx_1a, stx_1c, and stx_2b, resulted in a significant reduction in the Vero-d2EGFP fluorescent signal. These observations suggest that these non-O157 strains may have an enhanced ability to inhibit protein synthesis in Vero cells. Interestingly, analysis of the stx_2c-positive O157:H7 strains resulted in a high fluorescent signal, indicating a reduced toxicity in the Vero-d2EGFP cells. These findings indicate that the O157 and non-O157 STEC strains, recovered in the Culiacan Valley, display distinct virulence profiles and relative toxicities in mammalian cells and have provided information for evaluating risks associated with zoonotic STEC in this agricultural region in Mexico.

Introduction

Shiga toxin-producing Escherichia coli (STEC) is considered to be a major cause of foodborne disease and can cause a wide variety of disease symptoms in humans, ranging from watery and bloody diarrhea to the life-threatening diseases such as hemorrhagic colitis, and hemolytic uremic syndrome (HUS) (Tarr et al., 2005; Gyles, 2007; Karmali et al., 2010; Scallan et al., 2011; Melton-Celsa et al., 2012). Cattle are considered to be the major carrier of STEC strains (Gyles, 2007; Ferens and Hovde, 2011). However, additional studies that examined important animal reservoirs for these bacterial pathogens have indicated that small domestic ruminants, including sheep and goats, have been implicated as carriers of STEC (Ogden et al., 2005; Gyles, 2007; La Ragione et al., 2009; Ferens and Hovde, 2011; Mandrell, 2011). Furthermore, STEC strains have been also detected in other domestic and wild animals, including cats, dogs, rodents, deer, birds, feral pigs, chickens, and insects (Cooley et al., 2007; Ferens and Hovde, 2011; Mandrell, 2011).

Severe disease in humans has been associated with more than 100 serotypes of STEC (Gould et al., 2009; Mathusa et al., 2010). Serotype O157:H7 is responsible for most outbreaks in the United States (Karmali, 2009; Hoefer et al., 2011; Melton-Celsa et al., 2012). Additional epidemiological studies have indicated that six non-O157 serogroups, O26, O45, O103, O111, O121, and O145, have been associated with severe disease symptoms in North America (Johnson et al., 2006; Gould et al., 2009; Stigi et al., 2012). Additionally, STEC of serogroups, O91, O104, O113, and O128 have been reported to be significant causes of human infections worldwide (Brooks et al., 2005; Bettelheim, 2007; Mathusa et al., 2010; Beutin and Martin, 2012). Thus, these findings have indicated that strains with certain non-O157 serogroups may be potentially as virulent as strains with the O157:H7 serotype (Bettelheim, 2007; Coombes et al., 2011; Beutin and Martin, 2012; Stigi et al., 2012).

The production of Shiga toxins (Stx) by STEC contributes to the development of the life-threatening disease symptoms in humans (Karmali et al., 1983; Karmali, 1989). The Stx family has been categorized into two major types, Stx1 and Stx2. In particular, distinct subtypes of Stx1, Stx1a, Stx1c and Stx1d, have been identified (Scheutz and Strockbine, 2005; Scheutz et al., 2012). By contrast, the Stx2 group consists of a heterogeneous and diverse group of subtypes, and seven subtypes of Stx2, corresponding to Stx2a, Stx2b, Stx2c, Stx2d, Stx2e, Stx2f, and Stx2g, have been documented (Scheutz and Strockbine, 2005; Scheutz et al., 2012). Epidemiological and molecular genotyping studies of STEC have demonstrated that there is a strong correlation between strains with certain stx₂ subtypes and severe illness such as bloody diarrhea and HUS. STEC strains positive for the subtypes stx_2a, stx_2c, or stx_2d were found to be associated with an enhanced virulence and with the development of the HUS in humans (Friedrich et al., 2002; Beutin et al., 2004; Bielaszewska et al., 2006; Persson et al., 2007). Other subtypes of Stx1 and Stx2 appear to be associated with mild disease or asymptomatic carriage (Friedrich et al., 2002, 2003; Beutin et al., 2004; Bielaszewska et al., 2006; Scheutz et al., 2012).

