中国动物传染病学报
中國動物傳染病學報
중국동물전염병학보
CHINESE JOURNAL OF VETERINARY PARASITOLOGY
2014年
5期
21-27
,共7页
马明杰%郭翠平%焦玉祥%吕佳泓%孙振%张瑞华%陈君豪%谢之景%姜世金
馬明傑%郭翠平%焦玉祥%呂佳泓%孫振%張瑞華%陳君豪%謝之景%薑世金
마명걸%곽취평%초옥상%려가홍%손진%장서화%진군호%사지경%강세금
1型鸭甲肝病毒%VP1%变异%致弱
1型鴨甲肝病毒%VP1%變異%緻弱
1형압갑간병독%VP1%변이%치약
Duck hepatitis A virus tyre 1 (DHAV-1)%VP1%mutation%attenuation
为了解1型鸭甲肝病毒(Duck hepatitis A virus type 1)VP1基因在鸭胚传代中的变异规律,本研究将LY0801株DHAV-1在鸭胚体内传代至30代,分别对1~5、10、15、20、25、30代病毒进行VP1基因的克隆测序。各代次病毒分别以108copies/胚接种9日龄健康鸭胚,测定各组鸭胚的平均死亡时间和病毒在鸭胚尿囊液中的增殖拷贝数。结果表明:DHAV-1在鸭胚传代过程中,不同代次之间出现12个氨基酸的反复变异和同步变异,分别为R43M(K)、T48A、T101S、L169F、T180I、S181L、R183Q、E184A(K)、G187D、D193N、M213R、H219Y;在传代过程中,病毒致死鸭胚的时间逐渐延迟,但病毒在鸭胚内的增殖拷贝数未呈现稳定增长的趋势。
為瞭解1型鴨甲肝病毒(Duck hepatitis A virus type 1)VP1基因在鴨胚傳代中的變異規律,本研究將LY0801株DHAV-1在鴨胚體內傳代至30代,分彆對1~5、10、15、20、25、30代病毒進行VP1基因的剋隆測序。各代次病毒分彆以108copies/胚接種9日齡健康鴨胚,測定各組鴨胚的平均死亡時間和病毒在鴨胚尿囊液中的增殖拷貝數。結果錶明:DHAV-1在鴨胚傳代過程中,不同代次之間齣現12箇氨基痠的反複變異和同步變異,分彆為R43M(K)、T48A、T101S、L169F、T180I、S181L、R183Q、E184A(K)、G187D、D193N、M213R、H219Y;在傳代過程中,病毒緻死鴨胚的時間逐漸延遲,但病毒在鴨胚內的增殖拷貝數未呈現穩定增長的趨勢。
위료해1형압갑간병독(Duck hepatitis A virus type 1)VP1기인재압배전대중적변이규률,본연구장LY0801주DHAV-1재압배체내전대지30대,분별대1~5、10、15、20、25、30대병독진행VP1기인적극륭측서。각대차병독분별이108copies/배접충9일령건강압배,측정각조압배적평균사망시간화병독재압배뇨낭액중적증식고패수。결과표명:DHAV-1재압배전대과정중,불동대차지간출현12개안기산적반복변이화동보변이,분별위R43M(K)、T48A、T101S、L169F、T180I、S181L、R183Q、E184A(K)、G187D、D193N、M213R、H219Y;재전대과정중,병독치사압배적시간축점연지,단병독재압배내적증식고패수미정현은정증장적추세。
To survey the genetic variation of VP1 gene of Duck hepatitis A virus type I (DHAV-I), DHAV-1 LY0801 isolate was carried 30 serial passages in duck embryos. The VP1 gene of the first to fifth, tenth, fifteenth, twentieth, twenty-fifth and thirtieth passages was amplified and sequenced respectively. With the dose of 108 copies per embryo, each ten 9-day-old healthy duck embryos were inoculated with different passages of virus, and the mean death time of each group and the vial copies in duck embryo allantoic fluid were detected. The results showed that there were 12 amino acid mutation sites in VP1 gene in different passages, which were R43M(K), T48A, T101S, L169F, T180I, S181L, R183Q, E184A(K), G187D, D193N, M213R and H219Y. The 12 amino acid mutations appeared in different passages simultaneously and repeated the mutations in the first 30 passages. In the passaging process, the mean death time of duck embryos was increasing with increasing passage times, but the virus proliferation in duck embryos did not show a steady growth trend.