Condon K, Oakey J
Department of Primary Industries and Fisheries, Tropical & Aquatic Animal Health Laboratory, Oonoonba, Queensland, Australia.
Lett Appl Microbiol. 2007 Aug;45(2):121-7. doi: 10.1111/j.1472-765X.2007.02169.x.
The aim of this work was to develop a rapid molecular test for the detection of the Chlamydiaceae family, irrespective of the species or animal host.
The method described herein is a polymerase chain reaction targeting the 16S rRNA gene of the Chlamydiaceae family, and the results demonstrate that the test reacts with five reference Chlamydiaceae but none of the 19 other bacterial species or five uninfected animal tissues tested. The results also indicate the enhanced sensitivity of this test when compared with conventional culture or serology techniques. This is demonstrated through parallel testing of six real clinical veterinary cases and confirmatory DNA sequence analysis.
CONCLUSIONS, SIGNIFICANCE AND IMPACT OF THE STUDY: This test can be used by veterinary diagnostic laboratories for rapid detection of Chlamydiaceae in veterinary specimens, with no restriction of chlamydial species or animal host. The test does not differentiate chlamydial species, and if required, speciation must be carried out retrospectively using alternate methods. However, for the purpose of prescribing therapy for chlamydiosis, this test would be an invaluable laboratory tool.
本研究旨在开发一种快速分子检测方法,用于检测衣原体科,而不考虑其物种或动物宿主。
本文所述方法是针对衣原体科16S rRNA基因的聚合酶链反应,结果表明该检测方法与五种衣原体科参考菌株反应,但与其他19种细菌物种或五种未感染动物组织均无反应。结果还表明,与传统培养或血清学技术相比,该检测方法的灵敏度更高。通过对六个实际临床兽医病例的平行检测和验证性DNA序列分析得以证明。
研究的结论、意义及影响:兽医诊断实验室可使用该检测方法快速检测兽医标本中的衣原体科,不受衣原体物种或动物宿主的限制。该检测方法不能区分衣原体物种,如有需要,必须使用其他方法进行回顾性分类。然而,对于衣原体病的治疗处方而言,该检测方法将是一种非常有价值的实验室工具。