Many STEC strains that produce Stx do not cause HUS, demonstrating that additional virulence factors may be required to cause illness in humans (Bolton, 2011). For example, virulence factors present on pathogenicity islands, such as the locus of enterocyte effacement (LEE) and the non-LEE effectors, have been implicated in host colonization and disease (Bettelheim, 2007; Bolton, 2011; Coombes et al., 2011). In particular, a key virulence factor responsible for the attachment to intestinal epithelial cells is the LEE-encoded eae gene (Jerse et al., 1990; Kaper, 1998). An additional adhesin, Iha, the iron-regulated gene A homolog adhesin, may contribute to the attachment of LEE-positive and LEE-negative strains (Tarr et al., 2000; Schmidt et al., 2001). Moreover, the Nle effectors, not encoded by the LEE region, are proposed to be involved in altering the host cell response and have been linked to the disease severity associated with non-O157 STEC (Coombes et al., 2008; Karmali et al., 2010; Melton-Celsa et al., 2012). Other chromosomal and plasmid virulence genes, encoding proteases (espP), cytotoxins (subA), and adhesins (saa), may contribute to STEC pathogenesis by allowing bacterial attachment and colonization of the human epithelium (Karmali et al., 2010; Bolton, 2011; Melton-Celsa et al., 2012). The detection of these virulence genes in STEC strains would provide key information for the identification of risk factors that may potentially contribute to the development of human disease.

In the present study, a molecular characterization study was conducted to further examine the virulence potential of STEC strains, previously recovered from feces of domestic animals in small rural farms within the agricultural Culiacan Valley in Northwestern Mexico (Amézquita-López et al., 2012). The small rural farms were located in communities where the primary purpose of raising livestock is for local consumption (Amézquita-López et al., 2012). To determine the virulence profiles of STEC strains from animal reservoirs in this agricultural region in Mexico, the present study identified the stx subtypes as well as several virulence factors that have been associated with pathogenic STEC strains. The activity of the Stx subtypes, expressed by the tested STEC strains, was also further examined to obtain more detailed information on their ability to inhibit protein synthesis in mammalian cells.

Materials and methods

Bacterial strains and growth conditions

A subset of 29 STEC strains, previously recovered from various animal reservoirs in the Culiacan Valley in Mexico (Amézquita-López et al., 2012), was studied (Table 1). The subset of strains was selected based on serotype and on the recovery from distinct dates, sampling sites and animal reservoirs (Amézquita-López et al., 2012).

Table 1.

List of E. coli O157 and non-O157 strains analyzed in this study.

Strain	Serotypea	Sampling date	Source	Regionb
RM8744	O157:H7	18-Nov-08	Cattle	Iraguato
RM8745	O73:H4	02-Dec-08	Sheep	El Castillo
RM8747	O15:NT	22-Jul-08	Cattle	Agua Caliente
RM8748	O73:NT	22-Jul-08	Cattle	Agua Caliente
RM8749	O20:H4	12-Aug-08	Sheep	El Castillo
RM8752	O75:H8	07-Oct-08	Sheep	Cofradia de Navolato
RM8753	O157:H7	02-Dec-08	Sheep	Cofradia de Navolato
RM8755	O111:H8	20-Jan-09	Sheep	Cofradia de Navolato
RM8756	O146:H21	20-Jan-09	Sheep	Jotagua
RM8759	O157:H7	20-Jan-09	Sheep	Cofradia de Navolato
RM8760	O75:H8	20-Jan-09	Sheep	Cofradia de Navolato
RM8761	O146:H21	20-Jan-09	Sheep	El Castillo
RM8762	O146:H8	20-Jan-09	Sheep	El Castillo
RM8763	O75:H8	03-Feb-09	Sheep	Cofradia de Navolato
RM8768	O157:H7	20-Jan-09	Cattle	Cofradia de Navolato
RM8772	O8:H19	17-Feb-09	Cattle	El Castillo
RM8776	O8:H19	03-Feb-09	Cattle	Iraguato
RM8778	O75:H8	25-Feb-09	Sheep	Cofradia de Navolato
RM8781	O157:H7	25-Feb-09	Sheep	Cofradia de Navolato
RM8922	O157:H7	10-Mar-09	Cattle	Cofradia de Navolato
RM8923	O75:H8	10-Mar-09	Cattle	Cofradia de Navolato
RM8928	O157:H4	10-Mar-09	Cattle	El Castillo
RM8929	O75:H8	10-Mar-09	Sheep	Cofradia de Navolato
RM9450	O157:H7	10-Mar-09	Sheep	Cofradia de Navolato
RM9452	O157:H7	26-May-09	Sheep	Cofradia de Navolato
RM9454	O157:H7	26-May-09	Cattle	Cofradia de Navolato
RM9456	O157:H7	07-Apr-09	Cattle	Cofradia de Navolato
RM9458	O157:H7	24-Mar-09	Chicken	Agua Caliente
RM9462	O157:H7	03-Jun-09	Cattle	Iraguato
RM13865	O75:H8	07-Apr-09	Cattle	Cofradia de Navolato

