摘要
Recently, the incidence of<span> </span><i><span>Candida</span></i><span> infections has substantially increased. Conventional identification methods for </span><i><span>Candida</span></i><span> species are technically difficult to conduct and cannot accurately distinguish each species. The purpose of the present study was to design primers to identify and detect simultaneously</span><span> </span><span>eight medically important </span><i><span>Candida</span></i><span> species using one-step multiplex PCR. PCR primers were designed based on partial sequences of intergenic spacer (IGS) and internal transcribed spacer (ITS) genes of eight medically important </span><i><span>Candida</span></i><span> species. These primers were able to distinguish each </span><i><span>Candida</span></i><span> species and did not display cross-reactivity with representative </span><i><span>Candida </span></i><span>species other than the eight</span><i><span> Candida</span></i><span> species. Moreover, our developed one-step multiplex PCR method is accurate, specific, cost-effective, time-saving, and worked without requiring DNA extraction.</span>
Recently, the incidence of<span> </span><i><span>Candida</span></i><span> infections has substantially increased. Conventional identification methods for </span><i><span>Candida</span></i><span> species are technically difficult to conduct and cannot accurately distinguish each species. The purpose of the present study was to design primers to identify and detect simultaneously</span><span> </span><span>eight medically important </span><i><span>Candida</span></i><span> species using one-step multiplex PCR. PCR primers were designed based on partial sequences of intergenic spacer (IGS) and internal transcribed spacer (ITS) genes of eight medically important </span><i><span>Candida</span></i><span> species. These primers were able to distinguish each </span><i><span>Candida</span></i><span> species and did not display cross-reactivity with representative </span><i><span>Candida </span></i><span>species other than the eight</span><i><span> Candida</span></i><span> species. Moreover, our developed one-step multiplex PCR method is accurate, specific, cost-effective, time-saving, and worked without requiring DNA extraction.</span>
作者
Akira Fukatsu
Osamu Tsuzukibashi
Hidenori Suzuk
Katsuhiro Asaka
Yoshinori Ono
Mana Fuchigami
Taira Kobayashi
Satoshi Uchibori
Yuji Takahashi
Chiaki Komine
Yoshimi Konishi
Yuki Ogura
Hiroko Omori
Masanobu Wakami
Hiroshi Murakami
Masahiko Fukumoto
Akira Fukatsu;Osamu Tsuzukibashi;Hidenori Suzuk;Katsuhiro Asaka;Yoshinori Ono;Mana Fuchigami;Taira Kobayashi;Satoshi Uchibori;Yuji Takahashi;Chiaki Komine;Yoshimi Konishi;Yuki Ogura;Hiroko Omori;Masanobu Wakami;Hiroshi Murakami;Masahiko Fukumoto(Division of Laboratory Medicine for Dentistry, Department of Oral Health Science, Nihon University School of Dentistry at Matsudo, Chiba, Japan;Laboratory Medicine for Dentistry, Nihon University Graduate School of Dentistry at Matsudo, Chiba, Japan;Department of Fixed Prosthodontics and Oral Implantology, Nihon University School of Dentistry at Matsudo, Chiba, Japan;Division of Oral Function and Rehabilitation, Department of Oral Health Science, Nihon University School of Dentistry at Matsudo, Chiba, Japan)