• Journal of Microbiology and Biotechnology
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• 제26권12호
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• pp.2206-2213
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• 2016

Recently, several studies have revealed that commercial microbial identification systems do not accurately identify the uncommon causative species of candidiasis, including Candida famata, Meyerozyma guilliermondii, and C. auris. We investigated the accuracy of species-level identification in a collection of clinical isolates previously identified as C. famata (N = 38), C. lusitaniae (N = 1 2), and M. guilliermondii (N = 5) by the Vitek 2 system. All 55 isolates were re-analyzed by the Phoenix system (Becton Dickinson Diagnostics), two matrix-assisted laser desorption ionization-time of flight mass spectrometry analyzers (a Vitek MS and a Bruker Biotyper), and by sequencing of internal transcribed spacer (ITS) regions or 26S rRNA gene D1/D2 domains. Among 38 isolates previously identified as C. famata by the Vitek 2 system, the majority (27/38 isolates, 71.1%) were identified as C. tropicalis (20 isolates) or C. albicans (7 isolates) by ITS sequencing, and none was identified as C. famata. Among 20 isolates that were identified as C. tropicalis, 17 (85%) were isolated from urine. The two isolates that were identified as C. auris by ITS sequencing originated from ear discharge. The Phoenix system did not accurately identify C. lusitaniae, C. krusei, or C. auris. The correct identification rate for 55 isolates was 92.7% (51/55 isolates) for the Vitek MS and 94.6% (52/55 isolates) for the Bruker Biotyper, as compared with results from ITS sequencing. These results suggest that C. famata is very rare in Korea, and that the possibility of misidentification should be noted when an uncommon Candida species is identified.

• 대한임상검사과학회지
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• 제49권3호
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• pp.279-284
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• 2017

본 연구에서는 혈액배양에서 신속한 세균 동정과 항생제 감수성 시험(antibiotic susceptibility test, AST) 결과를 얻기 위해 혈액배양 양성배지에서 계대배양 없이 세균을 VITEK MS와 VITEK 2 시스템에 직접 접종하였으며, 도출된 결과를 표준방법과 비교하여, 그 신뢰도와 정확도를 평가하였다. 혈액배양 양성시료에서 직접 결과는 표준방법 AST 결과와 비교하였을 때, 97.9% (1,936/1,978)의 전체적인 일치율을 보였다. 그람양성 세균은 97.2% (1,051/1,081)의 일치율을 나타냈으며, 매우 중대한 오차율은 0.5% (5/1081), 중대한 오차율은 0.1% (1/1,081), 사소한 오차율은 2.2% (24/1,081)의 결과를 나타냈다. 두 방법 간 불일치의 주요 원인균은 Staphylococcus epidermidis이었고, 그 중 gentamicin (N=9)과 fusidic acid (N=8)에서 높은 오류를 나타냈다. 그람음성 세균 중 전체적인 일치율은 98.6%(885/897)였고, 사소한 오류는 1.4% (12/897)였다. 그람음성세균의 불일치 주요 원인균은 Escherichia coli와 Pseudomonas aeruginosa였으며, 그 중 amoxicillin/clavulanic acid(N=3)에서 높은 오류를 나타냈다. 직접법에 의한 AST 방법은 CLSI 기준을 충족하였고, 결과 보고 시간을 24시간 단축할 수 있었지만, 매우 큰 오류가 있는 항생제에 대해서는 디스크확산법으로 추가적인 검사를 시행한 후 보고해야 한다는 것을 알 수 있었다. 이러한 연구 결과들을 토대로 혈액배양 시료에서 직접 AST를 실시하는 방법은 정확하고 결과를 보고하는데 까지 소요되는 시간을 크게 감소시킬 수 있기 때문에 환자의 정확하고 효율적인 치료에 유용하게 활용될 수 있을 것으로 사료된다.

• 대한임상검사과학회지
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• 제49권4호
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• pp.407-412
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• 2017

본 연구에서는 계대배양과 세균 동정 시험에 소요되는 시간을 단축하고, 혈류감염의 새로운 검사 방법을 모색하여 간단하고 신속 정확한 동정 결과를 도출할 목적으로 질량분석기를 이용하여 다음과 같은 결과를 얻었다. 혈액배양에서 한 가지 세균만 배양된 검체는 총 254개였으며, Vitek 2에서 208주(81.8%)의 세균을 동정되었으며, 45주는 동정되지 않았다. 동정된 세균 중 그람양성 세균이 146개(57.5%), 그람음성 세균이 108개(42.5%)이었다. 전체적으로 233개는 종(species) 수준까지 동정 되었으며, 21개는 속(genus)수준까지 동정 되었다. 동정 오류는 Propionibacterium acnes를 Clostridium bifermentans로 동정 되었다. 균종별로는 enterobacteriaceae, glucose non-fermentative bacilli (GNFB), staphylococci의 정확도는 각각 81/83 (97.6%), 12/15 (80.0%), 72/85 (84.7%)로 나타났다. Vitek 2에 의한 표준법과 Vitek MS에 의한 직접법에 의한 동정의 일치율은 81.8%이었으며, 45주는 동정되지 않았다. 동정되지 않은 세균들의 대부분은 그람양성 세균(n=37)이었고, 그람양성 세균은 streptococci (14), coagulase-negative staphylococci (CNS) (11), enterococci (3), Staphylococcus aureus (2), Micrococcus spp. (2), Bacillus spp. (2) 그리고 Actinomyces odontolyticus, Finegoldia mag na, Peptostreptococcus spp.가 각각 1건씩 이었다. 결과 보고 시간은 기존의 검사 방법보다 24~72시간까지 단축되었다. 산소성 배양과 무산소성 배양 사이의 동정률의 차이는 없었으나 무산소성 배양을 사용하면 용해 과정이 필요 없어 검체 준비 시간을 단축할 수 있었다. 이상의 연구 결과로 혈액배양병에서 직접 동정하는 방법은 정확하고 결과 보고 시간이 신속하여 환자의 치료에 매우 유용할 것이라 생각된다. 향후 추가적인 연구에서는 본 연구에서 정확성이 부족했던 사슬알균(streptococci)과 혈장응고효소 음성 포도알균(CNS)을 동정하기 위한 방법을 더욱 개선할 필요가 있을 것으로 사료된다.

