| Literature DB >> 26597987 |
Turner Allen Conrad1, Siqi Gong1, Zhangsheng Yang1, Patrick Matulich2, Jonathon Keck2, Noah Beltrami2, Chaoqun Chen3, Zhou Zhou3, Jin Dai1, Guangming Zhong4.
Abstract
We previously associated a missense mutation of the tc0668 gene of serial in vitro-passaged Chlamydia muridarum, a murine model of human urogenital C. trachomatis, with severely attenuated disease development in the upper genital tract of female mice. Since these mutants also contained a TC0237 Q117E missense mutation that enhances their in vitro infectivity, an effort was made here to isolate and characterize a tc0668 single mutant to determine its individual contribution to urogenital pathogenicity. Detailed genetic analysis of C. muridarum passages revealed a truncated variant with a G216* nonsense mutation of the 408-amino-acid TC0668 protein that does not produce a detectable product. Intracellular growth and infectivity of C. muridarum in vitro remain unaffected in the absence of TC0668. Intravaginal inoculation of the TC0668 null mutant into C3H/HeJ mice results in a typical course of lower genital tract infection but, unlike a pathogenic isogenic control, is unable to elicit significant chronic inflammation of the oviduct and fails to induce hydrosalpinx. Thus, TC0668 is demonstrated as an important chromosome-encoded urogenital pathogenicity factor of C. muridarum and the first with these characteristics to be discovered for a Chlamydia pathogen.Entities:
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Year: 2015 PMID: 26597987 PMCID: PMC4730586 DOI: 10.1128/IAI.01171-15
Source DB: PubMed Journal: Infect Immun ISSN: 0019-9567 Impact factor: 3.441