http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
한국인의 치주질환 환자의 치은연하치면세균막에서 Prevotella intermedia와 Prevotella nigrescens의 검출율 비교
김미광 ( Mi Kwang Kim ),성진효 ( Jin Hyo Seong ),김동기 ( Dong Kie Kim ),손영남 ( Young Nam Son ),이장재 ( Jang Jae Lee ),김흥중 ( Heung Joong Kim ),박주철 ( Joo Cheol Park ),장현선 ( Hyun Seon Jang ),김병옥 ( Byung Ock Kim ),신 대한구강보건학회 2004 大韓口腔保健學會誌 Vol.28 No.2
분자생물학적 기법을 이용한 악골 골수염 병소의 세균 동정
김미성(Mi-Sung Kim),김수관(Su-Gwan Kim),정해만(Hae-Man Chung),김생곤(Sang-Gon Kim),국중기(Joong-Ki Kook),김미광(Mi-Kwang Kim),김화숙(Hwa-Sook Kim),유소영(So Young Yoo) 대한구강악안면외과학회 2003 대한구강악안면외과학회지 Vol.29 No.1
The purpose of this study was to isolate and identify the bacteria in osteomyelitis lesion of 3 patients. Two lesions were due to the post-infection after extraction. The other was resulted from mal-fixation of both sides of mandibular angles. Pus samples were collected by needle aspiration from the lesion and examined by culture method. Bacterial culture was performed in three culture systems (anaerobic, CO2, and aerobic incubator). Identification of the bacteria was performed by 16S rRNA gene cloning and nucleotide sequencing method. Our results showed that Streptococci species was predominantly isolated in both lesions of extraction socket. Only one species (Proteus vulagris) was detected in lesion of mandibular angle. This study was not sufficient to identify the causative bacteria in those osteomyelitis. However, our data may be offered the clue to solve the problem.
감염근관에서 분리 배양한 세균의 수종 항생제에 대한 감수성 조사
임상수,김미광,민정범,김민정,박순낭,황호길,국중기,Lim, Sang-Soo,Kim, Mi-Kwang,Min, Jeong-Beom,Kim, Min-Jung,Park, Soon-Nang,Hwang, Ho-Keel,Kook, Joong-Ki 한국미생물학회 2006 미생물학회지 Vol.42 No.3
본 연구는 치근관 감염병소에서 세균을 분리 및 동정하고, 8종의 항생제들에 대한 분리균주들의 감수성을 조사하기 위하여 실시하였다. 세균에 감염된 27개 치아의 괴사된 치근부 치부소직을 바비드 브로치나 페이퍼 포인트로 무균적으로 채취하였다. 치수가 채취된 부위의 바비드 브로치와 페이퍼 포인트를 500 ul의 $1{\times}PBS$ 용액에 담아 잘 혼합하고, 이를 5% 양혈이 포함된 BHI 한천배지(혈액한천배지)에 도말하여 $37^{\circ}C$ 혐기성 배양기에서 2-5일 동안 배양하였다. 혈액한천배지에서 자라난 세균은 16S rRNA 유전자(rDNA) 염기서열결정법을 이용하여 종수준으로 동정하였다. 이들 균주들의 8종 항상제에 대한 감수성은 최소성장억제농도 측정법으로 조사하였다. 본 연구결과, 101개의 세균 집락이 생겼고, Streptococcus spp. (29.7%)와 Actinomyces spp. (21.8%)가 가장 많이 검출되었다. 이들 균주들 중 9균주는 실험 도중 소실되거나 액체배지에 자라지 않아서 항생제 감수성 심험에서는 제외되었다. 각 항생제들에 대한 감수성을 조사한 결과, 분리된 균주들 중 80(87.0%) 균주가 클린다마이신에 감수성을 보였으며, 세프록심 아세틸과 테트라사이클린에 69(75.0%)가, 오그멘틴에 66(71.7%) 균주가, 페니실린 G에 63(68.5%) 균주가, 에리트로마이신에 61(66.3%) 균주가, 아목시실린에 41(44.6%) 균주가 감수성을 보였다. 그러나 시플록사신에는 29(31.5%) 균주만이 감수성을 보였다. 이러한 8종 항생제에 대한 균주들의 감수성 양상은 세균 종의 종류보다는 분리된 숙주에 따라 차이가 있었다. 