Development of TaqMan RT-qPCR for the detection of regulated citrus viruses and viroids in Aotearoa New Zealand

被引:4
作者
Yan, Juncong [1 ]
Tang, Joe [1 ]
Perez-Egusquiza, Zoila [1 ]
Thompson, Jeremy R. [1 ]
机构
[1] Minist Primary Ind, Plant Hlth & Environm Lab, 231 Morrin Rd, Auckland 1072, New Zealand
关键词
Citrus; Virus; Viroid; Real-time PCR; Detection; PSOROSIS-VIRUS; LEPROSIS; ASSAY;
D O I
10.1016/j.jviromet.2024.114950
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The major citrus species include several economically important fruits, such as orange, mandarin, lemon, limes, grapefruit and pomelos. Since the 1980 s, total production and consumption of citrus has grown strongly with the current annual worldwide production at over 105 million tonnes. New Zealand's citrus exports, for instance, had an estimated worth of NZ$ 11.6 million (approx. US$ 7 million) in 2020. Citrus plants are prone to viral diseases, which can lead to substantial economic losses. In New Zealand, the citrus Import Health Standard (IHS) has identified 22 viruses and viroids that are subject to regulation and requires citrus nursery stock to be free of these pathogens. As such, there is a need for reliable, sensitive, and rapid detection methods to screen for these viruses and viroids during post entry quarantine. In this study, we developed TaqMan RT-qPCR assays for the detection of nine of these regulated viruses and viroids, namely citrus leaf rugose virus (CiLRV), citrus leprosis virus C (CiLV-C), citrus leprosis virus C2 (CiLV-C2), citrus leprosis virus N (CiLV-N), citrus psorosis virus (CPsV), citrus yellow mosaic virus (CYMV), citrus bent leaf viroid (CBLVd), citrus viroid V (CVd-V), and citrus viroid VI (CVdVI). These assays have been validated and found to be highly sensitive, specific, and reliable. The implementation of these assays will facilitate the safe importation of citrus nursery stock, thus safeguarding the country's horticultural and economic interests.
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页数:6
相关论文
共 14 条
[1]   Citrus psorosis virus: nucleotide sequencing of the coat protein gene and detection by hybridization and RT-PCR [J].
Barthe, GA ;
Ceccardi, TL ;
Manjunath, KL ;
Derrick, KS .
JOURNAL OF GENERAL VIROLOGY, 1998, 79 :1531-1537
[2]   Production of mono-and polyclonal antibodies to Citrus leprosis virus C2 and their application in triple antibody sandwich ELISA and immunocapture RT-PCR diagnostic assays [J].
Choudhary, Nandlal ;
Roy, Avijit ;
Leon, M. G. ;
Wei, G. ;
Nakhla, M. K. ;
Levy, L. ;
Brlansky, R. H. .
JOURNAL OF VIROLOGICAL METHODS, 2017, 243 :177-181
[3]   Detection of Citrus leprosis virus C using specific primers and TaqMan probe in one-step real-time reverse-transcription polymerase chain reaction assays [J].
Choudhary, Nandlal ;
Wei, G. ;
Govindarajulu, A. ;
Roy, Avijit ;
Li, Wenbin ;
Picton, Deric D. ;
Nakhla, M. K. ;
Levy, L. ;
Brlansky, R. H. .
JOURNAL OF VIROLOGICAL METHODS, 2015, 224 :105-109
[4]  
Djelouah K., 2002, Int. Organ. Citrus Virol. Conf. Proc., V15
[5]  
Falaki F, 2023, Citrus Virus and Viroid Diseases
[6]   Simultaneous detection of six citrus viroids and Apple stem grooving virus from citrus plants by multiplex reverse transcription polymerase chain reaction [J].
Ito, T ;
Ieki, H ;
Ozaki, K .
JOURNAL OF VIROLOGICAL METHODS, 2002, 106 (02) :235-239
[7]   Development of a duplex one-step RT-qPCR assay for the simultaneous detection of Apple scar skin viroid and plant RNA internal control [J].
Khan, Subuhi ;
Mackay, John ;
Liefting, Lia ;
Ward, Lisa .
JOURNAL OF VIROLOGICAL METHODS, 2015, 221 :100-105
[8]   Brevipalpus-transmitted plant virus and virus-like diseases:: cytopathology and some recent cases [J].
Kitajima, EW ;
Chagas, CM ;
Rodrigues, JCV .
EXPERIMENTAL AND APPLIED ACAROLOGY, 2003, 30 (1-3) :135-160
[9]   Development and validation of a multiplex reverse transcription quantitative PCR (RT-qPCR) assay for the rapid detection of Citrus tristeza virus, Citrus psorosis virus, and Citrus leaf blotch virus [J].
Osman, Fatima ;
Hodzic, Emir ;
Kwon, Sun-Jung ;
Wang, Jinbo ;
Vidalakis, Georgios .
JOURNAL OF VIROLOGICAL METHODS, 2015, 220 :64-75
[10]  
Ramos-González PL, 2017, PHYTOPATHOLOGY, V107, P963, DOI [10.1094/PHYTO-02-17-0042-R, 10.1094/phyto-02-17-0042-r]