The Open Microbiology Journal




ISSN: 1874-2858 ― Volume 13, 2019

Presence of a Human Diarrheagenic Escherichia coli Clone in Captivity Kept Psittacidaes



Guilherme A Marietto-Gonçalves1, Silvia M de Almeida2, Josias Rodrigues1, *
1 Department of Microbiology and Immunology, IB-UNESP, Botucatu SP, Brazil
2 Floravida Institute, Botucatu SP, Brazil

Abstract

Bacterial cultures of cloaca swabs from 86 captivity kept psittacidaes revealed 17 Escherichia coli bearing birds sharing strains which, on the basis of enterobacterial repetitive intergenic consensus (ERIC) PCR analysis, proved to be genetically similar. Further, triplex PCR specific for the genetic markers chuA, yjaA, and TSPE4.C2 was used to assign the strains to the E. coli reference collection (EcoR) B2 group. One strain of each, from the enteropathogenic (EPEC), enteroaggregative (EAEC) and Shiga toxin (STEC) E. coli pathovars were found among these isolates.

Keywords: Shiga-toxin, diarrhea, parrots, parakeets, Escherichia coli.


Article Information


Identifiers and Pagination:

Year: 2011
Volume: 5
First Page: 72
Last Page: 75
Publisher Id: TOMICROJ-5-72
DOI: 10.2174/1874285801105010072

Article History:

Received Date: 30/4/2011
Revision Received Date: 10/5/2011
Acceptance Date: 12/5/2011
Electronic publication date: 20/7/2011
Collection year: 2011

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© Marietto-Gonçalves et al.; Licensee Bentham Open.

open-access license: This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.


* Address correspondence to this author at the Department of Microbiology and Immunology, Institute of Bioscience of the São Paulo State University in Botucatu, ZIP 18618-970, Botucatu, SP Brazil; Tel: 055 14 3811-6240; E-mail: josias@ibb.unesp.br





INTRODUCTION

Psittacidae comprise parrots and parakeets, which are often home cared as pets or found in many recreational zoos. In their natural habitats, they rarely have contact with the soil; their water supply comes from the fruits and some flowers rainfall deposits. As a consequence of this limited soil contact and eventual access to contaminated water, their alimentary tract´s microbiota shows a reduced presence of gram negative bacteria, such as E. coli [1Flammer K, Drewes LA. Species related differences in the incidence of gram-negative bacteria isolated from the cloaca of clinically normal psittacine birds Avian Dis 1988; 32: 79-83.-3Schremmer C, Lohr JE, Wastlhuber U, et al. Enteropathogenic Escherichia coli in Psittaciformes Avian Pathol 1999; 28: 349-54.]. In the case of home pets and institutional captivity kept birds, bacterial contamination is facilitated by contact with humans, aggregated animals and the environment [4Mattes BR, Consiglio SAS, Almeida BZ, et al. Influência da Biossegurança na colonização intestinal por Escherichia coli em Psitacídeos Arq Inst Biol 2005; 72: 13-6.]. In Brazil, illegally owned wild birds recovered by environmental police are usually kept in quarantine in Official Environmental Control Agencies or Non-Government Organizations facilities, which monitor eventual carriage of potential pathogens, before their re-introduction into natural habitats.

Pathogenic E. coli are classified in distinct categories according to their virulence properties, symptoms of diseases that they cause, species and age group where they are found. These criteria have been the basis for the division of human diarrheagenic E. coli (DEC) in at least five categories [5Nataro JP, Kaper JB. Diarrheagenic Escherichia coli Clin Microbiol Rev 1998; 11: 42-201.]: enteropathogenic (EPEC), enterotoxigenic (ETEC), enteroinvasive (EIEC), enterohemorrhagic (EHEC), and enteroaggregative (EAEC) E. coli. EPEC are an important agent of infantile diarrhea in developing countries; EIEC share several features with Shigella including the ability to cause dysentery in school-age children; EHEC potentially cause both hemorrhagic colitis and the hemolytic uremic syndrome; ETEC are a traveler’s cholera-like diarrhea agent; EAEC are an emerging agent of protracted diarrhea found in both developed and developing countries.

