Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1995 Nov;63(11):4423-8.
doi: 10.1128/iai.63.11.4423-4428.1995.

Enterotoxic activity of hemolysin BL from Bacillus cereus

Affiliations

Enterotoxic activity of hemolysin BL from Bacillus cereus

D J Beecher et al. Infect Immun. 1995 Nov.

Abstract

Bacillus cereus causes exotoxin-mediated diarrheal food poisoning. Hemolysin BL (HBL) is a well-characterized B. cereus toxin composed of three components (B, L1, and L2) that together possess hemolytic, cytotoxic, dermonecrotic, and vascular permeability activities. Here, we show that HBL causes fluid accumulation in ligated rabbit ileal loops at a dose of 5 micrograms of each component per loop. Maximal fluid responses occurred for combinations of all three components at > or = 25 micrograms of each component per loop. Individual components and binary combinations did not cause significant fluid accumulation at 25 micrograms of each component. Specific antisera to HBL components inhibited the fluid accumulation response of crude culture supernatant from B. cereus F837/76. These antisera were tested against an antiserum to a partially characterized multicomponent diarrheal toxin described previously by Thompson et al. (N. E. Thompson, M. J. Ketterhagen, M. S. Bergdoll, and E. J. Shantz, Infect. Immun. 43:887-894, 1984). Immunoblot and immunoprecipitation analyses indicate that HBL and that toxin are identical. These results confirm previous speculation that HBL is a tripartite enterotoxin that, as for all of its other known activities, requires all three components for maximal activity.

PubMed Disclaimer

References

    1. Infect Immun. 1994 Mar;62(3):980-6 - PubMed
    1. J Bacteriol. 1993 Nov;175(21):6760-6 - PubMed
    1. Appl Environ Microbiol. 1994 Dec;60(12):4614-6 - PubMed
    1. Infect Immun. 1995 Feb;63(2):632-9 - PubMed
    1. Infect Immun. 1995 Jun;63(6):2093-9 - PubMed

Publication types