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用于快速检测高毒力菌株的单重实时荧光定量PCR和双重PCR平台

Singleplex real-time PCR and duplex PCR platform for the rapid detection of hypervirulent .

作者信息

Wang Jiaqi, Wu Yishuai, Zhao Liying, Xing Mengran, Huang Yangyang, Peng Shengjie, Xu Chunyan, Yao Hong, Li Chenglong, Du Xiang-Dang

机构信息

International Joint Research Center of National Animal Immunology, College of Veterinary Medicine, Henan Agricultural University, Zhengzhou, China.

Ministry of Education Key Laboratory for Animal Pathogens and Biosafety, Henan Agricultural University, Zhengzhou, China.

出版信息

Front Vet Sci. 2025 Jul 17;12:1611750. doi: 10.3389/fvets.2025.1611750. eCollection 2025.

DOI:10.3389/fvets.2025.1611750
PMID:40746972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12312404/
Abstract

Hypervirulent (HvKP) is a notorious zoonotic pathogen that poses a significant threat to public health, as it can cause severe infections with high morbidity and mortality among young and healthy individuals. Commonly, a positive string test is primarily used to identify HvKP strains, but which is laborious and time-consuming. A rapid assay to identify HvKP is needed for public health personnel to track the spread of these strains and provide timely efforts for their control. Given this context, rapid SYBR Green I-based singleplex real-time PCR assays were developed for defining HvKP on the basis of the biomarkers , , and plasmid-borne , respectively. These four singleplex PCR assays all displayed a high degree of linearity ( 0.99) in the range of 10 to 10 cfu/mL, and the limit of detection (LOD) was 10 cfu/mL, which was equivalent to 10 cfu/reaction. To improve the efficiency and reduce the cost of diagnostic testing, SYBR Green I-based duplex PCR melting curve assays were developed with average melting temperatures of 85.0, 87.5, 76.0 and 78.5°C for , , and plasmid-borne , respectively. The LODs for the developed duplex PCRs for /, / and / combination were 10 cfu/mL (that was 10 cfu/reaction), 10 cfu/mL (that was 10 cfu/reaction) and 10 cfu/mL (that was 10 cfu/reaction), respectively. High specificity was shown when other bacterial pathogens were detected in this study. These assays could be used as rapid, sensitive and specific diagnostic tools for the practical identification of HvKP strains.

摘要

高毒力肺炎克雷伯菌(HvKP)是一种臭名昭著的人畜共患病原体,对公众健康构成重大威胁,因为它可在年轻健康个体中引起严重感染,发病率和死亡率很高。通常,阳性拉丝试验主要用于鉴定HvKP菌株,但该方法费力且耗时。公共卫生人员需要一种快速检测方法来追踪这些菌株的传播并及时采取控制措施。在此背景下,分别基于生物标志物、、和质粒携带的,开发了基于SYBR Green I的快速单重实时PCR检测方法来鉴定HvKP。这四种单重PCR检测方法在10至10 cfu/mL范围内均显示出高度线性( 0.99),检测限(LOD)为10 cfu/mL,相当于10 cfu/反应。为了提高诊断检测的效率并降低成本,开发了基于SYBR Green I的双重PCR熔解曲线检测方法,其针对、、和质粒携带的的平均熔解温度分别为85.0、87.5、76.0和78.5°C。所开发的用于/、/和/组合的双重PCR的LOD分别为10 cfu/mL(即10 cfu/反应)、10 cfu/mL(即10 cfu/反应)和10 cfu/mL(即10 cfu/反应)。本研究检测其他细菌病原体时显示出高特异性。这些检测方法可作为快速、灵敏和特异的诊断工具,用于实际鉴定HvKP菌株。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/443c/12312404/fe31b3fa9177/fvets-12-1611750-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/443c/12312404/a03dae759c5d/fvets-12-1611750-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/443c/12312404/cea5332d7a17/fvets-12-1611750-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/443c/12312404/333ddc11d1ed/fvets-12-1611750-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/443c/12312404/ef2d31e3e4d0/fvets-12-1611750-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/443c/12312404/fe31b3fa9177/fvets-12-1611750-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/443c/12312404/a03dae759c5d/fvets-12-1611750-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/443c/12312404/cea5332d7a17/fvets-12-1611750-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/443c/12312404/333ddc11d1ed/fvets-12-1611750-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/443c/12312404/ef2d31e3e4d0/fvets-12-1611750-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/443c/12312404/fe31b3fa9177/fvets-12-1611750-g005.jpg

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本文引用的文献

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