^aNT, Non-typeable H-antigen.

^bSampling sites correspond to regions in the Culiacan Valley, Sinaloa, Mexico (Amézquita-López et al., 2012).

The method employed to isolate the STEC strains (Table 1) from fecal samples from various domestic animals was previously described (Amézquita-López et al., 2012). The characteristics and sources of the STEC reference strains that were used in this study are described in Table 2. Bacteria were routinely propagated under aerobic conditions at 37°C on Luria-Bertani (LB) agar (Difco, Detroit, MI).

Table 2.

Shiga toxin-producing Escherichia coli reference strains used in this study.

Strain	Other strain designations	Serotype	Source	Location	Provider or referencea
RM2084	EDL-933; DEC 4f	O157:H7	Meat	United States	ECRC (Reid et al., 1999)
RM7004	E32511; TW02883	O157:H	Human	United States	The STEC Center (Schmitt et al., 1991)
RM7005	EH250; TW081611	O118:H12	Human	Belgium	The STEC Center (Piérard et al., 1998)
RM7006	B2F1; TW01393	O91:H21	Human	Canada	The STEC Center (Ito et al., 1990)
RM7110	NADC2228; S1191	O139:NM	Pig	United States	Evelyn Dean-Nystrom (Weinstein et al., 1988)
RM7203	SC-0012	O168:H8	Coyote	United States	Michael B. Cooley (Cooley et al., 2013)
RM7369	SP-0082-G9	ONT:H7	Pig	United States	Michael B. Cooley (Cooley et al., 2013)
RM7508	MA146B-A7	O128:H2	Deer	United States	Michael B. Cooley (Cooley et al., 2013)
RM7519	F260-H2	O113:H21	Cattle	United States	Michael B. Cooley (Cooley et al., 2013)

^aContact information of strain providers: ECRC, E. coli Reference Center, College of Agricultural Sciences, The Pennsylvania State University, University Park, PA, USA; The STEC Center, National Food Safety and Toxicology Center, Michigan State University, East Lansing, MI, USA; Michael B. Cooley, USDA/ARS, Western, Regional Research Center, Produce Safety and Microbiology Research Unit, Albany, CA, USA; Evelyn Dean-Nystrom, Iowa State University, National Animal Disease Center, Veterinary Microbiology and Preventive Medicine, Ames, Iowa, USA.

Polymerase chain reaction for amplification of stx subtypes and other virulence genes

For the detection of stx subtypes and other virulence genes, the following STEC reference strains (Table 2) were used as a control for the PCR amplification of ent/espL2, espK, espN, espP, etpD, ihA, katP, nleA, nleB, nleE, nleH1-2, sheA, stx_1a, and stx_2a (RM2084); stx_2c (RM7004); stx_2b (RM7005); saa and stx_2d (RM7006); stx_2f (RM7007); stx_2e (RM7110); stx_2g (RM7203); stx_1d (RM7369); stx_1c (RM7508); hlyA (RM10227). All PCR amplifications were performed by using primers as shown in Table 3. As template for the PCR reaction, cultures of the STEC strains were grown aerobically in tryptic soy broth (Beckton Dickinson, Sparks, MD) for 24 h with constant shaking (200 rpm) at 37°C, and 100 μL of the bacterial cultures were collected by centrifugation at 2000 ×g for 5 min. Cell pellets were resuspended in 100 μl of HyPure™ molecular biology-grade water (HyClone Laboratories, Inc., Logan, UT) and incubated at 95°C for 20 min, as in previous studies (Quiñones et al., 2011, 2012). The lysates were centrifuged at 2000 ×g for 5 min, and the supernatants were collected and frozen until further use. The PCR amplifications consisted of a 25 μl reaction mixture, each containing 5 μL of the bacterial crude lysate, 0.5 μM of each primer (Eurofins MWG Operon, Huntsville, AL), and 12.5 μl of 2× GoTaq® Green Master Mix (Promega Corporation, Madison, WI). The reaction mixtures were placed in a Dyad Peltier Thermal Cycler (Bio-Rad Laboratories, Hercules, CA), as in previous studies (Amézquita-López et al., 2012). The virulence genes were amplified with PCR cycling conditions, as described in the references listed in Table 3. Amplified products were analyzed in 2% agarose gels containing 0.04 μl/ml GelRed Nucleic Acid Stain (Phenix Research, Candler, NC).

