RISS 학술연구정보서비스

검색
다국어 입력

http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.

변환된 중국어를 복사하여 사용하시면 됩니다.

예시)
  • 中文 을 입력하시려면 zhongwen을 입력하시고 space를누르시면됩니다.
  • 北京 을 입력하시려면 beijing을 입력하시고 space를 누르시면 됩니다.
닫기
    인기검색어 순위 펼치기

    RISS 인기검색어

      KCI등재

      Real-time PCR과 Colony forming unit법을 이용한 타액 내 2종의 구강미생물 총량분석 = Analysis of total oral microorganisms in saliva using real-time PCR and colony forming unit

      한글로보기
      • 내보내기
      • 내책장담기
      • 공유하기
      • 오류접수

      부가정보

      다국어 초록 (Multilingual Abstract)

      Objectives: The purpose of this study was to compare colony forming unit (CFU) method and multiplex real-time polymerase chain reaction (MRT-PCR) method for accurate quantitative analysis of bacteria. Methods: We compared the CFU method and the MRT-PCR method, which are still used in Korea, for Prevotella intermedius (P. intermedius), a periodontal disease pathogen selected by MRT-PCR, and Streptococcus mutans (S. mutans), a dental caries causative organism. The subjects of this study were 30 patients who visited the C dental hospital. Results: Total microorganisms in MRT-PCR method were significantly higher in both types of bacteria (p<0.05), since DNA of dead bacteria was also analyzed. This was because the periodontal dise(-) anaerobes, and even dead bacteria contain large amounts of toxic substances called LPS in the extracellular membrane, and fimbriae and pili, which are motility structures, still remain as a strong toxic substance in periodontal tissue. Conclusions: Therefore, in terms of the total amount of bacteria found, the MRT-PCR method will be a useful technique for searching all the bacteria in the oral cavity including live bacteria, as well as sterilization.
      번역하기

      Objectives: The purpose of this study was to compare colony forming unit (CFU) method and multiplex real-time polymerase chain reaction (MRT-PCR) method for accurate quantitative analysis of bacteria. Methods: We compared the CFU method and the MRT-PC...

      Objectives: The purpose of this study was to compare colony forming unit (CFU) method and multiplex real-time polymerase chain reaction (MRT-PCR) method for accurate quantitative analysis of bacteria. Methods: We compared the CFU method and the MRT-PCR method, which are still used in Korea, for Prevotella intermedius (P. intermedius), a periodontal disease pathogen selected by MRT-PCR, and Streptococcus mutans (S. mutans), a dental caries causative organism. The subjects of this study were 30 patients who visited the C dental hospital. Results: Total microorganisms in MRT-PCR method were significantly higher in both types of bacteria (p<0.05), since DNA of dead bacteria was also analyzed. This was because the periodontal dise(-) anaerobes, and even dead bacteria contain large amounts of toxic substances called LPS in the extracellular membrane, and fimbriae and pili, which are motility structures, still remain as a strong toxic substance in periodontal tissue. Conclusions: Therefore, in terms of the total amount of bacteria found, the MRT-PCR method will be a useful technique for searching all the bacteria in the oral cavity including live bacteria, as well as sterilization.

      더보기

      참고문헌 (Reference)

      1 윤정호, "한국인 만성 치주염 환자에서 치주질환 원인균의 동정" 대한치주과학회 38 (38): 143-152, 2008

      2 장현선, "치주질환이 없는 청년의 치은연상 및 치은연하 치면세균막에 존재하는 치주질환 관련 4종 세균의 분포 비교" 대한치주과학회 33 (33): 159-166, 2003

      3 국중기, "치면세균막에서 분리한 뮤탄스 연쇄상구균 및 Streptococcus anginosus의 수종 항생제에 대한 감수성 조사" 대한치과보존학회 29 (29): 462-469, 2004

      4 김지훈, "중합효소연쇄반응법을 이용한 급성 치수 및 치근단 질환의 병원성 세균의 동정" 대한치과보존학회 28 (28): 178-183, 2003

      5 T. W. Ammann, "Validation of a quantitative real‐time PCR assay and comparison with fluorescence microscopy and selective agar plate counting for species‐specific quantification of an in vitro subgingival biofilm model" Wiley-Blackwell 48 (48): 517-526, 2013

      6 Kyung-Hui Moon, "The Influence on the Recognition for Periodontal Care to Oral Micro-Organism Changes in Dental Implant Patients" 대한예방치과학회 12 (12): 221-228, 2016

