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首页> 外文期刊>Infection and Drug Resistance >Cryptococcus neoformans/gattii Species Complexes from Pre-HIV Pandemic Era Contain Unusually High Rate of Non-Wild-Type Isolates for Amphotericin B
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Cryptococcus neoformans/gattii Species Complexes from Pre-HIV Pandemic Era Contain Unusually High Rate of Non-Wild-Type Isolates for Amphotericin B

机译:来自艾滋病毒前大流行时代的碱性核族种类/ Gattii物种复合物含有异常高的非野生型分离株,用于两性霉素B.

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Introduction: The Cryptococcus neoformans/gattii species complexes are a leading cause of fatality among HIV-infected patients. Despite the unavailability of clinical breakpoints (CBPs) for antifungal agents, epidemiological cutoff values (ECVs) were recently proposed, and non-wild-type isolates for polyenes and azoles are being increasingly reported. However, the distributions of the susceptibility patterns for pre-HIV-era isolates have not been studied. Methods: We determined the in vitro antifungal susceptibility patterns of 233 Cryptococcus isolates, collected at the National Institutes of Health, USA, in pre-HIV pandemic era, to study minimum inhibitory concentrations (MICs) to the important drugs for cryptococcosis and to compare the results with strain genotypes. Amphotericin B susceptibility was compared to published ECV of C. neoformans. Results: The 233 Cryptococcus strains consisted of 89.7% C. neoformans species complex and 10.3% C. gattii species complex. Most were from clinical sources (189, 81.1%), and the major molecular type was VNI (146, 62.7%). The highest geometric mean (GM) was observed for fluconazole (GM = 0.96 μg/mL) while the lowest was for itraconazole (GM = 0.10 μg/mL). MICs to fluconazole in C. gattii species complex were significantly higher than C. neoformans species complex ( p 0.001). Moreover, C. neoformans /VNI strains showed significantly higher MICs than others such as C. neoformans /VNII to fluconazole ( p 0.0001) and C. deneoformans /VNIV to amphotericin B ( p = 0.022) and fluconazole ( p = 0.008). In our collection of 167 clinical C. neoformans species complex strains, 85 (50.9%), 24 (14.4%), and 3 (1.8%) strains had an amphotericin B (AMB)-MIC of 1, 2, and 4 μg/mL, respectively. The high percentage (66.9%, 79/118 strains) of non-wild-type clinical C. neoformans VNI strains, using an AMB-ECV of 0.5 μg/mL, was found. Moreover, 25 of 28 (89.3%) C. neoformans VNI strains from environmental and veterinary sources also had AMB-MICs above 0.5 μg/mL. In general, there was no significant difference in GM AMB-MIC of the clinical strains isolated from patients with (35 patients) and without (78 patients) prior AMB treatment (0.85 vs 0.76; p = 0.624). GM MIC of the environmental strains was not significantly different from that of the prior AMB-treatment strains (0.98 vs 0.76, p = 0.159) and the post-AMB-treatment strains (0.98 vs 0.85, p = 0.488). Conclusion: The high rate of non-wild-type among these otherwise naive isolates to amphotericin B is unexpected. Confirmation with more strains from a later era is needed.
机译:介绍:隐性球菌新族裔/ Gattii物种复合物是艾滋病毒感染患者之间的致命原因。尽管临床断点(CBP)对于抗真菌剂(CBP),最近提出了流行病学截止值(ECV),并且越来越多地报道聚烯酶和氮杂的非野生型分离物。然而,尚未研究用于预艾滋病毒时代分离物的易感模式的分布。方法:确定在美国国家卫生大流行时代的国家卫生大学大学大学大学学习中收集的233次隐球菌的体外抗真菌敏感模式,以研究最小抑制浓度(MIC)对隐球菌的重要药物,并比较结果菌株基因型。将两性霉素B易感性与C. Neoformans的ECV进行了比较。结果:233个水蛭球菌菌株由89.7%C.Neoformans物种复合物和10.3%C. Gatti I物种复合物组成。大多数来自临床来源(189,81.1%),主要分子量为VNI(146,62.7%)。对于氟康唑(GM =0.96μg/ mL)观察到最高几何平均值(GM),而最低用于伊唑奈唑(GM =0.10μg/ mL)。在C. Gattii物种复合物中氟康唑的MIC明显高于C.Neoformans物种复合物(P <0.001)。此外,C.Neoformans / VNI菌株显示出比其他更高的麦克风,例如C. Neoformans / VNII至氟康唑(P <0.0001)和C.Deneoformans / VNIV至两性霉素B(P = 0.022)和氟康唑(p = 0.008)。在我们的167个临床C. Neoformans物种复合菌株中,85株(50.9%),24(14.4%)和3(1.8%)菌株的两性蛋白B(Amb)-MiC为1,2和4μg/分别。发现使用AMB-ECV为0.5μg/ mL的Neocric型临床C. Neoformormans VNI菌株的高百分比(66.9%,79/118株)。此外,来自环境和兽医源的25个(89.3%)C. neoformans VNI菌株也具有高于0.5μg/ mL的AMB-MIC。一般而言,从(35名患者)和没有(78名患者)之前的患者(35名患者)的临床菌株的GM AMB-MIC没有显着差异(78名患者)之前的AMB处理(0.85 Vs 0.76; p = 0.624)。 GM的环境菌株的MIC与先前的AMB处理菌株(0.98 Vs 0.76,P = 0.159)和后水后处理菌株(0.98 Vs 0.85,P = 0.488)显着不同。结论:对于两性统计蛋白B的这些别的分离物中的非野生型高速率意外。需要从后来的时代的更多菌株确认。

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