Table 3.

List of DNA oligonucleotides used in this study for PCR amplification.

Target genea	Forward sequence (5′ → 3′)	Reverse sequence (5′ → 3′)	Amplicon size (bp)	Reference
ent/espL2	CACATCATTAGAAGTTCATT	AGTCCTGCTCCCATAGCAAA	342	Quiñones et al., 2012
espK	GTAGCGCCACAGACAGCATA	ATCAGGCATCCCTTCAACAC	242	Kyle et al., 2012
espN	TTTCTTTCGTGACGCTGATG	GCACCGGAGAATCATCGTAT	155	Kyle et al., 2012
espP	GCACTGTCTGGCGGTGAATA	CGTCCAGATTCCCGTTTATG	202	Quiñones et al., 2012
etpD	TTGGATGACGGCGAAACTG	AGATGATACGCTGTTGGGAG	85	Bugarel et al., 2010b
hlyA	GTCTGCAAAGCAATCCGCTGCAAATAAA	CTGTGTCCACGAGTTGGTTGATTAG	561	Kerényi et al., 2005
iha	GTGATGATTGTCTCGGCATC	GTAACTGGCTGGCATTCCWC	207	Kyle et al., 2012
katP	GCGGAAGAGAAGATGACTGG	GCACCATGTGCTTTACCAAA	277	Quiñones et al., 2012
nleA	TGGATTAACDGCTCARGTDGTTCG	GCATTGGTAAGYARGGCATA	267	Kyle et al., 2012
nleB	GGAAGTTTGTTTACAGAGACG	AAAATGCCGCTTGATACC	297	Coombes et al., 2008
nleE	GTATAACCAGAGGAGTAGC	GATCTTACAACAAATGTCC	260	Coombes et al., 2008
nleH1-2	GCCTGATAATCGTGTTTTATC	CGCATAATCCACTGGAGGTAA	295	Kyle et al., 2012
saa	CCAATCAACAGTTTCGTCAA	GCAATAGCCTGTTCATCACG	166	Quiñones et al., 2012
sheA	GAGGCGAATGATTATGACTG	ACTTCAGGTACCTCAAAGAG	920	Kerényi et al., 2005
stx1a	CACGTTACAGCGTGTTGCA	CGCCCACTGAGATCATCC	219	Kyle et al., 2012
stx1c	GAACGAAATAATTTATATGT	CTCATTAGGTACAATTCT	555	Koch et al., 2001
stx1d	CTTTTCAGTTAATGCGATTGCT	AACCCCATGATATCGACTGC	192	Bürk et al., 2003
stx2a	AGATATCGACCCCTCTTGAA	GTCAACCTTCACTGTAAATG	969	Nakao et al., 2002
stx2b	TATACGATGACACCGGAAGAAG	CCTGCGATTCAGAAAAGCAGC	300	Nakao et al., 2002
stx2c	TTTTATATACAACGGGTA	GGCCACTTTTACTGTGAATGTA	163	Nakao et al., 2002; Zheng et al., 2008
stx2d	CTTTATATACAACGGGTG	CTGAATTGTGACACAGATTAC	359	Zheng et al., 2008
stx2e	CAGGAAGTTATATTTCCGTAGG	GTATTCTCTTCCTGACACCTTC	911	Nakao et al., 2002
stx2f	TTTACTGTGGATTTCTCTTCGC	TCAGTAAGATCCTGAGGCTTG	875	Nakao et al., 2002
stx2g	GTTATATTTCTGTGGATATC	GAATAACCGCTACAGTA	573	Leung et al., 2003
subA	CGGCTTATCATCCTGTCAGC	TATAGCTGTTGCTTCTGACG	233	Quiñones et al., 2012

