A B C D E F G H I J K L M N O P Q R S T U V W X Y Z All
Abbas, Hisham A.
- Biofilms: the Microbial Castle of Resistance
Authors
1 Department of Microbiology and Immunology-Faculty of Pharmacy-Zagazig University- Zagazig, EG
Source
Research Journal of Pharmacy and Technology, Vol 6, No 1 (2013), Pagination: 1-3Abstract
Biofilms are highly resistant to antimicrobial agents. As a consequence, biofilm-based infections are recalcitrant and their treatment is very difficult. Many factors contribute to the biofilm resistance to antimicrobials. The mechanisms of resistance include delayed diffusion of antibiotics through the biofilm matrix, low oxygen and nutrient, reduced growth rates and metabolism. Other resistance mechanisms involved are biofilm-specific phenotypic variants, stress response activation, over expression of efflux pumps, formation of persisters and quorum sensing.Keywords
Biofilm, Antimicrobial Resistance, Biofilm Matrix, Quorum Sensing, Persister Cells, Phenotypic Variants, Efflux PumpsReferences
- Costerton, JW et al. Bacterial biofilms: a common cause of persistent infections. Science. 284; 1999: 1318–1322.
- Branda SS et al. Biofilms: The matrix revisited. Trends in Microbiology. 13; 2005: 20–26.
- Bjarnsholt T and Givskov M. Quorum-sensing blockade as a strategy for enhancing host defenses against bacterial pathogens. Philosophical Transactions of the Royal Society B. 362; 2007: 1213–1222.
- Hall-Stoodley L and Stoodley P. Evolving concepts in biofilm infections. Cellular Microbiology. 11; 2009: 1034–1043.
- Mah TF and O’Toole GA. Mechanisms of biofilm resistance to antimicrobial agents. Trends in Microbiology. 9; 2001: 34–39.
- Costerton J W et al. Microbial biofilms. Annual Review of Microbiology. 49; 1995: 711–745.
- Xu KD et al. Spatial physiological heterogeneity in Pseudomonas aeruginosa biofilm is determined by oxygen availability. Applied and Environmental Microbiology. 64; 1998: 4035– 4039.
- Walters M C et al. Contributions of antibiotic penetration, oxygen limitation, and low metabolic activity to tolerance of Pseudomonas aeruginosa biofilms to ciprofloxacin and tobramycin. Antimicrobial Agents and Chemotherapy. 47; 2003: 317–323.
- Werner E et al. Stratified growth in Pseudomonas aeruginosa biofilms. Applied and Environmental Microbiology. 70; 2004: 6188–6196.
- Pamp SJ et al. Tolerance to the antimicrobial peptide colistin in Pseudomonas aeruginosa biofilms is linked to metabolically active cells, and depends on the prm and mexAB-oprM genes. Molecular Microbiology. 68; 2008: 223–240.
- Molin S and Tolker-Nielsen T. Gene transfer occurs with enhanced efficiency in biofilms and induces enhanced stabilisation of the biofilm structure. Current Opinion in Biotechnology. 14; 2003: 255–261.
- Driffield K et al. Increased mutability of Pseudomonas aeruginosa in biofilms. Journal of Antimicrobial Chemotherapy. 61; 2008:1053–1056.
- Jalal S et al. Molecular mechanisms of fluoroquinolone resistance in Pseudomonas aeruginosa isolates from cystic fibrosis patients. Antimicrobial Agents and Chemotherapy. 44; 2000: 710–712.
- Islam S et al. Chromosomal mechanisms of aminoglycoside resistance in Pseudomonas aeruginosa isolates from cystic fibrosis patients. Clinical Microbiology and Infection. 15; 2009: 60–66.
- Dibdin GH et al. Mathematical model of -lactam penetration into a biofilm of Pseudomonas aeruginosa while undergoing simultaneous inactivation by released -lactamases. Journal of Antimicrobial Chemotherapy. 38; 1996: 757–769.
- Donlan RM and Costerton JW. Biofilms: survival mechanisms of clinically relevant microorganisms. Clinical Microbiology Reviews. 15; 2002: 167–193.
- Lewis K. Riddle of biofilm resistance. Antimicrobial Agents and Chemotherapy. 45; 2001: 999–1007.
