Kumar Swati, Kutlin Andrei, Roblin Patricia, Kohlhoff Stephan, Bodetti Tracey, Timms Peter, Hammerschlag Margaret R
Department of Pediatrics, Division of Infectious Diseases, State University of New York, Downstate Medical Center, 450 Clarkson Ave., Brooklyn, NY 11203, USA.
J Clin Microbiol. 2007 Feb;45(2):392-4. doi: 10.1128/JCM.01726-06. Epub 2006 Nov 22.
A range of species of Chlamydiales have previously been detected in a variety of Australian marsupials, including koalas and western barred bandicoots. Thirty-seven ocular, urogenital, or nasal swabs were obtained from 21 wild western barred bandicoots. Chlamydia culture and antibiotic susceptibility testing were performed for cycloheximide-treated HEp-2 cells in 96-well microtiter plates. Chlamydia spp. were isolated from 11 specimens from 9 (42.8%) bandicoots. All isolates were identified as Chlamydiales by conventional PCR with 16S and 23S rRNA gene primers specific to Chlamydiales and were confirmed to be Chlamydia pneumoniae by a C. pneumoniae-specific ompA-based real-time PCR assay and 16S rRNA and 23S rRNA gene signature sequence analyses. The MICs of azithromycin, doxycycline, ciprofloxacin, and enrofloxacin for 10 C. pneumoniae isolates from these bandicoots ranged from 0.015 to 1 microg/ml, 0.25 to 1 microg/ml, 0.25 to 2 microg/ml, and 0.25 to 0.5 microg/ml, respectively. The MICs at which 90% of isolates were inhibited and the minimal bactericidal concentrations were within the ranges reported previously for human isolates of C. pneumoniae.
此前在包括考拉和西部斑纹袋狸在内的多种澳大利亚有袋动物中检测到了一系列衣原体目物种。从21只野生西部斑纹袋狸身上采集了37份眼、泌尿生殖道或鼻腔拭子。在96孔微量滴定板中对经放线菌酮处理的HEp-2细胞进行衣原体培养和抗生素敏感性测试。从9只(42.8%)袋狸的11份标本中分离出了衣原体属。通过使用衣原体目特异性的16S和23S rRNA基因引物进行常规PCR,将所有分离株鉴定为衣原体目,并通过基于肺炎衣原体特异性ompA的实时PCR检测以及16S rRNA和23S rRNA基因特征序列分析,确认其为肺炎衣原体。从这些袋狸中分离出的10株肺炎衣原体对阿奇霉素、强力霉素、环丙沙星和恩诺沙星的最低抑菌浓度分别为0.015至1微克/毫升、0.25至1微克/毫升、0.25至2微克/毫升和0.25至0.5微克/毫升。90%的分离株被抑制时的最低抑菌浓度以及最小杀菌浓度在先前报道的人类肺炎衣原体分离株的范围内。