^aThe stx₁ and stx₂ subtypes are listed with new stx nomenclature, as recently described (Feng et al., 2011; Scheutz et al., 2012)

Vero cell-based method to detect STX activity

The Stx activity of the STEC strains was measured using a Vero cell line, Vero-d2EGFP, that harbored a destabilized variant (t_1/2 = 2 h) of the enhanced green fluorescent protein (EGFP) (Quiñones et al., 2009; Quiñones and Swimley, 2011). To monitor the Stx-induced inhibition of protein synthesis, the tested STEC strains (Table 1), the Stx-expressing O157:H7 strain RM2084 (positive control) (Table 2), and the Stx-negative O157:H4 strain RM8928 (Amézquita-López et al., 2012) (negative control) were inoculated in 1 ml of sterile LB broth (Difco, Detroit, MI). All E. coli strains were grown aerobically for 24 h at 37°C with shaking at 200 rpm and were then centrifuged at 2000 ×g for 15 min. The culture supernatants were filter-sterilized using 0.45 μm polyvinylidene fluoride syringe filters (Durapore® membranes, Millipore Corporation, Billerica, MA) and were frozen at −20°C until further use (Quiñones and Swimley, 2011). One day prior to intoxication, the Vero-d2EGFP cells were seeded at 10,000 cells per well in Greiner black 96-well microplates with clear bottoms (VWR International, Aurora, CO) and were grown at 5% CO₂ and 37°C under humidified conditions in Ham's F-12 complete medium, supplemented with 10% fetal bovine serum and 1% penicillin-streptomycin (Gibco BRL, Grand Island, NY) (Quiñones et al., 2009; Quiñones and Swimley, 2011). The Vero-d2EGFP cells were then exposed to Ham's F-12 complete medium containing a tenfold dilution of the cell-free supernatants from each strain and were incubated for 16 h at 37°C in a 5% CO₂ humidified incubator. The EGFP fluorescence from the Vero-d2EGFP cells was measured using a Synergy HT Multi-Detection Microplate Reader (BioTek, Winooski, VT) with the 485/20 nm excitation filter and the 528/20 nm emission filter (Quiñones et al., 2009; Quiñones and Swimley, 2011). All measurements were performed in triplicate, and the results were expressed as percentages of the fluorescence values obtained for culture supernatant-treated Vero-d2EGFP cells when compared to the fluorescence values from control Vero-d2EGFP cells incubated without culture supernatants. To determine statistical differences in the Stx activity among the STEC strains, the results were analyzed by performing a k-means clustering using the Hartigan and Wong algorithm (Hartigan and Wong, 1979) with the R Statistical Software (version 3.0.1; R Foundation for Statistical Computing, Vienna, Austria) (R-Core Team, 2013). The distinct clusters were further validated by measuring the Dunn Index with the clValid R Package (Brock et al., 2008).

Results

Virulence gene profiles of STEC strains from domestic farm animals

To further characterize the virulence potential of STEC strains recovered from domestic farm animals in the agricultural Culiacan Valley region in Mexico, the presence of genes, associated with pathogenic STEC strains, was identified. Our initial analysis focused on the identification of the subtypes of Stx, a virulence factor that has been attributed to the development of serious disease symptoms in humans (Karmali et al., 2010; Bolton, 2011; Melton-Celsa et al., 2012). The results indicated that 97% (28/29) of the O157 and non-O157 STEC strains, recovered from sheep, cattle and chickens, were PCR-positive for genes encoding stx₂ subtypes (Table 4). By contrast, stx₁ subtypes were only identified in the non-O157 strains from sheep and cattle. Interestingly, the stx_2c subtype was detected in 51% (15/29) of the strains selected from the different animal sources and was predominantly identified in strains with the O157:H7 serotype (Table 4). Furthermore, the stx_2d subtype was only identified in the ovine strain RM8749 belonging to serotype O20:H4. Our results also demonstrated that 45% (13/29) of the recovered STEC strains were positive for more than one gene encoding stx subtypes in the same strain. In particular, strains with serotypes O73:H4, O75:H8, O146:H8, and O146:H21 were found to harbor the stx gene profile stx_1a, stx_1c, and stx_2b (Table 4). Moreover, the stx gene profile stx_1a, stx_2a, and stx_2c was exclusively found in the O8:H19 strains recovered from cattle. None of the STEC strains recovered from domestic animals in rural farms in the Culiacan Valley were PCR-positive for the stx subtypes stx_1d, stx_2e, stx_2f, or stx_2g.

