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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 3

Gene presence/absence map of the pangenome of 31 isolates from cholera toxin‒positive Vibrio cholerae serogroups. The red rectangle in the accessory genome indicates the conserved unique coding sequences that are specific to the serogroup O141. Each serogroup is associated with a color block: O37 (red), O1 (orange), O139 (dark blue), O141 (purple), O75 (Marron). Scale bar indicates nucleotide substitutions per site.

Figure 3. Gene presence/absence map of the pangenome of 31 isolates from cholera toxin‒positive Vibrio cholerae serogroups. The red rectangle in the accessory genome indicates the conserved unique coding sequences that are specific to the serogroup O141. Each serogroup is associated with a color block: O37 (red), O1 (orange), O139 (dark blue), O141 (purple), O75 (Marron). Scale bar indicates nucleotide substitutions per site.

Main Article

Page created: January 05, 2022
Page updated: February 21, 2022
Page reviewed: February 21, 2022
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