이러한 결과는 치근관 감염질환의 치료에 항생제가 필요할 경우 항생제 감수성검사를 병행하는 것이 효과적임을 시사한다. The aim of this study was to identify the bacteria isolated from endodontic lesions by cell culture and to determine the antimicrobial susceptibility of them against 8 antibiotics. The necrotic pulpal tissues were collected from 27 infected root canals, which were diagnosed as endodontic infection. Samples were collected aseptically from the infected pulpal tissue of the infected root canals using a barbed broach and a paper point. The cut barbed broaches and paper points were transferred to an eppendorf tube containing $500{\mu}l\;of\;1{\times}PBS$. The sample solution was briefly mixed and plated onto a BHI-agar plate containing 5% sheep blood. The agar plates were incubated in a $37^{\circ}C$ anaerobic chamber for 2 to 5 days. The bacteria grown on the agar plates were identified by comparison of 16S rRNA gene (rDNA) sequencing method at the species level. To test the sensitivity of the bacteria isolated from the infected root canals against 8 antibiotics, minimum inhibitory concentrations (MIC) were determined using broth dilution assay. The data showed that 101 bacterial strains were isolated and were identified. Streptococcus spp. (29.7%) and Actinomyces spp. (21.8%) were predominantly isolated. The 9 strains were excluded in antimicrobial susceptibility test because they were lost during the experiment or were not grown in broth culture. The percentage of bacteria susceptible for each antibiotic in this study was clindamycin, 87.0% (80 of 92); tetracycline, 75.0% (69 of 92); cefuroxime axetil, 75.0% (69 of 92); amoxicillin + clavulanic acid (5:1), 71.7% (66 of 92); penicillin G, 66.3% (61 of 92); erythromycin, 66.3% (61 of 92); amoxicillin, 44.6% (41 of 92); and ciprofloxacin, 31.5% (29 of 92). The susceptibility pattern of 8 antibiotics was dependent on the host of the bacteria strains rather than the kinds of bacterial species. These results indicate that antibiotic susceptibility test should be performed when antibiotics are needed for the treatment of infected root canals.
Prevotella nigrescens ATCC $33563^T$ 균주-특이 중합효소연쇄반응 프라이머 개발
송수근,유소영,김미광,김화숙,임선아,김도경,박재윤,국중기,Song, Soo-Keun,Yoo, So-Young,Kim, Mi-Kwang,Kim, Hwa-Sook,Lim, Sun-A,Kim, Do-Kyung,Park, Jae-Yoon,Kook, Joong-Ki 한국미생물학회 2008 미생물학회지 Vol.44 No.3