Table 4.

Identification of virulence genes in E. coli O157 and non-O157 strains used in this study.

Serotype	Strain	Source	Virulence profile
O8:H19	RM8772	Cattle	espP, saa, stx1a, stx2a, stx2c, subA
	RM8776	Cattle
O15:NT	RM8747	Cattle	ent/espL2, espP, katP, stx2c
O20:H4	RM8749	Sheep	stx2d
O73:NT	RM8748	Cattle	ent/espL2, espP, katP, stx2a
O73:H4	RM8745	Sheep	stx1a, stx1c, stx2b
O75:H8	RM8752	Sheep	iha, sheA, stx1a, stx1c, stx2b
	RM8760	Sheep
	RM8763	Sheep
	RM8778	Sheep
	RM8923	Cattle
	RM8929	Sheep
	RM13865	Cattle
O111:H8	RM8755	Sheep	ent/espL2, espK, espN, iha, nleA, nleB, nleE, nleH1-2, sheA, stx1a
O146:H8	RM8762	Sheep	iha, sheA, stx1a, stx1c, stx2b
O146:H21	RM8756	Sheep	iha, sheA, stx1a, stx1c, stx2b
	RM8761	Sheep
O157:H7	RM8744	Cattle	ent/espL2, espK, espN, espP, etpD, iha, katP, nleA, nleB, nleE, nleH1-2, sheA, stx2c
	RM8753	Sheep
	RM8759	Sheep
	RM8768	Cattle
	RM8781	Sheep
	RM8922	Cattle
	RM9450	Sheep
	RM9452	Sheep
	RM9454	Cattle
	RM9456	Cattle
	RM9458	Chicken
	RM9462	Cattle

Given that Stx is not the only virulence determinant that is responsible for full pathogenicity (Karmali et al., 2010; Bolton, 2011; Melton-Celsa et al., 2012), the STEC strains isolated from this agricultural region were further screened for the presence of additional markers encoding adhesins, cytotoxins, proteases, and other effectors. The virulence typing analysis revealed the presence of the non-LEE encoded effectors, nleA, nleB, nleE, and nleH1-2, in the recovered O157:H7 strains from sheep, cattle, and chicken as well as in the recovered O111:H8 strains from sheep (Table 4). Other effectors, espK, and espN, were also identified in the O157:H7 and O111:H8 strains. However, the plasmid-encoded etpD gene was only detected in the O157:H7 strains. Furthermore, saa and subA genes were exclusively identified in the O8:H19 cattle strains (Table 4). Finally, the iron-regulated adhesion gene (iha) and the cytolysin A gene (sheA) were both present in 79% (23/29) of the non-O157 and O157 strains. The ovine strains belonging to serotypes O20:H4 and O73:H4 were found to be negative for the presence of the accessory virulence determinants that were tested in the present study (Table 4).

STX activity in STEC strains isolated from domestic farm animals

A quantitative and sensitive cell-based assay was further employed to examine the activity of the Stxs expressed by the O157 and non-O157 strains recovered from domestic animals in the Culiacan Valley. A Vero cell line, Vero-d2EGFP, was employed to measure the inhibition of protein synthesis by Stx in mammalian cells (Quiñones et al., 2009; Quiñones and Swimley, 2011). Consequently, incubation with active Stx results in a reduction of the EGFP fluorescent signal that is detected from the Vero-d2EGFP cells (Quiñones et al., 2009; Quiñones and Swimley, 2011). Our results indicated low levels of fluorescence, ranging from 5.4 to 19.5%, were observed when the Vero-d2EGFP cells were incubated with culture supernatants from several STEC strains with the serotypes O8:H19, O75:H8, and O146:H8 (Figure 1), recovered from sheep and cattle. Further statistical analysis of the detected EGFP fluorescence indicated that these STEC strains with serotypes O8:H19, O75:H8 and O146:H8 belong to the same k-means cluster, suggesting that the Stx expressed by these non-O157 strains had similar effects on the EGFP fluorescence. Moreover, significantly reduced levels of EGFP fluorescence to approximately 16.7% were also observed after incubation with cell-free culture supernatants from the positive control O157:H7 strain RM2084 (Figure 1).

