TY - JOUR
T1 - Clinical and immunologic characteristics of vibrio cholerae o139 bengal infection in north american volunteers
AU - Morris, J. Glenn
AU - Losonsky, Genevieve E.
AU - Johnson, Judith A.
AU - Tacket, Carol O.
AU - Nataro, James P.
AU - Panigrahi, Pinaki
AU - Levin, Myron M.
N1 - Funding Information:
Received 25 August 1994; revised 22 November 1994. Presented in part: 32nd annual meeting. Infectious Diseases Society of America. Orlando. Florida. 7-10 October 1994. All studies were approved by the Institutional Review Board. University of Maryland at Baltimore. To ensure informed consent. volunteers had to pass a written examination containing questions on all aspects of the study. including risks. benefits. procedures. bacteriology. and immunology. Grant support: National Institutes of Health (AI-15096 to M.M.L. and AI-35729 to J.AJ.). Reprints or correspondence: Dr. J. Glenn Morris. VA Medical Center. 10 N. Greene St.. Baltimore. MD 2120I.
PY - 1995/4
Y1 - 1995/4
N2 - Vibrio cholerae O139 Bengal has recently emerged as a cause of epidemic cholera in Asia. To evaluate clinical and immunologic responses to infection, V. cholerae O139 Bengal AIl837 was administered to healthy adult North American volunteers. Two of 4 persons ingesting 104 cfu became ill (incubation period, 48 h; mean diarrheal stool, 1873 g), as did 7 of9 persons receiving 106 cfu (incubation period, 28 h; mean diarrheal stool, 4548 g). III volunteers did not demonstrate a vibriocidal antibody response to the challenge strain or other V. cholerae. Three months later, volunteers were rechallenged with the homologous O139 Bengal strain. Only 1 of 6 persons who had been ill on initial challenge had diarrhea, compared with 11 of 13 controls (P=.01; protective efficacy = 80%). V. cholerae O139 Bengal can cause severe diarrhea typical of cholera, with clinical characteristics and a dose-response similar to those seen with V. cholerae O1 E1 Tor. A moderately high level of protection against subsequent disease is provided by initial clinical infection.
AB - Vibrio cholerae O139 Bengal has recently emerged as a cause of epidemic cholera in Asia. To evaluate clinical and immunologic responses to infection, V. cholerae O139 Bengal AIl837 was administered to healthy adult North American volunteers. Two of 4 persons ingesting 104 cfu became ill (incubation period, 48 h; mean diarrheal stool, 1873 g), as did 7 of9 persons receiving 106 cfu (incubation period, 28 h; mean diarrheal stool, 4548 g). III volunteers did not demonstrate a vibriocidal antibody response to the challenge strain or other V. cholerae. Three months later, volunteers were rechallenged with the homologous O139 Bengal strain. Only 1 of 6 persons who had been ill on initial challenge had diarrhea, compared with 11 of 13 controls (P=.01; protective efficacy = 80%). V. cholerae O139 Bengal can cause severe diarrhea typical of cholera, with clinical characteristics and a dose-response similar to those seen with V. cholerae O1 E1 Tor. A moderately high level of protection against subsequent disease is provided by initial clinical infection.
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U2 - 10.1093/infdis/171.4.903
DO - 10.1093/infdis/171.4.903
M3 - Article
C2 - 7706818
AN - SCOPUS:0028949899
SN - 0022-1899
VL - 171
SP - 903
EP - 908
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 4
ER -