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Published in: Gut Pathogens 1/2017

Open Access 01-12-2017 | Short report

Incidence of Campylobacter concisus and C. ureolyticus in traveler’s diarrhea cases and asymptomatic controls in Nepal and Thailand

Authors: Oralak Serichantalergs, Sirigade Ruekit, Prativa Pandey, Sinn Anuras, Carl Mason, Ladaporn Bodhidatta, Brett Swierczewski

Published in: Gut Pathogens | Issue 1/2017

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Abstract

Background

Campylobacter concisus and C. ureolyticus have emerged in recent years as being associated with acute and prolonged gastroenteritis and implicated in the development of inflammatory bowel diseases. However, there are limited data on the prevalence of these microorganisms in Southeast Asia. In this study, 214 pathogen-negative stool samples after laboratory examination for common enteric pathogens to include C. jejuni and C. coli by culture from two case–control traveler’s diarrhea (TD) studies conducted in Thailand (cases = 26; controls = 30) and Nepal (cases = 83; controls = 75) respectively were assayed by PCR for the detection of Campylobacter 16S rRNA and two specific heat shock protein genes specific for C. concisus (cpn60) and C. ureolyticus (Hsp60) respectively.

Results

Campylobacter 16S rRNA was detected in 28.5% (61/214) of the pathogen-negative TD stool samples (CIWEC Travel Medicine Clinic, Kathmandu, Nepal: cases = 36, control = 14; Bamrungrad International Hospital, Bangkok, Thailand: cases = 9, controls = 2). C. consisus was identified significantly more often in TD cases in Nepal (28.9%; 24/83) as compared to controls (4%; 3/75) (OR = 9.76; 95% CI 2.80–34.02; P = 0.0003) while C. consisus was detected in only two cases (2/26; 7.7%) and none of the controls stool samples from Thailand. C. ureolyticus was detected in four cases (4.8%; 4/83) and four controls (5.3%; 4/75) and in one case (3.8%; 1/26) and one control (3.1%; 1/30) from Nepal and Thailand respectively. C. jejuni and C. coli were isolated in 18.3 and 3.4% of the cases and in 4.0 and 1.4% of the controls in stool samples from both Thailand and Nepal respectively while C. concisus nor C. ureolyticus were not tested for in these samples.

