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      Global Multilocus Sequence Type Analysis of Chlamydia trachomatis Strains from 16 Countries.

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          Abstract

          The Uppsala University Chlamydia trachomatis multilocus sequence type (MLST) database (http://mlstdb.bmc.uu.se) is based on five target regions (non-housekeeping genes) and the ompA gene. Each target has various numbers of alleles-hctB, 89; CT058, 51; CT144, 30; CT172, 38; and pbpB, 35-derived from 13 studies. Our aims were to perform an overall analysis of all C. trachomatis MLST sequence types (STs) in the database, examine STs with global spread, and evaluate the phylogenetic capability by using the five targets. A total of 415 STs were recognized from 2,089 specimens. The addition of 49 ompA gene variants created 459 profiles. ST variation and their geographical distribution were characterized using eBURST and minimum spanning tree analyses. There were 609 samples from men having sex with men (MSM), with 4 predominating STs detected in this group, comprising 63% of MSM cases. Four other STs predominated among 1,383 heterosexual cases comprising, 31% of this group. The diversity index in ocular trachoma cases was significantly lower than in sexually transmitted chlamydia infections. Predominating STs were identified in 12 available C. trachomatis whole genomes which were compared to 22 C. trachomatis full genomes without predominating STs. No specific gene in the 12 genomes with predominating STs could be linked to successful spread of certain STs. Phylogenetic analysis showed that MLST targets provide a tree similar to trees based on whole-genome analysis. The presented MLST scheme identified C. trachomatis strains with global spread. It provides a tool for epidemiological investigations and is useful for phylogenetic analyses.

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          Author and article information

          Journal
          J. Clin. Microbiol.
          Journal of clinical microbiology
          1098-660X
          0095-1137
          Jul 2015
          : 53
          : 7
          Affiliations
          [1 ] Section of Clinical Bacteriology, Department of Medical Sciences, Uppsala University, Uppsala, Sweden bjorn.herrmann@medsci.uu.se.
          [2 ] Section of Clinical Bacteriology, Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
          [3 ] Department of Organismal Biology, Uppsala University, Uppsala, Sweden.
          [4 ] Bioinformatics Infrastructure for Life Sciences (BILS) and Computational Life Science Cluster (CLiC), Department of Molecular Biology, Umeå University, Umeå, Sweden.
          [5 ] Public Health Laboratory, Public Health Service of Amsterdam, Amsterdam, the Netherlands.
          [6 ] Department of Microbiology and Infection Control, University Hospital of North Norway, Tromsø, Norway.
          Article
          JCM.00249-15
          10.1128/JCM.00249-15
          4473235
          25926497
          852fa04d-d33e-4c71-86a4-74781a6d5f17
          Copyright © 2015, American Society for Microbiology. All Rights Reserved.
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