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首页> 外文期刊>Journal of neurosurgical sciences >Detection of Echinocandin-Resistant Candida glabrata in Blood Cultures Spiked with Different Percentages of FKS2 Mutants
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Detection of Echinocandin-Resistant Candida glabrata in Blood Cultures Spiked with Different Percentages of FKS2 Mutants

机译:检测血液培养中的echInocandinin抗性念珠菌尖刺,掺入不同百分比的FKS2突变体

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Infections caused by the coexistence of Candida glabrata echinocandin-resistant and echinocandin-susceptible cells may be possible, and the detection of FKS mutants when the proportions of FKS mutants are underrepresented poses a problem. We assessed the role of EUCAST and methods directly performed on positive blood cultures-Etest (ETDIR) and anidulafungin-containing agar plate assays-for detecting resistance in C. glabrata isolates containing different amounts of echinocandin-susceptible and -resistant Candida glabrata isolates. We studied 10 pairs of C. glabrata isolates involving parental echinocandin-susceptible isolates and isogenic echinocandin-resistant FKS mutant isolates. Three inocula per pair (1 X 10(3) to 5 X 10(3), 1 X 10(2) to 5 X 10(2), and 10 to 50 CFU/ml) spanning suspensions with different amounts of susceptible/resistant isolates (9/1, 5/5, and 1/9 proportions for each the three inocula) were prepared. The suspensions were spiked in Bactec bottles and incubated until they were positive, and the three methods were compared. The EUCAST method showed echinocandin resistance when the bottles were spiked with susceptible/resistant isolates at 5/5 and 1/9 proportions; the results for the suspensions with a 9/1 proportion of susceptible/resistant isolates were susceptible for three pairs. We observed with the ETDIR resistance to both echinocandins in all pairs (resistance to micafungin and anidulafungin; MICs, >= 0.064 mg/liter and >= 0.125 mg/liter, respectively) and a double ring of growth inhibition in two pairs. The anidulafungin-containing plates showed fungal growth in the 90 spiked blood cultures at 48 h. Testing of echinocandin susceptibility with the ETDIR directly on the positive blood culture bottles is a reliable and rapid method to detect echinocandin resistance in C. glabrata. On the other hand, resistance can be missed with the EU-CAST method when resistant isolates are underrepresented.
机译:可能是由念珠菌的共存引起的感染抗性和埃希鞘素易受敏感细胞的,并且当FKS突变体的比例低于代表性的突变体的比例产生问题时,突变体突变体的检测。我们评估了肌肉和方法直接对阳性血液培养物的作用 - ETEST(etdir)和含anidulafungin的琼脂平板测定 - 用于检测含有不同量的Echinocandin-易感和 - 蛋白念珠菌和 - 念珠菌蛋白分离物的C.Glabrata分离物中的抗性。我们研究了涉及父母echinocandinand敏感的分离物和抗性echinocandinan抗性FKS突变分离物的10对C.Glabrata分离物。每对三个接种物(1×10(3)至5×10(3),1×10(2)至5×10(2),和10至50个CFU / mL),跨越不同量的易感/抗性的悬浮液制备分离物(每三个接种物的9/1,5 / 5和1/9比例)。将悬浮液掺入Bactec瓶中并孵育直至它们为阳性,并比较三种方法。当瓶子掺入5/5和1/9比例的易感/抗性分离株时,肉糖方法表现出升膜膜阻力;具有9/1比例易感/抗性分离物的悬浮液的结果易于三对。我们观察到所有对echinocandins的Etdir抗性(抵抗Micafungin和Anidulafungin; MICS,> = 0.064mg /升)分别和> = 0.125mg /升,两对生长抑制的双环。含有anidulafungin的板在48小时的90个尖刺血液培养中显示出真菌生长。直接对阳性血液培养瓶中与Etdir的echinocandin易感性测试是一种可靠且快速的方法,可检测C.Glabrata的echinocandin抗性。另一方面,当抗性分离物不足时,欧盟铸造方法可能会错过电阻。

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