Lyme borreliosis caused by diverse genospecies of Borrelia burgdorferi sensu lato in northeastern China X.-B. Ni, N. Jia, B.-G. Jiang, T. Sun, Y.-C.

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Lyme borreliosis caused by diverse genospecies of Borrelia burgdorferi sensu lato in northeastern China X.-B. Ni, N. Jia, B.-G. Jiang, T. Sun, Y.-C. Zheng, Q.-B. Huo, K. Liu, L. Ma, Q.-M. Zhao, H. Yang, X. Wang, J.-F. Jiang, W.-C. Cao Clinical Microbiology and Infection Volume 20, Issue 8, Pages 808-814 (August 2014) DOI: 10.1111/1469-0691.12532 Copyright © 2014 European Society of Clinical Infectious Diseases Terms and Conditions

FIG. 1 Phylogenetic trees obtained by the maximum likelihood method. (a) (253-bp) 5S-23S rRNA intergenic spacer gene; (b) (588-bp) flagellin gene; (c) (636-bp) outer surface protein C (ospC) gene; (d) (903-bp) 16S rRNA gene; (e) (307-bp) ospA gene. Numbers on the branches indicate percentage of replicates that reproduces the topology for each clade. Parentheses enclose GenBank numbers of the sequences used in the phylogenetic analysis, and brackets enclose the quantity of the same sequences as this strain. Boldface indicates sequences obtained from this study. The trees are drawn to scale, with branch lengths in the same units as those of the evolutionary distances (see scale bars) used to infer the phylogenetic tree. Positions containing gaps, missing data and primer sequences were eliminated from the dataset. Clinical Microbiology and Infection 2014 20, 808-814DOI: (10.1111/1469-0691.12532) Copyright © 2014 European Society of Clinical Infectious Diseases Terms and Conditions

FIG. 1 Phylogenetic trees obtained by the maximum likelihood method. (a) (253-bp) 5S-23S rRNA intergenic spacer gene; (b) (588-bp) flagellin gene; (c) (636-bp) outer surface protein C (ospC) gene; (d) (903-bp) 16S rRNA gene; (e) (307-bp) ospA gene. Numbers on the branches indicate percentage of replicates that reproduces the topology for each clade. Parentheses enclose GenBank numbers of the sequences used in the phylogenetic analysis, and brackets enclose the quantity of the same sequences as this strain. Boldface indicates sequences obtained from this study. The trees are drawn to scale, with branch lengths in the same units as those of the evolutionary distances (see scale bars) used to infer the phylogenetic tree. Positions containing gaps, missing data and primer sequences were eliminated from the dataset. Clinical Microbiology and Infection 2014 20, 808-814DOI: (10.1111/1469-0691.12532) Copyright © 2014 European Society of Clinical Infectious Diseases Terms and Conditions

FIG. 2 Erythema migrans (EM) in four patients. (a) EM near the axilla. It was a classic EM with central clearing. (b) EM at the back of the waist (20 cm in diameter) with vesicles in the centre. Borrelia afzelii was amplified from the patient's blood. (c) EM at the right flank with eschar in the centre. Borrelia garinii was identified from the patient. (d) EM on the right leg. Borrelia valaisiana-related EM was identified from the patient. Clinical Microbiology and Infection 2014 20, 808-814DOI: (10.1111/1469-0691.12532) Copyright © 2014 European Society of Clinical Infectious Diseases Terms and Conditions