Arun Thangave, C. Rajamanickam, O. Sahu, S. Ponnappan, Gezahegn Abawa, Abenezer Tadele
{"title":"耐甲氧西林凝固酶阴性葡萄球菌mecA基因的分子检测","authors":"Arun Thangave, C. Rajamanickam, O. Sahu, S. Ponnappan, Gezahegn Abawa, Abenezer Tadele","doi":"10.24896/JMBR.2017723","DOIUrl":null,"url":null,"abstract":"In the present research, a total of 27 Wound swab samples were collected for the isolation of Methicillin Resistant-Coagulase Negative Staphylococci. Out of these, 3.7% of the samples have been shown the presence of Methicillin Resistant-CoagulaseNegative Staphylococci (MR-CoNS). The preliminary coagulase activity has been identified by Coagulase slide and tube method. The HiCrome MeReSa agar medium has been used for the preliminary identification of Methicillin resistance. During the isolation, the other strains of Coagulase Negative Staphylococci (29.6%), Methicillin Sensitive Staphylococcus aureus (44.4%) have been also isolated. 6 samples (22.2%) were sterile. The genomic DNA was isolated from Methicillin resistant Coagulase Negative Staphylococciand other species of Staphylococcithrough Modified DNA extraction method. The isolated DNA was amplified through the thermal cycler using suitable forwardand reverse oligonucleotide primers, for the amplification of 527bp of mecA gene. The amplified DNA product has been identified by agarose gel electrophoresis using suitable 100bp ladder marker.","PeriodicalId":16482,"journal":{"name":"Journal of Microbiology and Biotechnology Research","volume":"4 1","pages":"11-16"},"PeriodicalIF":0.0000,"publicationDate":"2017-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Molecular detection of mecA gene from Methicillin Resistant Coagulase Negative Staphylococci\",\"authors\":\"Arun Thangave, C. Rajamanickam, O. Sahu, S. Ponnappan, Gezahegn Abawa, Abenezer Tadele\",\"doi\":\"10.24896/JMBR.2017723\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In the present research, a total of 27 Wound swab samples were collected for the isolation of Methicillin Resistant-Coagulase Negative Staphylococci. Out of these, 3.7% of the samples have been shown the presence of Methicillin Resistant-CoagulaseNegative Staphylococci (MR-CoNS). The preliminary coagulase activity has been identified by Coagulase slide and tube method. The HiCrome MeReSa agar medium has been used for the preliminary identification of Methicillin resistance. During the isolation, the other strains of Coagulase Negative Staphylococci (29.6%), Methicillin Sensitive Staphylococcus aureus (44.4%) have been also isolated. 6 samples (22.2%) were sterile. The genomic DNA was isolated from Methicillin resistant Coagulase Negative Staphylococciand other species of Staphylococcithrough Modified DNA extraction method. The isolated DNA was amplified through the thermal cycler using suitable forwardand reverse oligonucleotide primers, for the amplification of 527bp of mecA gene. The amplified DNA product has been identified by agarose gel electrophoresis using suitable 100bp ladder marker.\",\"PeriodicalId\":16482,\"journal\":{\"name\":\"Journal of Microbiology and Biotechnology Research\",\"volume\":\"4 1\",\"pages\":\"11-16\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-05-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Microbiology and Biotechnology Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.24896/JMBR.2017723\",\"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 Microbiology and Biotechnology Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.24896/JMBR.2017723","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Molecular detection of mecA gene from Methicillin Resistant Coagulase Negative Staphylococci
In the present research, a total of 27 Wound swab samples were collected for the isolation of Methicillin Resistant-Coagulase Negative Staphylococci. Out of these, 3.7% of the samples have been shown the presence of Methicillin Resistant-CoagulaseNegative Staphylococci (MR-CoNS). The preliminary coagulase activity has been identified by Coagulase slide and tube method. The HiCrome MeReSa agar medium has been used for the preliminary identification of Methicillin resistance. During the isolation, the other strains of Coagulase Negative Staphylococci (29.6%), Methicillin Sensitive Staphylococcus aureus (44.4%) have been also isolated. 6 samples (22.2%) were sterile. The genomic DNA was isolated from Methicillin resistant Coagulase Negative Staphylococciand other species of Staphylococcithrough Modified DNA extraction method. The isolated DNA was amplified through the thermal cycler using suitable forwardand reverse oligonucleotide primers, for the amplification of 527bp of mecA gene. The amplified DNA product has been identified by agarose gel electrophoresis using suitable 100bp ladder marker.