Molecular characterization of Aspergillus infections in an Iranian educational hospital using RAPD-PCR method
Objective(s): The nosocomial infections by Aspergillus species are associated with constructions and increased dust loads in hospital indoors. Our main object was to find the environmental sources of Aspergillus species causing hospital acquired infections. Materials and Methods: The clinical and en...
Main Authors: | , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Mashhad University of Medical Sciences
2014-09-01
|
Series: | Iranian Journal of Basic Medical Sciences |
Subjects: | |
Online Access: | http://ijbms.mums.ac.ir/pdf_3323_8a356552abcdaba298d7ccc8d1e260a0.html |
_version_ | 1819036043028987904 |
---|---|
author | Kambiz Diba Khadijeh Makhdoomi Hossein Mirhendi |
author_facet | Kambiz Diba Khadijeh Makhdoomi Hossein Mirhendi |
author_sort | Kambiz Diba |
collection | DOAJ |
description | Objective(s): The nosocomial infections by Aspergillus species are associated with constructions and increased dust loads in hospital indoors. Our main object was to find the environmental sources of Aspergillus species causing hospital acquired infections.
Materials and Methods: The clinical and environmental samplings were performed during 18 months from spring 2010 to summer 2011 in Imam educational hospital, Urmia, Iran. A morphological diagnosis was performed including microscopic characterization of isolated aspergillus from cultured specimens and polymerase chain reaction - restriction fragment length polymorphism (PCR-RFLP) for the identification in the level of species. Random amplified polymorphic DNA – PCR RAPD-PCR using random primers for rDNA gene was performed to compare Aspergillus isolates of clinical cases with the relevant environmental sources.
Results: Use of RAPD method resulted various differential patterns, so that some Aspergillus isolates from the clinical and hospital indoor were completely matched (matched pairs) and some other Aspergillus isolates were not matched. In the case of matched pairs, Aspergillus niger and A. flavus isolated from broncoalveolar lavage and sinus discharge were relevant to those of air conditioner and walls surfaces, respectively.
Conclusion: The hospital sources for the Aspergillus clinical isolates included air condition and walls. RAPD-PCR analysis can play a trivial role to find the hospital sources of Aspergillus clinical isolates. |
first_indexed | 2024-12-21T07:59:14Z |
format | Article |
id | doaj.art-5d46401bfb4e41c88d978465c7db6ac0 |
institution | Directory Open Access Journal |
issn | 2008-3866 2008-3874 |
language | English |
last_indexed | 2024-12-21T07:59:14Z |
publishDate | 2014-09-01 |
publisher | Mashhad University of Medical Sciences |
record_format | Article |
series | Iranian Journal of Basic Medical Sciences |
spelling | doaj.art-5d46401bfb4e41c88d978465c7db6ac02022-12-21T19:10:57ZengMashhad University of Medical SciencesIranian Journal of Basic Medical Sciences2008-38662008-38742014-09-011796466503323Molecular characterization of Aspergillus infections in an Iranian educational hospital using RAPD-PCR methodKambiz Diba0Khadijeh Makhdoomi1Hossein Mirhendi2Cellular and Molecular Research Center, Urmia University of Medical Sciences, Urmia, IranImam Educational Hospital, Urmia University of Medical Sciences, Urmia, IranEsfahan Institute of Public Health, Tehran University of Medical Sciences, Esfahan, IranObjective(s): The nosocomial infections by Aspergillus species are associated with constructions and increased dust loads in hospital indoors. Our main object was to find the environmental sources of Aspergillus species causing hospital acquired infections. Materials and Methods: The clinical and environmental samplings were performed during 18 months from spring 2010 to summer 2011 in Imam educational hospital, Urmia, Iran. A morphological diagnosis was performed including microscopic characterization of isolated aspergillus from cultured specimens and polymerase chain reaction - restriction fragment length polymorphism (PCR-RFLP) for the identification in the level of species. Random amplified polymorphic DNA – PCR RAPD-PCR using random primers for rDNA gene was performed to compare Aspergillus isolates of clinical cases with the relevant environmental sources. Results: Use of RAPD method resulted various differential patterns, so that some Aspergillus isolates from the clinical and hospital indoor were completely matched (matched pairs) and some other Aspergillus isolates were not matched. In the case of matched pairs, Aspergillus niger and A. flavus isolated from broncoalveolar lavage and sinus discharge were relevant to those of air conditioner and walls surfaces, respectively. Conclusion: The hospital sources for the Aspergillus clinical isolates included air condition and walls. RAPD-PCR analysis can play a trivial role to find the hospital sources of Aspergillus clinical isolates.http://ijbms.mums.ac.ir/pdf_3323_8a356552abcdaba298d7ccc8d1e260a0.htmlAspergillusHospitalMolecular identification |
spellingShingle | Kambiz Diba Khadijeh Makhdoomi Hossein Mirhendi Molecular characterization of Aspergillus infections in an Iranian educational hospital using RAPD-PCR method Iranian Journal of Basic Medical Sciences Aspergillus Hospital Molecular identification |
title | Molecular characterization of Aspergillus infections in an Iranian educational hospital using RAPD-PCR method |
title_full | Molecular characterization of Aspergillus infections in an Iranian educational hospital using RAPD-PCR method |
title_fullStr | Molecular characterization of Aspergillus infections in an Iranian educational hospital using RAPD-PCR method |
title_full_unstemmed | Molecular characterization of Aspergillus infections in an Iranian educational hospital using RAPD-PCR method |
title_short | Molecular characterization of Aspergillus infections in an Iranian educational hospital using RAPD-PCR method |
title_sort | molecular characterization of aspergillus infections in an iranian educational hospital using rapd pcr method |
topic | Aspergillus Hospital Molecular identification |
url | http://ijbms.mums.ac.ir/pdf_3323_8a356552abcdaba298d7ccc8d1e260a0.html |
work_keys_str_mv | AT kambizdiba molecularcharacterizationofaspergillusinfectionsinaniranianeducationalhospitalusingrapdpcrmethod AT khadijehmakhdoomi molecularcharacterizationofaspergillusinfectionsinaniranianeducationalhospitalusingrapdpcrmethod AT hosseinmirhendi molecularcharacterizationofaspergillusinfectionsinaniranianeducationalhospitalusingrapdpcrmethod |