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高毒力肺炎克雷伯菌 K1 血清型临床分离株在气液界面形成坚固的生物膜。

Hypervirulent Klebsiella pneumoniae serotype K1 clinical isolates form robust biofilms at the air-liquid interface.

机构信息

Department of Microbiology, Hospital Universitari de Bellvitge, Instituto de Investigación Biomédica de Bellvitge (IDIBELL), Barcelona, Spain.

Research Network for Respiratory Diseases (CIBERES), ISCIII, Madrid, Spain.

出版信息

PLoS One. 2019 Sep 18;14(9):e0222628. doi: 10.1371/journal.pone.0222628. eCollection 2019.

DOI:10.1371/journal.pone.0222628
PMID:31532800
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6750583/
Abstract

The prevalence of a new hypervirulent and hypermucoviscous K. pneumoniae phenotype (Hmv) is increasing worldwide, mainly linked to serotypes K1 and K2. Since capsular thickness can directly affect the capability to form biofilms, we aimed to evaluate the association between the Hmv phenotype with adhesion and biofilm formation in a collection of clinical K. pneumoniae isolates. We selected 38 Hmv clinical isolates [15 serotype K1; 9 serotype K2; 3 non-K1/K2 (rmpA+); 11 non-K1/K2 (rmpA-)] and 7 non-Hmv clinical isolates. The Hmv phenotype was assessed through the mucoviscosity test. Serum resistance was determined by bacterial viability tests in pooled human serum. Adhesion was evaluated with the Biofilm Ring Test®, and biofilm formation was identified by crystal violet staining (Solid-Liquid, SLI-biofilm) or visual examination (Air-Liquid, ALI-biofilm). This study linked for the first time the formation of robust ALI-biofilm plugs by K. pneumoniae to the capsular serotype K1, a group of hypervirulent strains which are generally highly susceptible to the antimicrobial agents. Among all the studied isolates, the capsular serotype K1 presented lower initial adhesion despite having the adhesins mrkD and fimH but higher ALI-biofilm formation than isolates with other capsular serotypes (K2 or non-K1/K2). This structure might confer increased resistance to a group of hypervirulent K. pneumoniae serotype K1.

摘要

一种新的高毒力、高黏液型肺炎克雷伯菌表型(Hmv)在全球范围内的流行率正在上升,主要与血清型 K1 和 K2 有关。由于荚膜厚度可以直接影响形成生物膜的能力,我们旨在评估 Hmv 表型与临床分离的肺炎克雷伯菌黏附与生物膜形成的相关性。我们选择了 38 株 Hmv 临床分离株[15 株血清型 K1;9 株血清型 K2;3 株非 K1/K2(rmpA+);11 株非 K1/K2(rmpA-)]和 7 株非 Hmv 临床分离株。Hmv 表型通过黏液性试验进行评估。血清抗性通过在混合人血清中的细菌活力试验确定。黏附通过生物膜环试验评估,生物膜形成通过结晶紫染色(固液,SLI-生物膜)或目视检查(气液,ALI-生物膜)进行鉴定。本研究首次将肺炎克雷伯菌形成坚固的 ALI-生物膜塞与荚膜血清型 K1 联系起来,K1 是一组高毒力菌株,通常对大多数抗菌药物高度敏感。在所有研究的分离株中,尽管具有 mrkD 和 fimH 粘附素,但荚膜血清型 K1 的初始粘附率较低,而其他荚膜血清型(K2 或非 K1/K2)的分离株的 ALI-生物膜形成率较高。这种结构可能赋予了一组高毒力的肺炎克雷伯菌血清型 K1 更高的耐药性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f06d/6750583/2e880aa256a1/pone.0222628.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f06d/6750583/e2b5a04f1325/pone.0222628.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f06d/6750583/be9e45cf9365/pone.0222628.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f06d/6750583/2e880aa256a1/pone.0222628.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f06d/6750583/e2b5a04f1325/pone.0222628.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f06d/6750583/be9e45cf9365/pone.0222628.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f06d/6750583/2e880aa256a1/pone.0222628.g003.jpg

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