The possibility of captivity-kept psittacidaes to harbor pathogenic DEC was here investigated by analyzing cloacae swabs of 16 white-eyed conure (Aratinga leucophthalmus) and 70 blue-fronted parrots (Amazonia aestiva). The birds were in a good health condition, fed with fruits and sunflower seeds and potable water and separated in groups of eight per regularly cleaned wired suspended cages. Originally recovered from illegal owners, they were under care and observation quarantine by experts from the Floravida Institute, Botucatu SP Brazil, for at least one year, in preparation for re-introduction into their natural habitats. Following collection, swabbed samples (one per bird) were pre-cultured overnight at 40ºC in alkaline peptone water and in selenite-cysteine broth. The enrichment cultures growth was then simultaneously streaked in Hektoen and MacConkey agars and incubated under the above culture condition. Finally, a number from 3-to-5 distinct and well-isolated colonies were individually subjected to biochemical tests for bacterial identification. This enabled the detection of E. coli in 4 of the 16 (25%) white-eyed conure and in 13 of the 70 (18.6%) blue-fronted parrots. The isolates were then cultured at 37ºC overnight in trypticase soy broth (TSB) and the resulting growth added with 20% glycerol (Sigma) and stored at -80°C.

When multiple isolates from single birds showed identical biochemical profiles, only a single isolate per bird was taken for subsequent analyses, which consisted of screening for the following virulence-related features: Congo red adsorption (CRA), antibiotic resistance, hemolytic activity, HEp-2 cells adhesion, and presence of DEC-specific virulence genes.

CRA and hemolytic activity tests were performed by streaking overnight TSB cultures respectively in Congo red and blood agar (Columbia agar base mixed with 5% de-fibrinated sheep blood) plates, incubation for 18-24h and observation of corresponding colonies phenotypes. Antibiotic bacterial resistance was tested by the disc-diffusion method against the following drugs: ciprofloxacin, chloramphenicol, enrofloxacin, gentamicin, streptomycin, sulphamycin, tetracycline and trimethoprim. Unless otherwise indicated, all the culture media employed were from Difco (Heidelberg, Germany) or Oxoid (Hampshire, UK).

HEp-2 cell adhesion tests were performed according to the original method of Cravioto et al. [6Cravioto A, Gross RJ, Scotland SM, Rowe B. An adhesive factor found in strains of Escherichia coli belonging to the traditional infantile enteropathogenic serotypes Curr Microbiol 1979; 3: 95-.]. Twenty microliters of overnight bacterial cultures in TSB were added to semi-confluent grown HEp-2 cell monolayers in chamber-slides (Nalge Nunc, Rochester, USA) containing 0.7 – 1.0 ml of Eagle essential minimum medium (Sigma, St. Louis, USA) supplied with 10% fetal calf serum (Cultilab, Campinas, Brazil) and added with 1% D-mannose (Sigma, St. Louis, USA). The preparations were incubated for 3h at 37°C in 5% CO2 atmosphere and then washed three times with phosphate buffered saline. Following methanol fixation, Giemsa staining, chamber removal and drying, the slides were observed at light microscope for cell monolayer attached bacteria. In surveys of at least 200 cells, adherent strains were those showing a minimum average number of 1 bacterium/HEp-2 cell. They were classified according to their adherent phenotypes in aggregative (AA), diffuse (DA) and localized (LA).