Conclusion

These findings suggest that C. concisus potentially is a pathogen associated with TD in Nepal. To our knowledge, this is the first report of C. concisus and C. ureolyticus detected from traveler’s diarrhea cases from travelers to Nepal and Thailand.
Literature
1.
go back to reference Whiley H, van den Akker B, Giglio S, Bentham R. The role of environmental reservoirs in human campylobacteriosis. Int J Environ Res Public Health. 2013;10:5886–907.CrossRefPubMedPubMedCentral Whiley H, van den Akker B, Giglio S, Bentham R. The role of environmental reservoirs in human campylobacteriosis. Int J Environ Res Public Health. 2013;10:5886–907.CrossRefPubMedPubMedCentral
3.
go back to reference Shah N, DuPont HL, Ramsey DJ. Global etiology of travelers’ diarrhea: systematic review from 1973 to the present. Am J Trop Med Hyg. 2009;80:609–14.PubMed Shah N, DuPont HL, Ramsey DJ. Global etiology of travelers’ diarrhea: systematic review from 1973 to the present. Am J Trop Med Hyg. 2009;80:609–14.PubMed
4.
go back to reference Pandey P, Bodhidatta L, Lewis M, et al. Travelers’ diarrhea in Nepal: an update on the pathogens and antibiotic resistance. J Travel Med. 2011;18:102–8.CrossRefPubMed Pandey P, Bodhidatta L, Lewis M, et al. Travelers’ diarrhea in Nepal: an update on the pathogens and antibiotic resistance. J Travel Med. 2011;18:102–8.CrossRefPubMed
5.
go back to reference Serichantalergs O, Pootong P, Dalsgaard A, et al. PFGE, Lior serotype, and antimicrobial resistance patterns among Campylobacter jejuni isolated from travelers and US military personnel with acute diarrhea in Thailand, 1998–2003. Gut Pathog. 2010;2:15.CrossRefPubMedPubMedCentral Serichantalergs O, Pootong P, Dalsgaard A, et al. PFGE, Lior serotype, and antimicrobial resistance patterns among Campylobacter jejuni isolated from travelers and US military personnel with acute diarrhea in Thailand, 1998–2003. Gut Pathog. 2010;2:15.CrossRefPubMedPubMedCentral
7.
go back to reference Fernandez H, Vera F, Villanueva MP, Garcia A. Occurrence of Campylobacter species in healthy well-nourished and malnourished children. Braz J Microbiol. 2008;39:56–8.CrossRefPubMedPubMedCentral Fernandez H, Vera F, Villanueva MP, Garcia A. Occurrence of Campylobacter species in healthy well-nourished and malnourished children. Braz J Microbiol. 2008;39:56–8.CrossRefPubMedPubMedCentral
8.
go back to reference Man SM. The clinical importance of emerging Campylobacter species. Nat Rev Gastroenterol Hepatol. 2011;8:669–85.CrossRefPubMed Man SM. The clinical importance of emerging Campylobacter species. Nat Rev Gastroenterol Hepatol. 2011;8:669–85.CrossRefPubMed
9.
go back to reference Taylor DN, Kiehlbauch JA, Tee W, Pitarangsi C, Echeverria P. Isolation of group 2 aerotolerant Campylobacter species from Thai children with diarrhea. J Infect Dis. 1991;163:1062–7.CrossRefPubMed Taylor DN, Kiehlbauch JA, Tee W, Pitarangsi C, Echeverria P. Isolation of group 2 aerotolerant Campylobacter species from Thai children with diarrhea. J Infect Dis. 1991;163:1062–7.CrossRefPubMed
10.
11.
go back to reference Lastovica AJ. Emerging Campylobacter spp.: the tip of the iceberg. Clin Microbiol Newsl. 2006;28:49–56.CrossRef Lastovica AJ. Emerging Campylobacter spp.: the tip of the iceberg. Clin Microbiol Newsl. 2006;28:49–56.CrossRef
12.
go back to reference Zhang L, Budiman V, Day AS, et al. Isolation and detection of Campylobacter concisus from saliva of healthy individuals and patients with inflammatory bowel disease. J Clin Microbiol. 2010;48:2965–7.CrossRefPubMedPubMedCentral Zhang L, Budiman V, Day AS, et al. Isolation and detection of Campylobacter concisus from saliva of healthy individuals and patients with inflammatory bowel disease. J Clin Microbiol. 2010;48:2965–7.CrossRefPubMedPubMedCentral
13.
go back to reference Nielsen HL, Engberg J, Ejlertsen T, Bucker R, Nielsen H. Short-term and medium-term clinical outcomes of Campylobacter concisus infection. Clin Microbiol Infect. 2012;18:E459–65.CrossRefPubMed Nielsen HL, Engberg J, Ejlertsen T, Bucker R, Nielsen H. Short-term and medium-term clinical outcomes of Campylobacter concisus infection. Clin Microbiol Infect. 2012;18:E459–65.CrossRefPubMed
