6 research outputs found
Detection of efflux pump activity among clinical isolates of Staphylococcus and Micrococcus species
Purpose: To detect efflux pump activity (EPA) and screening a suspected efflux pump inhibitor (EPI) [1- (3-(trifluoromethyl)benzyl]-piperazine (TFMBP)], which could help in reducing multi-drug resistance (MDR).Methods: Eighteen isolates, viz, 14 S. aureus, 2 S. lentus, 1 S. xylosus and 1 Micrococcus species from various hospital infections of admitted patients were screened for antibiotics susceptibility to 11 classes of antibiotics including oxacillin and β-lactamase production. Efflux pump activity (EPA) was determined by minimum inhibitory concentration (MIC) technique in the presence and absence of TFMBP, the isolates were also screened for MDR genes.Results: All the isolates were resistant to ampicillin (10 μg) and penicillin (10 μg), but sensitive to bacitracin (10 μg). Majority of the isolates were MDR 12/18 (66.7 %), 10 (55.6 %) were inducible β- lactamase producers and 3 (16.7 %) were intrinsic β-lactamase producers. Seven (38.9 %) were resistant to oxacillin and also produced carbapenemase enzyme. Eight (66.7 %) of the 12 MDR isolates gave evidence of EPA with TFMBP. However, no MDR genes were detected.Conclusion: Staphylococcus and Micrococcus species exhibit EPA in antibiotic resistance while a suitable EPI such as TFMBP when combined with specific antibiotics could help combat this menace.Keywords: [1-(3-(Trifluoromethyl)benzyl]-piperazine, Efflux pump activity, Oxacillin resistant S. aureus, Multidrug resistant, Carbapenemas
Molecular Characterization of the Circulating Strains of Vibrio cholerae during 2010 Cholera Outbreak in Nigeria
This study aimed at characterizing the phenotypic and toxigenic status
of circulating strains of cholera during outbreaks in Nigeria,
employing molecular typing techniques. Two hundred and one samples of
rectal swabs, stool, vomitus, water (from the well, borehole, sachet,
stream, and tap) and disinfectants (sodium hypochlorite) were collected
from three states in the country. The samples were inoculated on
thiosulphate-citrate bile salt-sucrose (TCBS), Cary-Blair transport
medium and smeared on glass slides for direct examination. The Vibrio
cholerae isolates were serotyped, biotyped, and characterized using
PCR of the cytotoxin gene A (ctxA), wbeO1, and wbfO139 gene primer. Of
the 201 samples screened, 96 were positive for V. cholerae O1 (48%),
with 69 (72%) positive for ctxA gene. The results from this study
showed that the circulating strains of cholera in Nigeria were of Ogawa
serotype, also observed in other outbreaks in Nigeria (1991, 1992, and
1996). However, the strains were of the Classical biotype and were
mainly (72%) ctxA gene-positive. This current investigation has
confirmed the production of cholera toxin by the circulating strains,
and this could be harnessed for possible cholera vaccine production in
Nigeria
Molecular Characterization of the Circulating Strains of Vibrio cholerae during 2010 Cholera Outbreak in Nigeria
This study aimed at characterizing the phenotypic and toxigenic status
of circulating strains of cholera during outbreaks in Nigeria,
employing molecular typing techniques. Two hundred and one samples of
rectal swabs, stool, vomitus, water (from the well, borehole, sachet,
stream, and tap) and disinfectants (sodium hypochlorite) were collected
from three states in the country. The samples were inoculated on
thiosulphate-citrate bile salt-sucrose (TCBS), Cary-Blair transport
medium and smeared on glass slides for direct examination. The Vibrio
cholerae isolates were serotyped, biotyped, and characterized using
PCR of the cytotoxin gene A (ctxA), wbeO1, and wbfO139 gene primer. Of
the 201 samples screened, 96 were positive for V. cholerae O1 (48%),
with 69 (72%) positive for ctxA gene. The results from this study
showed that the circulating strains of cholera in Nigeria were of Ogawa
serotype, also observed in other outbreaks in Nigeria (1991, 1992, and
1996). However, the strains were of the Classical biotype and were
mainly (72%) ctxA gene-positive. This current investigation has
confirmed the production of cholera toxin by the circulating strains,
and this could be harnessed for possible cholera vaccine production in
Nigeria