{"title":"铜绿假单胞菌临床样品生物膜形成的表型和分子研究。","authors":"Leila Dolatshah, Mohammad Tabatabaei","doi":"10.22099/mbrc.2021.41708.1673","DOIUrl":null,"url":null,"abstract":"<p><p><i>Pseudomonas aeruginosa</i> is identified as a versatile opportunistic microorganism with metabolic diversity contributing to a wide range of health burdens, especially in immunocompromised patients. This bacterium is the cause of 10 to 20% of nosocomial infections. In this study, we evaluated the phenotypic characterizations of biofilm formation in <i>P. aeruginosa</i> clinical isolates using micro-titer plate assay. Indeed, we estimated the prevalence of QS (<i>rhlI</i>, <i>rhlR</i>, <i>rhlAB</i>, <i>lasB</i>, <i>lasI</i>, <i>lasR, aprA</i>) and virulence genes (<i>pslA</i> and <i>cupA</i>) by PCR. The results showed that among 69% of the isolates forming biofilm, 9% were strong biofilm producers, whereas 13% and 47% of isolates produced moderate and low amounts of biofilm, respectively. All isolates possessed <i>cupA </i>and seven QS genes (<i>rhlI</i>, <i>rhlR</i>, <i>rhlAB</i>, <i>lasB</i>, <i>lasI</i>, <i>lasR</i>, <i>aprA</i>), while 92% of the isolates possessed the <i>pslA</i> gene. Identification of these genes and their association with biofilm formation can be advantageous in adopting therapeutic methods.</p>","PeriodicalId":19025,"journal":{"name":"Molecular Biology Research Communications","volume":null,"pages":null},"PeriodicalIF":1.5000,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798273/pdf/","citationCount":"0","resultStr":"{\"title\":\"A phenotypic and molecular investigation of biofilm formation in clinical samples of <i>Pseudomonas aeruginosa</i>.\",\"authors\":\"Leila Dolatshah, Mohammad Tabatabaei\",\"doi\":\"10.22099/mbrc.2021.41708.1673\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><i>Pseudomonas aeruginosa</i> is identified as a versatile opportunistic microorganism with metabolic diversity contributing to a wide range of health burdens, especially in immunocompromised patients. This bacterium is the cause of 10 to 20% of nosocomial infections. In this study, we evaluated the phenotypic characterizations of biofilm formation in <i>P. aeruginosa</i> clinical isolates using micro-titer plate assay. Indeed, we estimated the prevalence of QS (<i>rhlI</i>, <i>rhlR</i>, <i>rhlAB</i>, <i>lasB</i>, <i>lasI</i>, <i>lasR, aprA</i>) and virulence genes (<i>pslA</i> and <i>cupA</i>) by PCR. The results showed that among 69% of the isolates forming biofilm, 9% were strong biofilm producers, whereas 13% and 47% of isolates produced moderate and low amounts of biofilm, respectively. All isolates possessed <i>cupA </i>and seven QS genes (<i>rhlI</i>, <i>rhlR</i>, <i>rhlAB</i>, <i>lasB</i>, <i>lasI</i>, <i>lasR</i>, <i>aprA</i>), while 92% of the isolates possessed the <i>pslA</i> gene. Identification of these genes and their association with biofilm formation can be advantageous in adopting therapeutic methods.</p>\",\"PeriodicalId\":19025,\"journal\":{\"name\":\"Molecular Biology Research Communications\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2021-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798273/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular Biology Research Communications\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.22099/mbrc.2021.41708.1673\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Biology Research Communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22099/mbrc.2021.41708.1673","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
A phenotypic and molecular investigation of biofilm formation in clinical samples of Pseudomonas aeruginosa.
Pseudomonas aeruginosa is identified as a versatile opportunistic microorganism with metabolic diversity contributing to a wide range of health burdens, especially in immunocompromised patients. This bacterium is the cause of 10 to 20% of nosocomial infections. In this study, we evaluated the phenotypic characterizations of biofilm formation in P. aeruginosa clinical isolates using micro-titer plate assay. Indeed, we estimated the prevalence of QS (rhlI, rhlR, rhlAB, lasB, lasI, lasR, aprA) and virulence genes (pslA and cupA) by PCR. The results showed that among 69% of the isolates forming biofilm, 9% were strong biofilm producers, whereas 13% and 47% of isolates produced moderate and low amounts of biofilm, respectively. All isolates possessed cupA and seven QS genes (rhlI, rhlR, rhlAB, lasB, lasI, lasR, aprA), while 92% of the isolates possessed the pslA gene. Identification of these genes and their association with biofilm formation can be advantageous in adopting therapeutic methods.
期刊介绍:
“Molecular Biology Research Communications” (MBRC) is an international journal of Molecular Biology. It is published quarterly by Shiraz University (Iran). The MBRC is a fully peer-reviewed journal. The journal welcomes submission of Original articles, Short communications, Invited review articles, and Letters to the Editor which meets the general criteria of significance and scientific excellence in all fields of “Molecular Biology”.