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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:
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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