Banner

Phenotypic And Genotypic Methods For Detection Of Metallo-Beta-Lactamase (MβL) Producing Pseudomonas Aeruginosa

• 2015
العودة
معلومات البحث
المؤلفون Wafaa Ahmed EL-Shafei EL-Mosallamy, Ahmed Saied Osman, Hala Abd EL-Mageed Tabl and AL-Shaimaa Mahmood AL-Tabbakh
الكلمات المفتاحية Not Available
المجلة العلمية Not Available
الناشر Not Available
المجلد Not Available
العدد Not Available
الصفحات Not Available
publication.type International
رابط البحث Not Available
المواد المرفقة Not Available
الملخص
Carbapenems are among the best choices for treatment of infectionscaused by multidrug resistant Gram-negative rods
.
In recent years, Egypthas been considered among the countries that reported high rates of antimicrobial resistance
(Zafer et al., 2014)
.The occurrence of a Mβ-positive isolate in a hospital settingrepresents a therapeutic problem, as !ell as a serious concern for infection control management. The accurate identification and reportingof Mβ-producing
P. aeruginosa
!ill aid infection control practitioners in preventing the spread of these multidrug-resistant isolates
(Arunagiri et al., 2012)
.This study aimed to evaluate IM"- E#T$ C#T and IM"- E#T$##%T as phenotypic screening methods for Mβ detection in isolatedstrains of
P.aeruginosa
, detection of Mβ genes in those isolates andformulation of antibiotic policy for treatment of infections by Mβ producing
P.aeruginosa
.In this study a total number of &&' different samples !ere collectedfrom patients from (enha )niversity *ospital and (enha Teaching*ospital and +''
P.aeruginosa
strains ./0 !ere recovered fromthem.The isolated
P. aeruginosa
strains !ere sub1ected to2 +0$ntibiotic susceptibility by disc diffusion test.&0Mβ detection by both2a0 "henotypic method2 by both IM"- E#T$ C#T and IM"-E#T$ ##%T. b0 Genotypic method2 by multiple3 "C4
)131(


6-Summary and Conclusion
The present study revealed that2 5ut of +''
P.aeruginosa
isolates, & strains &/0 !ere imipenemresistant and + strains of them 6'/0 !ere carrying genes responsiblefor Mβ production +/ of the total number of
P.aeruginosa
0. Thirteenstrains +7/0 !ere carrying
VIM
gene !hile t!o strains &/0 !erecarrying both
VIM
and
SPM
genes together.
IMP, GIM-1, SIM-1
genes!ere not detected. 8one of the imipenem sensitive strains !ere carryinggenes of Mβ production.IM"- E#T$ C#T !as found to be more sensitive 97.7/0 than IM"-E#T$ ##%T 66.:/0. The specificity of both tests !as +''/ in relationto the gold standard "C4. 8early all
P.aeruginosa
strains !ere resistant to cefota3im,cefotria3one, cefopera;one, cefta;idime, cefepime and amo3icillinclavulanic acid !hile all strains !ere sensitive to colistin and polymy3in(. 8early all Mβ producers !ere resistant to most antibiotics used!hile +''/ of them !ere fully sensitive to colistin and polymy3in (.There !as insignificant relation bet!een Mβ production and each of patient age, patient se3 and site of infection.There !as significant decrease in the number of Mβ positive cases inshort periods of hospitali;ation. β-lactam antibiotic inta