Opsonophagocytic Activity and Other Serological Indications of Bordetella pertussis Infection in Military Recruits in Norway

Author:

Aase Audun1234,Herstad Tove Karin1234,Merino Samuel1234,Brandsdal Kari Torkildsen1234,Berdal Bjørn Peter1234,Aleksandersen Erja M.1234,Aaberge Ingeborg S.1234

Affiliation:

1. Department of Bacteriology and Immunology, Norwegian Institute of Public Health, Oslo, Norway

2. General Practice Branch, Armed Forces Medical Services, Oslo, Norway

3. Institute of Microbiology, Armed Forces Medical Services, Oslo, Norway

4. Ullevål University Hospital, Oslo, Norway

Abstract

ABSTRACT Bordetella pertussis is the causative agent of pertussis (whooping cough). Despite high vaccination coverage, pertussis remains a significant disease in many countries. Besides vaccination, transient carriage of Bordetella spp. or other cross-reacting organisms adds to the immunity against pertussis. However, the various immunological mechanisms conferring protection remain largely unknown. In this study, paired serum samples from 464 healthy Norwegian military recruits were collected, the first at enrolment and the second about 8 months later. The prevalence of pertussis during military service was examined by comparing the paired serum samples for immunoglobulin G (IgG) antibodies against pertussis toxin (PT) by enzyme-linked immunosorbent assay (ELISA). Seventy-eight percent of the recruits had low levels of IgG antibodies against PT in both samples. Conversely, 8.4% of the recruits demonstrated high anti-PT IgG levels in the first sample, indicative of recent pertussis prior to enrolment. One recruit experienced seroconversion, indicating pertussis during service. A subset of 248 serum samples with low, medium, and high anti-PT IgG titers were analyzed by a different ELISA kit for IgG and IgA antibodies against PT and filamentous hemagglutinin (FHA) and for opsonophagocytic activity (OPA), for induction of C3b deposition products, and for IgG binding with live B. pertussis as the antigen. We observed high correlations between OPA and IgG against live bacteria ( r = 0.83), between OPA and IgG anti-FHA ( r = 0.79), between OPA and anti-PT IgG ( r = 0.68), and between OPA and C3b binding ( r = 0.70) ( P < 0.0001 for all). Anti-PT IgA did not correlate closely with the other assays.

Publisher

American Society for Microbiology

Subject

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

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