Sykes J E, Studdert V P, Anderson G, Browning G F
University of Melbourne, Department of Veterinary Science, Parkville, Victoria, Australia.
Vet Rec. 1997 Mar 22;140(12):310-3. doi: 10.1136/vr.140.12.310.
Conjunctival swabs were taken from 168 cats with clinical signs of acute or chronic upper respiratory tract disease and tested for Chlamydia psittaci by the polymerase chain reaction (PCR) to amplify the ompA gene coding region. Twenty-two (13 per cent) were positive for C psittaci. The PCR products from positive samples were subjected to restriction endonuclease analysis with the restriction enzymes Alu I and Mse I. The fragments of DNA were detected on silver-stained polyacrylamide gels and the results were compared with the results obtained from chlamydial isolates from cats in Japan, France, the USA and the UK. All the strains had identical restriction patterns. When PCR is used as an epidemiological tool, feline chlamydial strains worldwide appear very similar.
从168只出现急性或慢性上呼吸道疾病临床症状的猫身上采集结膜拭子,通过聚合酶链反应(PCR)检测鹦鹉热衣原体,以扩增编码ompA基因的区域。22只(13%)猫的鹦鹉热衣原体检测呈阳性。对阳性样本的PCR产物用限制性内切酶Alu I和Mse I进行限制性内切酶分析。在银染聚丙烯酰胺凝胶上检测DNA片段,并将结果与从日本、法国、美国和英国的猫衣原体分离株获得的结果进行比较。所有菌株具有相同的限制性图谱。当PCR用作流行病学工具时,全球范围内的猫衣原体菌株似乎非常相似。