결핵균 배양에 대한 배양촉진물질(CPI-107)의 효과
Effect of culture-promoting ingredients (CPI-107) on the culture of Mycobacterium tuberculosis
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초록
Mycobacterium tuberculosis complex (M. tuberculosis complex) is a causative agent of contagious chronic disease in a wide range of mammalian hosts, mainly cattle, goat, pigs, wildlife, and humans. The definite diagnosis of tuberculosis is made based on culture of M. tuberculosis , but it takes a long time. In the present study, we analyzed whether the detection time of M. tuberculosis could be reduced when cultured in the medium containing the culture-promoting ingredients-107 (CPI-107) using the BacT/Alert 3D system, an automatic culture system. The time to detection (TTD) tended to decrease as the added concentration of CPI-107 increase. In the case of low numbers of M. tuber-culosis , it decreased by 21.0% at 1.2 mg/mL of CPI-107 and by 15.9% in the case of high numbers of M. tuberculosis . In the culture using clinically isolated M. tuberculosis strains, the shortening of the culture time by CPI was more evident. In conclusion, the detection time of M. tuberculosis was shortened in the medium added with CPI-107, and this could be used for isolation, culture and drug susceptibility test of M. tuberculosis .
Abstract
Mycobacterium tuberculosis complex (M. tuberculosis complex) is a causative agent of contagious chronic disease in a wide range of mammalian hosts, mainly cattle, goat, pigs, wildlife, and humans. The definite diagnosis of tuberculosis is made based on culture of M. tuberculosis , but it takes a long time. In the present study, we analyzed whether the detection time of M. tuberculosis could be reduced when cultured in the medium containing the culture-promoting ingredients-107 (CPI-107) using the BacT/Alert 3D system, an automatic culture system. The time to detection (TTD) tended to decrease as the added concentration of CPI-107 increase. In the case of low numbers of M. tuber-culosis , it decreased by 21.0% at 1.2 mg/mL of CPI-107 and by 15.9% in the case of high numbers of M. tuberculosis . In the culture using clinically isolated M. tuberculosis strains, the shortening of the culture time by CPI was more evident. In conclusion, the detection time of M. tuberculosis was shortened in the medium added with CPI-107, and this could be used for isolation, culture and drug susceptibility test of M. tuberculosis .
참고문헌 (21)
- Beste DJ, "The genetic requirements for fast and slow growth in mycobacteria", PLoS One, 4, pp.e5349~ (2009)
- Bird BR, "Changing practices in mycobacteriology : a follow-up survey of state and territorial public health laboratories", J Clin Microbiol, 34, pp.554~559 (1996)
- Cruciani M, "Meta-analysis of BACTEC MGIT 960 and BACTEC 460 TB, with or without solid media, for detection of mycobacteria", J Clin Microbiol, 42, pp.2321~2325 (2004)
- Denniston MM, "Contrast of survey results between state and a cohort of nonstate mycobacteriology laboratories : Changes in laboratory practices", J Clin Microbiol, 35, pp.422~426 (1997)
- Gruft H, "Enhancing effects of carbon dioxide on the primary isolation of acid-fast bacilli in a modified Lowenstein-Jensen medium", Appl Microbiol, 22, pp.944~945 (1971)
- Hoek KG, "Detecting drug-resistant tuberculosis : the importance of rapid testing", Mol Diagn Ther, 15, pp.189~194 (2011)
- Jaquess PA, "Enhanced growth of Mycobacterium tuberculosis in the presence of selenium", Am J Clin Pathol, 75, pp.209~210 (1981)
- Kim MN, "Mycobacterial Testing in Hospital Laboratories in Korea : Results of a Survey of 40 University or Tertiary-care Hospitals", Kor J Clin Pathol, 19, pp.86~91 (1999)
- Seung-Cheol Kim, "Effects of selenate and L-glutamate on the growth of Mycobacterium tuberculosis complex", 한국동물위생학회지, 41(4), pp.239~244 (2018), 한국동물위생학회[DOI]
- Koch A, "Mycobacterium tuberculosis", Trends Microbiol, 26, pp.555~556 (2018)
- 이기은, "항산균 배양 및 동정방법의 변화에 따른 양성률과 보고시간 변화", Annals of Laboratory Medicine, 25(1), pp.46~52 (2005), 대한진단검사의학회
- Machado D, "Advances in the molecular diagnosis of tuberculosis : From probes to genomes", Infec Genet Evol, 72, pp.93~112 (2019)
- Mok J, "Recent Advances in Diagnosis and treatment of Tuberculosis", J Kor Soc Health-Syst Pharm, pp.101~110 (2016)
- O’Grady J, "New and improved diagnostics for detection of drug-resistant pulmonary tuberculosis", Curr Opin Pulm Med, 17, pp.134~141 (2011)
- Orgeur M, "Evolution of virulence in the Mycobacterium tuberculosis complex", Curr Opin Microbiol, 41, pp.68~75 (2018)
- 박재석, "Issues Related to the Updated 2014 Korean Guidelines for Tuberculosis", Tuberculosis and Respiratory Diseases, 79(1), pp.1~4 (2016), 대한결핵및호흡기학회
- 박승규, "완전 자동화된 액체배양법과 기존의 고체배양법을 이용한 객담 내 mycobacterium의 신속검출에 대한 비교", Tuberculosis and Respiratory Diseases, 53(6), pp.635~643 (2002), 대한결핵및호흡기학회
- Sabagh BP, "Comparative study with two different enrichments in the culture media used in the disinfectant efficacy assay", J Microbiol Methods, 88, pp.255~262 (2012)
- Siddiqi SH, "Enhancement of Mycobacterial Growth in Middlebrook 7H12 Medium by Polyoxyethylene Stearate", Curr Microbiol, 17, pp.105~110 (1988)
- Wallace E, "Culturing Mycobacteria", Methods Mol Biol, 2314, pp.1~58 (2021)
- Global tuberculosis report 2022, "World Health Organization", WHO, ~ (2022)
