One-Step Multiplex Real-Time Fluorescent Quantitative Reverse Transcription PCR for Simultaneous Detection of Four Waterfowl Viruses

被引:0
|
作者
Wang, Chenchen [1 ]
Liu, Huixin [1 ]
Cheng, Junze [1 ]
Pan, Sijia [1 ]
Yang, Wenwen [1 ]
Wei, Xiaofang [1 ]
Cheng, Yue [1 ]
Xu, Ting [1 ]
Si, Hongbin [1 ]
机构
[1] Guangxi Univ, Coll Anim Sci & Technol, Guangxi Key Lab Anim Breeding Dis Control & Preven, Guangxi Grass Stn, Nanning 530004, Peoples R China
关键词
duck Tembusu virus; duck hepatitis virus; Muscovy duck reovirus; Muscovy duck parvovirus; real-time fluorescent quantitative reverse transcription PCR; MUSCOVY DUCK PARVOVIRUS; POLYMERASE CHAIN-REACTION; HEPATITIS-B VIRUS; HERICIUM-ERINACEUS POLYSACCHARIDE; NEWCASTLE-DISEASE VIRUS; TEMBUSU VIRUS; REOVIRUS INFECTION; GOOSE PARVOVIRUS; DIFFERENTIAL-DIAGNOSIS; DWARFISM SYNDROME;
D O I
10.3390/microorganisms12122423
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Duck Tembusu virus (DTMUV), duck hepatitis virus (DHV), Muscovy duck reovirus (MDRV), and Muscovy duck parvovirus (MDPV) represent four emergent infectious diseases impacting waterfowl, which can be challenging to differentiate due to overlapping clinical signs. In response to this, we have developed a one-step multiplex real-time fluorescence quantitative reverse transcription PCR (qRT-PCR) assay, capable of simultaneously detecting DTMUV, DHV, MDRV, and MDPV. This method exhibits high specificity, avoiding cross-reactivity with other viruses such as Fowl adenoviruses (FADV), infectious bursal disease virus (IBDV), infectious bronchitis virus (IBV), infectious laryngotracheitis virus (ILTV), Haemophilus paragallinarum (Hpg), duck circovirus (DUCV), goose astrovirus (GoAstV), and mycoplasma gallisepticum (MG). The limit of detection (LOD) established for DTMUV, DHV, MDRV, and MDPV was determined to be 27 copies/mu L. In the repeatability test, the intra-assay and inter-assay coefficients of variation (CVs) of the recombinant plasmid standard were less than 2%. Utilizing this method, we analyzed 326 clinical specimens sourced from Guangxi over the period spanning October 2021 through December 2023, yielding promising and precise outcomes. The qRT-PCR method established herein exhibits commendable specificity, sensitivity, and repeatability. Furthermore, it boasts a high clinical detection rate, making it a highly effective tool for diagnosing these pathogenic agents in waterfowl.
引用
收藏
页数:17
相关论文
共 50 条
  • [41] A probe-free four-tube real-time PCR assay for simultaneous detection of twelve enteric viruses and bacteria
    Zhang, Chen
    Niu, Peihua
    Hong, Yanying
    Wang, Ji
    Zhang, Jingyun
    Ma, Xuejun
    JOURNAL OF MICROBIOLOGICAL METHODS, 2015, 118 : 93 - 98
  • [42] Multiplex Real-Time PCR for Detection of Campylobacter, Salmonella, and Shigella
    Barletta, F.
    Mercado, E. H.
    Lluque, A.
    Ruiz, J.
    Cleary, T. G.
    Ochoa, T. J.
    JOURNAL OF CLINICAL MICROBIOLOGY, 2013, 51 (09) : 2822 - 2829
  • [43] A versatile internal control for use as DNA in real-time PCR and as RNA in real-time reverse transcription PCR assays
    Deer, D. M.
    Lampel, K. A.
    Gonzalez-Escalona, N.
    LETTERS IN APPLIED MICROBIOLOGY, 2010, 50 (04) : 366 - 372
  • [44] Evaluation of a duplex reverse-transcription real-time PCR assay for the detection of encephalomyocarditis virus
    Qin, Shaomin
    Underwood, Darren
    Driver, Luke
    Kistler, Carol
    Diallo, Ibrahim
    Kirkland, Peter D.
    JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 2018, 30 (04) : 554 - 559
  • [45] Development and Validation of One-Step SYBR Green Real-Time RT-PCR for the Rapid Detection of Newly Emerged Duck Tembusu Virus
    Liu, Zongliang
    Fu, Yuguang
    Ji, Yanhong
    Wei, Jianzhong
    Cai, Xuepeng
    Zhu, Qiyun
    AVIAN DISEASES, 2013, 57 (03) : 595 - 601
  • [46] Standardized One-Step Real-Time Reverse Transcription-PCR Assay for Universal Detection and Quantification of Hepatitis Delta Virus from Clinical Samples in the Presence of a Heterologous Internal-Control RNA
    Scholtes, Caroline
    Icard, Vinca
    Amiri, Majid
    Chevallier-Queyron, Philippe
    Trabaud, Mary-Anne
    Ramiere, Christophe
    Zoulim, Fabien
    Andre, Patrice
    Deny, Paul
    JOURNAL OF CLINICAL MICROBIOLOGY, 2012, 50 (06) : 2126 - 2128
  • [47] Screening Suitable Reference Genes for Normalization in Reverse Transcription Quantitative Real-Time PCR Analysis in Melon
    Kong, Qiusheng
    Yuan, Jingxian
    Niu, Penghui
    Xie, Junjun
    Jiang, Wei
    Huang, Yuan
    Bie, Zhilong
    PLOS ONE, 2014, 9 (01):
  • [48] TaqMan probe-based one-step multiplex real-time RT-PCR assay for the diagnosis of foot-and-mouth disease
    Biswal, Jitendra K.
    Mohapatra, Jajati K.
    Ranjan, Rajeev
    Rout, Manoranjan
    Dahiya, Shyam Singh
    Singh, Rabindra Prasad
    ACTA VIROLOGICA, 2023, 67
  • [49] Simultaneous detection of respiratory viruses in children with acute respiratory infection using two different multiplex reverse transcription-PCR assays
    Wang, Wei
    Ren, Peijun
    Sheng, Jun
    Mardy, Sek
    Yan, Huajie
    Zhang, Jing
    Hou, Lili
    Vabret, Astrid
    Buchy, Philippe
    Freymuth, Francois
    Deubel, Vincent
    JOURNAL OF VIROLOGICAL METHODS, 2009, 162 (1-2) : 40 - 45
  • [50] A multiplex TaqMan real-time PCR for detection and differentiation of four antigenic types of canine parvovirus in China
    Sun, Yaru
    Cheng, Yuening
    Lin, Peng
    Yi, Li
    Tong, Mingwei
    Cao, Zhigang
    Wang, Gaili
    Li, Shuang
    Cheng, Shipeng
    Yuan, Wanzhe
    Wang, Jianke
    MOLECULAR AND CELLULAR PROBES, 2018, 38 : 7 - 12