A spontaneous mutation in kdsD, a biosynthesis gene for 3 Deoxy-D-manno-Octulosonic Acid, occurred in a ciprofloxacin resistant strain of Francisella tularensis and caused a high level of attenuation in murine models of tularemia

Francisella tularensis, a gram-negative facultative intracellular bacterial pathogen, is the causative agent of tularemia and able to infect many mammalian species, including humans. Because of its ability to cause a lethal infection, low infectious dose, and aerosolizable nature, F. tularensis subs...

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Published inPloS one Vol. 12; no. 3; p. e0174106
Main Authors Chance, Taylor, Chua, Jennifer, Toothman, Ronald G, Ladner, Jason T, Nuss, Jonathan E, Raymond, Jo Lynne, Biot, Fabrice V, Demons, Samandra, Miller, Lynda, Halasohoris, Stephanie, Mou, Sherry, Koroleva, Galina, Lovett, Sean, Palacios, Gustavo, Vietri, Nicholas J, Worsham, Patricia L, Cote, Christopher K, Kijek, Todd M, Bozue, Joel A
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 01.03.2017
Public Library of Science (PLoS)
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Summary:Francisella tularensis, a gram-negative facultative intracellular bacterial pathogen, is the causative agent of tularemia and able to infect many mammalian species, including humans. Because of its ability to cause a lethal infection, low infectious dose, and aerosolizable nature, F. tularensis subspecies tularensis is considered a potential biowarfare agent. Due to its in vitro efficacy, ciprofloxacin is one of the antibiotics recommended for post-exposure prophylaxis of tularemia. In order to identify therapeutics that will be efficacious against infections caused by drug resistant select-agents and to better understand the threat, we sought to characterize an existing ciprofloxacin resistant (CipR) mutant in the Schu S4 strain of F. tularensis by determining its phenotypic characteristics and sequencing the chromosome to identify additional genetic alterations that may have occurred during the selection process. In addition to the previously described genetic alterations, the sequence of the CipR mutant strain revealed several additional mutations. Of particular interest was a frameshift mutation within kdsD which encodes for an enzyme necessary for the production of 3-Deoxy-D-manno-Octulosonic Acid (KDO), an integral component of the lipopolysaccharide (LPS). A kdsD mutant was constructed in the Schu S4 strain. Although it was not resistant to ciprofloxacin, the kdsD mutant shared many phenotypic characteristics with the CipR mutant, including growth defects under different conditions, sensitivity to hydrophobic agents, altered LPS profiles, and attenuation in multiple models of murine tularemia. This study demonstrates that the KdsD enzyme is essential for Francisella virulence and may be an attractive therapeutic target for developing novel medical countermeasures.
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Current address: Veterinary Pathology Services, Joint Pathology Center, Silver Spring, MD United States of America
Competing Interests: The authors have declared that no competing interests exist.
Conceptualization: JC JEN PLW TMK JAB.Data curation: JTL GK SL.Formal analysis: JTL JEN SD GK SL.Funding acquisition: GP PLW.Investigation: TC JC RGT JTL JEN JLR FVB SD LM SH SM GK SL CKC TMK JAB.Methodology: JC TMK JAB.Project administration: TC JTL SD GP NJV PLW TMK JAB.Resources: JEN GP.Supervision: TC JTL SD GP NJV PLW TMK JAB.Writing – original draft: TC JC JTL JEN JLR SD.Writing – review & editing: TC JC JTL JEN JLR SD CKC.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0174106