Pregled bibliografske jedinice broj: 926028
Antibiotic resistance in Enterobacteri cloacae with derepressed/partically derepressed/inducible AmpC and extended- spectrum beta-lactamase in Zenica-Doboj Canton, Bosnia and Herzegovina
Antibiotic resistance in Enterobacteri cloacae with derepressed/partically derepressed/inducible AmpC and extended- spectrum beta-lactamase in Zenica-Doboj Canton, Bosnia and Herzegovina // Online book of abstracts, IMED, 2016
Beč, 2016. str. 22-22 (poster, međunarodna recenzija, sažetak, ostalo)
CROSBI ID: 926028 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Antibiotic resistance in Enterobacteri cloacae with derepressed/partically derepressed/inducible AmpC and extended- spectrum beta-lactamase in Zenica-Doboj Canton, Bosnia and Herzegovina
Autori
Ibrahimagić, Amir ; Uzunović, Selma ; Bedenić, Branka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, ostalo
Izvornik
Online book of abstracts, IMED, 2016
/ - Beč, 2016, 22-22
Skup
International Meeting on Emerging Diseases and Surveillance
Mjesto i datum
Beč, Austrija, 04.11.2016. - 07.11.2016
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Enterobacter cloacae, AmpC beta-lactamase, extended-spectrum beta-lactamases, Bosnia and Herzegovina
Sažetak
Aim To investigate the prevalence of derepressed/partly derepressed/inducible and ESBL/AmpC-producing Enterobacter cloacae isolates and treatment options for infections associated with those isolates. Methods Antibiotic susceptibility was determined by disc diffusion and broth microdilution according to CLSI guidelines. Doubledisk synergy test (DDST) was performed in order to screen for ESBLs and combined disk test with phenylboronic acid to detect AmpC β - lactamases. PCR was used to detect blaESBL/blacarb genes. Genetic relatedness of the strains was determined by pulsed-fieldgel- electrophoresis (PFGE). Results Among 14 isolates with the ESBL positive E. cloaceae producing isolates, four (28.6%), nine (64.3%) and one (7.1%) isolates were derepressed/partly derepressed and inducible AmpC producers. Eleven (out of 14) isolates were resistant to cefotaxime, ceftazidime, ceftriaxone, aminoglycosides and fluoroquinolones. All isolates were susceptible to imipenem and meropenem, 79% to cefepime. Five (out of 14 ; 35.7%) isolates (four derepressed and one inducible AmpC carrying E. cloaceae) were negative in phenotypic test for ESBLs, but positive for broad spectrum TEM-1 β-lactamase. One (out of four derepressed) also produced CMY-2 β-lactamase. Four (out of nine) partly derepressed isolates were positive with the DDST, but did not yield PCR products with primers targeting TEM, SHV and CTX-M beta- lactamases. Four positive partly derepressed isolates carried a blaCTX-M-1 gene, two blaOXA- 1 one blaCTX-M-15, OXA-1 and one blaCTX-M-28, OXA-1 (n=1). Conclusion Microbiology laboratories must be able to detect and recognize AmpC-carrying isolates in a timely manner, especially those that are falsely susceptible in vitro to drugs that may be consideredfor therapy of infected patients.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
108-1080114-0015 - Mehanizmi rezistencije na antibiotike u Gram-negativnih bakterija (Bedenić, Branka, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Zagreb
Profili:
Branka Bedenić
(autor)