The E. coli isolates were screened by multiplex-PCR with primers specific for the following genetic markers [7Toma C, Lu Y, Higa N, et al. Multiplex PCR assay for identification of human diarrheagenic Escherichia coli J Clin Microbiol 2003; 41: 2669-71.]: ipaH, aggR, eae, stx and elt, respectively for EIEC, EAEC, EPEC, EHEC and ETEC. The reaction mixture, in a total volume of 50 μl, consisted of 1x reaction buffer, 0.15 mM MgCl2, 0.2 mM of dNTP mix (Promega, Madison, USA), 0.125 μM each of SK1, SK2, ipaIII, and ipaIV primers, 0.25 μM VTcom-u, VTcom-d, LTL, LTR, aggRks1 and aggRk2, 2.5 U Taq DNA polymerase (Promega, Madison, USA) and 5 μl of bacterial lysates. Reactions were run at 95°C/1min, 52°C/1min and 72°C/1min for 30 cycles and 72°C for 10 min in a Mastercycler pro S (Eppendorf, Hamburg, Germany). PCR products were submitted to electrophoresis in 1% agarose gels containing 104 X diluted GelRed (Biotium, California, USA) DNA stain and observed in an image capture device coupled UV transiluminator (Alpha Innotech, San Leandro, USA). In addition to the above mentioned genetic markers, PCR for the irp2 and shf – sequences commonly found in different pathogenic E. coli, particularly diffusely adhering strains and EAEC [8Czeczulin JR, Whittam TS, Henderson IR, Navarro-Garcia F, Nataro JP. Phylogenetic analysis of enteroaggregative and diffusely adherent Escherichia coli Infect Immun 1999; 67: 2692-9.,9Kahali S, Sarkar B, Rajendran K, et al. Virulence characteristics and molecular epidemiology of enteroaggregative Escherichia coli isolates from hospitalized diarrheal patients in Kolkata, India J Clin Microbiol 2004; 42: 4111-20.] – were performed. E. coli K12 HB101 strain was selected as a PCR-negative control and E2348-69, O42, 40T, EHY, and EIX, as EPEC, EAEC, ETEC, EHEC and EIEC positive controls, respectively. Genetic similarity among the strains were investigated by ERIC2-PCR [10Johnson JR, O’Bryan TT. Improved repetitive element PCR fingerprinting for resolving pathogenic and nonpathogenic phylogenetic groups within Escherichia coli Clin Diagn Lab Immunol 2000; 7: 265-73.], and their identity with E. coli reference (EcoR) groups [11Ochman H, Selander RK. Standard reference strains of Escherichia coli from natural populations J Bacteriol 1984; 157: 690-3.] analyzed on the basis of combination of distinct amplicons generated by triplex PCR specific for chuA, yjaA, and TSPE4.C2, as previously described [12Clermont O, Bonacorsi S, Bingen E. Rapid and simple determination of the Escherichia coli phylogenetic group Appl Environ Microbiol 2000; 66: 4555-8.].

When submitted to ERIC2-PCR, DNA of the 17 strains from distinct birds generated identical band profiles (Fig. 1). Genetic similarity could also be observed from the EcoR PCR typing results: all the strains had chuA, yjaA, and TSPE4.C2, a gene combination corresponding to the EcoR B2 group [12Clermont O, Bonacorsi S, Bingen E. Rapid and simple determination of the Escherichia coli phylogenetic group Appl Environ Microbiol 2000; 66: 4555-8.].

Fig. (1)

DNA fingerprints from ERIC2 PCR of 17 E. coli strains individually isolated from 17 distinct psittacidae birds.



Fig. (2)

Localized adhesion to HEp-2 cells expressed by the irp2-eae-bfpA+ strain (N° 8 labeled in Table 1), after a 3h incubation period of contact bacteria-cells. May-Grunwald/Giemsa dye stained preparation. Magnification: 1000x.



Table 1 presents the virulence features of psittacidae E. coli. Five strains expressed DA, one AA and one LA (Fig. 2). One strain caused cytotoxic effect, leading to HEp-2 cell fragmentation and detachment (Table 1). A high prevalence (70.5%) of CRA+ strains was observed within this E. coli population. Over 50% of psittacidae E. coli were hemolytic and the majority of strains harbored some of the virulence genes searched for. The cytotoxic effect causing strain was PCR positive for stx and the LA+ strain had eae (Table 1). Since along with bfpA, LA and eae distinguish EPEC, an additional PCR for the bundle forming pilus gene permitted the typing of the LA+ strain as belonging to the typical EPEC pathotype. Based on the above results, three DEC strains were recognized among the 17 psittacidae E. coli: one Shiga toxin E. coli (STEC), one atypical EAEC (AA+, aggR-), and one typical EPEC.

