MISC

2006年5月

Enterotoxigenicity of mature 45-kilodalton and processed 35-kilodalton forms of hemagglutinin protease purified from a cholera toxin gene-negative Vibrio cholerae non-O1, non-O139 strain

INFECTION AND IMMUNITY
  • A Ghosh
  • ,
  • DR Saha
  • ,
  • KM Hoque
  • ,
  • M Asakuna
  • ,
  • S Yamasaki
  • ,
  • H Koley
  • ,
  • SS Das
  • ,
  • MK Chakrabarti
  • ,
  • A Pal

74
5
開始ページ
2937
終了ページ
2946
記述言語
英語
掲載種別
DOI
10.1128/IAI.74.5.2937-2946.2006
出版者・発行元
AMER SOC MICROBIOLOGY

Cholera toxin gene-negative Fibrio cholerae non-O1, non-O139 strain PL-21 is the etiologic agent of cholera-like syndrome. Hemagglutinin protease (HAP) is one of the major secretory proteins of PL-21. The mature 45-kDa and processed 35-kDa forms of HAP were purified in the presence and absence of EDTA from culture supernatants of PL-21. Enterotoxigenicities of both forms of HAP were tested in rabbit ileal loop (RIL), Ussing chamber, and tissue culture assays. The 35-kDa HAP showed hemorrhagic fluid response in a dose-dependent manner in the RIL assay. Histopathological examination of 20 jig of purified protease-treated rabbit ileum showed the presence of erythrocytes and neutrophils in the upper part of the villous lamina propria. Treatment with 40 jig of protease resulted in gross damage of the villous epithelium with inflammation, hemorrhage, and necrosis. The 35-kDa form of HAP, when added to the lumenal surface of rat ileum loaded in an Ussing chamber, showed a decrease in the intestinal short-circuit current and a cell rounding effect on HeLa cells. The mature 45-kDa form of HAP showed an increase in intestinal short-circuit current in an Ussing chamber and a cell distending effect on HeLa cells. These results show that HAP may play a role in the pathogenesis of PL-21.

リンク情報
DOI
https://doi.org/10.1128/IAI.74.5.2937-2946.2006
CiNii Articles
http://ci.nii.ac.jp/naid/10028203811
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/16622232
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000237311200048&DestApp=WOS_CPL
ID情報
  • DOI : 10.1128/IAI.74.5.2937-2946.2006
  • ISSN : 0019-9567
  • eISSN : 1098-5522
  • CiNii Articles ID : 10028203811
  • PubMed ID : 16622232
  • Web of Science ID : WOS:000237311200048

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