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Comparative Genomic Analysis of Mannheimia haemolytica from Bovine Sources: e0149520
by
Rasmussen, Jay
, Zaheer, Rahat
, Xu, Yong
, Alexander, Trevor W
, Hendrick, Steve
, Potter, Andrew
, Klima, Cassidy L
, Cook, Shaun R
, Laing, Chad
, Gannon, Vick P
in
Mannheimia haemolytica
2016
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Comparative Genomic Analysis of Mannheimia haemolytica from Bovine Sources: e0149520
by
Rasmussen, Jay
, Zaheer, Rahat
, Xu, Yong
, Alexander, Trevor W
, Hendrick, Steve
, Potter, Andrew
, Klima, Cassidy L
, Cook, Shaun R
, Laing, Chad
, Gannon, Vick P
in
Mannheimia haemolytica
2016
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Comparative Genomic Analysis of Mannheimia haemolytica from Bovine Sources: e0149520
Journal Article
Comparative Genomic Analysis of Mannheimia haemolytica from Bovine Sources: e0149520
2016
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Overview
Bovine respiratory disease is a common health problem in beef production. The primary bacterial agent involved, Mannheimia haemolytica, is a target for antimicrobial therapy and at risk for associated antimicrobial resistance development. The role of M. haemolytica in pathogenesis is linked to serotype with serotypes 1 (S1) and 6 (S6) isolated from pneumonic lesions and serotype 2 (S2) found in the upper respiratory tract of healthy animals. Here, we sequenced the genomes of 11 strains of M. haemolytica, representing all three serotypes and performed comparative genomics analysis to identify genetic features that may contribute to pathogenesis. Possible virulence associated genes were identified within 14 distinct prophage, including a periplasmic chaperone, a lipoprotein, peptidoglycan glycosyltransferase and a stress response protein. Prophage content ranged from 2-8 per genome, but was higher in S1 and S6 strains. A type I-C CRISPR-Cas system was identified in each strain with spacer diversity and organization conserved among serotypes. The majority of spacers occur in S1 and S6 strains and originate from phage suggesting that serotypes 1 and 6 may be more resistant to phage predation. However, two spacers complementary to the host chromosome targeting a UDP-N-acetylglucosamine 2-epimerase and a glycosyl transferases group 1 gene are present in S1 and S6 strains only indicating these serotypes may employ CRISPR-Cas to regulate gene expression to avoid host immune responses or enhance adhesion during infection. Integrative conjugative elements are present in nine of the eleven genomes. Three of these harbor extensive multi-drug resistance cassettes encoding resistance against the majority of drugs used to combat infection in beef cattle, including macrolides and tetracyclines used in human medicine. The findings here identify key features that are likely contributing to serotype related pathogenesis and specific targets for vaccine design intended to reduce the dependency on antibiotics to treat respiratory infection in cattle.
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