Figure 1.

Effect of Escherichia coli O157 and non-O157 culture supernatants on Vero-d2EGFP fluorescence. Vero-d2EGFP cells were incubated in Ham's F-12 complete medium containing tenfold dilutions of cell-free culture supernatants from the tested Escherichia coli O157 and non-O157 strains (Table 1). Cell-free culture supernatants from the Stx-producing E. coli O157:H7 strain RM2084 and from the non-Stx producing E. coli O157:H4 strain RM8928 were used as positive and negative controls, respectively. The average ± standard deviation of three independent experiments with duplicate samples for each strain is shown. Bars with the same lowercase letter represent significantly distinct clusters according to the k-means clustering algorithm and the clValid R Software package (Brock et al., 2008; R-Core Team, 2013).

Intermediate levels of EGFP fluorescence, ranging from 22.9 to 32.4% were observed after incubation with culture supernatants from the ovine STEC strains belonging to serotypes O20:H4, O73:H4, O111:H8, and O146:H21. Interestingly, analysis of the culture supernatants from all O157:H7strains, recovered from sheep, cattle and chickens in the Culiacan Valley, resulted in significantly higher levels of EGFP fluorescence (Figure 1). The levels of EGFP fluorescence when testing the supernatants from the O157:H7 strains in the Vero-cell based assay ranged from 38.0 to 62.6%. High levels of EGFP fluorescence that also belong to the same k-means cluster group as the O157:H7 strains were also observed when testing culture supernatants from the O15:NT and O73:NT strains (Figure 1). No reduction of EGFP fluorescence, averaging 98% detected fluorescence, was observed after incubation with culture supernatants from the negative control O157:H4 strain RM8928 strain lacking an stx gene (Figure 1). The fluorescence in the Vero-d2EGFP cells still remained when testing culture supernatants from an stx-negative O157:H7 strain RM4876 (Quiñones et al., 2009) or after incubation with bacterial growth media without toxin added (data not shown).

Discussion

In the present study, a genotyping and functional analysis was conducted to further characterize STEC strains, recovered from domestic animals in rural farms in the Culiacan Valley, which is considered one of the most important agricultural regions in Mexico (Amézquita-López et al., 2012). Given that the rural farms were located in communities that may not follow efficient management of animal wastes (Jiménez et al., 2011; Amézquita-López et al., 2012), an understanding of the virulence potential of the STEC strains recovered from animal reservoirs in this agricultural region would assist in the development of control measures to prevent the dispersal and transmission of pathogens throughout the environment that could lead to human infections associated with STEC.

The virulence typing analysis revealed that all O157:H7 and O111:H8 STEC strains from domestic animal reservoirs in the Culiacan Valley were positive for several of the nle genes, known to be located in the genomic islands OI-122 and OI-71 (Coombes et al., 2008). A previous study showed that these O157 and O111 STEC strains were also positive for eae (Amézquita-López et al., 2012). Thus, these findings revealed that these STEC strains from the Culiacan Valley harbor the gene signature, eae, ent/espL2, nleA, nleB, nleF, and nleH1-2, which has been proposed to be present in STEC strains with high virulence for humans (Bugarel et al., 2010a). Moreover, EtpD, the pO157 plasmid-encoded type II secretory pathway protein (Burland et al., 1998), was exclusively identified in O157:H7 strains. Finally, the STEC autoagglutinating adhesin (Saa) and subtilase cytotoxin (SubA) were specifically detected in the O8:H19 cattle strains, previously shown to be eae-negative and to display a limited genomic diversity by multiple-locus variable-number tandem repeat analysis (Amézquita-López et al., 2012). The findings from the present study are in agreement with other reports that documented Saa and SubA to be associated with non-O157 LEE-negative strains (Paton et al., 2001; Jenkins et al., 2003; Kumar et al., 2004; Toma et al., 2004; Zweifel et al., 2004; Kobayashi et al., 2013).

