Accession Number : AD1015399


Title :   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 Causes a High Level of Attenuation in Murine Models of Tularemia


Descriptive Note : Journal Article


Corporate Author : USAMRIID Frederick United States


Personal Author(s) : Bozue, Joel A ; Chance,Taylor ; Chua,Jennifer ; Toothman,Ronald G ; Ladner,Jason T ; Nuss,Jonathan E ; Raymond,Jo L ; Biot,Fabrice V ; Demons,Samandra ; Miller,Lynda ; Mou,Sherry ; Koroleva,Galina ; Lovett,Sean ; Palacios,Gustavo ; Vietri,Nicholas ; Worsham,Patricia ; Cote,Christopher ; Kijek,Todd


Full Text : https://apps.dtic.mil/dtic/tr/fulltext/u2/1015399.pdf


Report Date : 30 Aug 2016


Pagination or Media Count : 64


Abstract : Francisella tularensis is a gramnegative facultative intracellular bacterial pathogen that can 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 determine additional genetic alterations that occurred during the selection process. The sequence of the CipR strain showed additional mutations which likely occurred spontaneously during the selection process. Of particular interest was a frameshift mutation within kdsD which encodes for an enzyme necessary for the production of 3-Deoxy-D50 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, it shared many phenotypic characteristics with the CipR strain, including growth defects under different conditions, sensitivity to hydrophobic agents, altered LPS profiles, and severe attenuation in multiple models of murine tularemia. This study demonstrates that the KdsD enzyme is an attractive therapeutic target for developing novel medical countermeasures.


Descriptors :   antibacterial agents , gramnegative bacteria , mutations , genes , antiinfective agents , enzymes


Distribution Statement : APPROVED FOR PUBLIC RELEASE