      7 김민정, "Strain-specific PCR Primers for the Detection of Prevotella intermedia ATCC 49046" 대한구강생물학회 36 (36): 79-82, 2011

      8 Eun AJ, "Simultaneous quantitation of two orchid viruses by the TaqMan real-time RT-PCR." 87 (87): 151-160, 2000

      9 Yano A, "Real-time PCR for quantification of Streptococcus mutans" 217 (217): 23-30, 2002

      10 Maeda H, "Quantitative real-time PCR using TaqMan and SYBR Green for Actinobacillus actinomycetemcomitans, Porphyromonas gingivalis, Prevotella intermedia, tetQ gene and total bacteria" 39 (39): 81-86, 2003

      1 윤정호, "한국인 만성 치주염 환자에서 치주질환 원인균의 동정" 대한치주과학회 38 (38): 143-152, 2008

      2 장현선, "치주질환이 없는 청년의 치은연상 및 치은연하 치면세균막에 존재하는 치주질환 관련 4종 세균의 분포 비교" 대한치주과학회 33 (33): 159-166, 2003

      3 국중기, "치면세균막에서 분리한 뮤탄스 연쇄상구균 및 Streptococcus anginosus의 수종 항생제에 대한 감수성 조사" 대한치과보존학회 29 (29): 462-469, 2004

      4 김지훈, "중합효소연쇄반응법을 이용한 급성 치수 및 치근단 질환의 병원성 세균의 동정" 대한치과보존학회 28 (28): 178-183, 2003

      5 T. W. Ammann, "Validation of a quantitative real‐time PCR assay and comparison with fluorescence microscopy and selective agar plate counting for species‐specific quantification of an in vitro subgingival biofilm model" Wiley-Blackwell 48 (48): 517-526, 2013

      6 Kyung-Hui Moon, "The Influence on the Recognition for Periodontal Care to Oral Micro-Organism Changes in Dental Implant Patients" 대한예방치과학회 12 (12): 221-228, 2016

      7 김민정, "Strain-specific PCR Primers for the Detection of Prevotella intermedia ATCC 49046" 대한구강생물학회 36 (36): 79-82, 2011

      8 Eun AJ, "Simultaneous quantitation of two orchid viruses by the TaqMan real-time RT-PCR." 87 (87): 151-160, 2000

      9 Yano A, "Real-time PCR for quantification of Streptococcus mutans" 217 (217): 23-30, 2002

      10 Maeda H, "Quantitative real-time PCR using TaqMan and SYBR Green for Actinobacillus actinomycetemcomitans, Porphyromonas gingivalis, Prevotella intermedia, tetQ gene and total bacteria" 39 (39): 81-86, 2003

      11 Lyons SR, "Quantitative real-time PCR for Porphyromonas gingivalis and total bacteria" 38 (38): 2362-2365, 2000

      12 Martin FE, "Quantitative microbiological study of human carious dentine by culture and real-time PCR: association of anaerobes with histopathological changes in chronic pulpitis" 40 (40): 1698-1704, 2002

      13 Kim JB, "Preventive Dentistry" Komoonsa 85-86, 2006

      14 Sastri A., "Plaque microorganism and periodontal disease" 27 (27): 88-92, 1977

      15 M. E. Reardon-Robinson, "Pilus hijacking by a bacterial coaggregation factor critical for oral biofilm development" Proceedings of the National Academy of Sciences 111 (111): 3835-3840, 2014

      16 Khalil Boutaga, "Periodontal pathogens: A quantitative comparison of anaerobic culture and real-time PCR" Oxford University Press (OUP) 45 (45): 191-199, 2005

      17 Löe H, "Periodontal disease in pregnancy I. Prevalence and severity" 21 : 533-551, 1963

      18 조홍범, "Multiplex Real-Time PCR을 이용하여 6종의 주요 잇몸질환 유발 미생물을 동시에 검출하는 기법" 한국미생물학회 49 (49): 292-296, 2013

      19 Rolph HJ, "Molecular identification of microorganisms from endodontic infections" 39 (39): 3282-3289, 2001

      20 Dymock D, "Molecular analysis of microflora associated with dentoalveolar abscesses" 34 : 537-542, 1996

      21 Loomer PM, "Microbiological diagnostic testing in the treatment of periodontal diseases" 34 : 49-56, 2004

      22 Amicosante M, "Inactivation of polymerase inhibitors for mycobacterium tuberculosis DNA amplification in sputum by using capture resin" 33 (33): 629-630, 1995

