Meningococcal Deduced Vaccine Antigen Reactivity (MenDeVAR) Index: a Rapid and Accessible Tool That Exploits Genomic Data in Public Health and Clinical Microbiology Applications

被引:46
作者
Rodrigues, Charlene M. C. [1 ,2 ]
Jolley, Keith A. [1 ]
Smith, Andrew [3 ,4 ]
Cameron, J. Claire [5 ]
Feavers, Ian M. [1 ]
Maiden, Martin C. J. [1 ]
机构
[1] Univ Oxford, Dept Zool, Oxford, England
[2] St Georges Univ Hosp NHS Fdn Trust, Paediat Infect Dis Unit, London, England
[3] Univ Glasgow, Glasgow Dent Sch, Glasgow, Lanark, Scotland
[4] NHS Greater Glasgow & Clyde, Scottish Microbiol Reference Lab, Glasgow, Lanark, Scotland
[5] Publ Hlth Scotland, Glasgow, Lanark, Scotland
基金
英国惠康基金;
关键词
meningococcal disease; Neisseria meningitidis; vaccines; Meningococcal Deduced Vaccine Antigen Reactivity (MenDeVAR); meningococcal antigen typing system (MATS); meningococcal antigen surface expression (MEASURE) assay; serum bactericidal activity assay; outbreaks; whole-genome sequencing; public health; BIVALENT RLP2086 VACCINE; SEROGROUP-B VACCINE; H BINDING-PROTEIN; PREDICTED STRAIN COVERAGE; MULTICOMPONENT VACCINE; BACTERICIDAL ACTIVITY; ACELLULAR PERTUSSIS; SINGLE-BLIND; IMMUNOGENICITY; DISEASE;
D O I
10.1128/JCM.02161-20
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
As microbial genomics makes increasingly important contributions to clinical and public health microbiology, the interpretation of whole-genome sequence data by nonspecialists becomes essential. In the absence of capsule-based vaccines, two protein-based vaccines have been used for the prevention of invasive serogroup B meningococcal disease (IMD) since their licensure in 2013 and 2014. These vaccines have different components and different levels of coverage of meningococcal variants. Hence, decisions regarding which vaccine to use in managing serogroup B IMD outbreaks require information about the index case isolate, including (i) the presence of particular vaccine antigen variants, (ii) the expression of vaccine antigens, and (iii) the likely susceptibility of its antigen variants to antibody-dependent bactericidal killing. To obtain this information requires a multitude of laboratory assays, impractical in real-time clinical settings, where the information is most urgently needed. To facilitate assessment for public health and clinical purposes, we synthesized genomic and experimental data from published sources to develop and implement the Meningococcal Deduced Vaccine Antigen Reactivity (MenDeVAR) Index, which is publicly available on PubMLST (https://pubmIst.org). Using whole-genome sequences or individual gene sequences obtained from IMD isolates or clinical specimens, the MenDeVAR Index provides rapid evidence-based information on the presence and possible immunological cross-reactivity of different meningococcal vaccine antigen variants. The MenDeVAR Index enables practitioners who are not genomics specialists to assess the likely reactivity of vaccines for individual cases, outbreak management, or the assessment of public health vaccine programs. The MenDeVAR Index has been developed in consultation with, but independently of, both the 4CMenB (Bexsero; Gsiq and rLP2086 (Trumenba; Pfizer, Inc.) vaccine manufacturers.
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页数:13
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