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首页> 外文期刊>Journal of Clinical Microbiology >Mycobactin analysis as an aid for the identification of Mycobacterium fortuitum and Mycobacterium chelonae subspecies.
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Mycobactin analysis as an aid for the identification of Mycobacterium fortuitum and Mycobacterium chelonae subspecies.

机译:霉菌素分析作为鉴定重组和骨髓术亚种的辅助。

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Mycobactin patterns from 65 Mycobacterium fortuitum and Mycobacterium chelonae strains have been determined by thin-layer chromatography. By use of a rich liquid medium containing an iron chelator (ethylenediamine-di-o-hydroxyphenylacetic acid [EDDA]) to ensure iron starvation, all strains were able to form mycobactins. The method developed here allows sensitive detection of mycobactin by thin-layer chromatography from as little as 5 ml of culture after a 2-week incubation. Within M. fortuitum two mycobactin patterns were identified, whereas within M. chelonae four were recognized. Comparisons with the subspecific identification performed by using biochemical tests showed that 73% of the M. fortuitum subsp. fortuitum strains shared the same mycobactin pattern (designated F), whereas 75% of the M. fortuitum subsp. peregrinum strains shared the other mycobactin pattern (designated P). Within the M. fortuitum strains that cannot be assigned to a subspecies on the basis of their biochemical features, only F and P patterns were determined. Similarly, 93% of the M. chelonae subsp. chelonae strains produced the so-called C1 and C2 patterns and 86% of the M. chelonae subsp. abscessus strains produced A1 and A2 patterns. C2 and A2 were the patterns most frequently encountered; they were represented by 65 and 50% of the M. chelonae subsp. chelonae and M. chelonae subsp. abscessus strains, respectively. Within the biochemically M. chelonae strains that did not fit any subspecies on the basis of biochemical test results, C1, C2, and A1 patterns were found. Whereas about 30% of both M. fortuitum and M. chelonae strains cannot be characterized to the subspecies level on the basis of biochemical tests, 100% of the strains of both species can be characterized on the basis of mycobactin patterns.
机译:通过薄层色谱法测定了65分枝杆菌和骨髓杆菌菌株的霉菌素图案。通过使用含有铁螯合剂的富液体介质(乙二胺-Di-O-羟基苯基乙酸[EDDA]),以确保铁饥饿,所有菌株都能够形成染色蛋白酶。此处开发的方法允许在2周孵育后,通过薄层色谱法通过薄层色谱法敏感检测薄层色谱。在M.Fortuitum中,鉴定了两种霉菌素图案,而在M. Chelonae 4内被认识到。通过使用生化试验进行的鉴定鉴定的比较显示,M.Fortuitum Subsp的73%。 Fortuitum菌株共享相同的霉菌模式(指定F),而75%的M.Fortuitum subsp。 Peregrinum Strins分享了其他霉菌模式(指定的P)。在M.Fortuitum菌株中,不能根据其生化特征分配给亚种,仅确定F和P模式。同样,93%的M. Chelonae亚数据。 Chelonae菌株产生所谓的C1和C2模式和86%的M.Chelonae Subsp。脓肿菌株产生A1和A2图案。 C2和A2最常遇到的模式;它们由65%和50%的M.Chelonae Subsp表示。 Chelonae和M. Chelonae subsp。脓肿菌株分别。在生物化学上,在生物化学测试结果的基础上不适合任何亚种的Chelonae菌株,发现C1,C2和A1模式。而大约30%的M.Fortuitum和M. Chelonae菌株不能在生化试验的基础上表征亚种水平,这两个物种的100%可以根据霉菌素模式表征。

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