伊朗烟曲霉临床和环境分离物的微卫星分子分型研究。

Q3 Medicine
Hamid Badali, Tahereh Shokohi, Sadegh Khodavaisy, Maryam Moazeni, Masoumeh Farhadi, Mojtaba Nabili
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引用次数: 1

摘要

背景与目的:由于曲霉感染的发病率越来越高,曲霉种类分型方法的应用越来越广泛。因此,研究从临床和环境分离的菌株,从单一宿主到大规模生态系统的传播和种群动态是非常必要的。在本研究中,我们对来自伊朗不同地区的分离株的9个微卫星位点进行了遗传分析,以比较和探讨环境和临床烟抽假单胞菌菌株的遗传多样性。材料与方法:从伊朗6个城市采集了66株临床分离株(n=43)和环境分离株(n= 23)。所有烟曲霉分离株均基于宏观和微观特征,在45°C以上生长的能力,并通过部分b-微管蛋白基因的DNA测序进行确认。对66株烟曲霉分离株进行了微卫星分型,采用3种不同的多重pcr方法对9个短串联重复序列(STR)进行了遗传亲缘性评价。结果:66株烟曲霉STR分型显示38个不同的基因型,分布在环境和临床分离株中。我们鉴定出12个克隆,包括40个不同的分离株,占所有分离株的60%,每个克隆包括2-7个分离株。结论:STR分型是研究烟熏假单胞菌分子流行病学和基因型多样性的有效方法。这些结果表明,伊朗烟曲霉分离株与伊朗境外烟曲霉分离株具有较高的遗传多样性,形成了一个独立的聚类。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Molecular typing of clinical and environmental Aspergillus fumigatus isolates from Iran using microsatellites.

Molecular typing of clinical and environmental Aspergillus fumigatus isolates from Iran using microsatellites.

Molecular typing of clinical and environmental Aspergillus fumigatus isolates from Iran using microsatellites.

Molecular typing of clinical and environmental Aspergillus fumigatus isolates from Iran using microsatellites.

Background and purpose: Because of the growing incidence of Aspergillus infection, typing methods of Aspergillus species are increasingly being used. Accordingly, studying the spread and population dynamics of strains isolating from clinical and environment, from a single host to large-scale ecosystems is definitely needed. In the current study, we carried out a genetic analysis of nine microsatellite loci in isolates from different regions of Iran to compare and explore the genetic diversity between environmental and clinical A. fumigatus strains.

Materials and methods: Sixty-six clinical (n=43) and environmental (n= 23) isolates of A. fumigatus, have collected from six cities of Iran. All A. fumigatus isolates identified based on macroscopic and microscopic characters, the ability to grow at above 45°C, and confirmed using DNA sequencing of the partial b-tubulin gene. Sixty-six A. fumigatus isolates were subjected by microsatellite typing using three separate multiplex PCRs with a panel of nine short tandem repeats (STR) to evaluate the genetic relatedness.

Results: The STR typing of 66 A. fumigatus isolates revealed 38 distinct genotypes distributed among environmental and clinical isolates. We identified 12 clones including 40 different isolates representing 60% of all isolates tested, which each clone included 2-7 isolates.

Conclusion: The STR typing is considered as a valuable tool with excellent discriminatory power to study the molecular epidemiology and genotypic diversity of A. fumigatus isolates. These findings show that the high genetic diversity observed of Iranian A. fumigatus isolates with those outside Iran and formed a separate cluster.

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来源期刊
Current Medical Mycology
Current Medical Mycology Medicine-Infectious Diseases
CiteScore
2.10
自引率
0.00%
发文量
16
审稿时长
4 weeks
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