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.

Msphere
|October 23, 2024
PubMed

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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