Table 1

Virulence Properties of 17 E. coli Strains Belonging to the EcoR B2 Group Isolated from Psittacidaes




Antibiotic resistance was observed for at least one of the eight drugs tested and a higher prevalence of resistant strains was for sulphamycin and chloramphenicol (82.3 and 70.6%, respectively). Multidrug resistant strains include EAEC and STEC, which were the single TetR and StrR-TriR strains detected, respectively (Table 1).

Although E. coli can be pathogenic for humans, the significance of their association with psittacidaes is controversial. Enteric microbiota in these birds is mostly comprised of gram-positive [1Flammer K, Drewes LA. Species related differences in the incidence of gram-negative bacteria isolated from the cloaca of clinically normal psittacine birds Avian Dis 1988; 32: 79-83.] and for some authors [2Grahan CL, Grahan DL. Occurrence of Escherichia coli in feces of Psittacine birds Avian Dis 1978; 22: 717-20.] the mere observation of E. coli in feces of a bird presented with enteritis could be significant enough to relate the bacteria with the symptoms. Yet, reports of E. coli isolation from psittacidaes are abundant, even in clinically healthy birds [1Flammer K, Drewes LA. Species related differences in the incidence of gram-negative bacteria isolated from the cloaca of clinically normal psittacine birds Avian Dis 1988; 32: 79-83.], sometimes in figures as high as 80% [4Mattes BR, Consiglio SAS, Almeida BZ, et al. Influência da Biossegurança na colonização intestinal por Escherichia coli em Psitacídeos Arq Inst Biol 2005; 72: 13-6.]. E. coli incidence varies according to the host psittacidae species [1Flammer K, Drewes LA. Species related differences in the incidence of gram-negative bacteria isolated from the cloaca of clinically normal psittacine birds Avian Dis 1988; 32: 79-83.], hygiene conditions and possibly the human contact [4Mattes BR, Consiglio SAS, Almeida BZ, et al. Influência da Biossegurança na colonização intestinal por Escherichia coli em Psitacídeos Arq Inst Biol 2005; 72: 13-6.]. The E. coli prevalence observed here – 25% for white-eyed conure and 18.6% for blue-fronted parrot – are not too different from previously reported results [1Flammer K, Drewes LA. Species related differences in the incidence of gram-negative bacteria isolated from the cloaca of clinically normal psittacine birds Avian Dis 1988; 32: 79-83.,3Schremmer C, Lohr JE, Wastlhuber U, et al. Enteropathogenic Escherichia coli in Psittaciformes Avian Pathol 1999; 28: 349-54.].

CRA, a frequently employed approach to identify chicken colisepticemic invasive E. coli, has previously been used to differentiate potentially virulent from innocuous psittacidae E. coli [13Styles K, Flammer K. Congo red binding of Escherichia coli from the cloacae of psittacine birds Avian Dis 1991; 35: 46-8.]. Accordingly, CRA+ isolates are found only in birds presenting clinical signs of illness, apparent behavioral change or physical debility. However data shown here do not support this conclusion, because, although 12 of 17 (70.5%) birds harbored CRA+ strains, all of them were in a good health and adapted to their condition at the time of sample collection.

