Devallois A, Rastogi N
Unité de la Tuberculose et des Mycobactéries, Institut Pasteur, Pointe-à-Pitre, Guadeloupe, French West Indies.
Res Microbiol. 1997 Nov;148(8):703-13. doi: 10.1016/S0923-2508(99)80069-2.
A total of 33 clinical isolates of the Mycobacterium avium complex from 25 patients, identified by means of biochemical and cultural characteristics, the Accuprobe system and DT1/DT6 PCR, were further analysed using novel insertion elements IS1245 and IS1311 in a French Caribbean setting. PvuII-cleaved DNA and non-radioactive Southern hybridization and detection systems were used for fingerprinting with both IS elements. The data confirmed the specificity of the two probes for M. avium in our setting and highlighted a significant proportion of M. intracellulare-infected patients in this region. Two distinct groups composed of 2-3 bands and 6-27 bands were found among M. avium isolates, and were composed of the same isolates both with IS1245 and IS1311. The computer analysis of polymorphic banding patterns identified two prevalent genotypes: one contained 4 isolates from 3 patients while a second 2-banded cluster was composed of 6 isolates from 4 patients; all the patients were from the same hospital in Guadeloupe. A single isolate from Martinique was falsely included in the 2-banded cluster initially upon IS1245 fingerprinting, but could be discriminated from other isolates on the basis of IS1311 fingerprinting of PvuII-cleaved DNA. These results were also confirmed upon IS1245 fingerprinting of PstI-digested DNA, as well as DT6 fingerprinting. A single case of polyclonal infection was also discovered in a patient at a 75-day interval. This is the first study comparing the two IS elements and constitutes a first description of disseminated M. avium complex disease from the Caribbean. We conclude that both elements possess a similar discriminatory potential for M. avium isolates. Coupled with computer analysis, this methodology would appear to be particularly suitable for larger epidemiological studies.
在法属加勒比地区,对通过生化和培养特征、Accuprobe系统以及DT1/DT6 PCR鉴定的来自25名患者的总共33株鸟分枝杆菌复合群临床分离株,使用新型插入元件IS1245和IS1311进行了进一步分析。用PvuII酶切的DNA以及非放射性Southern杂交和检测系统对这两种插入元件进行指纹分析。数据证实了这两种探针在我们的研究环境中对鸟分枝杆菌的特异性,并突出显示了该地区细胞内分枝杆菌感染患者的很大比例。在鸟分枝杆菌分离株中发现了由2 - 3条带和6 - 27条带组成的两个不同组,并且用IS1245和IS1311分析时由相同的分离株组成。对多态性条带模式的计算机分析确定了两种流行基因型:一种包含来自3名患者的4株分离株,而第二个2条带的簇由来自4名患者的6株分离株组成;所有患者均来自瓜德罗普岛的同一家医院。最初,来自马提尼克岛的一株分离株在基于IS1245指纹分析时被错误地归入2条带的簇中,但根据PvuII酶切DNA的IS1311指纹分析可将其与其他分离株区分开来。对PstI消化的DNA进行IS1245指纹分析以及DT6指纹分析时也证实了这些结果。还发现一名患者在75天的间隔内发生了一例多克隆感染。这是第一项比较这两种插入元件的研究,并且是对加勒比地区播散性鸟分枝杆菌复合群疾病的首次描述。我们得出结论,这两种元件对鸟分枝杆菌分离株具有相似的鉴别潜力。结合计算机分析,这种方法似乎特别适合更大规模的流行病学研究。