Loading…
Virulence gene profiling of porcine Pasteurella multocida isolates of Assam
The present study was conducted to detect and identify the virulence genes in isolates of porcine origin from Assam. A total of 21 porcine isolates were subjected to capsular typing and detection of virulence-associated genes ( , and ) using various polymerase chain reaction (PCR) methods reported e...
Saved in:
Published in: | Veterinary World 2018-03, Vol.11 (3), p.348-354 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | The present study was conducted to detect and identify the virulence genes in
isolates of porcine origin from Assam.
A total of 21 porcine
isolates were subjected to capsular typing and detection of virulence-associated genes (
, and
) using various polymerase chain reaction (PCR) methods reported elsewhere. Further, pathogenicity of the porcine isolates of
was studied in mice. For each strain of
selected for pathogenicity trial, the group of mice was injected intraperitoneally (i/p) with 0.1 ml of the inoculum prepared from respective field isolates, containing 10
organisms per ml.
Capsular typing of the isolates by multiplex PCR showed two capsular types, type A (66.66%) and type D (33.33%). All the isolates were positive for outer membrane protein genes,
and
genes. Iron acquisition genes,
and
, were detected in 14.28% and 19.04% of the isolates. The dermonecrotoxin encoding gene,
, was present in 23.80% of the isolates. Filamentous hemagglutinin encoding gene,
, was detected in 28.57%. The virulence gene distribution pattern of the isolates indicates the important role of the genes in disease pathogenesis.
From the present study, it can be concluded that
gene is an important marker gene for defining the pathogenic potential of
strains in swine. |
---|---|
ISSN: | 0972-8988 2231-0916 |
DOI: | 10.14202/vetworld.2018.348-354 |