Evaluation of Type-Specific Real-Time PCR Assays Using the LightCycler and JBAIDS for Detection of Adenoviruses in Species HAdV-C

被引:7
|
作者
Jones, Morris S. [1 ]
Hudson, Nolan Ryan [2 ]
Gibbins, Carl [2 ]
Fischer, Stephen L. [3 ]
机构
[1] Calif Dept Hlth Serv, Viral & Rickettsial Dis Lab, Richmond, CA USA
[2] David Grant Med Ctr, Clin Invest Facil, Travis AFB, CA USA
[3] Naval Hosp Camp Pendleton, Camp Pendleton, CA USA
来源
PLOS ONE | 2011年 / 6卷 / 10期
关键词
IDENTIFICATION; DISEASE; RECOMBINATION; QUANTITATION; MYOCARDITIS; SEROTYPE; CHILDREN;
D O I
10.1371/journal.pone.0026862
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Sporadically, HAdVs from species HAdV-C are detected in acute respiratory disease outbreaks. To rapidly type these viruses, we designed real-time PCR assays that detect and discriminate between adenovirus types HAdV-C1, -C2, -C5, and -C6. Sixteen clinical isolates from the California Department of Public Health were used to validate the new assays. Type-specific TaqMan real-time PCR assays were designed and used independently to successfully identify 16 representative specimens. The lower limit of detection for our LightCycler singleplex real-time PCR assays were calculated to be 100, 100, 100, and 50 genomic copies per reaction for HAdV-C1, HAdV-C2, HAdV-C5 and HAdV-C6, respectively. The results for the singleplex J.B.A.I.D.S. assays were similar. Our assays did not cross-react with other adenoviruses outside of species HAdV-C, respiratory syncytial virus, influenza, or respiratory disease causing bacteria. These assays have the potential to be useful as diagnostic tools for species HAdV-C infection.
引用
收藏
页数:6
相关论文
共 50 条
  • [41] Detection and identification of pathogenic dermatophytes using multiplex real-time PCR assays
    Wittig, Franziska
    Uhrlass, Silke
    Gaajetaan, Giel
    Dingemans, Gijs
    Krueger, Constanze
    Nenoff, Pietro
    MEDICAL MYCOLOGY, 2018, 56 : S82 - S82
  • [42] Detection and identification of pathogenic dermatophytes using multiplex real-time PCR assays
    Wittig, F.
    Uhriass, S.
    Gaajetaan, G.
    Dingemans, G.
    Krueger, C.
    Nenoff, P.
    MYCOSES, 2018, 61 : 25 - 25
  • [43] Rapid detection of leaf spot pathogens on spinach using PCR and real-time PCR assays
    Liu, B.
    Feng, C.
    Correll, J. C.
    PHYTOPATHOLOGY, 2018, 108 (10) : 69 - 69
  • [44] Rapid Detection of Pathogenic Fungi from Clinical Specimens Using LightCycler Real-Time Fluorescence PCR
    A. Imhof
    C. Schaer
    G. Schoedon
    D. J. Schaer
    R. B. Walter
    A. Schaffner
    M. Schneemann
    European Journal of Clinical Microbiology and Infectious Diseases , 2003, 22 : 558 - 560
  • [45] Rapid detection of pathogenic fungi from clinical specimens using LightCycler real-time fluorescence PCR
    Imhof, A
    Schaer, C
    Schoedon, G
    Schaer, DJ
    Walter, RB
    Schaffner, A
    Schneemann, M
    EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2003, 22 (09) : 558 - 560
  • [46] Rapid detection of Bordetella pertussis by real-time PCR using SYBR green I and a LightCycler instrument
    Poddar, SK
    JOURNAL OF CLINICAL LABORATORY ANALYSIS, 2004, 18 (05) : 265 - 270
  • [47] Improved detection of Clostridium difficile in animals by using enrichment culture followed by LightCycler real-time PCR
    Avbersek, Jana
    Zajc, Urska
    Micunovic, Jasna
    Ocepek, Matjaz
    VETERINARY MICROBIOLOGY, 2013, 164 (1-2) : 93 - 100
  • [48] Quantitative real-time PCR assays for species-specific detection and quantification of Baltic Sea spring bloom dinoflagellates
    Brink, Annica Marie
    Kremp, Anke
    Gorokhova, Elena
    FRONTIERS IN MICROBIOLOGY, 2024, 15
  • [49] Detection of 3199del6 mutation by real-time PCR using Roche LightCycler.
    Li, Q
    Sun, D
    GENETICS IN MEDICINE, 2004, 6 (04) : 355 - 355
  • [50] Quantitative real-time PCR on Lightcycler® for the detection of human immunodeficiency virus type 2 (HIV-2)
    Ruelle, J
    Mukadi, BK
    Schutten, M
    Goubau, P
    JOURNAL OF VIROLOGICAL METHODS, 2004, 117 (01) : 67 - 74