{"title":"肯尼亚Menengai火山口地热喷口放线菌抗生素提取物的体外致死测定","authors":"P. Waithaka","doi":"10.53411/jpadr.2022.3.3.05","DOIUrl":null,"url":null,"abstract":"Introduction: Drug resistance is the biggest threat to human existence today. This study was conducted to investigate the sensitivity of selected pathogenic microorganisms to antibiotic extracts from soils of Menengai crater geothermal vents in Kenya. \nMethod: Antibiotic-producing actinomycetes were isolated from geothermal vents of the crater. The isolates were identified using colony characteristics and biochemical means. Sensitivity of the selected pathogenic microorganism was carried out using primary and secondary screening techniques. Four actinomycetes coded PAN 9, PAN 18, PAN 117, and PAN 138 were selected for further analysis based on the size of the zone of inhibition and the broad spectrum of activity. Extraction of antibiotics from the selected actinomycetes was carried out using ethyl acetate. A sensitivity test of the pathogens to the extracts was done using Karby Bauer disk diffusion technique. Cytotoxicity of the antibiotic extracts was carried out using Brine shrimp lethality test and sheep blood hemolytic bioassays. The isolates presented typical actinomycetes characteristics. \nResults: A total of 20 actinomycete isolates showed antagonism against the test pathogenic microorganisms. The selected actinomycetes inhibited growth of Gram-positive and negative bacterial and fungal pathogens in both primary and secondary sensitivity tests. There was a significant difference in the diameters of zones of inhibition produced by the test pathogens when subjected to the antibiotic metabolites from the selected actinomycetes (F = 6.6046 P = 0.001338). \nDiscussion: The minimum inhibitory concentration and minimum bactericidal concentration/minimum fungicidal concentration did not vary significantly (F=0.4503, P = 0.7187). The LC50 values of the antibiotic extracts varied from 2.438±0.47µg in PAN 9 to 9.3455±0.41µg in PAN 138. PAN 18 and PAN 117 showed partial hemolysis while PAN 9 and PAN 138 exhibited complete hemolysis of sheep blood erythrocytes. Soils from Menengai crater geothermal vents have actinomycetes that produce antibiotics. The antibiotics are cytotoxic to brine shrimps. In addition, the antibiotics cause hemolysis of sheep blood erythrocytes. There is a need to purify the antibiotics and structure elucidate them. The active antibiotic extract needs to be evaluated to determine whether the hemolysis is due to the compound itself or some other chemical constituent.","PeriodicalId":388338,"journal":{"name":"Journal of Pharmacovigilance and Drug Research","volume":"94 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Determination of In vitro lethality of actinomycetes antibiotic extracts from Menengai crater geothermal vents, Kenya\",\"authors\":\"P. Waithaka\",\"doi\":\"10.53411/jpadr.2022.3.3.05\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction: Drug resistance is the biggest threat to human existence today. This study was conducted to investigate the sensitivity of selected pathogenic microorganisms to antibiotic extracts from soils of Menengai crater geothermal vents in Kenya. \\nMethod: Antibiotic-producing actinomycetes were isolated from geothermal vents of the crater. The isolates were identified using colony characteristics and biochemical means. Sensitivity of the selected pathogenic microorganism was carried out using primary and secondary screening techniques. Four actinomycetes coded PAN 9, PAN 18, PAN 117, and PAN 138 were selected for further analysis based on the size of the zone of inhibition and the broad spectrum of activity. Extraction of antibiotics from the selected actinomycetes was carried out using ethyl acetate. A sensitivity test of the pathogens to the extracts was done using Karby Bauer disk diffusion technique. Cytotoxicity of the antibiotic extracts was carried out using Brine shrimp lethality test and sheep blood hemolytic bioassays. The isolates presented typical actinomycetes characteristics. \\nResults: A total of 20 actinomycete isolates showed antagonism against the test pathogenic microorganisms. The selected actinomycetes inhibited growth of Gram-positive and negative bacterial and fungal pathogens in both primary and secondary sensitivity tests. There was a significant difference in the diameters of zones of inhibition produced by the test pathogens when subjected to the antibiotic metabolites from the selected actinomycetes (F = 6.6046 P = 0.001338). \\nDiscussion: