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Genome sequence analysis of the Indian strain Mannheimia haemolytica serotype A2 from ovine pneumonic pasteurellosis
Authors:Sahay  Swati  Shome  Rajeswari  Sankarasubramanian  Jagadesan  Vishnu  Udayakumar S.  Prajapati  Awadhesh  Natesan  Krithiga  Shome  Bibek Ranjan  Rahman   Habibur  Rajendhran   Jeyaprakash
Affiliation:1.Indian Council of Agricultural Research-National Institute of Veterinary Epidemiology and Disease informatics (ICAR-NIVEDI), Yelahanka, Bengaluru, 560064, India
;2.Department of Microbiology, Centre for Research in Pure and Applied Sciences, Jain University, Bangalore, 560011, India
;3.Department of Genetics, School of Biological Sciences, Madurai Kamaraj University, Madurai, Tamil Nadu, 625021, India
;4.International Livestock Research Institute, Block-C, First Floor, NASC Complex, CG Centre, DPS Marg, Pusa, New Delhi, 110012, India
;
Abstract:Mannheimia haemolytica is a leading causative agent of pasteurellosis in ruminants. Genome of M. haemolytica strains from different hosts has been sequenced worldwide to understand its pathogenesis. There are only few reports on the isolation of M. haemolytica in India with limited information on its molecular characteristics. The present study focuses on genome sequence analysis of a M. haemolytica strain isolated from pneumonic sheep. Mannheimia haemolytica A2 strain NIVEDI/MH/1 was isolated and identified by species and serotype-specific PCRs. Whole genome sequencing was performed using the Ion Torrent Personal Genome Machine. A comparative genomic analysis was performed to understand the virulence determinants of the Indian strain and its phylogenetic relationship with other global strains. Sequence data revealed a draft genome of 2,211,426 bp size with 41.3% GC content, assembled into 17 contigs, and contained 2379 genes. Five genomic islands identified in the genome showed high sequence identity with other respiratory pathogens of the Pasteurellaceae family. Phylogenetic analysis showed M. haemolytica A2 NIVEDI/MH/1 is very close to a M. haemolytica A2 strain from pneumonic calf. Further, the analysis revealed the presence of virulence, metal-, and multidrug resistance genes needed for pathogenesis and survival of the bacteria during infection. Also, we identified the presence of type I-C and type II-C of CRISPR-Cas arrays in the present sequenced genome. The study emphasizes the role of M. haemolytica in respiratory infections of ruminants in the Indian subcontinent and indicates the role of vertical and horizontal gene pools in pathogenicity and survivability of the bacteria.
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