fast detection of clostridium perfringens type a,b,c and d by multiplex pcr

Authors

مجتبی سعادتی

دانشگاه علوم پزشکی بقیه ا... (عج)- مرکزتحقیقات بیوتکنولوژی کاربردی و محیط زیست مهدی کمالی

دانشگاه علوم پزشکی بقیه ا... (عج)- مرکزتحقیقات بیوتکنولوژی کاربردی و محیط زیست محمدباقر صالحی

دانشگاه علوم پزشکی بقیه ا... (عج)- مرکزتحقیقات بیوتکنولوژی کاربردی و محیط زیست محمود تولایی

دانشگاه علوم پزشکی بقیه ا... (عج)- مرکزتحقیقات بیوتکنولوژی کاربردی و محیط زیست غلامرضا اولاد

abstract

clostridium perfringens is a part of the microflora of soil, and many reports have revealed the widespread occurrence of this organism in raw and processed foods. c. perfringens is classified into five types (types a to e), depending upon their ability to express alpha, beta, epsilon, and iota toxins in this study, a multiplex polymerase chain reaction (pcr) assay was developed for detection of c. perfringens types a, b, c and d. these strains have formerly been confirmed by the biochemical methods as well as serological test. for detection by pcr, four primer pairs with equal melting temperatures, were designed. dna amplification fragments of 1167 bp for c. perfringens type a alone (α toxin), 1167 bp, 1025 bp and 961 bp for c. perfringens type b (α, β and ε toxin) 1167 bp and 1025 bp for c. perfringens type c (α and β toxin), and 1167 bp and 961 bp for c. perfringens type d (α and ε toxin) were obtained. clostridium botulinum ued as negative control and did not yield a pcr product. these findings suggest that the assay is easy, timesaving, sensitive and specific and can use for detection of a, b, c and d types of c. perfringens.

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Journal title:
دامپزشکی

جلد ۲۲، شماره ۲، صفحات ۶۳-۷۱

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