| Literature DB >> 26429774 |
Tomohiro Yamazaki1, Junji Matsuo2, Satoshi Takahashi3, Shouta Kumagai2, Tomoko Shimoda4, Kiyotaka Abe5, Kunihiro Minami5, Hiroyuki Yamaguchi6.
Abstract
Although sexually transmitted disease due to Chlamydia trachomatis occurs similarly in both men and women, the female urogenital tract differs from that of males anatomically and physiologically, possibly leading to specific polymorphisms of the bacterial surface molecules. In the present study, we therefore characterized polymorphic features in a high-definition phylogenetic marker, polymorphic outer membrane protein (Pmp) F of C. trachomatis strains isolated from male urogenital tracts in Japan (Category: Japan-males, n = 12), when compared with those isolated from female cervical ducts in Japan (Category: Japan-females, n = 11), female cervical ducts in the other country (Category: Ref-females, n = 12) or homosexual male rectums in the other country (Category: Ref-males, n = 7), by general bioinformatics analysis tool with MAFFT software. As a result, phylogenetic reconstruction of the PmpF amino acid sequences showing three distinct clusters revealed that the Japan-males were limited into cluster 1 and 2, although there were only four clusters even though including an outgroup. Meanwhile, the phylogenetic distance values of PmpF passenger domain without hinge region, but not its full-length sequence, showed that the Japan-males were more stable and displayed less diversity when compared with the other categories, supported by the sequence conservation features. Thus, PmpF passenger domain is a useful phylogenetic maker, and the phylogenic features indicate that C. trachomatis strains isolated from male urogenital tracts in Japan may be unique, suggesting an adaptation depending on selective pressure, such as the presence or absence of microbial flora, furthermore possibly connecting to sexual differentiation.Entities:
Keywords: Chlamydia trachomatis; Male; Phylogenetic analysis; Polymorphic membrane protein F (PmpF); Polymorphism
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Year: 2015 PMID: 26429774 DOI: 10.1016/j.jiac.2015.08.016
Source DB: PubMed Journal: J Infect Chemother ISSN: 1341-321X Impact factor: 2.211