A Burkholderia pseudomallei protein microarray reveals serodiagnostic and cross-reactive antigens

被引:140
作者
Felgner, Philip L. [1 ,2 ,5 ]
Kayala, Matthew A. [2 ,3 ]
Vigil, Adam [1 ]
Burk, Chad [1 ]
Nakajima-Sasaki, Rie [1 ]
Pablo, Jozelyn [1 ]
Molina, Douglas M. [5 ]
Hirst, Siddiqua [1 ]
Chew, Janet S. W. [6 ]
Wang, Dongling [6 ]
Tan, Gladys [6 ]
Duffield, Melanie [7 ]
Yang, Ron [8 ]
Neel, Julien [2 ,3 ]
Chantratita, Narisara [11 ]
Bancroft, Greg [9 ]
Lertmemongkolchai, Ganjana [10 ]
Davies, D. Huw [1 ]
Baldi, Pierre [2 ,3 ,4 ]
Peacock, Sharon [11 ,12 ]
Titball, Richard W. [8 ,9 ]
机构
[1] Univ Calif Irvine, Dept Med, Div Infect Dis, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Inst Genom & Bioinformat, Irvine, CA 92067 USA
[3] Univ Calif Irvine, Dept Comp Sci, Irvine, CA 92067 USA
[4] Univ Calif Irvine, Dept Biol Chem, Irvine, CA 92067 USA
[5] Antigen Discovery Inc, Irvine, CA 92618 USA
[6] DSO Natl Labs, Def Med & Environm Res Inst, Singapore 117510, Singapore
[7] Def Sci & Technol Lab, Salisbury SP4 0JQ, Wilts, England
[8] Univ Exeter, Sch Biosci, Exeter EX4 4QD, Devon, England
[9] Univ London London Sch Hyg & Trop Med, Dept Infect & Trop Dis, London WC1E 7HT, England
[10] Khon Kaen Univ, Dept Clin Immunol, Khon Kaen 40002, Thailand
[11] Mahidol Univ, Fac Trop Med, Mahidol Oxford Trop Med Res Unit, Bangkok 10400, Thailand
[12] Univ Oxford, Nuffield Dept Clin Med, Ctr Clin Vaccinol & Trop Med, Churchill Hosp, Oxford CB2 0QQ, England
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
antigen discovery; melioidosis; diagnostic; antigen prediction; HEAT-SHOCK PROTEINS; IMMUNE-RESPONSE; ANTIBODY-RESPONSES; CAUSATIVE AGENT; VACCINE; MELIOIDOSIS; INFECTION; VIRULENCE; GROEL; IDENTIFICATION;
D O I
10.1073/pnas.0812080106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Understanding the way in which the immune system responds to infection is central to the development of vaccines and many diagnostics. To provide insight into this area, we fabricated a protein microarray containing 1,205 Burkholderia pseudomallei proteins, probed it with 88 melioidosis patient sera, and identified 170 reactive antigens. This subset of antigens was printed on a smaller array and probed with a collection of 747 individual sera derived from 10 patient groups including melioidosis patients from Northeast Thailand and Singapore, patients with different infections, healthy individuals from the USA, and from endemic and nonendemic regions of Thailand. We identified 49 antigens that are significantly more reactive in melioidosis patients than healthy people and patients with other types of bacterial infections. We also identified 59 cross-reactive antigens that are equally reactive among all groups, including healthy controls from the USA. Using these results we were able to devise a test that can classify melioidosis positive and negative individuals with sensitivity and specificity of 95% and 83%, respectively, a significant improvement over currently available diagnostic assays. Half of the reactive antigens contained a predicted signal peptide sequence and were classified as outer membrane, surface structures or secreted molecules, and an additional 20% were associated with pathogenicity, adaptation or chaperones. These results show that microarrays allow a more comprehensive analysis of the immune response on an antigen-specific, patient-specific, and population-specific basis, can identify serodiagnostic antigens, and contribute to a more detailed understanding of immunogenicity to this pathogen.
引用
收藏
页码:13499 / 13504
页数:6
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