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  4. Monkeypox virus A29L protein as the target for specific diagnosis and serological analysis
 
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Monkeypox virus A29L protein as the target for specific diagnosis and serological analysis

Journal
Applied Microbiology and Biotechnology
Journal Volume
108
Journal Issue
1
ISSN
0175-7598
1432-0614
Date Issued
2024-11-21
Author(s)
Chia-Yu Liang
TAI-LING CHAO  
Chong‐Syun Chao
Yu-Chen Cheng
WANG-DA LIU  
SUI-YUAN CHANG  
SHIH-CHUNG CHANG  
DOI
10.1007/s00253-024-13361-6
DOI
10.1007/s00253-024-13361-6
URI
https://www.scopus.com/record/display.uri?eid=2-s2.0-85209763393&origin=resultslist
https://scholars.lib.ntu.edu.tw/handle/123456789/723642
Abstract
The unexpected monkeypox (Mpox) outbreak has been reported in many non-endemic countries and regions since May 2022. The mutant strains of Mpox virus (MPXV) were found with higher infectivity and greater capability for sustained human-to-human transmission, posing a significant public health threat. MPXV A29L, a protein homolog of vaccinia virus (VACV) A27L, plays an important role in viral attachment to host cell membranes. Therefore, MPXV A29L is considered the diagnostic target and the potential vaccine candidate for eliciting neutralizing antibodies and protective immune responses. In response to the escalating Mpox outbreak, three monoclonal antibodies (mAbs) (2-9B, 3-8G, and 2-5H) targeting the different domains of MPXV A29L have been developed in the study. Among them, 2-5H is highly specific for MPXV A29L without exhibiting cross-reactivity with VACV A27L. The antibody pairing composed of 2-5H and 3-8G has been developed as the lateral flow immunochromatographic assay for specific detection of MPXV A29L. However, these three mAbs were unable to inhibit A29L binding to heparin column or prevent MPXV infection in the neutralization test assays. The results of the serological assays using the truncated A29L fragments as the antigens showed that the Mpox patient sera contained significantly lower levels of antibodies targeting the N-terminal 1–34 residues of A29L, suggesting that the N-terminal portion of A29L is less immunogenic upon natural infection. Key points: • MAbs 2-9B, 3-8G, and 2-5H neither interrupted A29L binding to heparin nor neutralized MPXV. • The LFIA composed of 3-8G and 2-5H can specifically distinguish MPXV A29L from VACV A27L. • Mpox patient sera contained lower levels of antibodies targeting the N-terminal portion of A29L.
Subjects
A29L protein
Lateral flow immunochromatographic assay
Monkeypox (Mpox)
Monkeypox virus (MPXV)
Monoclonal antibody
Serological assay
Publisher
Springer Science and Business Media LLC
Description
Article number 522
Type
journal article

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