A Pn10 DNA probe was introduced as a Prevotella nigrescens ATCC $33563^T$-specific DNA probe. In that study, the specificity of the Pn10 was tested with only type or reference strains of 5 oral bacterial species. The purpose of this study is to evaluate the specificity of the Pn10 using the wild type strains of P. nigrescens and is to develop the P. nigrescens ATCC $33563^T$-specific PCR primers based on the nucleotide sequence of the Pn10. The specificity of the Pn10 DNA probe was determined by Southern blot analysis. The nucleotide sequence of Pn10 DNA probes was determined by chain termination method. The PCR primers were designed based on the nucleotide sequence of cloned DNA fragment. The data showed that Pn10 DNA probe were hybridized with the genomic DNAs from P. nigrescens ATCC $33563^T$ and KB6. The Pn10 homologous region, KB6-Pn10, of P. nigrescens KB6 was cloned by PCR and sequenced. The Pn10 and KB6-Pn10 DNA fragments were consisted of 1,875 bp and 1,873 bp, respectively. The percent identity of the two was 98.8% and the divergence of them was 0.6%. The two primer sets (Pn10-F-AC/ Pn10-R-AC and Pn10-F-A/ Pn10-R-A), designed base on the nucleotide sequences of Pn10 DNA probe, were specific to the P. nigrescens ATCC $33563^T$. The two PCR primer sets could detect as little as 4 pg of genomic DNA of P. nigrescens ATCC $33563^T$. These results indicate that the two PCR primer sets have proven useful for the identification of P. nigrescens ATCC $33563^T$, especially with regard to the maintenance of the strain. 본 연구는 Prevotella nigrescens ATCC $33563^T$에 대한 균주 특이 DNA 프로브라고 보고된 Pn10 프로브의 균주 특이성을 한국인에서 분리된 P. nigrescens의 임상분리 균주를 이용하여 검증하고, P. nigrescens ATCC $33563^T$ 균주 특이 PCR 프라이머를 개발하고자 시행되었다. P. nigrescens와 유전학적으로 가장 가까운 Prevotella intermedia를 포함한 구강 내 치주질환 원인균종인 5균종의 표준균주 및 참고균주, 그리고 P. nigrescens와 P. intermedia의 임상분리 균주를 이용하여 Southern blot 분석법을 시행하였다. Southern blot 분석 결과 Pn10 DNA 프로브에 P. nigrescens ATCC $33563^T$ 및 ChDC KB6 두 균주 지놈 DNA가 검출되었다. P. nigrescens KB6 균주에서 Pn10 DNA 프로브와 상동성이 있는 부위를 PCR법으로 증폭(KB6-Pn10)하여 클로닝한 다음 Pn10 DNA프로브와 같이 핵산 염기서열을 결정하여 상동성을 비교하였다. 그 결과 Pn10과 KB6-Pn10의 핵산염기서열간의 Percent identity는 98.8%였으며, divergence는 0.6%였다. Pn10 DNA 프로브의 핵산염기서열을 바탕으로 두 중류 프라이머 쌍(Pn10-F-AC/Pn10-R-AC 및 Pn10-F-A/Pn10-R-A)을 설계 및 제작하여 P. nigrescens ATCC $33563^T$에 대한 균주 특이성을 PCR법으로 검증하였다. 이들 프라이머 쌍들의 민감도(sensitivity) 조사 결과, 이들은 P. nigrescens ATCC $33563^T$ 지놈 DNA 4 pg까지 검출할 수 있음을 알았다. 이상의 연구 결과를 종합하면, Pn10 DNA 핵산염기서열을 바탕으로 설계된 Pn10-F-AC/Pn10-R-AC 및 Pn10-F-A/Pn10-R-A 프라이머 쌍들은 P. nigrescens ATCC $33563^T$를 신속 정확하게 검출하는 수 있어, 균주의 보존적 측면에서 유용하게 이용될 수 있을 것으로 생각된다.
DNA probe Pn25를 이용한 Prevotella intermedia 및 Prevotella nigrescens의 동정
김화숙 ( Hwa Sook Kim ) , 김미광 ( Mi Kwang Kim ) , 유소영 ( So Young Yoo ) , 최민호 ( Min Ho Choi ) , 임상수 ( Sang Soo Lim ) , 박헌동 ( Heon Dong Park ) , 송수근 ( Soo Keun Song ) , 신환선 ( Hwan Seon Shin ) , 박슬희 ( Seul H 조선대학교 구강생물학연구소 2003 Oral Biology Research (Oral Biol Res) Vol.27 No.2
.
