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      KCI등재후보

      Genus-Specific Polymerase Chain Reaction to Detect Mycoplasma Species

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      https://www.riss.kr/link?id=A76198490

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      다국어 초록 (Multilingual Abstract)

      Mycoplasmas are highly fastidious bacteria, difficult to culture and slow growing. Many species of mycoplasma are important pathogens causing respiratory infection in laboratory animals and known to affect influencing experimental results obtained with contaminated animals. Screening of Mycoplasma species is particularly desirable, because they are prevalent in commercial and research animal facilities. A consensus polymerase chain reaction (PCR) analysis was employed to detect Mycoplasma species and typing of the species was performed on the basis of sequence analysis of the PCR product. The target nucleic acid fragments were specifically amplified by consensus PCR with 16S ribosomal DNA primers. The sequencing analyses of amplified DNAs showed the effective differentiation of Mycoplasma species. Nasal swabs collected from rats were submitted to detect Mycoplasma species and three cases of Mycoplasma pulmonis were detected. In this study, the consensus PCR was able to detect successfully mycoplasma species. This consensus PCR was recommended for monitoring Mycoplasma species in laboratory animals. PCR and direct sequencing approach is effective for detecting and typing of Mycoplasma species.
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      Mycoplasmas are highly fastidious bacteria, difficult to culture and slow growing. Many species of mycoplasma are important pathogens causing respiratory infection in laboratory animals and known to affect influencing experimental results obtained wit...

      Mycoplasmas are highly fastidious bacteria, difficult to culture and slow growing. Many species of mycoplasma are important pathogens causing respiratory infection in laboratory animals and known to affect influencing experimental results obtained with contaminated animals. Screening of Mycoplasma species is particularly desirable, because they are prevalent in commercial and research animal facilities. A consensus polymerase chain reaction (PCR) analysis was employed to detect Mycoplasma species and typing of the species was performed on the basis of sequence analysis of the PCR product. The target nucleic acid fragments were specifically amplified by consensus PCR with 16S ribosomal DNA primers. The sequencing analyses of amplified DNAs showed the effective differentiation of Mycoplasma species. Nasal swabs collected from rats were submitted to detect Mycoplasma species and three cases of Mycoplasma pulmonis were detected. In this study, the consensus PCR was able to detect successfully mycoplasma species. This consensus PCR was recommended for monitoring Mycoplasma species in laboratory animals. PCR and direct sequencing approach is effective for detecting and typing of Mycoplasma species.

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      목차 (Table of Contents)

      • Materials and Methods
      • Results
      • Discussion
      • Acknowledgments
      • References
      • Materials and Methods
      • Results
      • Discussion
      • Acknowledgments
      • References
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      유사연구자 (20) 활용도상위20명

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2026 평가예정 재인증평가 신청대상 (재인증)
      2020-01-01 평가 등재학술지 유지 (재인증) KCI등재
      2017-01-01 평가 등재학술지 유지 (계속평가) KCI등재
      2013-01-01 평가 등재 1차 FAIL (등재유지) KCI등재
      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2007-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2006-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2005-07-03 학술지명변경 한글명 : Korean Association For Laboratory Animal Science -> Laboratory Animal Research
      외국어명 : Korean Association For Laboratory Animal Science -> Laboratory Animal Research
      KCI등재후보
      2004-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.16 0.16 0.16
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.25 0.19 0.415 0.03
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