念珠菌属定植:在血液培养物中发现的一种基因型来源,可广泛传播。

IF 4.6 2区 医学 Q2 IMMUNOLOGY Frontiers in Cellular and Infection Microbiology Pub Date : 2024-11-07 eCollection Date: 2024-01-01 DOI:10.3389/fcimb.2024.1468692
Aina Mesquida, Pablo Martín-Rabadán, Luis Alcalá, Almudena Burillo, Elena Reigadas, Patricia Muñoz, Jesús Guinea, Pilar Escribano
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引用次数: 0

摘要

目的:我们以前的基因分型研究表明,某些解剖部位是可能导致念珠菌血症的基因型的储存库,因为我们在胃肠道或导管尖端分离物和血液培养物中发现了相同的基因型,相反,我们在阴道样本中没有发现血液培养物基因型。我们注意到,某些基因型在血培养物中的出现频率高于其他基因型,其中一些基因型被称为广泛基因型,因为在不同医院收治的无关病人中都曾发现过这些基因型。广泛存在的基因型之所以更常被发现,可能是因为它们容易导致念珠菌血症。我们研究了白念珠菌、副丝状念珠菌和热带念珠菌的定植基因型,以评估在血液培养物中发现的比例以及广泛基因型的比例:本文研究的分离菌株(n= 640 个念珠菌分离菌株,来自 323 名患者)来自格雷戈里奥马拉尼翁医院(西班牙马德里)临床微生物学和传染病部门在 2016 年 7 月 1 日至 2019 年 6 月 30 日期间处理的样本。使用物种特异性微卫星标记对白念球菌(n=486)、副丝状念球菌(n=94)和热带念球菌(n=60)分离株进行了基因分型,分离株来自血液(n=120)和定植解剖部位(n=520;导管[n=50]、下呼吸道[n=227]、皮肤/粘膜[n=132]和泌尿道[n=111])。基因型相同的分离株是指所有标记的等位基因都相同,或仅在某一标记的一个位点上存在差异。相同基因型还可进一步分为匹配型(在给定患者的不同组样本中发现相同基因型)或群组型(在≥2 名患者中发现相同基因型)。最后,单体是指检测到一次的基因型。然后,将发现的基因型与我们的内部数据库(包含格雷戈里奥-马拉尼翁医院(2007-2023 年)收治的 587 名患者的血液基因型)进行比较,以评估在定植样本中发现的基因型与在血液培养物中发现的基因型的比例。此外,由于我们内部数据库中的一些基因型已被标记为广泛分布的基因型,因此我们使用标准二项式方法比较了广泛分布的基因型的比例,以及在完全定植基因型、完全血液培养基因型和既定植又血液培养基因型中发现的匹配比例、集群比例和集群中涉及的患者比例:患者内分析仅针对从特定物种中分离出≥2个分离物的患者(n=225;69.7%)进行;完全定植患者的匹配比例低于念珠菌血症和定植基因型患者(87.3% vs. 94.1%;p = 0.126)。对所有患者(n=323)和来自第 1、第 2 和第 3 组的分离株(n=640)进行了患者间分析。总体而言,我们发现了 341 种基因型,其中 320 种为单基因型,21 种为群集基因型(6.16%)。集群涉及血液培养物和来自导管尖端(14.6%)、皮肤和粘膜(7.5%)、尿液(7.4%)和下呼吸道(4.6%)的定植分离物。集群患者并非同时入住同一病房。在 290 种定植基因型中,有 91 种(31.1%)也在血液培养物中发现,其中比例最高的是副丝状菌(P < 0.05);在血液培养物和导管尖端发现的相同基因型比例高于在血液培养物和其他定植样本中发现的相同基因型比例(79.2% 对 26.7%;P < 0.001)。在血液和定植样本中发现的基因型的广泛基因型比率明显高于仅在血液培养物或其他定植基因型中发现的基因型(分别为 31.9% vs. 7.1% vs. 3.7%;p < 0.001):我们观察到,94% 的念珠菌血症患者定植了导致感染的基因型;同样,31% 的定植基因型可在血液培养中检测到。最后,在定植样本和血液培养物中发现的相同基因型具有更高的广泛性。
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Candida spp. colonization: a genotype source found in blood cultures that can become widespread.