Approximately 79% of the O157 and non-O157 recovered STEC harbored both the iha and sheA genes. Previous studies demonstrated that iha, which codes for the iron-regulated gene A homolog adhesin, has been commonly observed in both LEE-positive as well as LEE-negative strains with different serotypes (Tarr et al., 2000; Schmidt et al., 2001). Moreover, sheA, encoding the cytolysin A or “silent hemolysin” has been shown to be prevalent in certain non-pathogenic E coli strains and in other enteropathogenic E. coli strains (Del Castillo et al., 1997; Fernández et al., 1998; Ludwig et al., 2004). All O157:H7 strains were positive for katP, a gene mostly identified in STEC strains belonging to seropathotypes associated with HUS (Bugarel et al., 2010b, 2011; Kobayashi et al., 2013). However, the present study also detected katP in O73:NT and O15:NT strains, belonging to serogroups not implicated in causing any human illness (Hussein, 2007).

To examine the relative toxicities of Stx subtypes expressed by the recovered STEC strains, the Vero-d2EGFP fluorescent assay was employed. The assay uses the Vero-d2EGFP cell line, expressing a destabilized variant of EGFP (Quiñones et al., 2009), and measures in mammalian cells the inhibition of protein synthesis by Stx (Quiñones et al., 2009; Quiñones and Swimley, 2011). Given that Vero cells are highly responsive to the effects of Stx (Keusch et al., 1995), the Vero-d2EGFP fluorescent assay is thus a sensitive and quantitative method to examine the potential relative toxicities of STEC strains. The results from the present study demonstrated that STEC strains with serotypes O8:H19, O75:H8, and O146:H8, serotypes previously associated with severe disease in humans (Boerlin et al., 1999; Blanco et al., 2003; Hussein, 2007), displayed a significant reduction in the EGFP signal from the Vero-d2EGFP cells to similar levels as the positive control O157:H7 strain RM2084. Moreover, the molecular typing study revealed that the stx gene profile stx_1a, stx_2a, and stx_2c was exclusively found in the O8:H19 cattle strains while the stx_1a, stx_1c, and stx_2b profile was detected in the O73:H4, O75:H8, O146:H8 and O146:H21 strains from cattle and sheep. In summary, these findings have indicated that these non-O157 strains, possessing multiple stx subtypes, appear to be more efficient at inhibiting protein synthesis in mammalian cells.

Interestingly, analysis of the Stx activity from the stx_2c-positive O157:H7 strains, recovered from chicken, cattle, and sheep in the Culiacan Valley, indicated that the Vero-d2EGFP fluorescence levels were on average threefold higher when compared to the positive control O157:H7 strain RM2084. These findings suggested that the O157:H7 strains from this region in Mexico may have a significantly lower ability to inhibit protein synthesis in mammalian cells. Previous reports have documented that the Stx2a, Stx2c, and Stx2d subtypes have been associated with severe disease symptoms, including HUS and bloody diarrhea, as well as with differential toxicities in mammalian cells (Friedrich et al., 2002; Ethelberg et al., 2004; Persson et al., 2007; Manning et al., 2008; Müthing et al., 2009; Fuller et al., 2011; Quiñones and Swimley, 2011). However, recent evidence has indicated that purified Stx2c appears to have a reduced potency at inhibiting protein synthesis and metabolic activity in mammalian cells and a lower toxicity in mice (Fuller et al., 2011). The findings from the present study have demonstrated that the stx_2c-positive O157:H7 strains from this region in Mexico, previously shown to be closely-related by multiple-locus variable-number tandem repeat analysis (Amézquita-López et al., 2012), were less toxic to Vero cells although they possessed other key accessory virulence factors.

Previous reports have documented that the amounts of Stx2 produced may define the severity of disease caused by STEC strains (Zhang et al., 2000; Dean-Nystrom et al., 2003; Muniesa et al., 2004), and the differential expression and induction of Stx2 subtypes appears to contribute to the relative virulence of the STEC strain (Muniesa et al., 2004; Zhang et al., 2005; De Sablet et al., 2008). Therefore, future work is aimed at further characterizing the amounts of Stx produced after induction under different conditions to obtain a more detail understanding of the pathogenic potential of O157 and non-O157 STEC strains from diverse sampling sites and sampling sources in the agricultural Culiacan Valley region in Mexico.

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.