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用于检测泛梅伯病毒的夹心酶联免疫吸附测定法的建立。

Establishment of a Sandwich ELISA for Detection of Pan-Merbecoviruses.

作者信息

Li Kaixin, Katayama Misa, Ichikawa Ayano, Matsugo Hiromichi, Wakabayashi Yuta, Takenaka-Uema Akiko, Sekine Wataru, Horimoto Taisuke, Murakami Shin

机构信息

Laboratory of Veterinary Microbiology, Graduate School of Agricultural and Life Sciences, University of Tokyo, Tokyo 113-8657, Japan.

Laboratory of Veterinary Public Health, Graduate School of Agricultural and Life Sciences, University of Tokyo, Tokyo 113-8657, Japan.

出版信息

Pathogens. 2025 Jun 19;14(6):605. doi: 10.3390/pathogens14060605.


DOI:10.3390/pathogens14060605
PMID:40559613
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12196402/
Abstract

, a subgenus of , includes MERS-CoV and multiple bat-derived viruses with zoonotic potential. Given the unpredictable emergence of these viruses and their genetic diversity, development of broad-spectrum diagnostic tools is expected. In this study, we established a sandwich ELISA targeting the nucleocapsid (N) protein of merbecoviruses. We generated monoclonal antibodies (mAbs) using recombinant N protein of a bat merbecovirus, VsCoV-1, and selected cross-reactive clones for other merbecoviruses. Three mAbs showed strong reactivities with multiple merbecoviruses but not with SARS-CoV-2 or endemic human coronaviruses. Pairwise ELISA screening identified 1A8/10H6 mAbs as the optimal combination for detection of N protein from six merbecoviruses-VsCoV-1, EjCoV-3, MERS-CoV, NeoCoV, HKU4, and HKU5-with limits of detection (LODs) below 7.81 ng/mL, including 1.25 ng/mL for VsCoV-1. Infectious bat merbecovirus EjCoV-3 was detected at 1.3 × 10 PFU/mL. No cross-reactivity was observed with non-merbecoviruses, indicating its high specificity. This sandwich ELISA offers a rapid, reproducible, and cost-effective diagnostic platform with potential for high-throughput screening and automation. Moreover, its design is amenable to adaptation into point-of-care formats such as lateral flow assays, highlighting its value for field-based surveillance and pandemic preparedness.

摘要

,的一个亚属,包括中东呼吸综合征冠状病毒(MERS-CoV)和多种具有人畜共患病潜力的蝙蝠源病毒。鉴于这些病毒的不可预测性出现及其遗传多样性,预计需要开发广谱诊断工具。在本研究中,我们建立了一种针对merbecoviruses核衣壳(N)蛋白的夹心酶联免疫吸附测定(ELISA)。我们使用蝙蝠merbecovirus VsCoV-1的重组N蛋白产生单克隆抗体(mAb),并选择对其他merbecoviruses具有交叉反应性的克隆。三种mAb对多种merbecoviruses表现出强反应性,但对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)或地方性人类冠状病毒无反应。成对ELISA筛选确定1A8/10H6 mAb是检测六种merbecoviruses(VsCoV-1、EjCoV-3、MERS-CoV、NeoCoV、HKU4和HKU5)N蛋白的最佳组合,检测限(LOD)低于7.81 ng/mL,其中VsCoV-1的检测限为1.25 ng/mL。在1.3×10 PFU/mL的浓度下检测到具有传染性的蝙蝠merbecovirus EjCoV-3。未观察到与非merbecoviruses的交叉反应,表明其具有高特异性。这种夹心ELISA提供了一个快速、可重复且经济高效的诊断平台,具有高通量筛选和自动化的潜力。此外,其设计易于改编为即时检测形式,如侧向流动分析,突出了其在现场监测和大流行防范中的价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9fe/12196402/78040325af13/pathogens-14-00605-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9fe/12196402/db2ac91536fd/pathogens-14-00605-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9fe/12196402/9620b764752c/pathogens-14-00605-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9fe/12196402/8f13b19c5088/pathogens-14-00605-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9fe/12196402/21cfafd994dd/pathogens-14-00605-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9fe/12196402/78040325af13/pathogens-14-00605-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9fe/12196402/db2ac91536fd/pathogens-14-00605-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9fe/12196402/9620b764752c/pathogens-14-00605-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9fe/12196402/8f13b19c5088/pathogens-14-00605-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9fe/12196402/21cfafd994dd/pathogens-14-00605-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9fe/12196402/78040325af13/pathogens-14-00605-g005.jpg

相似文献

[1]
Establishment of a Sandwich ELISA for Detection of Pan-Merbecoviruses.

Pathogens. 2025-6-19

[2]
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[4]
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[6]
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[7]
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Lancet Infect Dis. 2025-2

[8]
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[9]
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[10]
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本文引用的文献

[1]
and characterization of a bat merbecovirus with ACE2- and DPP4-independent cell entry.

J Virol. 2025-7-22

[2]
Bat-infecting merbecovirus HKU5-CoV lineage 2 can use human ACE2 as a cell entry receptor.

Cell. 2025-3-20

[3]
Sandwich ELISA for the Quantification of Nucleocapsid Protein of SARS-CoV-2 Based on Polyclonal Antibodies from Two Different Species.

Int J Mol Sci. 2023-12-26

[4]
Identification and Genetic Characterization of MERS-Related Coronavirus Isolated from Nathusius' Pipistrelle () near Zvenigorod (Moscow Region, Russia).

Int J Environ Res Public Health. 2023-2-19

[5]
Isolation of Bat Sarbecoviruses, Japan.

Emerg Infect Dis. 2022-12

[6]
Detection and genetic characterization of bat MERS-related coronaviruses in Japan.

Transbound Emerg Dis. 2022-11

[7]
Comparison of Titer and Signal to Noise (S/N) for Determination of Anti-drug Antibody Magnitude Using Clinical Data from an Industry Consortium.

AAPS J. 2022-7-12

[8]
Production of SARS-CoV-2 N Protein-Specific Monoclonal Antibody and Its Application in an ELISA-Based Detection System and Targeting the Interaction Between the Spike C-Terminal Domain and N Protein.

Front Microbiol. 2021-12-7

[9]
Ecology, evolution and spillover of coronaviruses from bats.

Nat Rev Microbiol. 2022-5

[10]
Development of double antibody sandwich ELISA as potential diagnostic tool for rapid detection of Crimean-Congo hemorrhagic fever virus.

Sci Rep. 2021-7-19

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