14.
go back to reference Nielsen HL, Engberg J, Ejlertsen T, Nielsen H. Clinical manifestations of Campylobacter concisus infection in children. Pediatr Infect Dis J. 2013;32:1194–8.CrossRefPubMed Nielsen HL, Engberg J, Ejlertsen T, Nielsen H. Clinical manifestations of Campylobacter concisus infection in children. Pediatr Infect Dis J. 2013;32:1194–8.CrossRefPubMed
15.
go back to reference Nielsen HL, Ejlertsen T, Engberg J, Nielsen H. High incidence of Campylobacter concisus in gastroenteritis in North Jutland, Denmark: a population-based study. Clin Microbiol Infect. 2013;19:445–50.CrossRefPubMed Nielsen HL, Ejlertsen T, Engberg J, Nielsen H. High incidence of Campylobacter concisus in gastroenteritis in North Jutland, Denmark: a population-based study. Clin Microbiol Infect. 2013;19:445–50.CrossRefPubMed
16.
go back to reference Underwood AP, Kaakoush NO, Sodhi N, et al. Campylobacter concisus pathotypes are present at significant levels in patients with gastroenteritis. J Med Microbiol. 2016;65:219–26.CrossRefPubMed Underwood AP, Kaakoush NO, Sodhi N, et al. Campylobacter concisus pathotypes are present at significant levels in patients with gastroenteritis. J Med Microbiol. 2016;65:219–26.CrossRefPubMed
17.
go back to reference Engberg J, On SL, Harrington CS, Gerner-Smidt P. Prevalence of Campylobacter, Arcobacter, Helicobacter, and Sutterella spp. in human fecal samples as estimated by a reevaluation of isolation methods for Campylobacters. J Clin Microbiol. 2000;38:286–91.PubMedPubMedCentral Engberg J, On SL, Harrington CS, Gerner-Smidt P. Prevalence of Campylobacter, Arcobacter, Helicobacter, and Sutterella spp. in human fecal samples as estimated by a reevaluation of isolation methods for Campylobacters. J Clin Microbiol. 2000;38:286–91.PubMedPubMedCentral
18.
go back to reference Van Etterijck R, Breynaert J, Revets H, et al. Isolation of Campylobacter concisus from feces of children with and without diarrhea. J Clin Microbiol. 1996;34:2304–6.PubMedPubMedCentral Van Etterijck R, Breynaert J, Revets H, et al. Isolation of Campylobacter concisus from feces of children with and without diarrhea. J Clin Microbiol. 1996;34:2304–6.PubMedPubMedCentral
19.
go back to reference Man SM, Zhang L, Day AS, Leach ST, Lemberg DA, Mitchell H. Campylobacter concisus and other Campylobacter species in children with newly diagnosed Crohn’s disease. Inflamm Bowel Dis. 2010;16:1008–16.CrossRefPubMed Man SM, Zhang L, Day AS, Leach ST, Lemberg DA, Mitchell H. Campylobacter concisus and other Campylobacter species in children with newly diagnosed Crohn’s disease. Inflamm Bowel Dis. 2010;16:1008–16.CrossRefPubMed
20.
go back to reference Hatanaka N, Shimizu A, Somroop S, et al. High prevalence of Campylobacter ureolyticus in stool specimens of children with diarrhea in Japan. Jpn J Infect Dis 2017;70(4):455–457CrossRefPubMed Hatanaka N, Shimizu A, Somroop S, et al. High prevalence of Campylobacter ureolyticus in stool specimens of children with diarrhea in Japan. Jpn J Infect Dis 2017;70(4):455–457CrossRefPubMed
21.
go back to reference Bullman S, Corcoran D, O’Leary J, O’Hare D, Lucey B, Sleator RD. Emerging dynamics of human campylobacteriosis in Southern Ireland. FEMS Immuno Med Microbiol. 2011;63:248–53.CrossRef Bullman S, Corcoran D, O’Leary J, O’Hare D, Lucey B, Sleator RD. Emerging dynamics of human campylobacteriosis in Southern Ireland. FEMS Immuno Med Microbiol. 2011;63:248–53.CrossRef
22.
go back to reference Bullman S, Corcoran D, O’Leary J, Lucey B, Byrne D, Sleator RD. Campylobacter ureolyticus: an emerging gastrointestinal pathogen? FEMS Immunol Med Microbiol. 2011;61:228–30.CrossRefPubMed Bullman S, Corcoran D, O’Leary J, Lucey B, Byrne D, Sleator RD. Campylobacter ureolyticus: an emerging gastrointestinal pathogen? FEMS Immunol Med Microbiol. 2011;61:228–30.CrossRefPubMed
23.
