Okuda Yo, Ono Masaaki, Shibata Isao, Sato Shizuo, Akashi Hiroomi
JA Zen-noh (National Federation of Agricultural Co-operative Associations), Institute of Animal Health, Sakura, Chiba, Japan.
J Vet Diagn Invest. 2006 Mar;18(2):162-7. doi: 10.1177/104063870601800204.
The fiber gene sequence and pathogenicity of the serotype-1 fowl adenovirus (FAdV-1) isolated from gizzard erosions and from clinically normal chickens were compared among isolates. The FAdV-99ZH strain, which induced gizzard erosions, had a nucleotide sequence of the long fiber gene that was different from that of the Ote strain, which did not induce gizzard erosions. The differences could be distinguished by use of polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis. The long fiber gene of 16 FAdV-1 isolates from gizzard erosions and 10 FAdV-1 isolates from the feces of clinically normal chickens was examined by use of PCR-RFLP analysis. All 16 FAdV-1 isolates from gizzard erosions had the same restriction patterns as those of strain 99ZH; however, 10 FAdV-1 isolates from normal chickens were classified into 3 groups. Specific-pathogen-free (SPF) chickens were inoculated orally with 2 FAdV-1 isolates from gizzard erosions or 3 FAdV-1 isolates from clinically normal chickens to determine the pathogenicity of each strain. Two of 2 FAdV-1 isolates from gizzard erosions induced gizzard erosions. Two of 3 FAdV-1 isolates from normal chickens had the same PCR-RFLP patterns as those of the Ote strain, but did not induce any gizzard erosions. However, 1 FAdV-1 isolate from clinically normal chickens had the same PCR-RFLP pattern as that of strain 99ZH and induced gizzard erosions. These results indicate that there are FAdV-1 strains that have different pathogenicity; one strain induces gizzard erosions, and the other does not. Use of PCR-RFLP analysis of long fiber genes may be able to distinguish between these two strains.
对从肌胃糜烂鸡和临床正常鸡中分离出的1型禽腺病毒(FAdV-1)的纤维基因序列和致病性进行了比较。引起肌胃糜烂的FAdV-99ZH毒株的长纤维基因核苷酸序列与不引起肌胃糜烂的Ote毒株不同。这些差异可通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析来区分。通过PCR-RFLP分析检测了16株来自肌胃糜烂鸡的FAdV-1和10株来自临床正常鸡粪便的FAdV-1的长纤维基因。所有16株来自肌胃糜烂鸡的FAdV-1分离株具有与99ZH毒株相同的限制性酶切图谱;然而,10株来自正常鸡的FAdV-1分离株被分为3组。用2株来自肌胃糜烂鸡的FAdV-1分离株或3株来自临床正常鸡的FAdV-1分离株经口接种无特定病原体(SPF)鸡,以确定各毒株的致病性。2株来自肌胃糜烂鸡的FAdV-1分离株中有2株引起了肌胃糜烂。3株来自正常鸡的FAdV-1分离株中有2株具有与Ote毒株相同的PCR-RFLP图谱,但未引起任何肌胃糜烂。然而,1株来自临床正常鸡的FAdV-1分离株具有与毒株99ZH相同的PCR-RFLP图谱,并引起了肌胃糜烂。这些结果表明,存在致病性不同的FAdV-1毒株;一种毒株引起肌胃糜烂,另一种则不引起。对长纤维基因进行PCR-RFLP分析可能能够区分这两种毒株。