Comparison of the utility of five commercial kits for extraction of DNA from Aspergillus fumigatus spores.
نویسندگان
چکیده
The aim of this study was to compare the efficiency of DNA extraction from water as well as from blood samples spiked with A. fumigatus spores, using selected commercial kits. Extraction of DNA according to manufacturer's protocols was preceded by blood cells lysis and disruption of fungal cells by enzymatic digestion or bead beating. The efficiency of DNA extraction was measured by PCR using Aspergillus-specific primers and SYBR Green I dye or TaqMan probes targeting 28S rRNA gene. All methods allowed the detection of Aspergillus at the lowest tested density of water suspensions of spores (10¹ cells/ml). The highest DNA yield was obtained using the ZR Fungal/Bacterial DNA kit, YeastStar Genomic DNA kit, and QIAamp DNA Mini kit with mechanical cell disruption. The ZR Fungal/Bacterial DNA and YeastStar kits showed the highest sensitivity in examination of blood samples spiked with Aspergillus (100 % for the detection of 10² spores and 75 % for 10¹ spores). Recently, the enzymatic method ceased to be recommended for examination of blood samples for Aspergillus, thus ZR Fungal/Bacterial DNA kit and QIAamp DNA Mini kit with mechanical cell disruption could be used for extraction of Aspergillus DNA from clinical samples.
منابع مشابه
Decolorization of Distillery Wastewater by UV irradiated spores of Aspergillus fumigatus
An efficient microbial technique for decolorizing distillery wastewater was achieved using irradiated spores of Aspergillus fumigatus. The fungus was isolated from soil samples taken from the local distillery processing unit. By using the irradiated spores, wastewater decolorization increased by 14.3% as compared to that of the control treatment (68.8% vs. 54.5%). In the presence of sodium nitr...
متن کاملComparison of six DNA extraction methods for recovery of fungal DNA as assessed by quantitative PCR.
The detection of fungal pathogens in clinical samples by PCR requires the use of extraction methods that efficiently lyse fungal cells and recover DNA suitable for amplification. We used quantitative PCR assays to measure the recovery of DNA from two important fungal pathogens subjected to six DNA extraction methods. Aspergillus fumigatus conidia or Candida albicans yeast cells were added to br...
متن کاملOptimization of the genomic DNA extraction in some mosses
The presence of organic compounds and high amount of secondary metabolites (polysaccharides, phenolic component, etc.) in mosses cause difficulties in DNA extraction that are followed by problems in PCR reactions. In lower plants, various methods have been used for DNA extraction including silica gel and different commercial kits. These methods mostly use hazardous (like phenol or liquid nitrog...
متن کاملSequences from the aspergillopepsin PEP gene of Aspergillus fumigatus: evidence on their use in selective PCR identification of Aspergillus species in infected clinical samples.
In immunodeficient patients, Aspergillus species emerge as circumstantial pathogens. Aspergillus fumigatus is a distant first among the pathogenic aspergilli, which cause deep-seated mycoses. Sequences of the pep gene of A. fumigatus as potential PCR primers, which have not been tested before, were used to identify this species and if possible, differentiate it from other, co-identified, clinic...
متن کاملبررسی بیوآئروسل ها در هوای معابر شهری و روستایی دامغان در زمستان 1390
Abstract Introduction: fungi exist all over the world and about as much as flowering plants are abundant and diverse. They reproduce through spores. Fungi can grow at body temperature and may easily infect susceptible people and make some infections. The study of fungal spores is one of the important indicators of biological air quality. So, it defined as the purpose of this study. Metho...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Acta biochimica Polonica
دوره 57 4 شماره
صفحات -
تاریخ انتشار 2010