- Stewart PS. Mechanisms of antibiotic resistance in bacterial biofilms. International Journal of Medical Microbiology. 292; 2002: 107–113.
- Gillis RJ et al. Molecular basis of azithromycin-resistant Pseudomonas aeruginosa biofilms. Antimicrobial Agents and Chemotherapy 49; 2005: 3858–3867.
- Zhang L and Mah TF. 2008. Involvement of a novel efflux system in biofilm-specific resistance to antibiotics. Journal of Bacteriology. 190; 2008: 4447–4452.
- Drenkard E. Antimicrobial resistance of Pseudomonas aeruginosa biofilms. Microbes and Infection. 5; 2003:1213- 1219.
- Sauer K et al. Pseudomonas aeruginosa displays multiple phenotypes during development as a biofilm. Journal of Bacteriology. 184; 2002: 1140–1154.
- Whiteley M et al. Gene expression in Pseudomonas aeruginosa biofilms. Nature. 413; 2001: 860–864.
- Spoering AL and Lewis K. Biofilms and planktonic cells of Pseudomonas aeruginosa have similar resistance to killing by antimicrobials. Journal of Bacteriology. 183; 2001: 6746–6751.
- Lewis, K. Riddle of biofilm resistance. Antimicrobial Agents and Chemotherapy. 45; 2001: 999–1007.
- Brooun A et al. A dose-response study of antibiotic resistance in Pseudomonas aeruginosa biofilms. . Antimicrobial Agents and Chemotherapy. 44; 2000: 640–646.
- De Gischolar_maine et al. Novel persistence genes in Pseudomonas aeruginosa identified by high throughput screening. FEMS Microbiology Letters. 297; 2009: 73–79.
- Drenkard E and Ausubel FM. Pseudomonas biofilm formation and antibiotic resistance are linked to phenotypic variation. Nature. 416; 2002: 740–743.
- Greenberg EP. Quorum sensing in Gram-negative bacteria. American Society of Microbiology News. 63; 1997: 371–377.
- Lindum PW et al. N-acyl-homoserine lactone autoinducers control production of an extracellular lipopeptide biosurfactant required for swarming motility of Serratia liquefaciens MG1. Journal of Bacteriology. 180; 1998: 6384–6388.
- Williams P et al. 2000. Quorum sensing and the populationdependent control of virulence. Philosophical Transactions of the Royal Society B. Biological Sciences. 355; 2000: 667–680.
- Davies DG et al. 1998. The involvement of cell-to-cell signals in the development of a bacterial biofilm. Science. 280; 1998: 295– 298.
- Bjarnsholt T et al. Pseudomonas aeruginosa tolerance to tobramycin, hydrogen peroxide and polymorphonuclear leukocytes is quorum-sensing dependent. Microbiology. 151; 2005: 373–383.
- Resistance of Escherichia coli and Klebsiella pneumoniae Isolated from different Sources to β-Lactam Antibiotics
Authors
1 Department of Microbiology and Immunology, Zagazig University, Zagazig, EG
2 Department of Microbiology and Biotechnology, Delta University for Science and Technology, Gamasa, Mansoura, EG
Source
Research Journal of Pharmacy and Technology, Vol 10, No 2 (2017), Pagination: 589-591Abstract
Escherichia coli and Klebsiella pneumoniae are important human pathogens that cause many infectious diseases. β-lactam antibiotics are commonly used in the treatment of these infections. However, resistance to such antibiotics complicates the treatment. Mechanisms of resistance to β-lactams include production of β-lactamases, efflux pumps, change in drug targets and outer membrane impermeability. This study was performed to investigate the resistance of Klebsiella pneumoniae and Escherichia coli to β-lactam antibiotics. The study was carried out from May 2014 to May 2015. Five hundred clinical isolates were collected from patients in Belquas Hospital and Mansoura University Hospitals. Three hundred isolates were identified as Klebsiella pneumoniae and Escherichia coli (one hundred and fifty isolates each). Klebsiella pneumoniae and Escherichia coli isolates showed high resistance to cefoperazone and ceftriaxone, intermediate resistance to cefoxitin, cefotaxime, ceftazidime and amoxicillin-clavulanic acid and low resistance to imipenem and meropenem. Klebsiella pneumoniae showed more resistance than Escherichia coli. Resistance of Klebsiella pneumoniae was higher to cefoperazone, ceftriaxone, ceftazidime, imipenem and meropenem. However, Escherichia coli was more resistant to cefotaxime and cefoxitin. The resistance to amoxicillin-clavulinic acid was more or less similar in both bacteria. In conclusion, the resistance of Klebsiella pneumoniae and Escherichia coli isolates to B-lactams was high and this needs a strict policy for antibiotic dispensing to reduce the emergence of resistance.
