°</sup>C 和NGRV( 86.5<sup>°</sup>C ,對常見的水禽流行疫病均未出現(xiàn)擴增,最低檢出為 6.466×10<sup>1</sup> 拷貝 /μLGRV 和 4.979×10<sup>1</sup> 拷貝 /μLNGRV ,組內(nèi)與組間變異系數(shù)均小于 0.55% 。結(jié)果表明,這個研究所建立基于染料法的雙重RT-qPCR檢測方法可以快速準(zhǔn)確地確定感染鵝群中不同型的GRV,為疾病的早期診斷、流行病學(xué)監(jiān)測和有效防控提供支持。-龍源期刊網(wǎng)" />

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經(jīng)典型和新型鵝呼腸孤病毒的雙重RT-qPCR檢測方法的建立和應(yīng)用

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關(guān)鍵詞:鵝呼腸孤病毒;GRV和NGRV;染料法;RT-qRCR;熔解曲線中圖分類號: S852.65+91 文獻標(biāo)識碼:A 文章編碼:1005-8567(2025)03-0096-09

Abstract:The Goose reovirus(GRV)comprises two distinct types:the classic(GRV)and the novel goose reovirus(NGRV).These two types exhibit diferences in theirepidemiological characteristicsandviral gene sequences.Thelack ofsensitiveandspecificassays forboth typesof viruses hasresulted indificultiesinaccurately diagnosing and timely intervening incases.Inorderto distinguish GRVfrom NGRV,adual RT-qPCR assy based on a dye-based method(SYBR Green I)was established.The results demonstrated that the method was capable of distinguishing GRV( 79.5°C )and NGRV( 86.5qC )based on their respective melting curves.Furthermore,no amplification was observed for any of the common waterfowl epidemics,the lowest detections were 6.466 × 101 copies/ (204號 μL GRV and 4.979×101 copies /μL NGRV. The results demonstrated that the dual RT-qPCR assay,based on a dyebased method,couldrapidlyandaccurately identifydifferent types of GRVs in infected geese.Theassay exhibiteda high degree of precision,with coefficients of variation less than 0.55% for both intra-and intergroups.This method has the potentialtosupport earlydiagnosis,epidemiological monitoring and efective preventionandcontrolofthedisease.

Keywords: Goose reovirus;GRV and NGRV;dye-based method;RT-qPCR;Melting curve

禽呼腸孤病毒是呼腸孤病毒科(Reoviridae)刺突呼腸孤病毒亞科(Spinareovirinae)正呼腸孤病毒屬(Orthoreovirus)的成員之一。(剩余10129字)

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