go back to reference Collado L, Gutierrez M, Gonzalez M, Fernandez H. Assessment of the prevalence and diversity of emergent campylobacteria in human stool samples using a combination of traditional and molecular methods. Diagn Microbiol Infect Dis. 2013;75:434–6.CrossRefPubMed Collado L, Gutierrez M, Gonzalez M, Fernandez H. Assessment of the prevalence and diversity of emergent campylobacteria in human stool samples using a combination of traditional and molecular methods. Diagn Microbiol Infect Dis. 2013;75:434–6.CrossRefPubMed
24.
go back to reference Mukhopadhya I, Thomson JM, Hansen R, Berry SH, El-Omar EM, Hold GL. Detection of Campylobacter concisus and other Campylobacter species in colonic biopsies from adults with ulcerative colitis. PLoS ONE. 2011;6:e21490.CrossRefPubMedPubMedCentral Mukhopadhya I, Thomson JM, Hansen R, Berry SH, El-Omar EM, Hold GL. Detection of Campylobacter concisus and other Campylobacter species in colonic biopsies from adults with ulcerative colitis. PLoS ONE. 2011;6:e21490.CrossRefPubMedPubMedCentral
25.
go back to reference Bodhidatta L, McDaniel P, Sornsakrin S, Srijan A, Serichantalergs O, Mason CJ. Case-control study of diarrheal disease etiology in a remote rural area in Western Thailand. Am J Trop Med Hyg. 2010;83:1106–9.CrossRefPubMedPubMedCentral Bodhidatta L, McDaniel P, Sornsakrin S, Srijan A, Serichantalergs O, Mason CJ. Case-control study of diarrheal disease etiology in a remote rural area in Western Thailand. Am J Trop Med Hyg. 2010;83:1106–9.CrossRefPubMedPubMedCentral
26.
go back to reference Meng CY, Smith BL, Bodhidatta L, et al. Etiology of diarrhea in young children and patterns of antibiotic resistance in Cambodia. Pediatr Infect Dis J. 2011;30:331–5.CrossRefPubMed Meng CY, Smith BL, Bodhidatta L, et al. Etiology of diarrhea in young children and patterns of antibiotic resistance in Cambodia. Pediatr Infect Dis J. 2011;30:331–5.CrossRefPubMed
27.
go back to reference Linton D, Owen RJ, Stanley J. Rapid identification by PCR of the genus Campylobacter and of five Campylobacter species enteropathogenic for man and animals. Res Microbiol. 1996;147:707–18.CrossRefPubMed Linton D, Owen RJ, Stanley J. Rapid identification by PCR of the genus Campylobacter and of five Campylobacter species enteropathogenic for man and animals. Res Microbiol. 1996;147:707–18.CrossRefPubMed
28.
go back to reference Bullman S, O’Leary J, Corcoran D, Sleator RD, Lucey B. Molecular-based detection of non-culturable and emerging campylobacteria in patients presenting with gastroenteritis. Epidemiol Infect. 2012;140:684–8.CrossRefPubMed Bullman S, O’Leary J, Corcoran D, Sleator RD, Lucey B. Molecular-based detection of non-culturable and emerging campylobacteria in patients presenting with gastroenteritis. Epidemiol Infect. 2012;140:684–8.CrossRefPubMed
29.
go back to reference Chaban B, Musil KM, Himsworth CG, Hill JE. Development of cpn60-based real-time quantitative PCR assays for the detection of 14 Campylobacter species and application to screening of canine fecal samples. Appl Environ Microbiol. 2009;75:3055–61.CrossRefPubMedPubMedCentral Chaban B, Musil KM, Himsworth CG, Hill JE. Development of cpn60-based real-time quantitative PCR assays for the detection of 14 Campylobacter species and application to screening of canine fecal samples. Appl Environ Microbiol. 2009;75:3055–61.CrossRefPubMedPubMedCentral
30.
go back to reference Murphy H, Pandey P. Pathogens for travelers’ diarrhea in Nepal and resistance patterns. Curr Infect Dis Rep. 2012;14:238–45.CrossRefPubMed Murphy H, Pandey P. Pathogens for travelers’ diarrhea in Nepal and resistance patterns. Curr Infect Dis Rep. 2012;14:238–45.CrossRefPubMed
31.
go back to reference Taylor DN, Echeverria P, Pitarangsi C, Seriwatana J, Bodhidatta L, Blaser MJ. Influence of strain characteristics and immunity on the epidemiology of Campylobacter infections in Thailand. J Clin Microbiol. 1988;26:863–8.PubMedPubMedCentral Taylor DN, Echeverria P, Pitarangsi C, Seriwatana J, Bodhidatta L, Blaser MJ. Influence of strain characteristics and immunity on the epidemiology of Campylobacter infections in Thailand. J Clin Microbiol. 1988;26:863–8.PubMedPubMedCentral