The minimum inhibitory concentration and minimum bactericidal concentration/minimum fungicidal concentration did not vary significantly (F=0.4503, P = 0.7187). The LC50 values of the antibiotic extracts varied from 2.438±0.47µg in PAN 9 to 9.3455±0.41µg in PAN 138. PAN 18 and PAN 117 showed partial hemolysis while PAN 9 and PAN 138 exhibited complete hemolysis of sheep blood erythrocytes. Soils from Menengai crater geothermal vents have actinomycetes that produce antibiotics. The antibiotics are cytotoxic to brine shrimps. In addition, the antibiotics cause hemolysis of sheep blood erythrocytes. There is a need to purify the antibiotics and structure elucidate them. The active antibiotic extract needs to be evaluated to determine whether the hemolysis is due to the compound itself or some other chemical constituent.\",\"PeriodicalId\":388338,\"journal\":{\"name\":\"Journal of Pharmacovigilance and Drug Research\",\"volume\":\"94 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Pharmacovigilance and Drug Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.53411/jpadr.2022.3.3.05\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pharmacovigilance and Drug Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.53411/jpadr.2022.3.3.05","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
导读:耐药性是当今人类生存的最大威胁。本研究旨在研究肯尼亚Menengai火山口地热喷口土壤中选定的病原微生物对抗生素提取物的敏感性。方法:从火山口地热喷口分离产生抗生素的放线菌。利用菌落特征和生化手段对分离菌株进行鉴定。采用一级筛选和二级筛选技术对所选病原微生物进行敏感性分析。根据抑制区大小和广谱活性,选择4个放线菌进行进一步分析,分别为PAN 9、PAN 18、PAN 117和PAN 138。采用乙酸乙酯法从所选放线菌中提取抗生素。采用卡比-鲍尔盘片扩散法进行病原菌对提取物的敏感性试验。采用盐水对虾致死试验和羊血溶血生物测定法对抗生素提取物进行细胞毒性研究。分离菌株具有典型的放线菌特征。结果:20株放线菌对试验病原菌有拮抗作用。在初级和次级敏感性试验中,选定的放线菌抑制革兰氏阳性和阴性细菌和真菌病原体的生长。所选放线菌的抗生素代谢物对试验病原菌产生的抑制带直径有显著差异(F = 6.6046 P = 0.001338)。讨论:最小抑菌浓度和最小杀菌浓度/最小杀真菌浓度无显著差异(F=0.4503, P = 0.7187)。抗生素提取物的LC50值在PAN 9中为2.438±0.47µg,在PAN 138中为9.3455±0.41µg。PAN 18和PAN 117表现为部分溶血,PAN 9和PAN 138表现为完全溶血。门能盖火山口地热喷口的土壤中含有能产生抗生素的放线菌。抗生素对卤虾有细胞毒性。此外,抗生素引起绵羊红细胞溶血。有必要对抗生素进行纯化和结构分析。需要对活性抗生素提取物进行评估,以确定溶血是由于化合物本身还是由于其他化学成分。
Determination of In vitro lethality of actinomycetes antibiotic extracts from Menengai crater geothermal vents, Kenya
Introduction: Drug resistance is the biggest threat to human existence today. This study was conducted to investigate the sensitivity of selected pathogenic microorganisms to antibiotic extracts from soils of Menengai crater geothermal vents in Kenya.
Method: Antibiotic-producing actinomycetes were isolated from geothermal vents of the crater. The isolates were identified using colony characteristics and biochemical means. Sensitivity of the selected pathogenic microorganism was carried out using primary and secondary screening techniques. Four actinomycetes coded PAN 9, PAN 18, PAN 117, and PAN 138 were selected for further analysis based on the size of the zone of inhibition and the broad spectrum of activity. Extraction of antibiotics from the selected actinomycetes was carried out using ethyl acetate. A sensitivity test of the pathogens to the extracts was done using Karby Bauer disk diffusion technique. Cytotoxicity of the antibiotic extracts was carried out using Brine shrimp lethality test and sheep blood hemolytic bioassays. The isolates presented typical actinomycetes characteristics.
Results: A total of 20 actinomycete isolates showed antagonism against the test pathogenic microorganisms. The selected actinomycetes inhibited growth of Gram-positive and negative bacterial and fungal pathogens in both primary and secondary sensitivity tests. There was a significant difference in the diameters of zones of inhibition produced by the test pathogens when subjected to the antibiotic metabolites from the selected actinomycetes (F = 6.6046 P = 0.001338).
Discussion: The minimum inhibitory concentration and minimum bactericidal concentration/minimum fungicidal concentration did not vary significantly (F=0.4503, P = 0.7187). The LC50 values of the antibiotic extracts varied from 2.438±0.47µg in PAN 9 to 9.3455±0.41µg in PAN 138. PAN 18 and PAN 117 showed partial hemolysis while PAN 9 and PAN 138 exhibited complete hemolysis of sheep blood erythrocytes. Soils from Menengai crater geothermal vents have actinomycetes that produce antibiotics. The antibiotics are cytotoxic to brine shrimps. In addition, the antibiotics cause hemolysis of sheep blood erythrocytes. There is a need to purify the antibiotics and structure elucidate them. The active antibiotic extract needs to be evaluated to determine whether the hemolysis is due to the compound itself or some other chemical constituent.