Fomitiporia mediterranea, a new basidiomycete species for mycobiota of Iran

During last decade, the decline of elm trees was observed in Fars province (Iran) due to a wood decaying agent in heartwood of the trees. Unknown basidiomycete isolates were frequently isolated from such trees. The objective of the present study was to identify the basidiomycete isolates by molecular phylogenetic analysis of the internal transcribed spacers of ribosomal DNA. For this purpose, isolates of a basidiomycete were recovered from infected elm trees with brown rot in heartwood in Fars province. The isolates developed buff-colored colonies with white margins which produced red-brownish pigments in both PDA and MEA media. Mycelial width was average ۲.۴–۳.۸ µm, with brown cell wall without clamp connections. No aerial mycelia were observed in any isolates and average growth rate of colonies was ۱.۳۵mm-۱ at ۲۵ °C. No sexual organs were observed after six months of incubation at ۲۵°C. Neighbor-joining phylogenetic analysis of internal transcribed spacers of rDNA (ITS) of sequences showed that the isolates belong to Fomitiporia mediterranea. This is the first report of F. mediterranea for Iran mycobiota. Small pieces of decaying wood from infected elm trees were placed on PDA and MEA at ۲۵ °C and recovered isolates were purified on WA by hyphal tip method. Isolates were grown in ۵۰ ml still culture of potato broth at ۲۵ ºC. Freeze-dried mycelia were homogenized using sea sand (Fluka, Germany) and a plastic disposable pestle. Freeze-dried plant materials were also homogenized using mortars and pestles. DNA was extracted from homogenized preparation using a Genomic DNA Purification kit, (Fermentas, UK) according to the manufacturer’s instructions. DNA of the internal transcribed spacer regions (ITS) were amplified using the universal primers ITS۱:۵'- TCC GTA GGT GAA CCT GCG G -۳' and ITS۴:۵'- TCC TCC GCT TAT TGA TAT GC -۳'. Amplifications were performed in a CG۱-۹۶ thermocycler (Korbett Research, Australia). The PCR mixture contained: ۱۰–۲۰ ng of template DNA, ۱ μM of each primer, ۱۰۰ μM of dNTPs, ۰.۴ U Taq DNApolymerase (CinnaGen, Iran), ۱.۵ mM of Mg Cl۲, ۲.۵ μl of ۱۰× PCR buffer, ۱۰۰ mM BSA, in a reaction volume of ۲۵ μl. All PCRs consisted of ۱ cycle of ۹۴ °C for ۳ min; ۳۰ cycles of ۹۵ °C for ۳۰ s, ۵۰ °C for ۳۰ s, ۷۲ °C for ۶۰ s; and a final cycle of ۷۲ °C for ۱۰ min. PCR products were sequenced. Sequences of the internal transcribed spacer regions including the ۵.۸S gene of rDNA were used to study phylogenetic relationships of the studied taxa. The internal transcribed spacers sequences of rDNA generated in this study were compared to those of other taxa obtained from GenBank. A preliminary alignment of sequences was made using ClustalX with subsequent visual adjustment. Neighbor-joining phylogenetic analysis of internal transcribed spacers of rDNA (ITS) of sequences showed that the isolates belong to Fomitiporia mediterranea M. Fisch. (Fig. ۱). The ۷۸۰ bp sequence of isolate EN۱ (GenBank Accession No.: HM۵۸۲۰۹۷) was ۹۹% similar to ITS sequence from fruit body of F. mediterranea (Pilotti et al. ۲۰۰۵, GenBank Accession No.: AY۶۲۰۹۹۷) with some differences in ۲۶۰ (T to C substitution) and ۷۷۴ (A to gap substitution) nucleotide sites. Fomitiporia mediterranea was distinct by the sequences of the ribosomal DNA (ITS) region and growth rates at temperatures between ۱۵ °C and ۳۵ °C (Elena et al. ۲۰۰۶). The isolates developed buff colored colonies with white margins which produced red-brownish pigments in both PDA and MEA media (Fig. ۲). Average mycelia width was ۲.۴–۳.۸ µm, with brown cell wall without clamp connections. No aerial mycelia were observed in any isolates and average growth rate of colonies was ۱.۳۵mm d-۱ at ۲۵ °C. No sexual organs were observed after six months of incubation at ۲۵ °C. The isolates were able to grow at all temperatures tested between ۱۵ °C and ۳۵ °C. This is the first report of F. mediterranea for Iran. Specimen examined: Iran: Fars province, Shiraz, Bajgah, isolate EN۱, recovered from elm trees, deposited at the Fungal Culture Collection of the Department of Plant Protection, Shiraz University, Shiraz, Iran (FT۰۱.۱۵.۰۱).