• 대한의생명과학회지
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• 제29권4호
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• pp.256-262
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• 2023

The purpose of this study is to investigate microbial contamination in water purifiers from two universities (A and B) in Chungcheong region and to evaluate about the harmfulness of the isolated bacteria to the human. The degree of microbiological contamination of six water purifiers at university A was investigated three times from July 2018 to September 2019, and nine water purifiers at university B were investigated in 2023. The isolated bacteria were biochemically identified using an API kit and Vitek-2 system, and then the bacteria were identified to the species level using MALDI-TOF MS. In addition, the possibility of human infection of the isolated bacteria was evaluated through a literature search. In July 2018 and September 2019, the number of bacteria isolated inside the faucet was below the acceptable standard for hot water, but exceed for cold water in all water purifiers. In January and September 2019, bacteria exceeding the acceptable standards were isolated nine times from the cold water of six water purifies (a total of 12 water purifiers). Bacteria identified by MALDI-TOF MS included anaerobic bacteria (Clostridium novyi, Clostridium themopalmarium etc.), Gram-positive bacilli (Microbacterium testaceum, Arthrobacter woluwensis etc.), and Gramnegative bacilli (Acinetobacter nosocomialis, Comamonas kerstersii etc.), which are difficult identify by biochemical methods. In conclusion, bacteria exceeding the acceptable standard were isolated from the cold water of most of the water purifiers. Most of the isolated bacteria were low-pathogenic bacteria from natural environment, but opportunistic bacteria that can cause infection in humans were also isolated from some water purifiers.

• 대한의생명과학회지
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• 제25권1호
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• pp.40-53
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• 2019

Of the Acinetobacter spp., A. baumannii (genospecies 2) is the most clinically significant in terms of hospital-acquired infections worldwide. It is difficult to perform Acinetobacter-related taxonomy using phenotypic characteristics and routine laboratory methods owing to clusters of closely related species. The ability to accurately identify Acinetobacter spp. is clinically important because antimicrobial susceptibility and clinical relevance differs significantly among the different genospecies. Based on the medical importance of pathogenic Acinetobacter spp., the distribution and characterization of Acinetobacter spp. isolates from 123 clinical samples was determined in the current study using four typically applied bacterial identification methods; partial rpoB gene sequencing, amplified rRNA gene restriction analysis (ARDRA) of the intergenic transcribed spacer (ITS) region of the 16~23S rRNA, the $VITEK^{(R)}$ 2 system (an automated microbial identification system) and matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS). A. baumannii isolates (74.8%, 92/123) were the most common species, A. nosocomialis (10.6%, 13/123) and A. pittii isolates (7.5%, 9/123) were second and third most common strains of the A. calcoaceticus-A. baumannii (ACB) complex, respectively. A. soli (5.0%, 6/123) was the most common species of the non-ACB complex. RpoB gene sequencing and ARDRA of the ITS region were demonstrated to lead to more accurate species identification than the other methods of analysis used in this study. These results suggest that the use of rpoB genotyping and ARDRA of the ITS region is useful for the species-level identification of Acinetobacter isolates.

• 한국환경보건학회지
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• 제50권2호
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• pp.93-101
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• 2024

Background: As pollutants caused by non-point sources flow into rivers, river water quality monitoring for fecal pollution is becoming increasingly important. Objectives: This study was conducted to investigate the distribution of microbial communities in the Yeongsangang River water system and sewage treatment plants in Gwangju and to evaluate their antibiotic resistance. Methods: In the experiment, samples were distributed to five selective media at each point and then cultured for 18 to 24 hours. When bacteria were observed, they were sub-cultured by size and shape and identified using MALDI-TOF MS equipment. When identification was completed, 17 types of antibiotic susceptibility tests were performed using VITEK II equipment, focusing on gram-negative dominant species among the identified strains. Results: During the study period, a total of 266 strains were isolated from 39 samples. Gram-positive bacteria were 37 strains in four genera, or 13.9% of the total, and Gram-negative bacteria were 229 strains in 23 genera, or 86.1% of the total. Antibiotic susceptibility testing of 23 strains, the major dominant species, showed that one strain (4.3%) was resistant to only one antibiotic, and two strains (8.7%) were 100% susceptible to the 17 antibiotics tested. The other 20 strains (87.0%) were multidrug resistant bacteria resistant to two or more antibiotics. There were various types of multidrug resistance. Among them, penicillin and cephalosporin series showed the highest resistance. Conclusions: Based on the results of this study, it was found that the bacterial community structure changed according to regional and environmental factors, and it was judged that continuous research such as genetic analysis of antibiotic-resistant bacteria present in natural rivers is necessary.