TY - JOUR
T1 - Polymorphisms influencing expression of dermonecrotic toxin in Bordetella bronchiseptica
AU - Okada, Keisuke
AU - Abe, Hiroyuki
AU - Ike, Fumio
AU - Ogura, Yoshitoshi
AU - Hayashi, Tetsuya
AU - Fukui-Miyazaki, Aya
AU - Nakamura, Keiji
AU - Shinzawa, Naoaki
AU - Horiguchi, Yasuhiko
N1 - Publisher Copyright:
© 2015 Okada et al.
PY - 2015/2/2
Y1 - 2015/2/2
N2 - Bordetella bronchiseptica is a pathogenic bacterium causing respiratory infections in a broad range of mammals. Recently, we determined the whole genome sequence of B. bronchiseptica S798 strain isolated from a pig infected with atrophic rhinitis and found four single-nucleotide polymorphisms (SNPs) at positions -129, -72, +22, and +38 in the region upstream of dnt encoding dermonecrotic toxin (DNT), when compared with a rabbit isolate, RB50. DNT is known to be involved in turbinate atrophy observed in atrophic rhinitis. Immunoblotting, quantitative real-time PCR, and β-galactosidase reporter assay revealed that these SNPs resulted in the increased promoter activity of dnt and conferred the increased ability to produce DNT on the bacteria. Similar or identical SNPs were also found in other pig isolates kept in our laboratory, all of which produce a larger amount of DNT than RB50. Our analysis revealed that substitution of at least two of the four bases, at positions -72 and +22, influenced the promoter activity for dnt. These results imply that these SNPs are involved in the pathogenicity of bordetellae specific to pig diseases.
AB - Bordetella bronchiseptica is a pathogenic bacterium causing respiratory infections in a broad range of mammals. Recently, we determined the whole genome sequence of B. bronchiseptica S798 strain isolated from a pig infected with atrophic rhinitis and found four single-nucleotide polymorphisms (SNPs) at positions -129, -72, +22, and +38 in the region upstream of dnt encoding dermonecrotic toxin (DNT), when compared with a rabbit isolate, RB50. DNT is known to be involved in turbinate atrophy observed in atrophic rhinitis. Immunoblotting, quantitative real-time PCR, and β-galactosidase reporter assay revealed that these SNPs resulted in the increased promoter activity of dnt and conferred the increased ability to produce DNT on the bacteria. Similar or identical SNPs were also found in other pig isolates kept in our laboratory, all of which produce a larger amount of DNT than RB50. Our analysis revealed that substitution of at least two of the four bases, at positions -72 and +22, influenced the promoter activity for dnt. These results imply that these SNPs are involved in the pathogenicity of bordetellae specific to pig diseases.
UR - http://www.scopus.com/inward/record.url?scp=84922496586&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84922496586&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0116604
DO - 10.1371/journal.pone.0116604
M3 - Article
C2 - 25642712
AN - SCOPUS:84922496586
SN - 1932-6203
VL - 10
JO - PloS one
JF - PloS one
IS - 2
M1 - e0116604
ER -