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Molecular characterization of extended-spectrum beta lactamase (ESBL) producing klebsiella pneumoniae and escherichia coli among hospitalized patients in Oman
Hospital-acquired infections due to ESBL-producing gram-negative rods are a worldwide healthcare problem causing substantial patient morbidity and mortality. In the Middle East, a significant increase in incidence and prevalence has been reported recently due to the misuse of antibiotics and lack o...
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2011
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| access_status_str | Open Access |
| author | Mourad, Lobna |
| author_browse | Mourad, Lobna |
| author_facet | Mourad, Lobna |
| author_sort | Mourad, Lobna |
| collection | Thesis |
| dc_rights_str_mv | The author retains all rights with regard to copyright. The author certifies that written permission from the owner(s) of third-party copyrighted matter included in the thesis, dissertation, paper, or record of study has been obtained. The author further certifies that IRB approval has been obtained for this thesis, or that IRB approval is not necessary for this thesis. Insofar as this thesis, dissertation, paper, or record of study is an educational record as defined in the Family Educational Rights and Privacy Act (FERPA) (20 USC 1232g), the author has granted consent to disclosure of it to anyone who requests a copy. |
| description | Hospital-acquired infections due to ESBL-producing gram-negative rods are a worldwide healthcare problem causing substantial patient morbidity and mortality. In the Middle East, a significant increase in incidence and prevalence has been reported recently due to the misuse of antibiotics and lack of coherent antimicrobial resistance (AR) surveillance programs. The aim of the study was to determine the level of genotypic diversity and mechanism of AR of E. coli and K. pneumoniae ESBL-producing isolates from nosocomial infections among patients in Oman. 35 E. coli and 14 K. pneumoniae isolates were used in the study. Antibiotic susceptibility testing (AST) and ESBL screening was conducted via disk diffusion and E-test following CLSI (Clinical and Laboratory Standards Institute) guidelines. ESBL producers were screened for blaCTX-M, blaSHV, blaOXA, and blaTEM resistance markers via PCR. All PCR amplicons were sequenced to determine their allelic variants. In order to demonstrate overall genotypic diversity, Pulsed-Field Gel Electrophoresis (PFGE) analyses were done separately for all E. coli and K. pneumoniae isolates. 40 (80%) isolates were determined to be ESBL producing bacteria (27 E. coli and 13 K. pneumoniae). The highest level of AR (>70%) was against tetracycline, ampicillin, nalidixic acid, cephalothin, and cefpodoxime. The lowest level of AR was against chloramphenicol, amikacin and ticarcillin-clavulanic acid. Resistance against imipenem was not detected. Similarity of K. pneumoniae isolates ranged from 61% to 100%. Three K. pneumoniae clusters (n= 7; 58%) had â ¥ 80% similarity suggesting high level of similarity. E. coli PFGE analyses showed an overall similarity of 64% with 4 clusters (n= 14; 54%) showing 80% similarity. No correlation was demonstrated between the AR pattern and genotypic similarity for either species. Percentages of isolates with genetic markers for blaCTX-M, blaSHV, blaTEM, and blaOXA were 73%, 24%, 68%, and 60% respectively. DNA sequencing analyses revealed that the most common AR mechanism in these ESBL isolates is due to blaCTX-M-15 marker. In addition, SHV-1, SHV-11, SHV-12, TEM-1, and OXA-1 contribute to the overall AR mechanisms in nosocomial ESBL isolates from Oman. This is the first study characterizing the AR mechanism of ESBL's isolates from hospital-acquired infections in Oman. The results showed that hospital-acquired E. coli isolates from Oman are more diverse than K. pneumoniae. The blaCTX-M-15 is the most abundant mechanism conferring ESBL phenotype on E. coli and K. pneumoniae, while the ESBL-SHV-type was the least abundant. |
| format | Thesis |
| id | oai:fount.aucegypt.edu:etds-2186 |
| institution | American University in Cairo (Egypt) |
| last_indexed | 2026-06-10T12:35:47.730Z |
| license_str | Other — see source repository |
| provenance_str_mv | Harvested via OAI-PMH from AUC Knowledge Fountain — bepress |
| publishDate | 2011 |
| publishDateRange | 2011 |
| publishDateSort | 2011 |
| publisher | AUC Knowledge Fountain |
| publisherStr | AUC Knowledge Fountain |
| record_format | dspace |
| source_str | AUC Knowledge Fountain — bepress |
