Aminoglycoside Resistance Rates, Phenotypes, and Mechanisms of Gram-Negative Bacteria from Infected Patients in Upper Egypt

被引:42
作者
Gad, Gamal F. [1 ]
Mohamed, Heba A. [1 ]
Ashour, Hossam M. [2 ,3 ]
机构
[1] Minia Univ, Dept Microbiol & Immunol, Fac Pharm, Al Minya, Egypt
[2] Cairo Univ, Dept Microbiol & Immunol, Fac Pharm, Cairo, Egypt
[3] Wayne State Univ, Eugene Applebaum Coll Pharm & Hlth Sci, Detroit, MI USA
关键词
PSEUDOMONAS-AERUGINOSA; ANTIBIOTICS; COMBINATION; PREVALENCE; THERAPY; MEXXY; MONOTHERAPY; ENZYMES;
D O I
10.1371/journal.pone.0017224
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
With the re-emergence of older antibiotics as valuable choices for treatment of serious infections, we studied the aminoglycoside resistance of Gram-negative bacteria isolated from patients with ear, urinary tract, skin, and gastrointestinal tract infections at Minia university hospital in Egypt. Escherichia coli (mainly from urinary tract and gastrointestinal tract infections) was the most prevalent isolate (28.57%), followed by Pseudomonas aeruginosa (25.7%) (mainly from ear discharge and skin infections). Isolates exhibited maximal resistance against streptomycin (83.4%), and minimal resistance against amikacin (17.7%) and intermediate degrees of resistance against neomycin, kanamycin, gentamicin, and tobramycin. Resistance to older aminoglycosides was higher than newer aminoglycoides. The most common aminoglycoside resistance phenotype was that of streptomycin resistance, present as a single phenotype or in combination, followed by kanamycin-neomycin as determined by interpretative reading. The resistant Pseudomonas aeruginosa strains were capable of producing aminoglycoside-modifying enzymes and using efflux as mechanisms of resistance. Using checkerboard titration method, the most frequently-observed outcome in combinations of aminoglycosides with beta-lactams or quinolones was synergism. The most effective combination was amikacin with ciprofloxacin (100% Synergism), whereas the least effective combination was gentamicin with amoxicillin (53.3% Synergistic, 26.7% additive, and 20% indifferent FIC indices). Whereas the studied combinations were additive and indifferent against few of the tested strains, antagonism was never observed. The high resistance rates to aminoglycosides exhibited by Gram-negative bacteria in this study could be attributed to the selective pressure of aminoglycoside usage which could be controlled by successful implementation of infection control measures.
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共 36 条
[1]   Multiplex-PCR and PCR-RFLP assays to monitor water quality against pathogenic bacteria [J].
Abd-El-Haleem, D ;
Kheiralla, ZH ;
Zaki, S ;
Rushdy, AA ;
Abd-El-Rahiem, W .
JOURNAL OF ENVIRONMENTAL MONITORING, 2003, 5 (06) :865-870
[2]   Chronobiology and chronotoxicology of antibiotics and aminoglycosides [J].
Beauchamp, Denis ;
Labrecque, Gaston .
ADVANCED DRUG DELIVERY REVIEWS, 2007, 59 (9-10) :896-903
[3]   R-FACTOR MEDIATED GENTAMICIN RESISTANCE - NEW ENZYME WHICH MODIFIES AMINOGLYCODIDE ANTIBIOTICS [J].
BENVENISTE, R ;
DAVIES, J .
FEBS LETTERS, 1971, 14 (05) :293-+
[4]   In vitro activities of tachyplesin III against Pseudomonas aeruginosa [J].
Cirioni, Oscar ;
Giacometti, Andrea ;
Kamysz, Wojciech ;
Silvestri, Carmela ;
Riva, Alessandra ;
Della Vittoria, Agnese ;
Abbruzzetti, Alessandra ;
Lukasiak, Jerzy ;
Scalise, Giorgio .
PEPTIDES, 2007, 28 (04) :747-751
[5]  
*CLSI, 2007, M100S15 CLSI
[6]   Bacterial resistance to aminoglycoside antibiotics [J].
Davies, J ;
Wright, GD .
TRENDS IN MICROBIOLOGY, 1997, 5 (06) :234-240
[7]  
Drusano G.L., 2007, CLIN INFECT DIS, V45, P753, DOI DOI 10.1086/520991
[8]   Potential of old-generation antibiotics to address current need for new antibiotics [J].
Falagas, Matthew E. ;
Grammatikos, Alexandros P. ;
Michalopoulos, Argyris .
EXPERT REVIEW OF ANTI-INFECTIVE THERAPY, 2008, 6 (05) :593-600
[9]   Old antibiotics for infections in critically ill patients [J].
Falagas, Matthew E. ;
Kopterides, Petros .
CURRENT OPINION IN CRITICAL CARE, 2007, 13 (05) :592-597
[10]  
FOSSE T, 1983, PATHOL BIOL, V31, P483