福建畜牧兽医
福建畜牧獸醫
복건축목수의
FUJIAN JOURNAL OF ANIMAL HUSBANDRY AND VETERINARY
2012年
1期
9-12
,共4页
刘阳%孔繁德%彭小莉%徐淑菲%吴德峰%林方
劉暘%孔繁德%彭小莉%徐淑菲%吳德峰%林方
류양%공번덕%팽소리%서숙비%오덕봉%림방
副溶血弧菌%纳米PCR
副溶血弧菌%納米PCR
부용혈호균%납미PCR
Vibrio parahaemolyticus Nanogold-assisted PCR
纳米金PCR是在普通PCR基础上发展起来的新技术,它能够明显提高普通PCR的灵敏度和特异性。根据副溶血弧菌(VP)的toxR基因序列,应用primer6.0设计一对特异性引物,建立了纳米金PCR方法,并对该方法的最佳反应条件、循环数、特异性和灵敏度进行测定。采用2.0%琼脂糖电泳进行检测,结果表明能扩增得到与试验设计相符的208bp(vP)的特异性奈带;与溶藻弧菌、霍乱弧菌、麦氏弧菌、沙门氏菌、枸橼酸杆菌没有交叉反应;纯培养细菌检测灵敏度为3cfta&应体系。与普通PCR法进行比较,该方法检测灵敏度比普通PCR高10倍。经临床检测,从150份带鱼、鱿鱼和鱼粉中检出5份阳性样品,与常规细菌分离鉴定方法符合率100%。该试验方法的建立对于加强进出口水产品中VP的检验检癌具有十分奄娶白白意义.
納米金PCR是在普通PCR基礎上髮展起來的新技術,它能夠明顯提高普通PCR的靈敏度和特異性。根據副溶血弧菌(VP)的toxR基因序列,應用primer6.0設計一對特異性引物,建立瞭納米金PCR方法,併對該方法的最佳反應條件、循環數、特異性和靈敏度進行測定。採用2.0%瓊脂糖電泳進行檢測,結果錶明能擴增得到與試驗設計相符的208bp(vP)的特異性奈帶;與溶藻弧菌、霍亂弧菌、麥氏弧菌、沙門氏菌、枸櫞痠桿菌沒有交扠反應;純培養細菌檢測靈敏度為3cfta&應體繫。與普通PCR法進行比較,該方法檢測靈敏度比普通PCR高10倍。經臨床檢測,從150份帶魚、魷魚和魚粉中檢齣5份暘性樣品,與常規細菌分離鑒定方法符閤率100%。該試驗方法的建立對于加彊進齣口水產品中VP的檢驗檢癌具有十分奄娶白白意義.
납미금PCR시재보통PCR기출상발전기래적신기술,타능구명현제고보통PCR적령민도화특이성。근거부용혈호균(VP)적toxR기인서렬,응용primer6.0설계일대특이성인물,건립료납미금PCR방법,병대해방법적최가반응조건、순배수、특이성화령민도진행측정。채용2.0%경지당전영진행검측,결과표명능확증득도여시험설계상부적208bp(vP)적특이성내대;여용조호균、곽란호균、맥씨호균、사문씨균、구연산간균몰유교차반응;순배양세균검측령민도위3cfta&응체계。여보통PCR법진행비교,해방법검측령민도비보통PCR고10배。경림상검측,종150빈대어、우어화어분중검출5빈양성양품,여상규세균분리감정방법부합솔100%。해시험방법적건립대우가강진출구수산품중VP적검험검암구유십분엄취백백의의.
Nanogold-assisted PCR(NP-PCR) is a new technology developed on the basis of ordinary PCR, it can obviously improve the sensitivity and specificity of ordinary PCR.Nanogold-assisted PCR was established and optimized to detect Vibrio parahaemolytictts (VP).One set of specific primers were designed according to the toxR sequence of VP in the GenBank by primer 6.0.The reaction conditions, cycle numbers, sensitivity and specialty of the method was optimized and assessed. It was showed that all samples which contained VP could be amplified by the nanogold-assisted PCR using this set primers. One specific band of VP 208 bp was detected using 2.0% agarose gel electrophoresis in this nanogold -assisted PCR and accorded with designed result, other bacterial (such as Vibrio alginolyticus, V.cholera, Vibrio metschnikovii,salmonella, Citro Bacter)controls gave negative results. The nanogold-assisted PCR was able to detect as little as 3 cfu/reaction system for VP from pure culture samples and more sensitive than polymerase chain reaction. The experiment proved that NP-PCR is 10 times than ordinary PCR in sensitivity.The method provides a fast and reliable way of identifying ~P.5 from 150 samples were positive by two methods and their coincidence rate was 100% .The method could prove very useful for identification and inspection of VP from fishery product in import and export.