Stanley W A, Hofacre C L, Speksnijder G, Kleven S H, Aggrey S E
Poultry Diagnostic and Research Center, Department of Avian Medicine, College of Veterinary Medicine, Athens, GA 30602, USA.
Avian Dis. 2001 Apr-Jun;45(2):534-9.
Three experimental strains of breeder chickens were accidentally exposed to Mycoplasma gallisepticum (MG) and Mycoplasma synoviae (MS), presumably from a newly introduced group of leghorn-type pullets. The experimental strains subsequently became infected and were diagnosed positive for MG and MS by the serum plate agglutination (SPA) test and confirmed by the hemagglutination inhibition (HI) test and the polymerase chain reaction (PCR) of tracheal swabs. Treatment with 10 mg/kg enrofloxacin via drinking water for 14 days was elected. Before and after initiation of treatment, MG and MS were monitored for changes by SPA, HI, PCR, and culture, with sampling intervals ranging from 1 wk to 7 wk. MG and MS SPA, HI, PCR, and culture were performed at each sampling period, with the exception of weeks 1.0 and 6.5. Week 1.0 included SPA and His for MG and MS. Week 6.5 included PCR and culture for MG and MS. The MG and MS SPA results were positive throughout the 29-wk trial period. MG HI titers declined until the last sampling, whereas the MS HI titers did not decline significantly. PCR for MG yielded only one positive result, which occurred before treatment. MS PCR remained positive throughout the trial period. MG was never isolated from any sample; however, one MS organism was isolated during treatment. The treatment regimen was effective for MG on the basis of PCR results. Treatment with enrofloxacin did not eliminate SPA reactions during the 29-wk trial period. MG HI titers remained in the suspicious range throughout the remainder of the trial period. Four weeks after the treatment ended, MG HIs were reduced by approximately 40%, with MS HIs remaining high throughout the 29-wk period. PCR appeared to be a sensitive and specific test on the basis of correlation with HIs. On the basis of the isolation of MS during treatment and continued subsequent PCR positive reactions, the treatment for MS with enrofloxacin was not as efficacious as for MG.
三种种鸡实验菌株意外接触到鸡毒支原体(MG)和滑液支原体(MS),推测是来自新引入的一组来航型小母鸡。这些实验菌株随后被感染,并通过血清平板凝集(SPA)试验诊断为MG和MS阳性,经血凝抑制(HI)试验和气管拭子聚合酶链反应(PCR)确认。选择通过饮水给予10mg/kg恩诺沙星治疗14天。在开始治疗前后,通过SPA、HI、PCR和培养监测MG和MS的变化,采样间隔为1周至7周。除第1.0周和6.5周外,在每个采样期进行MG和MS的SPA、HI、PCR和培养。第1.0周包括MG和MS的SPA和HI检测。第6.5周包括MG和MS的PCR和培养。在整个29周的试验期内,MG和MS的SPA结果均为阳性。MG的HI滴度在最后一次采样前下降,而MS的HI滴度没有显著下降。MG的PCR仅产生一个阳性结果,发生在治疗前。MS的PCR在整个试验期内均保持阳性。从未从任何样本中分离出MG;然而,在治疗期间分离出一株MS菌。根据PCR结果,该治疗方案对MG有效。在29周的试验期内,恩诺沙星治疗并未消除SPA反应。在试验期的剩余时间内,MG的HI滴度一直处于可疑范围内。治疗结束四周后,MG的HI降低了约40%,而MS的HI在整个29周内一直保持较高水平。基于与HI的相关性,PCR似乎是一种灵敏且特异的检测方法。基于治疗期间MS的分离以及随后持续的PCR阳性反应,恩诺沙星对MS的治疗效果不如对MG。