{"title":"糖尿病创面相关大肠杆菌的研究多重耐药和尼日利亚西南部β -内酰胺酶生产的发生","authors":"I. Ibeh, O. Florence, Omorodion Nosa Tery","doi":"10.15406/oajs.2018.02.00109","DOIUrl":null,"url":null,"abstract":"The β-Lactam agents such as penicillins,2 cephalosporin’s, monobactams and carbapenems, are among the most frequently prescribed antibiotics worldwide. In Gram-negative pathogens, β-lactamases remain the most important contributing factor to β-lactam resistance,3 and their increasing prevalence as well as their alarming evolution seem to be directly linked to the clinical use of novel sub-classes of β-lactams.4 β-Lactamases are bacterial enzymes that inactivate β-lactam antibiotics by hydrolysis, which result in ineffective compounds.5 At least 400 different types of β-lactamases, originating from clinical isolates, have been described and a website has been created to monitor the latest developments among the newer types of b-lactamases.6 Several excellent reviews have recently been published describing the microbiology, characteristics, and structure, epidemiology and treatment options of organisms producing newer types of b-lactamases. This report does not aim to be comprehensive, but rather to illustrate that extended-spectrum b-lactamase-(ESBL) producing bacteria are emerging pathogens in the community, and that clinical laboratories play a critical role for their detection and control. Many genera of gram-negative bacteria possess a naturally occurring, chromosomally mediated β-lactamase. These enzymes are thought to have evolved from penicillin-binding proteins, with which they show some sequence homology. This development was likely due to the selective pressure exerted by β-lactam-producing soil organisms found in the environment.7 The first plasmid-mediated β-lactamase in gram-negatives, TEM-1, was described in the early 1960s.5 The TEM-1 enzyme was originally found in a single strain of E. coli isolated from a blood culture from a patient named Temoniera in Greece, hence the designation TEM.8,9 Being plasmid and transposon mediated has facilitated the spread of TEM-1 to other species of bacteria. Within a few years after its first isolation, the TEM1 β-lactamase spread worldwide and is now found in many different species of members of the family Enterobacteriaceae, Pseudomonas aeruginosa, Haemophilus influenzae, and Neisseria gonorrhoeae. Another common plasmid-mediated β-lactamase found in Klebsiella pneumoniae and E. coli is SHV-1 (for sulphurhydryl variable). The SHV-1 β-lactamase is chromosomally encoded in the majority of isolates of K. pneumoniae but is usually plasmid mediated in E. coli.10","PeriodicalId":19581,"journal":{"name":"Open Access Journal of Science","volume":"276 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-11-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Studies on Escherichia coli associated with diabetic wounds; multi drug resistance and the occurrence of beta lactamase production in south-western Nigeria\",\"authors\":\"I. Ibeh, O. Florence, Omorodion Nosa Tery\",\"doi\":\"10.15406/oajs.2018.02.00109\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The β-Lactam agents such as penicillins,2 cephalosporin’s, monobactams and carbapenems, are among the most frequently prescribed antibiotics worldwide. In Gram-negative pathogens, β-lactamases remain the most important contributing factor to β-lactam resistance,3 and their increasing prevalence as well as their alarming evolution seem to be directly linked to the clinical use of novel sub-classes of β-lactams.4 β-Lactamases are bacterial enzymes that inactivate β-lactam antibiotics by hydrolysis, which result in ineffective compounds.5 At least 400 different types of β-lactamases, originating from clinical isolates, have been described and a website has been created to monitor the latest developments among the newer types of b-lactamases.6 Several excellent reviews have recently been published describing the microbiology, characteristics, and structure, epidemiology and treatment options of organisms producing newer types of b-lactamases. This report does not aim to be comprehensive, but rather to illustrate that extended-spectrum b-lactamase-(ESBL) producing bacteria are emerging pathogens in the community, and that clinical laboratories play a critical role for their detection and control. Many genera of gram-negative bacteria possess a naturally occurring, chromosomally mediated β-lactamase. These enzymes are thought to have evolved from penicillin-binding proteins, with which they show some sequence homology. This development was likely due to the selective pressure exerted by β-lactam-producing soil organisms found in the environment.7 The first plasmid-mediated β-lactamase in gram-negatives, TEM-1, was described in the early 1960s.5 The TEM-1 enzyme was originally found in a single strain of E. coli isolated from a blood culture from a patient named Temoniera in Greece, hence the designation TEM.8,9 Being plasmid and transposon mediated has facilitated the spread of TEM-1 to other species of bacteria. Within a few years after its first isolation, the TEM1 β-lactamase spread worldwide and is now found in many different species of members of the family Enterobacteriaceae, Pseudomonas aeruginosa, Haemophilus influenzae, and Neisseria gonorrhoeae. Another common plasmid-mediated β-lactamase found in Klebsiella pneumoniae and E. coli is SHV-1 (for sulphurhydryl variable). The SHV-1 β-lactamase is chromosomally encoded in the majority of isolates of K. pneumoniae but is usually plasmid mediated in E. coli.10\",\"PeriodicalId\":19581,\"journal\":{\"name\":\"Open Access Journal of Science\",\"volume\":\"276 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-11-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Open Access Journal of Science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15406/oajs.2018.02.00109\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Open Access Journal of Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15406/oajs.2018.02.00109","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Studies on Escherichia coli associated with diabetic wounds; multi drug resistance and the occurrence of beta lactamase production in south-western Nigeria
The β-Lactam agents such as penicillins,2 cephalosporin’s, monobactams and carbapenems, are among the most frequently prescribed antibiotics worldwide. In Gram-negative pathogens, β-lactamases remain the most important contributing factor to β-lactam resistance,3 and their increasing prevalence as well as their alarming evolution seem to be directly linked to the clinical use of novel sub-classes of β-lactams.4 β-Lactamases are bacterial enzymes that inactivate β-lactam antibiotics by hydrolysis, which result in ineffective compounds.5 At least 400 different types of β-lactamases, originating from clinical isolates, have been described and a website has been created to monitor the latest developments among the newer types of b-lactamases.6 Several excellent reviews have recently been published describing the microbiology, characteristics, and structure, epidemiology and treatment options of organisms producing newer types of b-lactamases. This report does not aim to be comprehensive, but rather to illustrate that extended-spectrum b-lactamase-(ESBL) producing bacteria are emerging pathogens in the community, and that clinical laboratories play a critical role for their detection and control. Many genera of gram-negative bacteria possess a naturally occurring, chromosomally mediated β-lactamase. These enzymes are thought to have evolved from penicillin-binding proteins, with which they show some sequence homology. This development was likely due to the selective pressure exerted by β-lactam-producing soil organisms found in the environment.7 The first plasmid-mediated β-lactamase in gram-negatives, TEM-1, was described in the early 1960s.5 The TEM-1 enzyme was originally found in a single strain of E. coli isolated from a blood culture from a patient named Temoniera in Greece, hence the designation TEM.8,9 Being plasmid and transposon mediated has facilitated the spread of TEM-1 to other species of bacteria. Within a few years after its first isolation, the TEM1 β-lactamase spread worldwide and is now found in many different species of members of the family Enterobacteriaceae, Pseudomonas aeruginosa, Haemophilus influenzae, and Neisseria gonorrhoeae. Another common plasmid-mediated β-lactamase found in Klebsiella pneumoniae and E. coli is SHV-1 (for sulphurhydryl variable). The SHV-1 β-lactamase is chromosomally encoded in the majority of isolates of K. pneumoniae but is usually plasmid mediated in E. coli.10