首页> 美国卫生研究院文献>Scientific Reports >In Vitro generation of Panton-Valentine leukocidin (PVL) in clinical Methicillin-Resistant Staphylococcus aureus (MRSA) and its correlation with PVL variant clonal complex infection type
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In Vitro generation of Panton-Valentine leukocidin (PVL) in clinical Methicillin-Resistant Staphylococcus aureus (MRSA) and its correlation with PVL variant clonal complex infection type

机译:临床耐甲氧西林金黄色葡萄球菌(MRSA)中Panton-Valentine leukocidin(PVL)的体外产生及其与PVL变异克隆复合体感染类型的相关性

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摘要

The amount of Panton-Valentine leukocidin (PVL) is diverse among Staphylococcus aureus isolates from different geographical regions, and its significance in some infections is disputed. However, data concerning this information in China are limited. Fifty-one lukSF-PV+ methicillin-resistant Staphylococcus aureus (MRSA) isolates gathered from varying infections were used for PVL production using enzyme-linked immunosorbent assay, and the quantity was analyzed in correlation with PVL isoform, genetic background of the isolate, and disease category. All isolates generated PVL with a range of 0.43–360.87 μg/mL, of which 56.9% isolates (29/51) generated 51–200 μg/mL of PVL; 11.8% (6/51) yielded PVL more than 200 μg/mL, and the rest (31.4%, 16/51) produced PVL of ≤50 μg/mL. The amount of PVL was not related to its variant and infection type, although isolates from skin and soft tissue infection had relatively high mean and median. Clonal complex (CC) 22 isolates might be the producer of relatively high concentrations of PVL; however, the difference among CCs was not analyzed due to a small number of CC isolates. The relevance of PVL production with the infection type, toxin isoform, and genetic characteristic of isolates may vary by clone type and also needs to be further evaluated using a large sample size and best concentration on in vivo environment.
机译:在来自不同地理区域的金黄色葡萄球菌分离株中,Panton-Valentine leukocidin(PVL)的数量是不同的,并且其在某些感染中的重要性还存在争议。但是,在中国有关此信息的数据有限。用酶联免疫吸附法将五十种来自不同感染的lukSF-PV + 耐甲氧西林金黄色葡萄球菌(MRSA)分离株用于PVL生产,并分析其数量与PVL亚型的相关性,分离物的遗传背景和疾病类别。所有分离物产生的PVL范围为0.43–360.87μg / mL,其中56.9%的分离株(29/51)产生51–200μg / mL的PVL; 11.8%(6/51)的PVL大于200μg/ mL,其余(31.4%,16/51)的PVL≤50μg/ mL。尽管从皮肤和软组织感染中分离出的PVL的平均值和中位数相对较高,但PVL的数量与其变异和感染类型无关。克隆复合物(CC)22分离株可能是相对较高浓度PVL的产生者。但是,由于分离出的CC数量少,因此未分析CC之间的差异。 PVL产量与感染类型,毒素同工型和分离株遗传特征的相关性可能因克隆类型而异,并且还需要使用较大的样本量和体内最佳浓度进行进一步评估。

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