Visual detection of H3 subtype avian influenza viruses by reverse transcription loop-mediated isothermal amplification assay

• Published in: Virology journal Vol. 8; no. 1; p. 337
• Main Authors: Peng, Yi, Xie, Zhixun, Liu, Jiabo, Pang, Yaoshan, Deng, Xianwen, Xie, Zhiqin, Xie, Liji, Fan, Qing, Feng, Jiaxun, Khan, Mazhar I
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 05.07.2011; BioMed Central; BMC
• Subjects: Animals; Assaying; avian influenza; Avian influenza viruses; Birds; Cross Reactions; DNA Primers - genetics; Genetic aspects; H3 subtype; Hemagglutinin Glycoproteins, Influenza Virus - genetics; Humans; Influenza A virus - genetics; Influenza A virus - isolation & purification; Influenza in Birds - diagnosis; Influenza in Birds - virology; Influenza, Human - diagnosis; Influenza, Human - virology; Loop-mediated isothermal amplification; Methodology; Nucleic Acid Amplification Techniques - methods; Physiological aspects; Reverse Transcription; Sensitivity and Specificity; Virology - methods; United States; China
• ISSN: 1743-422X; 1743-422X
• DOI: 10.1186/1743-422X-8-337

Recent epidemiological investigation of different HA subtypes of avian influenza viruses (AIVs) shows that the H3 subtype is the most predominant among low pathogenic AIVs (LPAIVs), and the seasonal variations in isolation of H3 subtype AIVs are consistent with that of human H3 subtype influenza viruses. Consequently, the development of a rapid, simple, sensitive detection method for H3 subtype AIVs is required. The loop-mediated isothermal amplification (LAMP) assay is a simple, rapid, sensitive and cost-effective nucleic acid amplification method that does not require any specialized equipment. A reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay was developed to detect the H3 subtype AIVs visually. Specific primer sets target the sequences of the hemagglutinin (HA) gene of H3 subtype AIVs were designed, and assay reaction conditions were optimized. The established assay was performed in a water bath for 50 minutes, and the amplification result was visualized directly as well as under ultraviolet (UV) light reflections. The detection limit of the RT-LAMP assay was 0.1pg total RNA of virus, which was one hundred-fold higher than that of RT-PCR. The results on specificity indicated that the assay had no cross-reactions with other subtype AIVs or avian respiratory pathogens. Furthermore, a total of 176 clinical samples collected from birds at the various live-bird markets (LBMs) were subjected to the H3-subtype-specific RT-LAMP (H3-RT-LAMP). Thirty-eight H3 subtype AIVs were identified from the 176 clinical samples that were consistent with that of virus isolation. The newly developed H3-RT-LAMP assay is simple, sensitive, rapid and can identify H3 subtype AIVs visually. Consequently, it will be a very useful screening assay for the surveillance of H3 subtype AIVs in underequipped laboratories as well as in field conditions.