Abstract

The virulence of chlamydial infection in wild koalas is highly variable between individuals. Some koalas can be infected (PCR positive) with Chlamydia for long periods but remain asymptomatic, whereas others develop clinical disease. Chlamydia in the koala has traditionally been studied without regard to coinfection with other pathogens, although koalas are usually subject to infection with koala retrovirus (KoRV). Retroviruses can be immunosuppressive, and there is evidence of an immunosuppressive effect of KoRV in vitro. Originally thought to be a single endogenous strain, a new, potentially more virulent exogenous variant (KoRV-B) was recently reported. We hypothesized that KoRV-B might significantly alter chlamydial disease outcomes in koalas, presumably via immunosuppression. By studying sub-groups of Chlamydia and KoRV infected koalas in the wild, we found that neither total KoRV load (either viraemia or proviral copies per genome), nor chlamydial infection level or strain type, was significantly associated with chlamydial disease risk. However, PCR positivity with KoRV-B was significantly associated with chlamydial disease in koalas (p = 0.02961). This represents an example of a recently evolved virus variant that may be predisposing its host (the koala) to overt clinical disease when co-infected with an otherwise asymptomatic bacterial pathogen (Chlamydia).

Highlights

  • Chlamydia is an obligate intracellular bacterium with a unique biphasic developmental cycle

  • The results of this study further provide new evidence to support a role for koala retrovirus (KoRV)-B in chlamydial disease pathogenesis in the koala

  • We found that infection with the KoRV-B variant was a significant predictor of the development of chlamydial disease in koalas infected with a variety of chlamydial ompA genotypes

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Summary

Introduction

Chlamydia is an obligate intracellular bacterium with a unique biphasic developmental cycle. Some Chlamydia infected animals present with clinical disease, whereas others remain asymptomatic[3]. What causes this variation in clinical outcomes is unclear. Many retroviruses, including human immunodeficiency virus (HIV) and feline leukemia virus (FeLV) can induce immunosuppression in their hosts[14, 15] This increases the host’s susceptibility to opportunistic infections, such as fungal infections (Cryptococcus) and tuberculosis, which are commonly associated with, and exacerbated by retroviruses[16,17,18,19]. We used a model selection approach[22] to examine the relationship between Chlamydia disease outcome and a number of variables, including KoRV load (genomic DNA and viral RNA load) and KoRV variant (KoRV-A and KoRV-B), chlamydial infectious load and genotype, as well as koala age and sex. We present here the variables that best predict overt signs of clinical chlamydial disease in the koala

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