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Detection of influenza A virus RNA in birds by optimized Real-Time PCR system
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作者:

Ilinykh, Ph A.
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h-index: 0
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State Res Ctr Virol & Biotechnol Vector, Koltsov 630559, Novosibirsk Reg, Russia State Res Ctr Virol & Biotechnol Vector, Koltsov 630559, Novosibirsk Reg, Russia

Shestopalova, E. M.
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State Res Ctr Virol & Biotechnol Vector, Koltsov 630559, Novosibirsk Reg, Russia State Res Ctr Virol & Biotechnol Vector, Koltsov 630559, Novosibirsk Reg, Russia

Khripko, Yu, I
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h-index: 0
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State Res Ctr Virol & Biotechnol Vector, Koltsov 630559, Novosibirsk Reg, Russia State Res Ctr Virol & Biotechnol Vector, Koltsov 630559, Novosibirsk Reg, Russia

Durimanov, A. G.
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h-index: 0
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State Res Ctr Virol & Biotechnol Vector, Koltsov 630559, Novosibirsk Reg, Russia State Res Ctr Virol & Biotechnol Vector, Koltsov 630559, Novosibirsk Reg, Russia

Sharshov, K. A.
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State Res Ctr Virol & Biotechnol Vector, Koltsov 630559, Novosibirsk Reg, Russia State Res Ctr Virol & Biotechnol Vector, Koltsov 630559, Novosibirsk Reg, Russia

Shestopalov, A. M.
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h-index: 0
机构:
State Res Ctr Virol & Biotechnol Vector, Koltsov 630559, Novosibirsk Reg, Russia State Res Ctr Virol & Biotechnol Vector, Koltsov 630559, Novosibirsk Reg, Russia
机构:
[1] State Res Ctr Virol & Biotechnol Vector, Koltsov 630559, Novosibirsk Reg, Russia
关键词:
Influenza A virus RNA;
Real-Time PCR;
MDCK cell culture;
Virus surveillance;
Wild birds;
WILD MIGRATORY BIRDS;
AVIAN INFLUENZA;
QUANTITATIVE PCR;
H5N1;
IDENTIFICATION;
PREVALENCE;
PATTERNS;
SUBTYPES;
ALASKA;
ASSAY;
D O I:
10.1016/S1995-7645(10)60082-X
中图分类号:
R1 [预防医学、卫生学];
学科分类号:
1004 ;
120402 ;
摘要:
Objective: To evaluate the use of Real Time PCR system based on specific amplification of matrix protein gene fragment for influenza A virus RNA detection in cloacal swabs from wild birds. Methods: Sensitivity, specificity and reproducibility of analysis results were identified. Study of cloacal swabs from wild birds for influenza A virus presence was performed. Results: Reproducibility of low concentrations of virus detection in samples by Real-Time PCR was significantly higher than that of detection based on cytopathic effect of viruses grown on MOCK cell culture. Conclusions: Real-time PCR system for influenza A virus RNA detection is developed and applied for virus surveillance study.
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页码:337 / 340
页数:4
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