» Articles » PMID: 36226942

Functional Activities of O-Polysaccharide and Hemolysin Coregulated Protein 1 Specific Antibodies Isolated from Melioidosis Patients

Overview
Journal Infect Immun
Date 2022 Oct 13
PMID 36226942
Authors
Affiliations
Soon will be listed here.
Abstract

Melioidosis is a fatal tropical disease caused by the environmental Gram-negative bacterium, Burkholderia pseudomallei. This bacterium is intrinsically resistant to several antibiotics and treatment of melioidosis requires prolonged antibiotic administration. To date, there are no vaccines available for melioidosis. Previous studies have shown that humoral immunity is critical for surviving melioidosis and that O-polysaccharide (OPS) and hemolysin coregulated protein 1 (Hcp1) are important protective antigens in animal models of melioidosis. Our previous studies revealed that melioidosis patients had high levels of OPS- and Hcp1-specific antibodies and that IgG against OPS (IgG-OPS) and Hcp1 (IgG-Hcp1) were associated with patient survival. In this study, we characterized the potential function(s) of IgG-OPS and IgG-Hcp1 from melioidosis patients. IgG-OPS and IgG-Hcp1 were purified from pooled serum obtained from melioidosis patients using immuno-affinity chromatography. Antibody-dependent cellular phagocytosis assays were performed with pooled serum from melioidosis patients and compared with serum obtained from healthy controls. Serum from melioidosis patients significantly enhanced B. pseudomallei uptake into the human monocytic cell line THP-1 compared with pooled serum from healthy donors. Enhanced opsonization was observed with IgG-OPS and IgG-Hcp1 in a dose-dependent manner. Antibody-dependent complement deposition assays were performed with IgG-OPS and IgG-Hcp1 using flow cytometry and showed that there was enhanced C3b deposition on the surface of B. pseudomallei treated with IgG-OPS but to a lesser degree with IgG-Hcp1. This study provides insight into the function of IgG-OPS and IgG-Hcp1 in human melioidosis and supports that OPS and Hcp1 are potential vaccine antigens for immunization against melioidosis.

Citing Articles

Burkholderia pseudomallei and melioidosis.

Meumann E, Limmathurotsakul D, Dunachie S, Wiersinga W, Currie B Nat Rev Microbiol. 2023; 22(3):155-169.

PMID: 37794173 DOI: 10.1038/s41579-023-00972-5.

References
1.
Chaichana P, Jenjaroen K, Chumseng S, Sumonwiriya M, Rongkard P, Kronsteiner B . Role of Burkholderia pseudomallei-Specific IgG2 in Adults with Acute Melioidosis, Thailand. Emerg Infect Dis. 2021; 27(2):463-470. PMC: 7853568. DOI: 10.3201/eid2702.200213. View

2.
Burtnick M, DeShazer D, Nair V, Gherardini F, Brett P . Burkholderia mallei cluster 1 type VI secretion mutants exhibit growth and actin polymerization defects in RAW 264.7 murine macrophages. Infect Immun. 2009; 78(1):88-99. PMC: 2798217. DOI: 10.1128/IAI.00985-09. View

3.
Chaowagul W, White N, Dance D, Wattanagoon Y, Naigowit P, Davis T . Melioidosis: a major cause of community-acquired septicemia in northeastern Thailand. J Infect Dis. 1989; 159(5):890-9. DOI: 10.1093/infdis/159.5.890. View

4.
Charuchaimontri C, Suputtamongkol Y, Nilakul C, Chaowagul W, Chetchotisakd P, Lertpatanasuwun N . Antilipopolysaccharide II: an antibody protective against fatal melioidosis. Clin Infect Dis. 1999; 29(4):813-8. DOI: 10.1086/520441. View

5.
Scott A, Laws T, DElia R, Stokes M, Nandi T, Williamson E . Protection against experimental melioidosis following immunization with live Burkholderia thailandensis expressing a manno-heptose capsule. Clin Vaccine Immunol. 2013; 20(7):1041-7. PMC: 3697456. DOI: 10.1128/CVI.00113-13. View