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An investigation of carbapenemase-encoding genes in Burkholderia cepacia and Aeromonas sobria nosocomial infections among Iraqi patients
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Abstract
Burkholderia cepacia
and
Aeromonas sobria
are difficult to eradicate due to their innate resistance to a variety of medications, and cause various diseases. The aim of this study was to investigate the occurrence of carbapenemase genes and patterns of antibiotic resistance in isolates of
B. cepacia
and
A. sobria.
A cross-sectional study was conducted in the Ramadi Teaching Hospitals in the Al-Anbar Governorate in 2024. Various study samples, were used to collect the studied bacteria. The antibiotic resistance was detected by the VITEK®2 System. The presence of carbapenemase genes was confirmed via PCR technique. In this investigation, seventy-five (75) isolates of
A. sobria
and
B. cepacia
were assessed. Of these,
A. sobria
made up 16.6% (n = 20) while
B. cepacia
accounted for 45.8% (n = 55). The study isolates showed highest antimicrobial resistance to piperacillin, cefepime, ceftriaxone (100%), ceftazidime (97.3%), and lowest antimicrobial resistance to imipenem (36%). The result showed 55/57
recA
gene positive for differentiated
B. cepacia complex
from other Burkholderia spp. The overall prevalence of carbapenemase genes was 92.8%% (52/56) with
bla
KPC
accounting for 80.8% (42/52) and
bla
GES
for 19.2% (10/52) of the total. The 42
B. cepacia
isolates that tested positive for carbapenem resistance were constituted of 38
bla
KPC
(n = 38) and two
bla
GES
(n = 2); in contrast, four
bla
KPC
(n = 4) and eight
bla
GES
(n = 8) were present in the
A. sobria
isolates that tested positive for carbapenems resistance. None of isolates studied tested positive for the
bla
IMP
gene. The recent study concluded that
recA
gene identification was more sensitive and specific technique for detection
B. cepacia complex
isolates. There was a notable predominance of
bla
KPC
and
bla
GES
carbapenemase producers among the isolates under investigation. The
bla
IMP
gene was not found in any of the research isolates.
Title: An investigation of carbapenemase-encoding genes in
Burkholderia cepacia
and
Aeromonas sobria
nosocomial infections among Iraqi patients
Description:
Abstract
Burkholderia cepacia
and
Aeromonas sobria
are difficult to eradicate due to their innate resistance to a variety of medications, and cause various diseases.
The aim of this study was to investigate the occurrence of carbapenemase genes and patterns of antibiotic resistance in isolates of
B.
cepacia
and
A.
sobria.
A cross-sectional study was conducted in the Ramadi Teaching Hospitals in the Al-Anbar Governorate in 2024.
Various study samples, were used to collect the studied bacteria.
The antibiotic resistance was detected by the VITEK®2 System.
The presence of carbapenemase genes was confirmed via PCR technique.
In this investigation, seventy-five (75) isolates of
A.
sobria
and
B.
cepacia
were assessed.
Of these,
A.
sobria
made up 16.
6% (n = 20) while
B.
cepacia
accounted for 45.
8% (n = 55).
The study isolates showed highest antimicrobial resistance to piperacillin, cefepime, ceftriaxone (100%), ceftazidime (97.
3%), and lowest antimicrobial resistance to imipenem (36%).
The result showed 55/57
recA
gene positive for differentiated
B.
cepacia complex
from other Burkholderia spp.
The overall prevalence of carbapenemase genes was 92.
8%% (52/56) with
bla
KPC
accounting for 80.
8% (42/52) and
bla
GES
for 19.
2% (10/52) of the total.
The 42
B.
cepacia
isolates that tested positive for carbapenem resistance were constituted of 38
bla
KPC
(n = 38) and two
bla
GES
(n = 2); in contrast, four
bla
KPC
(n = 4) and eight
bla
GES
(n = 8) were present in the
A.
sobria
isolates that tested positive for carbapenems resistance.
None of isolates studied tested positive for the
bla
IMP
gene.
The recent study concluded that
recA
gene identification was more sensitive and specific technique for detection
B.
cepacia complex
isolates.
There was a notable predominance of
bla
KPC
and
bla
GES
carbapenemase producers among the isolates under investigation.
The
bla
IMP
gene was not found in any of the research isolates.
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