Chlamydia trachomatis persistence in vitro: an overview.
Chlamydia trachomatis persistence in vitro: an overview.
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DOI:
10.1086/652394
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发表时间:
2010-06-15
期刊:
影响因子:
--
通讯作者:
Wyrick PB
中科院分区:
文献类型:
--
作者:
Wyrick PB
Chlamydiae growing in target mucosal human epithelial cells in vitro can transition from their normal developmental cycle progression -- alternating between infectious but metabolically-inactive elementary bodies (EB) to metabolically-active but non-infectious reticulate bodies (RB) and back to EB -- into a state of “persistence”. Persistence in vitro is defined as “viable but non-cultivable chlamydiae” involving “morphologically enlarged, aberrant, non-dividing RB”. The condition is “reversible” to yield infectious EB on removal of the inducers, including penicillin, interferon-gamma, iron/nutrient starvation, concomitant herpes infection, or maturation of the host cell into its physiologically-differentiated state. All aberrant RB phenotypes are not the same due to differing up/down regulated chlamydial gene sets and subsequent host responses. While all persistence-inducing conditions exist in vivo, key questions include whether or not (i) aberrant chlamydial RB occur in vivo during the alternating acute-silent chronic-acute chlamydial infection scenario that exists in infected patients and animals and (ii) if such aberrant RB can contribute to prolonged, chronic inflammation, fibrosis and scarring .
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