Meerabai Manoharan, Ajit Ramesh Sawant, K Prashanth, Sujatha Sistla
{"title":"全基因组测序检测溶血葡萄球菌耐利奈唑胺多种机制。","authors":"Meerabai Manoharan, Ajit Ramesh Sawant, K Prashanth, Sujatha Sistla","doi":"10.1099/jmm.0.001737","DOIUrl":null,"url":null,"abstract":"<p><p><b>Introduction.</b> Linezolid is an effective therapeutic option for treating severe infections caused by multidrug-resistant Gram-positive organisms. Several mechanisms have been reported to be responsible for resistance to this antibiotic.<b>Hypothesis or Gap Statement.</b> Although several mechanisms of linezolid resistance have been reported in <i>Staphylococcus haemolyticus</i>, the prevalence and potential for horizontal transfer of resistance genes have not been fully characterized, particularly among <i>S. haemolyticus</i> isolates from India.<b>Aim.</b> To perform whole-genome sequencing (WGS) of linezolid-resistant <i>S. haemolyticus</i> isolates to characterize the resistance mechanisms.<b>Methodology.</b> WGS was performed for 16 linezolid-resistant <i>S. haemolyticus</i> isolates to check for the presence of <i>cfr</i>, <i>optrA</i> and <i>poxtA</i> genes and mutations in 23S rRNA and ribosomal proteins (L3, L4 and L22) that are possible mechanisms implicated in linezolid resistance. Sequence types were identified using MLST finder. The minimum inhibitory concentration (MIC) of linezolid was determined using the E-test method. Polymerase chain reaction (PCR) was carried out for the detection of the <i>cfr</i> gene.<b>Results.</b> The study documented three different mechanisms of linezolid resistance in <i>S. haemolyticus</i>. Thirteen of the 16 isolates were phenotypically resistant to linezolid, of which 12 were positive for the <i>cfr</i> gene. The G2603T mutation in 23S rRNA was found in the majority of the isolates (<i>n</i>=13). Ten isolates had the R138V mutation in L3 ribosomal protein. Twelve isolates with the <i>cfr</i> gene in combination with either G2603T or R138V mutations displayed extremely high MIC values. Surprisingly, three phenotypically sensitive isolates were found to be positive for the <i>cfr</i> gene but negative for other resistance mechanisms. Importantly, in almost half of the isolates the <i>cfr</i> gene was present on a plasmid. ST3 and ST1 were found to be the predominant sequence types.<b>Conclusion.</b> All phenotypically resistant isolates exhibited two or three linezolid resistance mechanisms. The <i>cfr</i> gene was found on plasmids in many isolates, demonstrating its potential for horizontal transfer to more pathogenic organisms.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":"72 7","pages":""},"PeriodicalIF":4.6000,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Multiple mechanisms of linezolid resistance in <i>Staphylococcus haemolyticus</i> detected by whole-genome sequencing.\",\"authors\":\"Meerabai Manoharan, Ajit Ramesh Sawant, K Prashanth, Sujatha Sistla\",\"doi\":\"10.1099/jmm.0.001737\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Introduction.</b> Linezolid is an effective therapeutic option for treating severe infections caused by multidrug-resistant Gram-positive organisms. Several mechanisms have been reported to be responsible for resistance to this antibiotic.<b>Hypothesis or Gap Statement.</b> Although several mechanisms of linezolid resistance have been reported in <i>Staphylococcus haemolyticus</i>, the prevalence and potential for horizontal transfer of resistance genes have not been fully characterized, particularly among <i>S. haemolyticus</i> isolates from India.<b>Aim.</b> To perform whole-genome sequencing (WGS) of linezolid-resistant <i>S. haemolyticus</i> isolates to characterize the resistance mechanisms.<b>Methodology.</b> WGS was performed for 16 linezolid-resistant <i>S. haemolyticus</i> isolates to check for the presence of <i>cfr</i>, <i>optrA</i> and <i>poxtA</i> genes and mutations in 23S rRNA and ribosomal proteins (L3, L4 and L22) that are possible mechanisms implicated in linezolid resistance. Sequence types were identified using MLST finder. The minimum inhibitory concentration (MIC) of linezolid was determined using the E-test method. Polymerase chain reaction (PCR) was carried out for the detection of the <i>cfr</i> gene.<b>Results.</b> The study documented three different mechanisms of linezolid resistance in <i>S. haemolyticus</i>. Thirteen of the 16 isolates were phenotypically resistant to linezolid, of which 12 were positive for the <i>cfr</i> gene. The G2603T mutation in 23S rRNA was found in the majority of the isolates (<i>n</i>=13). Ten isolates had the R138V mutation in L3 ribosomal protein. Twelve isolates with the <i>cfr</i> gene in combination with either G2603T or R138V mutations displayed extremely high MIC values. Surprisingly, three phenotypically sensitive isolates were found to be positive for the <i>cfr</i> gene but negative for other resistance mechanisms. Importantly, in almost half of the isolates the <i>cfr</i> gene was present on a plasmid. ST3 and ST1 were found to be the predominant sequence types.<b>Conclusion.</b> All phenotypically resistant isolates exhibited two or three linezolid resistance mechanisms. The <i>cfr</i> gene was found on plasmids in many isolates, demonstrating its potential for horizontal transfer to more pathogenic organisms.</p>\",\"PeriodicalId\":2,\"journal\":{\"name\":\"ACS Applied Bio Materials\",\"volume\":\"72 7\",\"pages\":\"\"},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2023-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Bio Materials\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1099/jmm.0.001737\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1099/jmm.0.001737","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
Multiple mechanisms of linezolid resistance in Staphylococcus haemolyticus detected by whole-genome sequencing.
Introduction. Linezolid is an effective therapeutic option for treating severe infections caused by multidrug-resistant Gram-positive organisms. Several mechanisms have been reported to be responsible for resistance to this antibiotic.Hypothesis or Gap Statement. Although several mechanisms of linezolid resistance have been reported in Staphylococcus haemolyticus, the prevalence and potential for horizontal transfer of resistance genes have not been fully characterized, particularly among S. haemolyticus isolates from India.Aim. To perform whole-genome sequencing (WGS) of linezolid-resistant S. haemolyticus isolates to characterize the resistance mechanisms.Methodology. WGS was performed for 16 linezolid-resistant S. haemolyticus isolates to check for the presence of cfr, optrA and poxtA genes and mutations in 23S rRNA and ribosomal proteins (L3, L4 and L22) that are possible mechanisms implicated in linezolid resistance. Sequence types were identified using MLST finder. The minimum inhibitory concentration (MIC) of linezolid was determined using the E-test method. Polymerase chain reaction (PCR) was carried out for the detection of the cfr gene.Results. The study documented three different mechanisms of linezolid resistance in S. haemolyticus. Thirteen of the 16 isolates were phenotypically resistant to linezolid, of which 12 were positive for the cfr gene. The G2603T mutation in 23S rRNA was found in the majority of the isolates (n=13). Ten isolates had the R138V mutation in L3 ribosomal protein. Twelve isolates with the cfr gene in combination with either G2603T or R138V mutations displayed extremely high MIC values. Surprisingly, three phenotypically sensitive isolates were found to be positive for the cfr gene but negative for other resistance mechanisms. Importantly, in almost half of the isolates the cfr gene was present on a plasmid. ST3 and ST1 were found to be the predominant sequence types.Conclusion. All phenotypically resistant isolates exhibited two or three linezolid resistance mechanisms. The cfr gene was found on plasmids in many isolates, demonstrating its potential for horizontal transfer to more pathogenic organisms.