鲍曼不动杆菌的鉴定方法。色氨酸及其亚生物变体A和B

E. P. Sivolodskii, L. Kraeva, E. Melnikova, G. Gorelova
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引用次数: 0

摘要

本研究的目的是提高鲍曼不动杆菌的诊断敏感性。并评估该生物变体及其亚生物变体在鲍曼不动杆菌临床分离株中的流行率。在基洛夫(S.M. Kirov)命名的军事医学科学院细菌学实验室,检测了20212022年分离的鲍曼不动杆菌210株,其中42株为鲍曼不动杆菌。tryptophandestruens。采用苯甲酸钠在高密度营养培养基(g/l)上的显色生物转化法鉴定色氨酸destruens生物变异菌;氯化钠5.0;FeCl3 6H2O(10%水溶液)0.11 ml;溴百里酚蓝(1.6%水溶液)3 ml;琼脂15.0;NaOH(4%溶液)2.63 ml;蒸馏水1升;所有组分加热溶解后加入苯甲酸钠(CAS 532-32-1) 1.02.0;调整pH值7.20.2;在121С上消毒,倒入培养皿中。用添加l -色氨酸(1.02.0 g/l)代替苯甲酸钠的相同营养培养基对l -色氨酸进行显色生物转化,鉴定了生物变种色氨酸destruens亚生物变种A和B细菌。两种培养基同时使用。a . baumannii文化研究与循环对媒体的部门被播种在斑块的形式,在37С耗氧孵化1824个小时,和最终的数据分析如下:深棕色的颜色带细菌草坪周围的营养培养基苯甲酸钠,L-tryptophan-containing介质表示检测subbiovar tryptophandestruens的生物变型;本研究首次揭示了苯甲酸钠(苯甲酸)的显色生物转化作用及其作为鲍曼a.p ormannii色氨酸生物变异标记物的重要性。发现色氨酸降解菌的两个亚生物变体A和B。建立了一种利用苯甲酸钠和l -色氨酸的显色生物转化法鉴定鲍曼不动杆菌及其亚生物变体A和B的方法,通过检测亚生物变体B,提高了诊断灵敏度。测定了2021 - 2022年鲍曼不动杆菌临床分离株中色氨酸不动杆菌生物变体的分布频率:210株鲍曼不动杆菌中有42株(20.03.5%)为bv。色氨酸原亚型a27 (12.92.3%), b15(7.11.7%)。
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Method for identification of acinetobacter baumannii bv. tryptophandestruens and its subbiovars A and B
The aim of the study was to increase diagnostic sensitivity for identification of A. baumannii bv. tryptophandestruens bacteria and assess prevalence of this biovar and its subbiovars among A. baumannii clinical isolates. There were examined 210 primary strains of A. baumannii isolated in 20212022 at Bacteriological Laboratory of the Military Medical Academy named after S.M. Kirov, of which 42 strains were A. baumannii bv. tryptophandestruens. Tryptophandestruens biovar bacteria were identified by chromogenic biotransformation of sodium benzoate on a dense nutrient medium (g/l): peptone enzymatic 5.0; NaCl 5.0; FeCl3 6H2O (10% aqueous solution) 0.11 ml; bromothymol blue (1.6% aqueous solution) 3 ml; agar 15.0; NaOH (4% solution) 2.63 ml; distilled water 1 l; all components were dissolved by heating and added with sodium benzoate (CAS 532-32-1) 1.02.0; adjusted pH 7.20.2; sterilized at 121С, poured into Petri dishes. Bacteria of subbiovars A and B of biovar tryptophandestruens were identified by chromogenic biotransformation of L-tryptophan using the same nutrient medium supplemented with L-tryptophan (1.02.0 g/l) instead of sodium benzoate. Both nutrient media were used simultaneously. The A. baumannii cultures studied were seeded with a loop on the media sectors in the form of a plaque, incubated aerobically at 37С for 1824 hours, and analyzed final data as follows: the presence of a dark brown color zone of the nutrient medium around bacterial lawn on sodium benzoate- and L-tryptophan-containing medium indicated detection of subbiovar A of the tryptophandestruens biovar; in case of dark brown zone on sodium benzoate- but not L-tryptophan-containing medium around bacterial lawn identified biovar tryptophandestruens subbiovar B. The study revealed for the first time the chromogenic biotransformation of sodium benzoate (benzoic acid) and its importance as a marker for the biovar tryptophandestruens A. baumannii. Two subbiovars A and B of the tryptophandestruens biovar were found. A method was developed to identify the biovar tryptophandestruens A. baumannii and its subbiovars A and B by chromogenic biotransformation of sodium benzoate and L-tryptophan, which enhances diagnostic sensitivity by detecting the subbiovar B. The frequency of tryptophandestruens biovar distribution among primary clinical isolates of A. baumannii in 20212022 was determined: out of 210 strains of A. baumannii were 42 (20.03.5%) strains of bv. tryptophandestruens including subbiovar A 27 (12.92.3%), subbiovar B 15 (7.11.7%).
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