A Multiplex Real-Time Polymerase Chain Reaction Assay to Diagnose Epiphyas postvittana (Lepidoptera: Tortricidae)

被引:17
|
作者
Barr, N. B. [1 ]
Ledezma, L. A. [1 ]
Farris, R. E. [1 ]
Epstein, M. E. [2 ]
Gilligan, T. M. [3 ]
机构
[1] USDA APHIS, Mission Lab, Ctr Plant Hlth Sci & Technol, Edinburg, TX 78541 USA
[2] Calif Dept Food & Agr, Plant Pest Diagnost Branch, Sacramento, CA 95832 USA
[3] Colorado State Univ, Dept Bioagr Sci & Pest Management, Ft Collins, CO 80523 USA
关键词
Tortricidae; barcodes; internal transcribed spacer; real-time polymerase chain reaction; BROWN APPLE MOTH; INTRAGENOMIC VARIATION; RIBOSOMAL DNA; IDENTIFICATION; PCR; ITS2; TEPHRITIDAE; CALIFORNIA; NEMATODES; DIPTERA;
D O I
10.1603/EC11093
中图分类号
Q96 [昆虫学];
学科分类号
摘要
A molecular assay for diagnosis of light brown apple moth, Epiphyas postvittana (Walker) (Lepidoptera: Tortricidae), in North America is reported. The assay multiplexes two TaqMan real-time polymerase chain reaction (RT-PCR) probe systems that are designed to target DNA segments of the internal transcribed spacer region 2 (ITS2) and 18S rRNA gene. The RT-PCR probe designed for the 18S target recognizes a DNA sequence conserved in all of the moths included in the study and functions as a control in the assay. The second probe recognizes a segment of the ITS2 specifically found in E. postvittana and not found in the other moths included in the study, i.e., this segment is not conserved. Inclusion of the two markers in a single multiplex reaction did not affect assay performance. The assay was tested against 637 moths representing >90 taxa in 15 tribes in all three subfamilies in the Tortricidae. The assay generated no false negatives based on analysis of 355 E. postvittana collected from California, Hawaii, England, New Zealand, and Australia. Analysis of a data set including 282 moths representing 41 genera generated no false positives. Only three inconclusive results were generated from the 637 samples. Spike experiments demonstrated that DNA contamination in the assay can affect samples differently. Contaminated samples analyzed with the ITS2 RT-PCR assay and DNA barcode methodology by using the cytochrome oxidase I gene can generate contradictory diagnoses.
引用
收藏
页码:1706 / 1719
页数:14
相关论文
共 50 条
  • [1] Real-time polymerase chain reaction to diagnose lymphogranuloma venereum
    Morré, SA
    Spaargaren, J
    Fennerna, JSA
    de Vries, HJC
    Coutinho, RA
    Peña, AS
    EMERGING INFECTIOUS DISEASES, 2005, 11 (08) : 1311 - 1312
  • [2] A new multiplex real-time polymerase chain reaction assay for the diagnosis of periprosthetic joint infection
    Kawamura, Masaki
    Kobayashi, Naomi
    Inaba, Yutaka
    Choe, Hyonmin
    Tezuka, Taro
    Kubota, So
    Saito, Tomoyuki
    MODERN RHEUMATOLOGY, 2017, 27 (06) : 1072 - 1078
  • [3] Detection of bovine pestiviruses by a multiplex real-time polymerase chain reaction
    Nefedchenko, Aleksey, V
    Koteneva, Svetlana, V
    Glotova, Tatyana, I
    Glotov, Alexander G.
    VOPROSY VIRUSOLOGII, 2020, 65 (02) : 95 - 102
  • [4] Multiplex real-time quantitative polymerase chain reaction assay for rapid and sensitive detection of hematopoietic chimerism
    Nadvornikova, Sylvie
    Leontovycova, Monika
    Pegova, Kristyna
    Hrabakova, Pavla
    Prerovska, Renata
    Cechova, Hana
    HLA, 2018, 92 (04) : 215 - 223
  • [5] Results of Real-time Multiplex Polymerase Chain Reaction Assay in Renal Transplant Recipients With Sterile Pyuria
    Sarier, M.
    Demir, M.
    Goktas, S.
    Duman, I.
    Buyukkinaci, M.
    Yuksel, Y.
    Tekin, S.
    Yavuz, A. H.
    Sengul, A.
    TRANSPLANTATION PROCEEDINGS, 2017, 49 (06) : 1307 - 1311
  • [6] Evaluation of a multiplex real-time polymerase chain reaction assay for the detection of influenza and respiratory syncytial viruses
    Esposito, Susanna
    Scala, Alessia
    Tagliabue, Claudia
    Zampiero, Alberto
    Bianchini, Sonia
    Principi, Nicola
    DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2016, 84 (01) : 40 - 42
  • [7] Quantitative multiplex real-time polymerase chain reaction assay for the detection of Helicobacter pylori and clarithromycin resistance
    Kim, Ilsoo
    Maeng, Lee-So
    Kim, Joon Sung
    Kim, Byung-Wook
    Cheung, Dae Young
    Kim, Jin Il
    Park, Soo-heon
    BMC MICROBIOLOGY, 2023, 23 (01)
  • [8] A real-time 16S rRNA gene polymerase chain reaction assay to diagnose septic peritonitis
    Brown, AJ
    Gorman, R
    Rankin, SC
    CRITICAL CARE MEDICINE, 2005, 33 (12) : A164 - A164
  • [9] Correction: Quantitative multiplex real-time polymerase chain reaction assay for the detection of Helicobacter pylori and clarithromycin resistance
    Ilsoo Kim
    Lee-So Maeng
    Joon Sung Kim
    Byung-Wook Kim
    Dae Young Cheung
    Jin Il Kim
    Soo-heon Park
    BMC Microbiology, 23
  • [10] Evaluation of a Real-Time Multiplex Polymerase Chain Reaction Assay for Simultaneous Detection of Respiratory Pathogens in Nasopharyngeal Specimens
    Alturkmani, R.
    Southard, D.
    Branson, L.
    Jaime, A.
    Katrangi, W.
    CLINICAL CHEMISTRY, 2024, 70