S. Khanthawong, Peeranut Vongthanayodh, Supattra Pruanjarern, Apichaya Taengrom, Kanchana Usuwanthim, Pachuen Potup, Y. Thongsri
{"title":"盘片扩散法测定内生脓胞癣菌的抗菌药物敏感性","authors":"S. Khanthawong, Peeranut Vongthanayodh, Supattra Pruanjarern, Apichaya Taengrom, Kanchana Usuwanthim, Pachuen Potup, Y. Thongsri","doi":"10.33165/rmj.2024.47.1.267191","DOIUrl":null,"url":null,"abstract":"Background: Pythiosis is a life-threatening disease caused by the fungus-like organism Pythium insidiosum. It causes disease in both animals and humans. Amphotericin B antifungal is less effective because it lacks ergosterol, a drug target in the cell membrane.\nObjective: To evaluate antimicrobial susceptibility test of P. insidiosum isolated from human pythiosis by disc diffusion method.\nMethods: The antimicrobial drug susceptibility test by disc diffusion method was tested against 10 clinical isolated strains of P. insidiosum. Antimicrobial drugs comprise of 8 antibiotics (chloramphenicol, cefotaxime, ciprofloxacin, gentamycin, tetracycline, meropenem, oxacillin, and vancomycin) and 2 antifungal drugs (itraconazole and amphotericin B) which were included in the test.\nResults: Antimicrobial drugs susceptibility tests were performed on 10 clinically isolated strains of P. insidiosum. Six of them showed susceptibility to antimicrobial drugs. The cutaneous pythiosis strain (SIMI 8569) showed the highest number of susceptibilities to antimicrobial agents (chloramphenicol, ciprofloxacin, gentamycin, tetracycline, vancomycin, and itraconazole). In addition, 4 strains of P. insidiosum (M 29, SIMI 6666, SIMI 7873, and SIMI 2989-42) were not inhibited by all antimicrobial drugs.\nConclusions: This result concluded that chloramphenicol, tetracycline, and itraconazole inhibited the mycelial growth of P. insidiosum better than the other drugs. The inhibition effects of these drugs were observed in 40% - 60% of the strains. Further experiments should be carried out to evaluate the tested drugs in various concentrations with other more susceptible methods to get more precise concentrations exposed to P. insidiosum isolates such as broth dilution or dilution assays.\n ","PeriodicalId":500652,"journal":{"name":"Ramathibodi Medical Journal","volume":" 1138","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Antimicrobial Drug Susceptibility Test of Pythium insidiosum by Disc Diffusion Method\",\"authors\":\"S. Khanthawong, Peeranut Vongthanayodh, Supattra Pruanjarern, Apichaya Taengrom, Kanchana Usuwanthim, Pachuen Potup, Y. Thongsri\",\"doi\":\"10.33165/rmj.2024.47.1.267191\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: Pythiosis is a life-threatening disease caused by the fungus-like organism Pythium insidiosum. It causes disease in both animals and humans. Amphotericin B antifungal is less effective because it lacks ergosterol, a drug target in the cell membrane.\\nObjective: To evaluate antimicrobial susceptibility test of P. insidiosum isolated from human pythiosis by disc diffusion method.\\nMethods: The antimicrobial drug susceptibility test by disc diffusion method was tested against 10 clinical isolated strains of P. insidiosum. Antimicrobial drugs comprise of 8 antibiotics (chloramphenicol, cefotaxime, ciprofloxacin, gentamycin, tetracycline, meropenem, oxacillin, and vancomycin) and 2 antifungal drugs (itraconazole and amphotericin B) which were included in the test.