32.
go back to reference Walz SE, Baqar S, Beecham HJ, et al. Pre-exposure anti-Campylobacter jejuni immunoglobulin a levels associated with reduced risk of Campylobacter diarrhea in adults traveling to Thailand. Am J Trop Med Hyg. 2001;65:652–6.CrossRefPubMed Walz SE, Baqar S, Beecham HJ, et al. Pre-exposure anti-Campylobacter jejuni immunoglobulin a levels associated with reduced risk of Campylobacter diarrhea in adults traveling to Thailand. Am J Trop Med Hyg. 2001;65:652–6.CrossRefPubMed
33.
go back to reference Vandamme P, Debruyne L, De Brandt E, Falsen E. Reclassification of Bacteroides ureolyticus as Campylobacter ureolyticus comb. nov., and emended description of the genus Campylobacter. Int J Syst Evol Microbiol. 2010;60:2016–22.CrossRefPubMed Vandamme P, Debruyne L, De Brandt E, Falsen E. Reclassification of Bacteroides ureolyticus as Campylobacter ureolyticus comb. nov., and emended description of the genus Campylobacter. Int J Syst Evol Microbiol. 2010;60:2016–22.CrossRefPubMed
34.
go back to reference Varavithya W, Vathanophas K, Bodhidatta L, et al. Importance of Salmonellae and Campylobacter jejuni in the etiology of diarrheal disease among children less than 5 years of age in a community in Bangkok, Thailand. J Clin Microbiol. 1990;28:2507–10.PubMedPubMedCentral Varavithya W, Vathanophas K, Bodhidatta L, et al. Importance of Salmonellae and Campylobacter jejuni in the etiology of diarrheal disease among children less than 5 years of age in a community in Bangkok, Thailand. J Clin Microbiol. 1990;28:2507–10.PubMedPubMedCentral
35.
go back to reference Serichantalergs O, Dalsgaard A, Bodhidatta L, et al. Emerging fluoroquinolone and macrolide resistance of Campylobacter jejuni and Campylobacter coli isolates and their serotypes in Thai children from 1991 to 2000. Epidemiol Infect. 2007;135:1299–306.CrossRefPubMedPubMedCentral Serichantalergs O, Dalsgaard A, Bodhidatta L, et al. Emerging fluoroquinolone and macrolide resistance of Campylobacter jejuni and Campylobacter coli isolates and their serotypes in Thai children from 1991 to 2000. Epidemiol Infect. 2007;135:1299–306.CrossRefPubMedPubMedCentral
37.
38.
go back to reference Lee S, Lee J, Ha J, et al. Clinical relevance of infections with zoonotic and human oral species of Campylobacter. J Microbiol. 2016;54:459–67.CrossRefPubMed Lee S, Lee J, Ha J, et al. Clinical relevance of infections with zoonotic and human oral species of Campylobacter. J Microbiol. 2016;54:459–67.CrossRefPubMed
39.
go back to reference Kalischuk LD, Inglis GD. Comparative genotypic and pathogenic examination of Campylobacter concisus isolates from diarrheic and non-diarrheic humans. BMC Microbiol. 2011;11:53.CrossRefPubMedPubMedCentral Kalischuk LD, Inglis GD. Comparative genotypic and pathogenic examination of Campylobacter concisus isolates from diarrheic and non-diarrheic humans. BMC Microbiol. 2011;11:53.CrossRefPubMedPubMedCentral
40.
go back to reference Kaakoush NO, Man SM, Lamb S, et al. The secretome of Campylobacter concisus. FEBS J. 2010;277:1606–17.CrossRefPubMed Kaakoush NO, Man SM, Lamb S, et al. The secretome of Campylobacter concisus. FEBS J. 2010;277:1606–17.CrossRefPubMed
41.
go back to reference Man SM, Kaakoush NO, Leach ST, et al. Host attachment, invasion, and stimulation of proinflammatory cytokines by Campylobacter concisus and other non-Campylobacter jejuni Campylobacter species. J Infect Dis. 2010;202:1855–65.CrossRefPubMed Man SM, Kaakoush NO, Leach ST, et al. Host attachment, invasion, and stimulation of proinflammatory cytokines by Campylobacter concisus and other non-Campylobacter jejuni Campylobacter species. J Infect Dis. 2010;202:1855–65.CrossRefPubMed
42.
