Detection and Identification of Aspergillus fumigatus in BAL Samples of Patients with Suspected Tuberculosis by Nested-PCR

Background and Aim: Aspergillus fumigatus is the cause of more than 90% of invasive pulmonary aspergillosis. The aim of this study is identification and detection of A.fumigatus in bronchoalveolar lavage (BAL) samples patients suspected to have tuberculosis by using of Nested-PCR. Materials and Meth...

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Main Authors: Farzaneh Amini, Hossein Mirhendi, Reza Kachuei, Fatemeh Noorbakhsh
Format: Article
Language:English
Published: Farname 2014-08-01
Series:Iranian Journal of Medical Microbiology
Subjects:
Online Access:http://www.ijmm.ir/browse.php?a_code=A-10-37-2&slc_lang=en&sid=1
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author Farzaneh Amini
Hossein Mirhendi
Reza Kachuei
Fatemeh Noorbakhsh
author_facet Farzaneh Amini
Hossein Mirhendi
Reza Kachuei
Fatemeh Noorbakhsh
author_sort Farzaneh Amini
collection DOAJ
description Background and Aim: Aspergillus fumigatus is the cause of more than 90% of invasive pulmonary aspergillosis. The aim of this study is identification and detection of A.fumigatus in bronchoalveolar lavage (BAL) samples patients suspected to have tuberculosis by using of Nested-PCR. Materials and Methods: In this assay, a set of 100 BAL samples which were collected in 9 month, between the years 2012-2013, from patients with suspected tuberculosis in Tehran hospital, were examined by direct, culture and molecular tests. Manual phenol-chloroform method was used in order to extract DNA. Specific primers of Aspergillus genus and beta-actin primers were used for duplex-PCR. A pairs of internal primers were utilized in order to identification of A.fumigatus (Nested-PCR method). Finally, some of the PCR-products were sequenced for confirming results. Results: Overall, 12 samples (12%) were aspergillus-positive by molecular test while 11% and 10% samples were positive by direct and culture test, respectively. The sensitivities and specificities of PCR method compare with direct examination was 100% and 98.8%, respectively. The study also showed that sensitivities and specificities of PCR method compare with culture was 100% and 97.7%, respectively. After sequencing PCR product sample, isolated species were recognized as A. fumigatus. Conclusions: This study showed that PCR method in compare with the direct method and the culture has a higher sensitivity in the detection of Aspergillus species, also Present study displayed that can be consider Aspergillus species and A. fumigatus in suspicious to tuberculosis BAL samples
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spelling doaj.art-3ed4041dd9f248f99ab0a0cd6a2001e72022-12-21T22:32:10ZengFarnameIranian Journal of Medical Microbiology1735-86122345-43422014-08-01821421Detection and Identification of Aspergillus fumigatus in BAL Samples of Patients with Suspected Tuberculosis by Nested-PCRFarzaneh Amini0Hossein Mirhendi1Reza Kachuei2Fatemeh Noorbakhsh3 1. Depatment of Biology, Islamic Azad University, Varamin-pishva Branch, Tehran, Iran. 2. Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran Molecular Biology Research Center,Baqiyatallah University of Medical Sciences, Tehran, Iran 1. Depatment of Biology, Islamic Azad University, Varamin-pishva Branch, Tehran, Iran. Background and Aim: Aspergillus fumigatus is the cause of more than 90% of invasive pulmonary aspergillosis. The aim of this study is identification and detection of A.fumigatus in bronchoalveolar lavage (BAL) samples patients suspected to have tuberculosis by using of Nested-PCR. Materials and Methods: In this assay, a set of 100 BAL samples which were collected in 9 month, between the years 2012-2013, from patients with suspected tuberculosis in Tehran hospital, were examined by direct, culture and molecular tests. Manual phenol-chloroform method was used in order to extract DNA. Specific primers of Aspergillus genus and beta-actin primers were used for duplex-PCR. A pairs of internal primers were utilized in order to identification of A.fumigatus (Nested-PCR method). Finally, some of the PCR-products were sequenced for confirming results. Results: Overall, 12 samples (12%) were aspergillus-positive by molecular test while 11% and 10% samples were positive by direct and culture test, respectively. The sensitivities and specificities of PCR method compare with direct examination was 100% and 98.8%, respectively. The study also showed that sensitivities and specificities of PCR method compare with culture was 100% and 97.7%, respectively. After sequencing PCR product sample, isolated species were recognized as A. fumigatus. Conclusions: This study showed that PCR method in compare with the direct method and the culture has a higher sensitivity in the detection of Aspergillus species, also Present study displayed that can be consider Aspergillus species and A. fumigatus in suspicious to tuberculosis BAL sampleshttp://www.ijmm.ir/browse.php?a_code=A-10-37-2&slc_lang=en&sid=1Aspergillus fumigatus Bronchoalveolar lavage (BAL) PCR
spellingShingle Farzaneh Amini
Hossein Mirhendi
Reza Kachuei
Fatemeh Noorbakhsh
Detection and Identification of Aspergillus fumigatus in BAL Samples of Patients with Suspected Tuberculosis by Nested-PCR
Iranian Journal of Medical Microbiology
Aspergillus fumigatus
Bronchoalveolar lavage (BAL)
PCR
title Detection and Identification of Aspergillus fumigatus in BAL Samples of Patients with Suspected Tuberculosis by Nested-PCR
title_full Detection and Identification of Aspergillus fumigatus in BAL Samples of Patients with Suspected Tuberculosis by Nested-PCR
title_fullStr Detection and Identification of Aspergillus fumigatus in BAL Samples of Patients with Suspected Tuberculosis by Nested-PCR
title_full_unstemmed Detection and Identification of Aspergillus fumigatus in BAL Samples of Patients with Suspected Tuberculosis by Nested-PCR
title_short Detection and Identification of Aspergillus fumigatus in BAL Samples of Patients with Suspected Tuberculosis by Nested-PCR
title_sort detection and identification of aspergillus fumigatus in bal samples of patients with suspected tuberculosis by nested pcr
topic Aspergillus fumigatus
Bronchoalveolar lavage (BAL)
PCR
url http://www.ijmm.ir/browse.php?a_code=A-10-37-2&slc_lang=en&sid=1
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AT rezakachuei detectionandidentificationofaspergillusfumigatusinbalsamplesofpatientswithsuspectedtuberculosisbynestedpcr
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