中国动物检疫
中國動物檢疫
중국동물검역
CHINA ANMAL QUARANTINE
2014年
9期
64-68
,共5页
徐保娟%郭伟伟%宫晓%李陆梅%宋新宇%范根成
徐保娟%郭偉偉%宮曉%李陸梅%宋新宇%範根成
서보연%곽위위%궁효%리륙매%송신우%범근성
鸭肝炎病毒%VP1基因%序列分析%血清型%分离%鉴定
鴨肝炎病毒%VP1基因%序列分析%血清型%分離%鑒定
압간염병독%VP1기인%서렬분석%혈청형%분리%감정
duck hepatitis virus%VP1 gene%sequence analysis%serotype%isolation%identification
1999-2008年从山东、河南、浙江、江苏、广西、山西、江西、广东、福建和辽宁等地有典型鸭病毒性肝炎症状的病死雏鸭中共分离得到22株病毒。用鸭肝炎病毒(DHV)Ⅰ型(DHV-1)抗血清和新型DHV (N-DHV)抗血清对分离的22株病毒进行血清中和试验;对22株病毒的抗原相关VP1基因进行RT-PCR扩增和测序,然后对VP1基因的核苷酸与推导的氨基酸序列进行分析。结果表明,目前我国存在DHV-1和N-DHV两种血清型。其中分离到的12株为DHV-1,10株为N-DHV。依据VP1基因序列同源性进行的血清型分型结果与根据抗原性鉴定进行的血清型分型结果一致。12株DHV-1的氨基酸序列同源性为95%左右,10株N-DHV的氨基酸同源性为98%左右;DHV-1分离株与N-DHV分离株间氨基酸同源性为72%~77%。同血清型病毒株间的VP1基因变异很小,表明DHV的抗原性稳定。
1999-2008年從山東、河南、浙江、江囌、廣西、山西、江西、廣東、福建和遼寧等地有典型鴨病毒性肝炎癥狀的病死雛鴨中共分離得到22株病毒。用鴨肝炎病毒(DHV)Ⅰ型(DHV-1)抗血清和新型DHV (N-DHV)抗血清對分離的22株病毒進行血清中和試驗;對22株病毒的抗原相關VP1基因進行RT-PCR擴增和測序,然後對VP1基因的覈苷痠與推導的氨基痠序列進行分析。結果錶明,目前我國存在DHV-1和N-DHV兩種血清型。其中分離到的12株為DHV-1,10株為N-DHV。依據VP1基因序列同源性進行的血清型分型結果與根據抗原性鑒定進行的血清型分型結果一緻。12株DHV-1的氨基痠序列同源性為95%左右,10株N-DHV的氨基痠同源性為98%左右;DHV-1分離株與N-DHV分離株間氨基痠同源性為72%~77%。同血清型病毒株間的VP1基因變異很小,錶明DHV的抗原性穩定。
1999-2008년종산동、하남、절강、강소、엄서、산서、강서、엄동、복건화료녕등지유전형압병독성간염증상적병사추압중공분리득도22주병독。용압간염병독(DHV)Ⅰ형(DHV-1)항혈청화신형DHV (N-DHV)항혈청대분리적22주병독진행혈청중화시험;대22주병독적항원상관VP1기인진행RT-PCR확증화측서,연후대VP1기인적핵감산여추도적안기산서렬진행분석。결과표명,목전아국존재DHV-1화N-DHV량충혈청형。기중분리도적12주위DHV-1,10주위N-DHV。의거VP1기인서렬동원성진행적혈청형분형결과여근거항원성감정진행적혈청형분형결과일치。12주DHV-1적안기산서렬동원성위95%좌우,10주N-DHV적안기산동원성위98%좌우;DHV-1분리주여N-DHV분리주간안기산동원성위72%~77%。동혈청형병독주간적VP1기인변이흔소,표명DHV적항원성은정。
22 strains of duck hepatitis virus(DHV) were isolated from sick or died ducks with typical symptoms of duck hepatitis in Shandong,Henan,Zhejiang,Jiangsu,Guangxi,Shanxi,Jiangxi,Guangdong,Fujian and Lia-oning Provinces from 1999 to 2008. Serum neutralization test were conducted using duck hepatitis virus I type(DHV-1) antiserum and the new DHV(N-DHV) antiserum with these 22 strains. The VP1 genes of the isolated strains were amplified using RT-PCR and then sequenced. Amino acid sequences of VP1 were then deduced and analyzed. The results showed that there were two serotypes of DHV in China. Among the 22 strains,12 strains were in DHV-1 and 10 strains in N-DHV. The serotyping result based on the homology of VP1 gene sequences was identical to the result based on the antigenicity serotyping. Amino acid sequence homology was 95% within 12 DHV-1 strains and 98% within 10 N-DHV strains respectively. The amino acid homology of VP1 gene was 72~77% between DHV-1 and N-DHV strains. The less variation of VP1 gene in the same serotype strains suggested that the antigenicity of DHV was stable.