CTX-M β-lactamases and associated integrons: their dissemination in Gram-negative bacteria
dc.contributor.advisor
Amyes, Sebastian
en
dc.contributor.advisor
Doherty, Catherine
en
dc.contributor.author
Dimude, Juachi
en
dc.date.accessioned
2015-11-16T14:40:34Z
dc.date.available
2015-11-16T14:40:34Z
dc.date.issued
2013-06-29
dc.description.abstract
Gram-negative bacteria are able to cause many infections including blood stream
infections (BSI).These bacteria may become resistant to antibiotics, often by
acquiring genes in the presence of antibiotic selection pressure. Multi drug resistant
Gram-negative bacteria have become an increasing problem worldwide. A study of
antibiotic resistance in Gram-negative bacteria isolated from blood cultures from
patients in the New Royal Infirmary of Edinburgh (NRIE) was performed. In addition,
a study was performed on isolates from patients in an intensive care unit in Egypt. All
isolates were investigated for susceptibility to an extensive range of antibiotics.
Gram-negative bacteria from Edinburgh found to be resistant to either cefotaxime or
ceftazidime were investigated further. Among the cefotaxime/ceftazidime resistant
isolates, Polymerase Chain Reaction (PCR) analysis revealed the presence of CTX-M-
β-lactamases. Seven E.coli isolates were found to have CTX-M-15 β-lactamases while
the CTX-M-14 β-lactamase was detected in six Enterobacter cloacae. The insertion
sequence ISEcp1 was detected upstream of the blaCTX-M-15 gene in some isolates while
IS26 was found truncating the ISEcp1 in other isolates. Conjugation experiments
found the blaCTX-M-15 gene was transferable to E. coli J62-2. All the isolates had
detectable plasmids, a plasmid ~260kb carried the blaCTX-M-15 gene. Analysis of the
-containing isolates by PFGE shows that those carrying the CTX-M-14
β-lactamase were identical indicating cross infection within the hospital. The CTX-M-
15 β-lactamase-containing isolates showed four isolates had ≥85% similarity but the
others were diverse. Class 1 integrons were found in eight of the CTX-M β-lactamase containing
isolates with the associated gene cassette and sul1 gene.
The isolates from Egypt were found to be resistant to carbapenem, which is the final
mainstream antibiotic option in the treatment of multidrug resistant Gram-negative
bacteria. Further analysis revealed all carried the CTX-M-14 β-lactamase and two
additionally carried the VIM-4 metallo β-lactamase, which accounted for the
resistance to the carbapenems. Furthermore, the insertion sequence ISEcp1 was found
upstream of the blaCTX-M-14 gene in two of the isolates. The blaVIM-4 gene was found to
be part of the gene cassette in the class 1 integron associate with complex ISCR1.
Two of the Egyptian isolates had a detectable plasmid, ~300kb in size, which carried
both blaCTX-M-14 and blaVIM-4 genes.
All the blood culture isolates were examined to ascertain the persistence of
sulphonamide resistance despite the long-term prescribing reduction on this
antibacterial. PCR was performed to detect sul1, sul2 and sul3 genes in all the
isolates. Of the sulphonamide resistant isolates 25 carried the sul1, 27 carried the sul2
and none carried the sul3 genes. Eight isolates had both the sul1 and sul2 genes. Most
of the isolates carried sul1 had Int1 as part of the same class 1 integron. Interestingly
three isolates were PCR negative for sul1 but positive for sul2 and int1. Int2 and 3
were found in 3 and 2 isolates respectively. The class 1 integron contained different
insert gene cassettes; dfrA (dfrA17, dfrA16, dfrA15), aadA (aadA5, aadA2, aadA1)
and blaOXA-1 families in addition to the resident sul gene.
In conclusion this thesis shows the diversity of the genetic environment and carriers
of the CTX-M β-lactamases within the same hospital. Sulphonamide resistance in
Gram-negatives persists despite the prescribing reduction of this antibacterial in a
Scottish hospital and the recommended constraint on the use of sulphonamide.
en
dc.identifier.uri
http://hdl.handle.net/1842/11729
dc.language.iso
en
dc.publisher
The University of Edinburgh
en
dc.relation.hasversion
Juachi u Dimude & S.G.B Amyes. Molecular diversity associated with the dissemination of CTX-M-15 β-lactamase gene in blood culture isolates of Escherichia coli from Edinburgh (2013).Scandinavian Journal of Infectious Diseases Vol 45 No 1 Pages 32 - 37.
en
dc.relation.hasversion
Juachi Dimude & SGB Amyes. Molecular characterisation of CTX-M β–lactamase among blood stream isolate of Enterobacteriaceae September (2011). Presented at SGM York conference. Abstract YO07/04
en
dc.relation.hasversion
Juachi Dimude & SGB Amyes. Characterisation of IncFIA, IncFIB, IncF11 and IncN plasmids carrying the CTX-M-15, TEM-1, OXA-1 β-lactamase genes and the acc (6’)-IB-cr gene in Escherichia coli (2012). Clinical Microbiology and Infection. Vol 18 Issue Supplementry 3 page 734 Abstract no R2459. 22nd ECCMID Conference London
en
dc.relation.hasversion
Juachi Dimude & SGB Amyes. Molecular characterization and diversity in Enterobacter cloacae from Edinburgh and Egypt carrying blaCTX-M-14 and blaVIM-4 β- lactamase genes (2013) International Journal of Antimicrobial Agent. Vol 41 Pages 574 - 577.
en
dc.subject
CTX-M
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dc.subject
integrons
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dc.subject
sul genes
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dc.title
CTX-M β-lactamases and associated integrons: their dissemination in Gram-negative bacteria
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dc.type
Thesis or Dissertation
en
dc.type.qualificationlevel
Doctoral
en
dc.type.qualificationname
PhD Doctor of Philosophy
en
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