Objective: Our previous genotyping studies suggest that some anatomical locations act as reservoirs of genotypes that may cause further candidemia, since we found identical genotypes in gastrointestinal tract or catheter tip isolates and blood cultures, in contrast, we did not find blood culture genotypes in vagina samples. We observed that some genotypes can be found in blood cultures more frequently than others, some of them being called widespread genotypes because have been found in unrelated patients admitted to different hospitals. The presence of widespread genotypes may be more frequently found because of their predisposition to cause candidemia. It is unclear whether genotypes colonizing other anatomical sites different from the gastrointestinal tract can also be detected in this way; we studied C. albicans, C. parapsilosis, and C. tropicalis colonizing genotypes to assess what proportion could be found in blood cultures and the proportion of widespread genotypes.

Methods: The isolates (n= 640 Candida isolates from 323 patients) studied herein were obtained from samples processed at the Clinical Microbiology and Infectious Diseases Department of the Gregorio Marañón Hospital (Madrid, Spain) from July 1, 2016, to June 30, 2019. C. albicans (n=486), C. parapsilosis (n=94), and C. tropicalis (n=60) isolates were genotyped using species-specific microsatellite markers and sourced from blood (n=120) and colonized anatomical sites (n=520; catheter [n=50], lower respiratory tract [n=227], skin/mucosa [n=132], and urinary tract [n=111]). Isolates with identical genotypes were those presenting the same alleles for all markers or with only differences at one locus of a given marker. Identical genotypes were further classified as a match (identical genotype found in different groups of samples from a given patient) or as a cluster (identical genotype found in ≥2 patients). Finally, singletons were genotypes detected once. The genotypes found were then compared with our in-house database containing 587 blood genotypes from patients admitted to the Gregorio Marañón Hospital (2007-2023) to assess the proportion of genotypes found in colonized samples that were also found in blood cultures. Moreover, since some of our in-house database genotypes had been tagged as widespread genotypes, we compared the proportions of widespread genotypes as well as the proportions of matches, clusters, and patients involved in clusters found among exclusively colonizing genotypes, exclusively blood culture genotypes, and both colonizing and blood culture genotypes using a standard binomial method.

Results: Intra-patient analysis was conducted exclusively on those patients (n=225; 69.7%) who had ≥2 isolates from a given species; the proportion of patients with matches was lower in exclusively colonized patients than in patients with candidemia and colonizing genotypes (87.3% vs. 94.1%; p = 0.126). Inter-patient analysis was conducted considering all patients (n=323) and isolates from groups 1, 2, and 3 (n=640). Overall, we detected 341 genotypes, of which 320 were singletons and 21 were clusters (6.16%). Clusters involving blood cultures and colonizing isolates sourced from catheter tips (14.6%), skin and mucosa (7.5%), urine (7.4%), and lower respiratory tract (4.6%). Cluster-involved patients had not been admitted to the same ward at the same time. Of the 290 colonizing genotypes, 91 (31.1%) were also found in blood cultures, the highest proportion being C. parapsilosis (p < 0.05); proportions of identical genotypes found in blood cultures and catheter tips were higher than those found in blood cultures and other colonized samples (79.2% vs. 26.7%; p < 0.001). Widespread genotype ratios were significantly higher among genotypes found in both blood and colonized samples than among genotypes found exclusively in either blood culture or other colonizing genotypes (31.9% vs. 7.1% vs. 3.7%, respectively; p < 0.001).

Conclusion: We observed that 94% of patients with candidemia were colonized by a genotype causing the infection; likewise, a total of 31% of colonizing genotypes were detectable in blood cultures. Finally, identical genotypes found in both colonized samples and blood cultures had a higher probability of being widespread.

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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
1817
审稿时长
14 weeks
期刊介绍: Frontiers in Cellular and Infection Microbiology is a leading specialty journal, publishing rigorously peer-reviewed research across all pathogenic microorganisms and their interaction with their hosts. Chief Editor Yousef Abu Kwaik, University of Louisville is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Cellular and Infection Microbiology includes research on bacteria, fungi, parasites, viruses, endosymbionts, prions and all microbial pathogens as well as the microbiota and its effect on health and disease in various hosts. The research approaches include molecular microbiology, cellular microbiology, gene regulation, proteomics, signal transduction, pathogenic evolution, genomics, structural biology, and virulence factors as well as model hosts. Areas of research to counteract infectious agents by the host include the host innate and adaptive immune responses as well as metabolic restrictions to various pathogenic microorganisms, vaccine design and development against various pathogenic microorganisms, and the mechanisms of antibiotic resistance and its countermeasures.
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