Concomitant Enterotoxigenic Escherichia coli Infection Induces Increased Immune Responses to Vibrio cholerae O1 Antigens in Patients with Cholera in Bangladesh

Author:

Chowdhury Fahima1,Begum Yasmin A.1,Alam Mohammad Murshid1,Khan Ashraful I.1,Ahmed Tanvir1,Bhuiyan M. Saruar1,Harris Jason B.23,LaRocque Regina C.23,Faruque Abu S. G.1,Endtz Hubert1,Ryan Edward T.234,Cravioto Alejandro1,Svennerholm Ann-Mari5,Calderwood Stephen B.23,Qadri Firdausi1

Affiliation:

1. International Centre for Diarrheal Disease Research, Dhaka, Bangladesh

2. Massachusetts General Hospital, Boston, Massachusetts

3. Harvard Medical School, Boston, Massachusetts

4. Harvard School of Public Health, Boston, Massachusetts

5. Institute of Biomedicine, Dept. of Microbiology and Immunology, University of Gothenburg, Gothenburg, Sweden

Abstract

ABSTRACT Vibrio cholerae O1 and enterotoxigenic Escherichia coli (ETEC) are major bacterial pathogens that cause dehydrating disease requiring hospitalization of children and adults. The cholera toxin (CT) produced by V. cholerae O1 and the heat-labile toxin (LT) and/or heat-stable toxin (ST) of ETEC are responsible for secretory diarrhea. We have observed that about 13% of hospitalized diarrheal patients are concomitantly infected with V. cholerae O1 and ETEC. In order to understand the outcome of such dual infections on the clinical and immunological responses in cholera patients, we studied patients infected with V. cholerae O1 (group VC; n = 25), those infected with both V. cholerae O1 and ETEC (group VCET; n = 25), and those infected with ETEC only (group ET; n = 25). The VCET group showed more severe dehydration and had a higher intake of intravenous fluid and more vomiting than the ETEC group ( P = 0.01 to 0.003). The VCET patients showed higher vibriocidal responses and increased antibody titers to cholera toxin and lipopolysaccharide (LPS) in plasma than did the V. cholerae O1 patients ( P = 0.02 to <0.001). All responses in the V. cholerae O1 and in the VCET groups were more robust than those seen in the group infected with ETEC only ( P = 0.01 to <0.001). We thus show that concomitant colonization with ETEC induces immune responses to V. cholerae antigens that are more robust than those seen with V. cholerae O1 infection alone. It is possible that LT or other factors expressed by ETEC may play a role as a mucosal adjuvant in enhancing the immune responses to V. cholerae O1.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

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