isolation of mucorales from biological environment and identification of rhizopus among the isolates using pcr-rflp

Background and aims: mucorales are fungi belonging to the category of zygomycetes, found much in nature. culturebased methods for clinical samples are often negative, difficult and timeconsuming and mainly identify isolates to the genus level, and sometimes only as mucorales. therefore, applying fast and accurate diagnosis methods such as molecular approaches seems necessary. this study aims at isolating mucorales for determination of rhizopus genus between the isolates using molecular methods. methods: in this descriptive observational study, a total of 500 samples were collected from air and different surfaces and inoculated on sabouraud dextrose agar supplemented with chloramphenicol. then, the fungi belonging to mucorales were identified and their pure culture was provided. dna extraction was done using extraction kit and the chloroform method. after amplification, the samples belonging to mucorales were identified by observing 830 bp bands. for enzymatic digestion, enzyme bmgb1 was applied for identification of rhizopus species by formation of 593 and 235 bp segments. results: one hundred pure colonies belonging to mucorales were identified using molecular methods and after enzymatic digestion, 21 isolates were determined as rhizopus species. the sequencing of pcr products and macroscopic and microscopic studies confirmed the existence of r. stolonifera, r. oryzae and r. caespitosus in the samples. conclusion: generally, developing a reliable method for determining zygomycete species can be a useful tool for better understanding of the epidemiology of mucoromycosis.

Isolation of Mucorales from biological environment and identification of Rhizopus among the isolates using PCRRFLP

Background and aims: Mucorales are fungi belonging to the category of Zygomycetes, found much in nature. Culturebased methods for clinical samples are often negative, difficult and timeconsuming and mainly identify isolates to the genus level, and sometimes only as Mucorales. Therefore, applying fast and accurate diagnosis methods such as molecular approaches seems necessary. This study aims at isolating Mucorales for determination of Rhizopus genus between the isolates using molecular methods. Methods: In this descriptive observational study, a total of 500 samples were collected from air and different surfaces and inoculated on Sabouraud Dextrose Agar supplemented with chloramphenicol. Then, the fungi belonging to Mucorales were identified and their pure culture was provided. DNA extraction was done using extraction kit and the chloroform method. After amplification, the samples belonging to Mucorales were identified by observing 830 bp bands. For enzymatic digestion, enzyme BmgB1 was applied for identification of Rhizopus species by formation of 593 and 235 bp segments. Results: One hundred pure colonies belonging to Mucorales were identified using molecular methods and after enzymatic digestion, 21 isolates were determined as Rhizopus species. The sequencing of PCR products and macroscopic and microscopic studies confirmed the existence of R. stolonifera, R. oryzae and R. caespitosus in the samples. Conclusion: Generally, developing a reliable method for determining Zygomycete species can be a useful tool for better understanding of the epidemiology of mucoromycosis.