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Multicolor Flow Cytometry Analyses of Cellular Immune Response in Rhesus Macaques
Published on: April 22, 2010
Diversity of Campylobacter spp. circulating in a rhesus macaque (Macaca mulatta) breeding colony using culture and
Rebecca L Bacon1, Carolyn L Hodo2, Jing Wu1,3
1Department of Veterinary Pathobiology, School of Veterinary Medicine & Biomedical Sciences, Texas A&M University, College Station, Texas, USA.
Abstract:
Campylobacter jejuni and Campylobacter coli represent the leading causes of bacterial gastroenteritis in humans, and infections can produce post-infectious irritable bowel syndrome (PI-IBS). Rhesus macaques (Macaca mulatta) (RM) are similarly susceptible to acute campylobacteriosis and represent a potential model of PI-IBS. We characterized the Campylobacter species circulating in an RM breeding colony using culture, qPCR, and whole genome sequencing (WGS). We also compared the C. jejuni and C. coli prevalence in RM as detected with qPCR versus culture and identified risk factors for bacteria presence and intestinal disease. Culture of 275 samples yielded C. coli (103) and C. jejuni (8), of which 21.6% were resistant to quinolones and 3.6% were resistant to macrolides. Multidrug-resistant isolates were obtained exclusively from animals exhibiting diarrhea or with histologically confirmed chronic enterocolitis. WGS revealed a non-clonal population of Campylobacter spp. Genotypic predictions of resistance were excellent except for aminoglycosides. All sequenced isolates contained genes for all subunits of cytolethal distending toxin. qPCR detected a prevalence of 45.9% for C. coli and 29.6% for C. jejuni. The quantity of either bacteria was significantly higher (P < 0.05) in animals with intestinal disease compared to healthy animals, though only young age was significantly associated with the presence of Campylobacter sp. or intestinal disease. Significantly more C. jejuni positive animals were detected with qPCR than with culture. These results provide a comprehensive characterization of Campylobacter spp. circulating in a breeding colony of RM in the United States and suggest that qPCR is superior for the detection of C. jejuni in RM.
Importance:
Gastrointestinal disease is one of the most common reasons for hospitalization in non-human primate colonies and accounts for over one-third of non-research related euthanasia. In rhesus macaques, this manifests as both acute diarrhea and chronic enterocolitis (CE), a syndrome of chronic diarrhea resulting in poor weight gain or weight loss which is minimally responsive to treatment. Campylobacter spp. are major causes of acute enterocolitis in rhesus macaques and may predispose individuals to the development of CE, similar to post-infectious irritable bowel syndrome in humans. Despite these concerns, there are few studies characterizing Campylobacter in rhesus macaque colonies, in particular utilizing whole genome sequencing and assessing findings with respect to the health status of the host. Our findings provide insight into Campylobacter strains circulating in rhesus macaque colonies, which can improve clinical monitoring, assist in treatment decisions, and provide new avenues of investigation into campylobacteriosis as a catalyst for CE.
Insights
This study characterized Campylobacter in rhesus macaques, finding qPCR superior for detecting C. jejuni and linking infections to intestinal disease. These findings aid in monitoring and treating bacterial gastroenteritis in these primates.
Area of Science:
- Veterinary microbiology
- Primate infectious diseases
- Gastroenterology
Background:
- Gastrointestinal diseases are common in non-human primate colonies, leading to hospitalization and euthanasia.
- Campylobacter species cause acute enterocolitis in rhesus macaques (RM) and may contribute to chronic enterocolitis (CE), similar to post-infectious irritable bowel syndrome in humans.
- Limited studies characterize Campylobacter in RM colonies, especially using whole genome sequencing (WGS) and correlating with host health.
Purpose of the Study:
- To characterize Campylobacter species in an RM breeding colony.
- To compare the prevalence of C. jejuni and C. coli detected by qPCR versus culture.
- To identify risk factors for Campylobacter presence and intestinal disease in RM.
Main Methods:
- Culture, quantitative PCR (qPCR), and whole genome sequencing (WGS) were used to analyze 275 samples from RM.
- Prevalence, antimicrobial resistance, and virulence genes (cytolethal distending toxin) were assessed.
- Risk factors for Campylobacter presence and intestinal disease were identified.
Main Results:
- Culture identified C. coli and C. jejuni, with significant quinolone and macrolide resistance in some isolates, particularly from diseased animals.
- WGS revealed a diverse population of Campylobacter spp. with predicted resistance patterns.
- qPCR detected higher prevalence rates for both C. coli (45.9%) and C. jejuni (29.6%) compared to culture.
- Campylobacter quantity was higher in animals with intestinal disease, and young age was associated with infection and disease.
- qPCR detected significantly more C. jejuni positive animals than culture.
Conclusions:
- This study provides a comprehensive characterization of Campylobacter spp. in a US RM breeding colony.
- qPCR is a more sensitive method than culture for detecting C. jejuni in RM.
- Understanding Campylobacter prevalence and characteristics can improve clinical monitoring and treatment strategies for gastrointestinal diseases in RM.
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