\\nResults: Antimicrobial drugs susceptibility tests were performed on 10 clinically isolated strains of P. insidiosum. Six of them showed susceptibility to antimicrobial drugs. The cutaneous pythiosis strain (SIMI 8569) showed the highest number of susceptibilities to antimicrobial agents (chloramphenicol, ciprofloxacin, gentamycin, tetracycline, vancomycin, and itraconazole). In addition, 4 strains of P. insidiosum (M 29, SIMI 6666, SIMI 7873, and SIMI 2989-42) were not inhibited by all antimicrobial drugs.\\nConclusions: This result concluded that chloramphenicol, tetracycline, and itraconazole inhibited the mycelial growth of P. insidiosum better than the other drugs. The inhibition effects of these drugs were observed in 40% - 60% of the strains. 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引用次数: 0
摘要
背景:恙虫病是一种由类真菌恙虫引起的危及生命的疾病。它可导致动物和人类患病。两性霉素 B 的抗真菌效果较差,因为它缺乏麦角甾醇,而麦角甾醇是细胞膜上的一个药物靶点:通过碟片扩散法评估从人类脓疱病中分离出的内生脓疱癣菌的抗菌药物敏感性试验:方法:用盘扩散法对 10 株临床分离的脓疱疮脓疱疮菌进行抗菌药物药敏试验。抗菌药物包括 8 种抗生素(氯霉素、头孢他啶、环丙沙星、庆大霉素、四环素、美罗培南、氧西林和万古霉素)和 2 种抗真菌药物(伊曲康唑和两性霉素 B):结果:对 10 株临床分离的内生痢疾杆菌进行了抗菌药物药敏试验。其中 6 株对抗菌药物呈敏感性。皮肤脓毒血症菌株(SIMI 8569)对抗菌药物(氯霉素、环丙沙星、庆大霉素、四环素、万古霉素和伊曲康唑)的敏感性最高。此外,4 株 P. insidiosum(M 29、SIMI 6666、SIMI 7873 和 SIMI 2989-42)未被所有抗菌药物抑制:结论:氯霉素、四环素和伊曲康唑对内生豌豆菌菌丝生长的抑制作用优于其他药物。这些药物对 40% - 60% 的菌株有抑制作用。应开展进一步的实验,用其他更易受影响的方法(如肉汤稀释法或稀释法)评估不同浓度的受试药物,以获得更精确的抑制内生癣菌分离物的浓度。
Antimicrobial Drug Susceptibility Test of Pythium insidiosum by Disc Diffusion Method
Background: Pythiosis is a life-threatening disease caused by the fungus-like organism Pythium insidiosum. It causes disease in both animals and humans. Amphotericin B antifungal is less effective because it lacks ergosterol, a drug target in the cell membrane.
Objective: To evaluate antimicrobial susceptibility test of P. insidiosum isolated from human pythiosis by disc diffusion method.
Methods: The antimicrobial drug susceptibility test by disc diffusion method was tested against 10 clinical isolated strains of P. insidiosum. Antimicrobial drugs comprise of 8 antibiotics (chloramphenicol, cefotaxime, ciprofloxacin, gentamycin, tetracycline, meropenem, oxacillin, and vancomycin) and 2 antifungal drugs (itraconazole and amphotericin B) which were included in the test.
Results: Antimicrobial drugs susceptibility tests were performed on 10 clinically isolated strains of P. insidiosum. Six of them showed susceptibility to antimicrobial drugs. The cutaneous pythiosis strain (SIMI 8569) showed the highest number of susceptibilities to antimicrobial agents (chloramphenicol, ciprofloxacin, gentamycin, tetracycline, vancomycin, and itraconazole). In addition, 4 strains of P. insidiosum (M 29, SIMI 6666, SIMI 7873, and SIMI 2989-42) were not inhibited by all antimicrobial drugs.
Conclusions: This result concluded that chloramphenicol, tetracycline, and itraconazole inhibited the mycelial growth of P. insidiosum better than the other drugs. The inhibition effects of these drugs were observed in 40% - 60% of the strains. Further experiments should be carried out to evaluate the tested drugs in various concentrations with other more susceptible methods to get more precise concentrations exposed to P. insidiosum isolates such as broth dilution or dilution assays.