Apart from the role played by these bacteria in their bird host, the virulence markers that they possess grant the recognition of them as human pathogens. Significant difference is observed in E. coli prevalence between birds kept under strict hygiene rules and limited human contact and those of public recreational parks and zoos, with very higher figures for the later [4Mattes BR, Consiglio SAS, Almeida BZ, et al. Influência da Biossegurança na colonização intestinal por Escherichia coli em Psitacídeos Arq Inst Biol 2005; 72: 13-6.], in an indication of birds’ bacterial contamination from humans. The identification of three DEC bearing birds here demonstrates that they can be carriers of these enteropathogens, configuring a public health problem. It should also be noted that one E. coli-free bird harbored a Salmonella enterica serovar Enteritidis isolate (data not shown). Since geographical distribution of psittacidae species is restricted, unmonitored commerce may turn them potential and generalized transmitters of these enteropathogens. In fact, EPEC a particular diarrhea agent from developing countries have been detected in a pscittacidae of unknown origin in Germany [3Schremmer C, Lohr JE, Wastlhuber U, et al. Enteropathogenic Escherichia coli in Psittaciformes Avian Pathol 1999; 28: 349-54.]. Besides the detection of EPEC, the finding of a stx+ strain in psittacidae was also of great significance in the present work, since strains with this marker has usually been found only in mammalian hosts. Although assays were not conducted on Vero cells, which is the appropriate model for Shiga cytotoxins detection, phenotypic evidence could be inferred from the bacterial action on HEp-2 cells in the adhesion test and the strain hemolytic activity. This strain was resistant to five of the eight antibiotics tested. The third detected DEC was EAEC, presently recognized as a universal enteropathogen [14Kaper JB, Nataro JP, Mobley HLT. Pathogenic Escherichia coli Nature Rev Microbiol 2004; 2: 123-40.] and apparently assuming a more significant role as an infantile diarrhea agent than EPEC in developing countries [15Rodrigues J, Thomazini CM, Morelli A, Batista GCM. Reduced etiological role for enteropathogenic Escherichia coli in cases of diarrhea in Brazilian infants J Clin Microbiol 2004; 42: 398-400.]. The ability to express the aggregative adhesion is the shared E. coli phenotype of this group of strains, which nevertheless are very heterogeneous with respect to other features. Some are usually isolated from feces of normal subjects and the clinical significance of isolation depends on a more complete strain characterization, besides adhesion assays. A number of genetic markers have been identified in EAEC, which based on the presence of aggR, a plasmid encoded transcriptional activator of virulence factors, have been classified in typical (aggR+) and atypical (aggR-) [14Kaper JB, Nataro JP, Mobley HLT. Pathogenic Escherichia coli Nature Rev Microbiol 2004; 2: 123-40.]. The role of atypical EAEC in human disease is as yet unclear. It has been found that shf+ atypical EAEC are associated with diarrheal cases [16Zamboni A, Fabbricotti SH, Fagundes-Neto U, Scaletsky ICA. Enteroaggregative virulence factors are found to be associated with infantile diarrhea in Brazil J Clin Microbiol 2004; 42: 058-63.], but none of the psittacidae strains was positive for this marker. However, the atypical EAEC of this study was multidrug resistant (Table 1), a feature adding some significance to its finding. The DA phenotype and the irp2 gene were very common among the psittacidae strains (Table 1). The later is part of the yersiniabactin operon, is relatively ubiquitous among EAEC and DAEC strains [8Czeczulin JR, Whittam TS, Henderson IR, Navarro-Garcia F, Nataro JP. Phylogenetic analysis of enteroaggregative and diffusely adherent Escherichia coli Infect Immun 1999; 67: 2692-9.,] and seems to be involved in biofilm formation [17Mohamed JA, Huang DB, Jiang Z, et al. Association of putative enteroaggregative Escherichia coli virulence genes and biofilm production in isolates from travelers to developing countries J Clin Microbiol 2007; 45: 21-6.]. Like EAEC, DAEC is a very heterogeneous bacterial group including at least some pathogenic strains. No particular DAEC marker other than HEp-2 cell adhesion was investigated in these strains, thus limiting the interpretation of their high prevalence among the investigated strains.

Virulence of E. coli is a clonally distributed feature within its natural populations. Commensal strains are mostly assigned to EcoR A and B1 phylogenetic groups and those bearing pathogenicity markers to B2 and D [18Restieri C, Garriss G, Locas M-C, Dozois CM. Autotransporter-encoding sequences are phylogenetically distributed among clinical Escherichia coli clinical isolates and reference strains Appl Environ Microbiol 2007; 73: 1553-62.]. Strains belonging to the later groups are suspected of being associated with inflammatory bowel diseases cases [19Kotlowski R, Bernstein CN, Sepehri S, Krause DO. High prevalence of Escherichia coli belonging to the B2+D phylogenetic group in inflamamatory bowel disease Gut 2007; 56: 669-75.]. Thus, the present finding of a genetically homogeneous E. coli population of the EcoR B2 group, including traditional human pathotypes in psittacidaes suggests a role for these birds as potential reservoirs of these bacteria, and might represent an alert for the adoption of more strict control measures to prevent their carriage not only of E. coli but of other human bacterial pathogens.