| spelling | oai:fount.aucegypt.edu:etds-2186 Molecular characterization of extended-spectrum beta lactamase (ESBL) producing klebsiella pneumoniae and escherichia coli among hospitalized patients in Oman Mourad, Lobna Hospital-acquired infections due to ESBL-producing gram-negative rods are a worldwide healthcare problem causing substantial patient morbidity and mortality. In the Middle East, a significant increase in incidence and prevalence has been reported recently due to the misuse of antibiotics and lack of coherent antimicrobial resistance (AR) surveillance programs. The aim of the study was to determine the level of genotypic diversity and mechanism of AR of E. coli and K. pneumoniae ESBL-producing isolates from nosocomial infections among patients in Oman. 35 E. coli and 14 K. pneumoniae isolates were used in the study. Antibiotic susceptibility testing (AST) and ESBL screening was conducted via disk diffusion and E-test following CLSI (Clinical and Laboratory Standards Institute) guidelines. ESBL producers were screened for blaCTX-M, blaSHV, blaOXA, and blaTEM resistance markers via PCR. All PCR amplicons were sequenced to determine their allelic variants. In order to demonstrate overall genotypic diversity, Pulsed-Field Gel Electrophoresis (PFGE) analyses were done separately for all E. coli and K. pneumoniae isolates. 40 (80%) isolates were determined to be ESBL producing bacteria (27 E. coli and 13 K. pneumoniae). The highest level of AR (>70%) was against tetracycline, ampicillin, nalidixic acid, cephalothin, and cefpodoxime. The lowest level of AR was against chloramphenicol, amikacin and ticarcillin-clavulanic acid. Resistance against imipenem was not detected. Similarity of K. pneumoniae isolates ranged from 61% to 100%. Three K. pneumoniae clusters (n= 7; 58%) had â ¥ 80% similarity suggesting high level of similarity. E. coli PFGE analyses showed an overall similarity of 64% with 4 clusters (n= 14; 54%) showing 80% similarity. No correlation was demonstrated between the AR pattern and genotypic similarity for either species. Percentages of isolates with genetic markers for blaCTX-M, blaSHV, blaTEM, and blaOXA were 73%, 24%, 68%, and 60% respectively. DNA sequencing analyses revealed that the most common AR mechanism in these ESBL isolates is due to blaCTX-M-15 marker. In addition, SHV-1, SHV-11, SHV-12, TEM-1, and OXA-1 contribute to the overall AR mechanisms in nosocomial ESBL isolates from Oman. This is the first study characterizing the AR mechanism of ESBL's isolates from hospital-acquired infections in Oman. The results showed that hospital-acquired E. coli isolates from Oman are more diverse than K. pneumoniae. The blaCTX-M-15 is the most abundant mechanism conferring ESBL phenotype on E. coli and K. pneumoniae, while the ESBL-SHV-type was the least abundant. 2011-02-01T08:00:00Z thesis application/pdf https://fount.aucegypt.edu/etds/1187 https://fount.aucegypt.edu/context/etds/article/2186/viewcontent/FINAL_20MS_20Thesis_20__20Lobna.pdf The author retains all rights with regard to copyright. The author certifies that written permission from the owner(s) of third-party copyrighted matter included in the thesis, dissertation, paper, or record of study has been obtained. The author further certifies that IRB approval has been obtained for this thesis, or that IRB approval is not necessary for this thesis. Insofar as this thesis, dissertation, paper, or record of study is an educational record as defined in the Family Educational Rights and Privacy Act (FERPA) (20 USC 1232g), the author has granted consent to disclosure of it to anyone who requests a copy. Theses and Dissertations AUC Knowledge Fountain |
| spellingShingle | Mourad, Lobna Molecular characterization of extended-spectrum beta lactamase (ESBL) producing klebsiella pneumoniae and escherichia coli among hospitalized patients in Oman |
| title | Molecular characterization of extended-spectrum beta lactamase (ESBL) producing klebsiella pneumoniae and escherichia coli among hospitalized patients in Oman |
| title_full | Molecular characterization of extended-spectrum beta lactamase (ESBL) producing klebsiella pneumoniae and escherichia coli among hospitalized patients in Oman |
| title_fullStr | Molecular characterization of extended-spectrum beta lactamase (ESBL) producing klebsiella pneumoniae and escherichia coli among hospitalized patients in Oman |
| title_full_unstemmed | Molecular characterization of extended-spectrum beta lactamase (ESBL) producing klebsiella pneumoniae and escherichia coli among hospitalized patients in Oman |
| title_short | Molecular characterization of extended-spectrum beta lactamase (ESBL) producing klebsiella pneumoniae and escherichia coli among hospitalized patients in Oman |
| title_sort | molecular characterization of extended spectrum beta lactamase esbl producing klebsiella pneumoniae and escherichia coli among hospitalized patients in oman |
| url | https://fount.aucegypt.edu/etds/1187 https://fount.aucegypt.edu/context/etds/article/2186/viewcontent/FINAL_20MS_20Thesis_20__20Lobna.pdf |
| work_keys_str_mv | AT mouradlobna molecularcharacterizationofextendedspectrumbetalactamaseesblproducingklebsiellapneumoniaeandescherichiacoliamonghospitalizedpatientsinoman |