Antigen Discovery for Next-Generation Pertussis Vaccines Using Immunoproteomics and Transposon-Directed Insertion Sequencing

Author:

Gregg Kelsey A1,Wang Yihui1,Warfel Jason1,Schoenfeld Elizabeth1,Jankowska Ewa1,Cipollo John F1ORCID,Mayho Matthew2,Boinett Christine2,Prasad Deepika1,Brickman Timothy J3,Armstrong Sandra K3,Parkhill Julian2,Da Silva Antunes Ricardo4,Sette Alessandro45,Papin James F6,Wolf Roman6,Merkel Tod J1

Affiliation:

1. Division of Bacterial, Parasitic, and Allergenic Products, Center for Biologics Evaluation and Research, US Food and Drug Administration , Silver Spring, Maryland , USA

2. Wellcome Sanger Institute , Hinxton , United Kingdom

3. Department of Microbiology and Immunology, University of Minnesota , Minneapolis, Minnesota , USA

4. Division of Vaccine Discovery, La Jolla Institute for Immunology , La Jolla, California , USA

5. Department of Medicine, University of California, San Diego , La Jolla, California , USA

6. Department of Pathology, University of Oklahoma Health Sciences Center , Oklahoma City, Oklahoma , USA

Abstract

Abstract Background Despite high vaccination rates, the United States has experienced a resurgence in reported cases of pertussis after switching to the acellular pertussis vaccine, indicating a need for improved vaccines that enhance infection control. Methods Bordetella pertussis antigens recognized by convalescent-baboon serum and nasopharyngeal wash were identified by immunoproteomics and their subcellular localization predicted. Genes essential or important for persistence in the baboon airway were identified by transposon-directed insertion-site sequencing (TraDIS) analysis. Results In total, 314 B. pertussis antigens were identified by convalescent baboon serum and 748 by nasopharyngeal wash. Thirteen antigens were identified as immunogenic in baboons, essential for persistence in the airway by TraDIS, and membrane-localized: BP0840 (OmpP), Pal, OmpA2, BP1485, BamA, Pcp, MlaA, YfgL, BP2197, BP1569, MlaD, ComL, and BP0183. Conclusions The B. pertussis antigens identified as immunogenic, essential for persistence in the airway, and membrane-localized warrant further investigation for inclusion in vaccines designed to reduce or prevent carriage of bacteria in the airway of vaccinated individuals.

Funder

United States Food and Drug Administration

National Institutes of Health

Wellcome Trust

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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