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Volume 28, Number 3—March 2022
Research

Genomic and Phenotypic Insights for Toxigenic Clinical Vibrio cholerae O141

Yaovi M.G. HounmanouComments to Author , Brandon Sit, Bolutife Fakoya, Matthew K. Waldor, and Anders Dalsgaard
Author affiliations: University of Copenhagen, Frederiksberg, Denmark (Y.M.G. Hounmanou, A. Dalsgaard); Brigham & Women’s Hospital, Boston, Massachusetts, USA (B. Sit, B. Fakoya, M.K. Waldor); Harvard Medical School, Boston (B. Sit, B. Fakoya, M.K. Waldor)

Main Article

Figure 1

Maximum-likelihood phylogenetic tree for Vibrio cholerae O141 in a global context for 38 isolates from Ctx-positive V. cholerae and Ctx-negative serogroups. Numbers along branches are bootstrap values. Scale bar indicates nucleotide substitutions per site. Ctx, cholera toxin.

Figure 1. Maximum-likelihood phylogenetic tree for Vibrio cholerae O141 in a global context for 38 isolates from Ctx-positive V. cholerae and Ctx-negative serogroups. Numbers along branches are bootstrap values. Scale bar indicates nucleotide substitutions per site. Ctx, cholera toxin.

Main Article

Page created: January 05, 2022
Page updated: February 21, 2022
Page reviewed: February 21, 2022
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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