dc.contributor.author |
Ahmed Mohammed, Ahmed |
|
dc.contributor.author |
Mohammed, Hitham |
|
dc.contributor.author |
Saeed Mohammed, Saeed Abdelgadir |
|
dc.contributor.author |
Musa, Ahmed |
|
dc.date.accessioned |
2019-04-24T15:07:36Z |
|
dc.date.available |
2019-04-24T15:07:36Z |
|
dc.date.issued |
2019-03 |
|
dc.identifier.issn |
2589-8698 |
|
dc.identifier.issn |
2589-868X |
|
dc.identifier.uri |
http://hdl.handle.net/123456789/611 |
|
dc.description |
Background: Extended spectrum β-lactamase (ESBL)-producing Escherichia coli (ESBL-EC) constitute an emerging public-health concern. Consider that ESBL genes type CTX-M types has been increased significantly in most parts of the world. Few data are available on the CTX-M variants circulating in Sudan. Objective: This study used polymerase chain reaction (PCR) and bioinformatics tools to identify blaCTX-M and its variants for Extended-spectrum β-lactamase (ESBLs) producing clinical isolates of Escherichia coli (E. coli) obtained from hospitals in Khartoum-Sudan. Methods: A total of 216 nonrepetitive isolates were selected during 2007-2018. The phenotypic identification of ESBL production was confirmed according to CLSI guidelines. CTX-M genotype was analyzed by uniplex PCRs reactions subsequently sequences performed later sequences were analyzed using bioinformatics tools with nBLAST program, multiple alignments to determine CTX-M genotype variants . Nucleotide sequences were submitted to Gen Bank and accession numbers were obtained. Result: ESBL phenotype among 212 confirmed E.coli isolates was (34.9% of 212,n=74). (62.2% of 74, n=46) strains carried bla CTXM genes, CTX-M genotype variants identified in this study as followed: blaCTX-M-15 gene was the most prevalent one (78.6%) followed by blaCTX 90 (14.3%) and CTX-M55 (7.1%), Conclusion: This study reveled high ESBL occurrence among E.coli isolates, with CTX-M 15 the predominant variants and highlights the incidence of CTX-M-55 for the first time from Sudan. |
en_US |
dc.description.abstract |
Background: Extended spectrum β-lactamase (ESBL)-producing Escherichia coli (ESBL-EC) constitute an emerging public-health concern. Consider that ESBL genes type CTX-M types has been increased significantly in most parts of the world. Few data are available on the CTX-M variants circulating in Sudan. Objective: This study used polymerase chain reaction (PCR) and bioinformatics tools to identify blaCTX-M and its variants for Extended-spectrum β-lactamase (ESBLs) producing clinical isolates of Escherichia coli (E. coli) obtained from hospitals in Khartoum-Sudan. Methods: A total of 216 nonrepetitive isolates were selected during 2007-2018. The phenotypic identification of ESBL production was confirmed according to CLSI guidelines. CTX-M genotype was analyzed by uniplex PCRs reactions subsequently sequences performed later sequences were analyzed using bioinformatics tools with nBLAST program, multiple alignments to determine CTX-M genotype variants . Nucleotide sequences were submitted to Gen Bank and accession numbers were obtained. Result: ESBL phenotype among 212 confirmed E.coli isolates was (34.9% of 212,n=74). (62.2% of 74, n=46) strains carried bla CTXM genes, CTX-M genotype variants identified in this study as followed: blaCTX-M-15 gene was the most prevalent one (78.6%) followed by blaCTX 90 (14.3%) and CTX-M55 (7.1%), Conclusion: This study reveled high ESBL occurrence among E.coli isolates, with CTX-M 15 the predominant variants and highlights the incidence of CTX-M-55 for the first time from Sudan. |
en_US |
dc.language.iso |
en_US |
en_US |
dc.publisher |
International Journal of Medical and Biomedical Studies |
en_US |
dc.relation.ispartofseries |
Volume 3, Issue 3;;March: 2019; Page No.146-157 |
|
dc.subject |
E. coli |
en_US |
dc.subject |
PCR |
en_US |
dc.subject |
ESBLs |
en_US |
dc.subject |
CTX-M |
en_US |
dc.subject |
bioinformatics |
en_US |
dc.subject |
Sudan |
en_US |
dc.title |
CTX-M Β-LACTAMASE–PRODUCING ESCHERICHIA COLI IN SUDAN TERTIARY HOSPITALS: DETECTION GENOTYPES VARIANTS AND BIOINFORMATICS ANALYSIS |
en_US |
dc.type |
Article |
en_US |