Suppr超能文献

聚合酶链反应-限制性片段长度多态性与真菌培养用于评估[疾病名称]患者真菌种类的比较研究

A Comparative Study of Polymerase Chain Reaction-Restriction Fragment Length Polymorphism and Fungal Culture for the Evaluation of Fungal Species in Patients with .

作者信息

Hazlianda Cut, Muis Kamaliah, Lubis Isma

机构信息

Universitas Sumatera Utara, Fakultas Kedokteran, Dermatology and Venereology, Medan, Indonesia.

出版信息

Open Access Maced J Med Sci. 2017 Nov 21;5(7):844-847. doi: 10.3889/oamjms.2017.197. eCollection 2017 Dec 15.

Abstract

BACKGROUND

Tinea cruris is the second most common dermatophytosis in the world and the most common in Indonesia. The conventional laboratory tests for dermatophyte infection are slow and less specific. Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RFLP) is a PCR method with the addition of enzyme after amplification, therefore enabling for more specific results.

AIM

This study aimed to find whether the PCR-RFLP test could yield the same fungal species result as a fungal culture.

METHODS

The specimens were skin scrapings from thirty-one patients suspected tinea cruris. The tools and materials that were used were Sabaroud's dextrose agar media, primer ITS 1 and ITS 4 and MvaI.

RESULTS

The equation percentage of the test result species between PCR-RFLP and fungal culture was 50% of 12 subjects whose the test results were both positive from the fungal culture and PCR-RFLP. The percentage of the test result with fungal culture the fungal species were found, but in the PCR-RFLP test which the fungal species was not found, the percentage was 50% of 12 subjects which the test results were both positive as fungi from the culture and PCR-RFLP test.

CONCLUSIONS

The species from PCR-RFLP examination was the same with the fungal culture.

摘要

背景

股癣是世界上第二常见的皮肤癣菌病,在印度尼西亚最为常见。传统的皮肤癣菌感染实验室检测方法耗时且特异性较低。聚合酶链反应-限制性片段长度多态性(PCR-RFLP)是一种在扩增后添加酶的PCR方法,因此能够获得更具特异性的结果。

目的

本研究旨在探究PCR-RFLP检测能否得出与真菌培养相同的真菌种类结果。

方法

标本为31例疑似股癣患者的皮肤刮屑。使用的工具和材料有沙氏葡萄糖琼脂培养基、引物ITS 1和ITS 4以及MvaI。

结果

在12名真菌培养和PCR-RFLP检测结果均为阳性的受试者中,PCR-RFLP与真菌培养检测结果物种的符合率为50%。在12名真菌培养检测出真菌种类但PCR-RFLP检测未发现真菌种类的受试者中,该比例为50%,这些受试者的真菌培养和PCR-RFLP检测结果均为阳性。

结论

PCR-RFLP检测出的真菌种类与真菌培养结果相同。

相似文献

1
2
Characterizing the clinical isolates of dermatophytes in Hamadan city, Central west of Iran, using PCR-RLFP method.
J Mycol Med. 2018 Mar;28(1):101-105. doi: 10.1016/j.mycmed.2017.11.009. Epub 2018 Feb 11.
5
Polymerase Chain Reaction-Restriction Fragment Length Polymorphism as a Confirmatory Test for Onychomycosis.
Open Access Maced J Med Sci. 2018 Feb 14;6(2):280-283. doi: 10.3889/oamjms.2018.098. eCollection 2018 Feb 15.
6
Use of Restriction Fragment Length Polymorphism to Rapidly Identify Dermatophyte Species Related to Dermatophytosis.
Jundishapur J Microbiol. 2015 Jun 30;8(6):e17296. doi: 10.5812/jjm.8(5)2015.17296. eCollection 2015 Jun.
7
Epidemiological Aspects of Dermatophytosis in Khuzestan, southwestern Iran, an Update.
Mycopathologia. 2016 Aug;181(7-8):547-53. doi: 10.1007/s11046-016-9990-x. Epub 2016 Feb 17.
9
Characterization of clinically important dermatophytes in North of Iran using PCR-RFLP on ITS region.
J Mycol Med. 2016 Dec;26(4):345-350. doi: 10.1016/j.mycmed.2016.06.006. Epub 2016 Aug 3.

本文引用的文献

2
Identification of dermatophytes using multiplex polymerase chain reaction.
Ann Dermatol. 2011 Aug;23(3):304-12. doi: 10.5021/ad.2011.23.3.304. Epub 2011 Aug 6.
4
Introduction of a dermatophyte polymerase chain reaction assay to the diagnostic mycology service in Scotland.
Br J Dermatol. 2011 May;164(5):966-72. doi: 10.1111/j.1365-2133.2010.10186.x.
5
Tinea cruris in children.
Cutis. 2009 Sep;84(3):133-7.
6
Rapid detection of dermatophytes from skin and hair.
BMC Res Notes. 2009 Apr 18;2:60. doi: 10.1186/1756-0500-2-60.
7
Epidemiological trends in skin mycoses worldwide.
Mycoses. 2008 Sep;51 Suppl 4:2-15. doi: 10.1111/j.1439-0507.2008.01606.x.
8
Common tinea infections in children.
Am Fam Physician. 2008 May 15;77(10):1415-20.
9
What is the best way to treat tinea cruris?
J Fam Pract. 2006 Mar;55(3):256-8.
10
Rapid identification and differentiation of fungal DNA in dermatological specimens by LightCycler PCR.
J Med Microbiol. 2004 Dec;53(Pt 12):1207-1214. doi: 10.1099/jmm.0.45779-0.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验