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Specific PCR-primers for detection of Picoa lefebvrei desert truffle in Carex stenophylla roots

عنوان مقاله: Specific PCR-primers for detection of Picoa lefebvrei desert truffle in Carex stenophylla roots
شناسه ملی مقاله: JR_ROST-16-2_008
منتشر شده در در سال 1394
مشخصات نویسندگان مقاله:

صمد جمالی - Assistant Prof., Mycology, Department of Plant Protection, College of Agriculture, Razi University, Kermanshah, Iran (jamali۴۵۴@yahoo.com)

خلاصه مقاله:
Picoa species are hypogeous desert truffles, which can be found in semi-arid ranges of North Africa, West Asian, South of Europe and Middle East, including Iran (Moreno et al. ۲۰۰۰, Jamali & Banihashemi ۲۰۱۲, ۲۰۱۳). Picoa species form symbiosis mainly on roots of annual and perennial herbaceous plants of the Helianthemum, including H. ledifolium and H. salicifolium var. salicifolium (Jamali & Banihashemi ۲۰۱۲, ۲۰۱۳), H. nummularium (Riousset et al. ۱۹۸۹, ۱۹۹۶), H. sessiliflorum (Sbissi et al. ۲۰۱۰), H. squamatum and H. kahiricum (Moreno et al. ۲۰۰۰). In Iran, mycorrhizal association between sedge and desert truffles is little known. Ammarellou et al. (۲۰۰۷) isolated the sedge roots (Kobresia bellardii) directly from under zone of Terfezia boudieri. During ۲۰۱۳–۱۴, roots of Carex stenophylla Wahlenb were collected from various rangeland sites in Iran. The field and anatomical studies showed that, C. stenophylla have ectomycorrhizal associations with P. lefebvrei in the studied areas. In general, external mycelium was observed around all the mycorrhizal plants. The ITS۱-۵.۸S-ITS۲ gene region was amplified with the genomic DNA extracted from roots by nested polymerase chain reaction using the universal fungal primer pair ITS۱/ITS۴ and specific primer pair FLE (۵´GTA CCT TAC CTG TTG CTT CCG TG) and RLE (۵´ATC CCT ACC TGA GCC GAG GTC AA) which were designed based on ITS۱-۵.۸S-ITS۲ gene region of Picoa lefebvrei. Nested PCR of ITS۱/ITS۴ amplified product with FLE/RLE primers resulted in amplification of ۵۰۰ bp products in C. stenophylla roots. Sequences of PCR products amplified by FLE/RLE in two randomly root samples were similar (۱۰۰%) with previously published DNA sequences of P. lefebvrei specimens and confirmed the existence of P. lefebvrei in mycorrhizal roots of C. stenophylla in the rangelands of Iran. Moreover, nested PCR increased the sensitivity of FLE/RLE primers to ۱۰ fg DNA concentration. lant life cycle. On the other hand, correlation coefficient between spore population and root colonization was very low for Torbat specimens, which could be related to other factors e.g. environmental and geographical conditions.  

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صفحه اختصاصی مقاله و دریافت فایل کامل: https://civilica.com/doc/1537265/