Salmonella enterica Serovar Typhi-Specific Immunoglobulin A Antibody Responses in Plasma and Antibody in Lymphocyte Supernatant Specimens in Bangladeshi Patients with Suspected Typhoid Fever

Author:

Sheikh Alaullah1,Bhuiyan M. Saruar1,Khanam Farhana1,Chowdhury Fahima2,Saha Amit1,Ahmed Dilruba1,Jamil K. M. A.1,LaRocque Regina C.2,Harris Jason B.2,Ahmad Mian Mashhud3,Charles Richelle2,Brooks W. Abdullah1,Calderwood Stephen B.245,Cravioto Alejandro1,Ryan Edward T.246,Qadri Firdausi1

Affiliation:

1. International Centre for Diarrhoeal Disease Research, Bangladesh (ICDDR,B), Dhaka, Bangladesh

2. Division of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts

3. Dhaka Medical College Hospital, Dhaka, Bangladesh

4. Department of Medicine, Harvard Medical School, Boston, Massachusetts

5. Department of Microbiology and Molecular Center, Harvard Medical School, Boston, Massachusetts

6. Department of Immunology and Infectious Diseases, Harvard School of Public Health, Boston, Massachusetts

Abstract

ABSTRACT Many currently available diagnostic tests for typhoid fever lack sensitivity and/or specificity, especially in areas of the world where the disease is endemic. In order to identify a diagnostic test that better correlates with typhoid fever, we evaluated immune responses to Salmonella enterica serovar Typhi (serovar Typhi) in individuals with suspected typhoid fever in Dhaka, Bangladesh. We enrolled 112 individuals with suspected typhoid fever, cultured day 0 blood for serovar Typhi organisms, and performed Widal assays on days 0, 5, and 20. We harvested peripheral blood lymphocytes and analyzed antibody levels in supernatants collected on days 0, 5, and 20 (using an antibody-in-lymphocyte-supernatant [ALS] assay), as well as in plasma on these days. We measured ALS reactivity to a serovar Typhi membrane preparation (MP), a formalin-inactivated whole-cell preparation, and serovar Typhi lipopolysaccharide. We measured responses in healthy Bangladeshi, as well as in Bangladeshi febrile patients with confirmed dengue fever or leptospirosis. We categorized suspected typhoid fever individuals into different groups (groups I to V) based on blood culture results, Widal titer, and clinical features. Responses to MP antigen in the immunoglobulin A isotype were detectable at the time of presentation in the plasma of 81% of patients. The ALS assay, however, tested positive in all patients with documented or highly suspicious typhoid, suggesting that such a response could be the basis of improved diagnostic point-of-care-assay for serovar Typhi infection. It can be important for use in epidemiological studies, as well as in difficult cases involving fevers of unknown origin.

Publisher

American Society for Microbiology

Subject

Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy

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