go back to reference Bullman S, Lucid A, Corcoran D, Sleator RD, Lucey B. Genomic investigation into strain heterogeneity and pathogenic potential of the emerging gastrointestinal pathogen Campylobacter ureolyticus. PLoS ONE. 2013;8:e71515.CrossRefPubMedPubMedCentral Bullman S, Lucid A, Corcoran D, Sleator RD, Lucey B. Genomic investigation into strain heterogeneity and pathogenic potential of the emerging gastrointestinal pathogen Campylobacter ureolyticus. PLoS ONE. 2013;8:e71515.CrossRefPubMedPubMedCentral
43.
go back to reference Buchan BW, Olson WJ, Pezewski M, et al. Clinical evaluation of a real-time PCR assay for identification of Salmonella, Shigella, Campylobacter (Campylobacter jejuni and C. coli), and shiga toxin-producing Escherichia coli isolates in stool specimens. J Clin Microbiol. 2013;51:4001–7.CrossRefPubMedPubMedCentral Buchan BW, Olson WJ, Pezewski M, et al. Clinical evaluation of a real-time PCR assay for identification of Salmonella, Shigella, Campylobacter (Campylobacter jejuni and C. coli), and shiga toxin-producing Escherichia coli isolates in stool specimens. J Clin Microbiol. 2013;51:4001–7.CrossRefPubMedPubMedCentral
44.
go back to reference Schuurman T, de Boer RF, van Zanten E, et al. Feasibility of a molecular screening method for detection of Salmonella enterica and Campylobacter jejuni in a routine community-based clinical microbiology laboratory. J Clin Microbiol. 2007;45:3692–700.CrossRefPubMedPubMedCentral Schuurman T, de Boer RF, van Zanten E, et al. Feasibility of a molecular screening method for detection of Salmonella enterica and Campylobacter jejuni in a routine community-based clinical microbiology laboratory. J Clin Microbiol. 2007;45:3692–700.CrossRefPubMedPubMedCentral
45.
go back to reference Wohlwend N, Tiermann S, Risch L, Risch M, Bodmer T. Evaluation of a multiplex real-time PCR assay for detecting major bacterial enteric pathogens in fecal specimens: intestinal inflammation and bacterial load are correlated in Campylobacter infections. J Clin Microbiol. 2016;54:2262–6.CrossRefPubMedPubMedCentral Wohlwend N, Tiermann S, Risch L, Risch M, Bodmer T. Evaluation of a multiplex real-time PCR assay for detecting major bacterial enteric pathogens in fecal specimens: intestinal inflammation and bacterial load are correlated in Campylobacter infections. J Clin Microbiol. 2016;54:2262–6.CrossRefPubMedPubMedCentral
46.
go back to reference Platts-Mills JA, Liu J, Gratz J, et al. Detection of Campylobacter in stool and determination of significance by culture, enzyme immunoassay, and PCR in developing countries. J Clin Microbiol. 2014;52:1074–80.CrossRefPubMedPubMedCentral Platts-Mills JA, Liu J, Gratz J, et al. Detection of Campylobacter in stool and determination of significance by culture, enzyme immunoassay, and PCR in developing countries. J Clin Microbiol. 2014;52:1074–80.CrossRefPubMedPubMedCentral
47.
go back to reference Gradel KO, Nielsen HL, Schonheyder HC, Ejlertsen T, Kristensen B, Nielsen H. Increased short- and long-term risk of inflammatory bowel disease after Salmonella or Campylobacter gastroenteritis. Gastroenterology. 2009;137:495–501.CrossRefPubMed Gradel KO, Nielsen HL, Schonheyder HC, Ejlertsen T, Kristensen B, Nielsen H. Increased short- and long-term risk of inflammatory bowel disease after Salmonella or Campylobacter gastroenteritis. Gastroenterology. 2009;137:495–501.CrossRefPubMed
48.
go back to reference Riddle MS, Gutierrez RL, Verdu EF, Porter CK. The chronic gastrointestinal consequences associated with Campylobacter. Curr Gastroenterol Rep. 2012;14:395–405.CrossRefPubMed Riddle MS, Gutierrez RL, Verdu EF, Porter CK. The chronic gastrointestinal consequences associated with Campylobacter. Curr Gastroenterol Rep. 2012;14:395–405.CrossRefPubMed
Metadata
Title
Incidence of Campylobacter concisus and C. ureolyticus in traveler’s diarrhea cases and asymptomatic controls in Nepal and Thailand
Authors
Oralak Serichantalergs
Sirigade Ruekit
Prativa Pandey
Sinn Anuras
Carl Mason
Ladaporn Bodhidatta
Brett Swierczewski
Publication date
01-12-2017
Publisher
BioMed Central
Published in
Gut Pathogens / Issue 1/2017
Electronic ISSN: 1757-4749
DOI
https://doi.org/10.1186/s13099-017-0197-6

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