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通过ITS区域测序和扩增片段长度多态性分析对科威特近平滑念珠菌复合体分离株进行简单、低成本检测及对正平滑念珠菌菌株进行分子指纹识别

Simple, Low-Cost Detection of Candida parapsilosis Complex Isolates and Molecular Fingerprinting of Candida orthopsilosis Strains in Kuwait by ITS Region Sequencing and Amplified Fragment Length Polymorphism Analysis.

作者信息

Asadzadeh Mohammad, Ahmad Suhail, Hagen Ferry, Meis Jacques F, Al-Sweih Noura, Khan Ziauddin

机构信息

Department of Microbiology, Faculty of Medicine, Kuwait University, Safat, Kuwait.

Department of Medical Microbiology and Infectious Diseases, Canisius Wilhelmina Hospital, Nijmegen, The Netherlands.

出版信息

PLoS One. 2015 Nov 18;10(11):e0142880. doi: 10.1371/journal.pone.0142880. eCollection 2015.

Abstract

Candida parapsilosis has now emerged as the second or third most important cause of healthcare-associated Candida infections. Molecular studies have shown that phenotypically identified C. parapsilosis isolates represent a complex of three species, namely, C. parapsilosis, C. orthopsilosis and C. metapsilosis. Lodderomyces elongisporus is another species phenotypically closely related to the C. parapsilosis-complex. The aim of this study was to develop a simple, low cost multiplex (m) PCR assay for species-specific identification of C. parapsilosis complex isolates and to study genetic relatedness of C. orthopsilosis isolates in Kuwait. Species-specific amplicons from C. parapsilosis (171 bp), C. orthopsilosis (109 bp), C. metapsilosis (217 bp) and L. elongisporus (258 bp) were obtained in mPCR. Clinical isolates identified as C. parapsilosis (n = 380) by Vitek2 in Kuwait and an international collection of 27 C. parapsilosis complex and L. elongisporus isolates previously characterized by rDNA sequencing were analyzed to evaluate mPCR. Species-specific PCR and DNA sequencing of internal transcribed spacer (ITS) region of rDNA were performed to validate the results of mPCR. Fingerprinting of 19 clinical C. orthopsilosis isolates (including 4 isolates from a previous study) was performed by amplified fragment length polymorphism (AFLP) analysis. Phenotypically identified C. parapsilosis isolates (n = 380) were identified as C. parapsilosis sensu stricto (n = 361), C. orthopsilosis (n = 15), C. metapsilosis (n = 1) and L. elongisporus (n = 3) by mPCR. The mPCR also accurately detected all epidemiologically unrelated C. parapsilosis complex and L. elongisporus isolates. The 19 C. orthopsilosis isolates obtained from 16 patients were divided into 3 haplotypes based on ITS region sequence data. Seven distinct genotypes were identified among the 19 C. orthopsilosis isolates by AFLP including a dominant genotype (AFLP1) comprising 11 isolates recovered from 10 patients. A rapid, low-cost mPCR assay for detection and differentiation of C. parapsilosis, C. orthopsilosis, C. metapsilosis and L. elongisporus has been developed.

摘要

近平滑念珠菌现已成为医疗保健相关念珠菌感染的第二或第三大重要病因。分子研究表明,表型鉴定的近平滑念珠菌分离株代表了三个物种的复合体,即近平滑念珠菌、正平滑念珠菌和间平滑念珠菌。长孢洛德酵母是另一个在表型上与近平滑念珠菌复合体密切相关的物种。本研究的目的是开发一种简单、低成本的多重(m)PCR检测方法,用于近平滑念珠菌复合体分离株的种特异性鉴定,并研究科威特正平滑念珠菌分离株的遗传相关性。在多重PCR中获得了来自近平滑念珠菌(171 bp)、正平滑念珠菌(109 bp)、间平滑念珠菌(217 bp)和长孢洛德酵母(258 bp)的种特异性扩增子。对科威特通过Vitek2鉴定为近平滑念珠菌的临床分离株(n = 380)以及先前通过rDNA测序表征的27株近平滑念珠菌复合体和长孢洛德酵母的国际菌株进行分析,以评估多重PCR。进行种特异性PCR和rDNA内部转录间隔区(ITS)区域的DNA测序以验证多重PCR的结果。通过扩增片段长度多态性(AFLP)分析对19株临床正平滑念珠菌分离株(包括先前一项研究中的4株分离株)进行指纹图谱分析。通过多重PCR,表型鉴定的近平滑念珠菌分离株(n = 380)被鉴定为狭义近平滑念珠菌(n = 361)、正平滑念珠菌(n = 15)、间平滑念珠菌(n = 1)和长孢洛德酵母(n = 3)。多重PCR还准确检测了所有流行病学上不相关的近平滑念珠菌复合体和长孢洛德酵母分离株。根据ITS区域序列数据,从16名患者中获得的19株正平滑念珠菌分离株被分为3个单倍型。通过AFLP在19株正平滑念珠菌分离株中鉴定出7种不同的基因型,其中包括一种优势基因型(AFLP1),由从10名患者中分离出的11株分离株组成。已开发出一种快速、低成本的多重PCR检测方法,用于检测和区分近平滑念珠菌、正平滑念珠菌、间平滑念珠菌和长孢洛德酵母。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e13/4651534/5b4644178865/pone.0142880.g001.jpg

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