상악동염 병소 부위에서 세균의 분리 동정 및 항생제 감수성에 대한 연구
최영옥(Young-Og Choi),김수관(Su-Gwan Kim),김학균(Hak-Kyun Kim),김영종(Yong-Jong Kim),최동국(Dong-Kook Choi),김미광(Mi-Kwang Kim),박순낭(Soon-Nang Park),김민정(Min-Jung Kim),국중기(Joong-Ki Kook) 대한구강악안면외과학회 2006 대한구강악안면외과학회지 Vol.32 No.5
The purpose of this study was to isolate and identify the bacteria in chronic maxillary sinusitis (CMS) lesions from 3 patients and to determine the antimicrobial susceptibility of them against 10 antibiotics. One of them was odontogenic origin and the others were non-odontogenic origin. Pus samples were collected by needle aspiration from the lesions and examined by culture method. Bacterial culture was performed in three culture systems (anaerobic, CO2, and aerobic incubator). Identification of the bacteria was performed by 16S rRNA gene (16S rDNA) nucleotide sequencing method. To test the sensitivity of the bacteria isolated from the maxillary sinusitis lesions against seven antibiotics, penicillin G, amoxicillin, tetracycline, ciprofloxacin, cefuroxime, erythromycin, clindamycin, and vancomycin, minimum inhibitory concentration (MIC) was performed using broth dilution assay. Our data showed that enterobacteria such as Enterobacter aerogenes (30%), Klebsiella pneumoniae (25%), and Serratia marcescens (15%) were predominately isolated from the lesion of non-odontogenic CMS of senile patient (70 year old). Streptococcus spp. (40.3%), Actinomyces spp. (27.4%), P. nigrescens, M. micros, and P. anaerobius strains were isolated in the lesion of odontogenic CMS. In the lesion of non-odontogenic CMS, Streptococcus spp. (68.4%), Rothia spp. (13.2%), and Actinomyces sp. (10.5%) were isolated. The susceptibility pattern of 10 antibiotics was determined according to the host of the bacteria strains ratter than the kinds of bacterial species. Even though the number of CMS was limited as three, these results indicate that antibiotic susceptibility test must be accompanied with treatment of CMS. The combined treatment of two or more antibiotics is better than single antibiotic treatment in the presence of multidrug-resistant bacteria in the CMS lesions.
한국인의 치은연하 치태에서 Fusobacterium nucleatum의 분리
장현선,김세훈,김화숙,국중기,김미광,유소영,김병옥,Jang, Hyun-Seon,Kim, Seo-Hoon,Kim, Hwa-Sook,Kook, Joong-Ki,Kim, Mi-Kwang,Yoo, So-Young,Kim, Byung-Ock 대한치주과학회 2003 Journal of Periodontal & Implant Science Vol.33 No.2
The purpose of this study was to isolate and characterize the Fusohacrerium nucleatum (F. nucleatum) from subgingival plaque in Korean periodontitis patients. The subgingival plaque samples of periodontitis patient were collected with sterilized paper point. The paper point was put into reduced transfer medium and then immediately transferred to laboratory. The subgingival samples were diluted by 10,000 folds and plated on F. nucleatum-selective media agar plate. The plates were incubated at 37$^{\circ}C$ in an anaerobic chamber for 3 days. The violet-colored colonies were selected and subjected to further verification whether those are F. nucleatum or not. For further confirmation, 16S rRNA genes (rDNA) were cloned from each of bacterial clones and determined sequence of 16S rDNA. In this study, we found 17 distinct clinical isolates of F. nucleatum from subgingival plaque. The clinical isolates will be a useful in various studies in periodontology.
DNA probe Pn25를 이용한 Prevotella intermedia 및 Prevotella nigrescens의 동정
김화숙 ( Hwa Sook Kim ),김미광 ( Mi Kwang Kim ),유소영 ( So Young Yoo ),최민호 ( Min Ho Choi ),임상수 ( Sang Soo Lim ),박헌동 ( Heon Dong Park ),송수근 ( Soo Keun Song ),신환선 ( Hwan Seon Shin ),박슬희 ( Seul Hee Park ),임선아 ( 조선대학교 구강생물학연구소 2003 口腔生物學硏究 Vol.27 No.2