中国动物检疫
中國動物檢疫
중국동물검역
CHINA ANMAL QUARANTINE
2015年
6期
69-74
,共6页
张玲%唐小千%绳秀珍%战文斌
張玲%唐小韆%繩秀珍%戰文斌
장령%당소천%승수진%전문빈
克氏原螯虾(Procambarus clarkii)%白斑症病毒(WSSV)%实时荧光定量PCR%病毒增殖
剋氏原螯蝦(Procambarus clarkii)%白斑癥病毒(WSSV)%實時熒光定量PCR%病毒增殖
극씨원오하(Procambarus clarkii)%백반증병독(WSSV)%실시형광정량PCR%병독증식
Procambarus clarkii%white spot syndrome virus%quantitative real-time PCR%virus proliferation
本文建立了白斑症病毒(WSSV)实时荧光定量PCR标准曲线,结果显示其线性关系良好,利用建立的WSSV实时荧光定量PCR技术检测感染了WSSV后克氏原螯虾(Procambarus clarkii)组织内病毒数量的时序动态变化。注射WSSV粗提液感染克氏原螯虾,在感染后0h、3h、6h、12h、24h、36h、48h、60h和72h分别取螯虾鳃、血淋巴、心脏、附肢、造血组织和肌肉,提取组织DNA,实时荧光定量PCR测定WSSV浓度,发现感染后3h在附肢、鳃、血淋巴和造血组织中检测到病毒,12h时在各组织中皆检测到病毒,但浓度较低;24~48h内WSSV浓度呈指数增长,此时螯虾出现少量死亡;60~72h内WSSV数量缓慢增长达到平台期,螯虾累计死亡率快速升高。不同组织中的WSSV浓度有较大差异,附肢中浓度最高,血淋巴、鳃、心脏和造血组织稍低,肌肉中WSSV浓度最低;附肢中WSSV动态变化代表了WSSV增殖变化规律,是很好的病毒检测与病程进展评估材料。本文结果可为WSSV的早期诊断提供技术支持,为阐明WSSV感染增殖规律提供资料。
本文建立瞭白斑癥病毒(WSSV)實時熒光定量PCR標準麯線,結果顯示其線性關繫良好,利用建立的WSSV實時熒光定量PCR技術檢測感染瞭WSSV後剋氏原螯蝦(Procambarus clarkii)組織內病毒數量的時序動態變化。註射WSSV粗提液感染剋氏原螯蝦,在感染後0h、3h、6h、12h、24h、36h、48h、60h和72h分彆取螯蝦鰓、血淋巴、心髒、附肢、造血組織和肌肉,提取組織DNA,實時熒光定量PCR測定WSSV濃度,髮現感染後3h在附肢、鰓、血淋巴和造血組織中檢測到病毒,12h時在各組織中皆檢測到病毒,但濃度較低;24~48h內WSSV濃度呈指數增長,此時螯蝦齣現少量死亡;60~72h內WSSV數量緩慢增長達到平檯期,螯蝦纍計死亡率快速升高。不同組織中的WSSV濃度有較大差異,附肢中濃度最高,血淋巴、鰓、心髒和造血組織稍低,肌肉中WSSV濃度最低;附肢中WSSV動態變化代錶瞭WSSV增殖變化規律,是很好的病毒檢測與病程進展評估材料。本文結果可為WSSV的早期診斷提供技術支持,為闡明WSSV感染增殖規律提供資料。
본문건립료백반증병독(WSSV)실시형광정량PCR표준곡선,결과현시기선성관계량호,이용건립적WSSV실시형광정량PCR기술검측감염료WSSV후극씨원오하(Procambarus clarkii)조직내병독수량적시서동태변화。주사WSSV조제액감염극씨원오하,재감염후0h、3h、6h、12h、24h、36h、48h、60h화72h분별취오하새、혈림파、심장、부지、조혈조직화기육,제취조직DNA,실시형광정량PCR측정WSSV농도,발현감염후3h재부지、새、혈림파화조혈조직중검측도병독,12h시재각조직중개검측도병독,단농도교저;24~48h내WSSV농도정지수증장,차시오하출현소량사망;60~72h내WSSV수량완만증장체도평태기,오하루계사망솔쾌속승고。불동조직중적WSSV농도유교대차이,부지중농도최고,혈림파、새、심장화조혈조직초저,기육중WSSV농도최저;부지중WSSV동태변화대표료WSSV증식변화규률,시흔호적병독검측여병정진전평고재료。본문결과가위WSSV적조기진단제공기술지지,위천명WSSV감염증식규률제공자료。
A real-time quantitative PCR was developed and the absolute copy number of WSSV VP28 gene was quan-tified based on a standard curve in Procambarus clarkii infected with WSSV. Following intramuscular injection with WSSV,the gill,hemolymph,heart,muscle,pleopods and hemopoietic tissue of Procambarus clarkii were sampled at 0,3,6,12,24,36,48,60 and 72 h post infection(hpi),DNA was extracted from the samples and the viral load was analyzed. It was found that WSSV was detected in pleopod,gill hemolymph and hemopoietic tissue at 3 hpi, and in all sampled tissues at 12hpi with low absolute copy number of WSSV;then the WSSV copies increased logarith-mically from 24 to 48hpi and a low mortality rate was observed. Thereafter,the WSSV propagation went into the pla-teau phase and massive mortality appeared from 60 to 72hpi,showing a positive correlation between the viral load and cumulative mortality of Procambarus clarkii. Obvious difference in WSSV copy numbers were found in tested tissues, and WSSV copies in pleopod were the highest,followed by hemolymph,gill,heart and hemopoietic tissue,and the lowest in muscle. The dynamic changes of the amount of WSSV in pleopods could well represent all sampled tissues of Procambarus clarkii,so pleopods could be a reliable tissue for WSSV detection. This study might provide technical support for early diagnosis of WSSV infection and important basic data for better understanding of WSSV proliferation rules in shrimp.