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Published on: December 1, 2017
Ascending Reproductive Tract Infection in Pig-Tailed Macaques Inoculated with Mycoplasma genitalium
Laarni Kendra T Aguila1, Dorothy L Patton2, German G Gornalusse2
1Department of Medicine, Division of Allergy and Infectious Diseases, University of Washingtongrid.34477.33, Seattle, Washington, USA.
Abstract:
Mycoplasma genitalium is a sexually transmitted bacterial pathogen that causes urogenital disease in men and women. M. genitalium infections can persist for months to years and can ascend to the upper reproductive tract in women where it is associated with serious sequelae including pelvic inflammatory disease, tubal factor infertility, and preterm birth. An animal model is needed to understand immune evasion strategies that allow persistence, mechanisms of ascending infection, and factors associated with clearance. In earlier studies, we determined that pig-tailed macaques are susceptible to cervical infection; however, not all primates were successfully infected, persistence varied between animals, and ascension to the upper reproductive tract was not observed after 4 or 8 weeks of follow-up. Building on our previous findings, we refined our inoculation methods to increase infection rates, extended observation to 18 weeks, and comprehensively sampled the upper reproductive tract to detect ascending infection. With these improvements, we established infection in all (3/3) primates inoculated with M. genitalium and demonstrated lower tract persistence for 16 to 18 weeks. Ascension to the upper reproductive tract at endpoint was observed in two out of three primates. All three primates developed serum and local antibodies reacting primarily to the MgpB and MgpC adherence proteins. Elevated genital polymorphonuclear leukocytes (PMNs) and inflammatory cytokines and chemokines, erythema of the ectocervix in one primate, and histologic evidence of vaginitis and endocervicitis in two primates suggest a mild to moderate inflammatory response to infection. This model will be valuable to understand the natural history of M. genitalium infection including mechanisms of persistence, immune evasion, and ascension to the upper reproductive tract.
Insights
A new pig-tailed macaque model successfully establishes persistent Mycoplasma genitalium infection, showing upper reproductive tract ascension. This model aids research into genital Mycoplasma persistence and immune evasion strategies.
Area of Science:
- Reproductive infectious diseases
- Microbiology
- Animal models
Background:
- Mycoplasma genitalium is a significant sexually transmitted pathogen causing urogenital disease.
- Persistent infections can lead to severe reproductive health issues like pelvic inflammatory disease and infertility.
- Existing animal models have limitations in fully recapitulating M. genitalium infection dynamics.
Purpose of the Study:
- To develop and validate an improved animal model for studying Mycoplasma genitalium infection.
- To investigate M. genitalium persistence, immune response, and ascending infection in a primate model.
- To understand factors influencing M. genitalium clearance and pathogenesis.
Main Methods:
- Refined inoculation techniques in pig-tailed macaques (Macaca nemestrina).
- Extended observation period to 18 weeks with comprehensive upper reproductive tract sampling.
- Monitored infection establishment, persistence, ascension, and host immune responses (antibodies, inflammatory markers).
Main Results:
- All inoculated macaques (3/3) developed M. genitalium infection with lower tract persistence for 16-18 weeks.
- Ascension to the upper reproductive tract was observed in 2 out of 3 primates.
- Infection elicited serum and local antibodies against MgpB/MgpC proteins and a mild-moderate inflammatory response.
Conclusions:
- The refined pig-tailed macaque model effectively replicates persistent M. genitalium infection and allows for the study of ascending infection.
- This model provides a valuable platform for investigating M. genitalium pathogenesis, immune evasion, and potential therapeutic strategies.