      23 H. P. Horz, "Evaluation of Universal Probes and Primer Sets for Assessing Total Bacterial Load in Clinical Samples: General Implications and Practical Use in Endodontic Antimicrobial Therapy" American Society for Microbiology 43 (43): 5332-5337, 2005

      24 Gouet P, "ESPript: analysis of multiple sequence alignments in PostScript" 15 (15): 305-308, 1999

      25 Bernard J. Moncla, "Direct detection of Porphyromonas gingivalis in Macaca fascicularis dental plaque samples using an oligonucleotide probe" Wiley-Blackwell 65 (65): 398-403, 1994

      26 Soon-Nang Park, "Development of quantitative real-time PCR primers for detecting 42 oral bacterial species" Springer Nature 195 (195): 473-482, 2013

      27 박순낭, "Development of Quantitative Real-Time PCR Primers for the Detection of Aggregatibacter actinomycetemcomitans" 대한구강생물학회 36 (36): 1-6, 2011

      28 Nadkarni MA, "Determination of bacterial load by real-time PCR using a broad-range (universal) probe and primers set" 148 (148): 257-266, 2002

      29 Mättö J, "Detection of Porphyromonas gingivalisfrom saliva by PCR by using a simple sample-processing method" 36 (36): 157-160, 1998

      30 Mättö J, "Detection of Porphyromonas gingivalis from Saliva by PCR by using a simple sample-processing method" 36 (36): 157-160, 1998

      31 Lovegrove JM, "Dental plaque revisited: bacteria associated with periodontal disease" 87 : 7-21, 2004

      32 Boutaga K, "Comparison of real-time PCR and culture for detection of Porphyromonas gingivalis in subgingival plaque samples" 41 (41): 4950-4954, 2003

      33 P.-M. Jervoe-Storm, "Comparison of culture and real-time PCR for detection and quantification of five putative periodontopathogenic bacteria in subgingival plaque samples" Wiley-Blackwell 32 (32): 778-783, 2005

      34 Ali RW, "Comparative detection frequency of 6 putative periodontal pathogens in Sudanese and Norwegian adult periodontitis patients" 65 (65): 1046-1052, 1994

      35 C. Verner, "Carpegen real‐time polymerase chain reaction vs. anaerobic culture for periodontal pathogen identification" Wiley-Blackwell 21 (21): 341-346, 2006

      36 Kroes I, "Bacterial diversity within the human subgingival crevice" 96 (96): 14547-14552, 1996

      37 A. D. Haffajee, "Association of Eubacterium nodatum and Treponema denticola with human periodontitis lesions" Wiley-Blackwell 21 (21): 269-282, 2006

      38 Johnson SR, "Alterations in sample preparation increase sensitivity of PCR assay for diagnosis of chancroid" 33 (33): 1036-1038, 1995

      더보기

      동일학술지(권/호) 다른 논문

      분석정보

      View

      상세정보조회

      0

      Usage

      원문다운로드

      0

      대출신청

      0

      복사신청

      0

      EDDS신청

      0

      동일 주제 내 활용도 TOP

      더보기

      주제

      연도별 연구동향

      연도별 활용동향

      연관논문

      연구자 네트워크맵

      공동연구자 (7)

      유사연구자 (20) 활용도상위20명

      인용정보 인용지수 설명보기

      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2027 평가예정 재인증평가 신청대상 (재인증)
      2021-01-01 평가 등재학술지 유지 (재인증) KCI등재
      2018-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2015-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2011-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2010-06-23 학회명변경 한글명 : 한국치위생교육학회 -> 한국치위생학회
      영문명 : The Journal of Korean Academy of Dental Hygiene Education -> Korean Society of Dental Hygiene
      KCI등재후보
      2010-06-23 학술지명변경 한글명 : 한국치위생교육학회지 -> 한국치위생학회지
      외국어명 : The Journal of Korean Academy of Dental Hygiene Education -> Journal of Korean society of Dental Hygiene
      KCI등재후보
      2010-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2008-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
      더보기

      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.89 0.89 0.93
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.92 0.94 1.058 0.24
      더보기

      이 자료와 함께 이용한 RISS 자료

      나만을 위한 추천자료

      해외이동버튼