ACKNOWLEDGEMENT

This work was supported by Fapesp Grant Nº 2008/10975-0 given to J.R.

REFERENCES

[1] Flammer K, Drewes LA. Species related differences in the incidence of gram-negative bacteria isolated from the cloaca of clinically normal psittacine birds Avian Dis 1988; 32: 79-83.
[2] Grahan CL, Grahan DL. Occurrence of Escherichia coli in feces of Psittacine birds Avian Dis 1978; 22: 717-20.
[3] Schremmer C, Lohr JE, Wastlhuber U, et al. Enteropathogenic Escherichia coli in Psittaciformes Avian Pathol 1999; 28: 349-54.
[4] Mattes BR, Consiglio SAS, Almeida BZ, et al. Influência da Biossegurança na colonização intestinal por Escherichia coli em Psitacídeos Arq Inst Biol 2005; 72: 13-6.
[5] Nataro JP, Kaper JB. Diarrheagenic Escherichia coli Clin Microbiol Rev 1998; 11: 42-201.
[6] Cravioto A, Gross RJ, Scotland SM, Rowe B. An adhesive factor found in strains of Escherichia coli belonging to the traditional infantile enteropathogenic serotypes Curr Microbiol 1979; 3: 95-.
[7] Toma C, Lu Y, Higa N, et al. Multiplex PCR assay for identification of human diarrheagenic Escherichia coli J Clin Microbiol 2003; 41: 2669-71.
[8] Czeczulin JR, Whittam TS, Henderson IR, Navarro-Garcia F, Nataro JP. Phylogenetic analysis of enteroaggregative and diffusely adherent Escherichia coli Infect Immun 1999; 67: 2692-9.
[9] Kahali S, Sarkar B, Rajendran K, et al. Virulence characteristics and molecular epidemiology of enteroaggregative Escherichia coli isolates from hospitalized diarrheal patients in Kolkata, India J Clin Microbiol 2004; 42: 4111-20.
[10] Johnson JR, O’Bryan TT. Improved repetitive element PCR fingerprinting for resolving pathogenic and nonpathogenic phylogenetic groups within Escherichia coli Clin Diagn Lab Immunol 2000; 7: 265-73.
[11] Ochman H, Selander RK. Standard reference strains of Escherichia coli from natural populations J Bacteriol 1984; 157: 690-3.
[12] Clermont O, Bonacorsi S, Bingen E. Rapid and simple determination of the Escherichia coli phylogenetic group Appl Environ Microbiol 2000; 66: 4555-8.
[13] Styles K, Flammer K. Congo red binding of Escherichia coli from the cloacae of psittacine birds Avian Dis 1991; 35: 46-8.
[14] Kaper JB, Nataro JP, Mobley HLT. Pathogenic Escherichia coli Nature Rev Microbiol 2004; 2: 123-40.
[15] Rodrigues J, Thomazini CM, Morelli A, Batista GCM. Reduced etiological role for enteropathogenic Escherichia coli in cases of diarrhea in Brazilian infants J Clin Microbiol 2004; 42: 398-400.
[16] Zamboni A, Fabbricotti SH, Fagundes-Neto U, Scaletsky ICA. Enteroaggregative virulence factors are found to be associated with infantile diarrhea in Brazil J Clin Microbiol 2004; 42: 058-63.
[17] Mohamed JA, Huang DB, Jiang Z, et al. Association of putative enteroaggregative Escherichia coli virulence genes and biofilm production in isolates from travelers to developing countries J Clin Microbiol 2007; 45: 21-6.
[18] Restieri C, Garriss G, Locas M-C, Dozois CM. Autotransporter-encoding sequences are phylogenetically distributed among clinical Escherichia coli clinical isolates and reference strains Appl Environ Microbiol 2007; 73: 1553-62.
[19] Kotlowski R, Bernstein CN, Sepehri S, Krause DO. High prevalence of Escherichia coli belonging to the B2+D phylogenetic group in inflamamatory bowel disease Gut 2007; 56: 669-75.

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