Abstract:
BACKGROUND:Human cutaneous infection caused by a homogeneous group of keratinophilic fungi called dermatophytes. These fungi are the most common infectious agents in humans that are free of any population and geographic area. Microsporum canis is a cause of dermatophytosis (Tinea) in recent years in Iran and atypical strain has been isolated in Iran. Its cases occur sporadically due to M. canis transmission from puppies and cats to humans. Since this pathogenic dermatophyte is eukaryotes, chemical treatment with antifungal drugs may also affect host tissue cells. OBJECTIVES:The aim of the current study was to find a new antifungal agent of soil-Actinomycetes from Kerman province against M. canis and Actinomycete isolates were identified by PCR. MATERIALS AND METHODS:A number of hundred Actinomycete isolated strains were evaluated from soil of Kerman province, for their antagonistic activity against the M. canis. M. canis of the Persian Type Culture Collection (PTCC) was obtained from the Iranian Research Organization for Science and Technology (IROST). Electron microscope studies of these isolates were performed based on the physiological properties of these antagonists including lipase, amylase, protease and chitinase activities according to the relevant protocols and were identified using gene 16SrDNA. RESULTS:In this study the most antagonist of Actinomycete isolates with antifungal activity against M. canis isolates of L1, D5, Ks1m, Km2, Kn1, Ks8 and Ks1 were shown in vitro. Electron microscopic studies showed that some fungal strains form spores, mycelia and spore chain. Nucleotide analysis showed that Ks8 had maximum homology (98%) to Streptomyces zaomyceticus strain xsd08149 and L1 displayed 100% homology to Streptomyces sp. HVG6 using 16SrDNA studies. CONCLUSIONS:Our findings showed that Streptomyces has antifungal effects against M. canis.
journal_name
Jundishapur J Microbioljournal_title
Jundishapur journal of microbiologyauthors
Keikha N,Ayatollahi Mousavi SA,Nakhaei AR,Yadegari MH,Shahidi Bonjar GH,Amiri Sdoi
10.5812/jjm.8(5)2015.14874subject
Has Abstractpub_date
2015-05-31 00:00:00pages
e14874issue
5eissn
2008-3645issn
2008-4161journal_volume
8pub_type
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