血液感染肺炎克雷伯氏菌的毒力与碳青霉烯耐药表型之间的关系:一种碳青霉烯耐药和高毒力菌株的鉴定。

Quanfeng Liao, Weili Zhang, Jin Deng, Siying Wu, Ya Liu, Yuling Xiao, Mei Kang
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引用次数: 0

摘要

研究目的研究血液感染肺炎克雷伯菌毒力与碳青霉烯耐药表型的关系,鉴定碳青霉烯耐药和高病毒性肺炎克雷伯菌(CR-HVKP)菌株:从2016年至2019年血液感染患者血液培养中分离出肺炎克雷伯菌株共192株,其中96株为耐碳青霉烯类肺炎克雷伯菌(CRKP),96株为碳青霉烯类敏感肺炎克雷伯菌(CSKP)。采用 VITEK-2 型全自动微生物分析仪检测药敏性,聚合酶链式反应检测碳青霉烯酶基因、毒力基因和胶囊分型,串联试验检测菌株的高粘度表型,全基因组测序检测 CR-HVKP 的基因组特征。通过血清杀灭试验和生物膜形成试验进一步验证了CR-HVKP的毒力:结果:除米诺环素外,CSKP 和 CRKP 分离物(均为 PblaKPC-2)对常见抗生素的耐药性存在明显差异。串联测试结果显示,CRKP 的 4 个分离株和 CSKP 的 36 个分离株(CSKP 组的 PKfu、aerobictin、iutA、ybtS、rmpA、magA、allS 和胶囊抗原 K1 和 K2 均显著高于 CRKP 组(全部为 PPiutA、entB、mrkD、fimH 和 rmpA 毒力基因)呈阳性,并表现出很强的生物膜形成能力,血清抗药性显著增强。全基因组测序结果显示,该CR-HVKP分离株携带blaSHV-145、blaTEM-1、blaCTX-M-3、fosA6、oqxA5、oqxB26和aac(3)-IId耐药基因,并伴有外膜蛋白K(OmpK)35和OmpK36的异常:CRKP的耐药性明显高于CSKP,而与CSKP相比,CRKP携带的毒力基因在数量和类型上都较少。发现了一种新的耐碳青霉烯类药物和高病毒性肺炎克雷伯菌株的 MLST 类型,需要引起临床注意并进行流行病学监测。
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Relationship between virulence and carbapenem resistance phenotype of Klebsiella pneumoniae from blood infection: identification of a carbapenem-resistant and hypervirulent strain.

Objectives: To investigate the relationship between the virulence and the carbapenem resistance phenotype of Klebsiella pneumoniae from blood infection, and to identify carbapenem-resistant and hypervirulent Klebsiella pneumoniae (CR-HVKP)strains.

Methods: A total of 192 Klebsiella pneumoniae strains were isolated from blood culture of patients with bloodstream infections from 2016 to 2019, of which 96 isolates were carbapenem-resistant Klebsiella pneumoniae (CRKP) and 96 were carbapenem-sensitive Klebsiella pneumoniae (CSKP). The drug susceptibility was detected by VITEK-2 automatic microbial analyzer; carbapenemase genes, virulence genes and capsule typing were detected by polymerase chain reaction; the high viscosity phenotype of strains was detected by string test, and the genome characteristics of CR-HVKP were detected by whole genome sequencing. Serum killing and biofilm formation test were used to further verify the virulence of CR-HVKP.

Results: There were significant differences in drug resistance to common antibiotics, except for minocycline between CSKP and CRKP isolates (all P<0.05). 92 out of 96 CRKP isolates carried carbapenemase genes, mainly blaKPC-2. The string tests were positive in 4 isolates of CRKP and 36 isolates of CSKP (P<0.05). The detection rates of virulence genes Kfu, aerobictin, iutA, ybtS, rmpA, magA, allS, and capsule antigen K1 and K2 in CSKP group were significantly higher than those in CRKP group (all P<0.05). One HVKP strain was detected in the CRKP group (CR-HVKP) and 36 HVKP was detected in the CSKP group (P<0.05). The CR-HVKP strain belonged to the MLST412, serotype K57, expressed iutA, entB, mrkD, fimH, and rmpA virulence genes, and showed strong biofilm formation and significantly increased serum resistance. Whole genome sequencing results showed that this CR-HVKP isolate carried blaSHV-145, blaTEM-1, blaCTX-M-3, fosA6, oqxA5, oqxB26, and aac(3)-IId resistance genes, accompanied by abnormalities in outer membrane protein K (OmpK) 35 and OmpK36.

Conclusions: The drug resistance of CRKP is significantly higher than that of CSKP, while CRKP carrying fewer virulence genes in both number and types compared to CSKP. A new MLST type of carbapenem-resistant and hypervirulent Klebsiella pneumoniae strain has been detected, which requires clinical awareness and epidemiological monitoring.

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