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.
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页数:6
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