Keywords
β-Lactams, Resistance, Klebsiella pneumoniae, Escherichia coli.- Antimicrobial Resistance Patterns of Proteus mirabilis Isolates from Urinary Tract, Burn Wound and Diabetic Foot Infections
Authors
1 Zagazig, Zagazig University, Department of Microbiology and Immunology, EG
Source
Research Journal of Pharmacy and Technology, Vol 11, No 1 (2018), Pagination: 249-252Abstract
Proteus mirabilis is a common etiologic agent of urinary tract, burn wound and diabetic foot infections. Resistance to Proteus mirabilis is also common and represents a challenge to antibiotic therapy. This study aimed to investigate the antibiotic resistance of Proteus mirabilis isolated from three sources; urinary tract infections, burn wound infections in addition to diabetic foot infections. Forty-five clinical isolates of Proteus mirabilis (15 from each source) were used in this study. Complete resistance was found with each of ampicillin and tetracycline. High resistance was exhibited with cefepime. The resistance was intermediate against ceftazidime, cefotaxime, sulfamethoxazole-trimethoprim, amoxicillin-clavulinic, chloramphenicol, cefoperazone, aztreonam and ampicillin-sulbactam. Low resistance was found with piperacillin. These low resistance rates were also shown against tested aminoglycosides and fluoroquinolones. Very little resistance was found to imipenem, while no resistance was exhibited against piperacillin- tazobactam. The resistance pattern showed variation among different sources. Generally, burn wound isolates showed the highest resistance rates followed by diabetic foot isolates, while urinary tract isolates were the least resistant. High resistance was found with cefepime only in isolates from urinary tract infections and no diabetic foot isolate was highly resistant to any of the tested antibiotics. However, such resistance was observed with amoxicillin-clavulinic acid, cefepime, ceftazidime, cefotaxime and sulphamethoxazole-trimethoprim in burn wound isolates. Multidrug resistance (MDR) was also found with varying rates in isolates from different sources. MDR was more common in burn wound isolates than in diabetic foot isolates or urinary tract isolates. This study suggests that there is a variation in antibiotic resistance of Proteus mirabilis among different sources and alarms against high resistance especially in burn wound isolates that requires a strict policy in antibiotic dispensing to minimize such tesistance.Keywords
Proteus mirabilis, Burn Infection, Urinary Tract Infection, Diabetic Foot Infection, Antibiotic Resistance.References
- Rozalski A, Sidorczyk Z and Kotelko K. Potential Virulence Factors of Proteus Bacilli. Microbiology and Molecular Biology Reviews. 61; 1997: 65-89.
- O'Hara CM, Brenner FW and Miller JM. Classification, Identification and Clinical Significance of Proteus, Providencia, and Morganella. Clinical Microbiology Reviews. 13(4); 2000: 534–546.
- Warren JW et al. A prospective microbiologic study of bacteriuria in patients with chronic indwelling urethral catheters. Journal of Infectious Diseases.146; 1982:719–723.
- Warren JW. Catheter-associated urinary tract infections. Infectious Disease Clinicsof North America. 1(4); 1987:823-854.
- Jacobsen SM et al. Complicated Catheter-Associated Urinary Tract Infections Due to Escherichia coli and Proteus mirabilis. Clinical Microbiology Reviews. 21(1); 2008: 26-59.
- Shanmugam P, Jeya M and Linda Susan S. The Bacteriology of Diabetic Foot Ulcers, with a Special Reference to Multidrug Resistant Strain. Journal of Clinial and Diagnosti Research. 7(3); 2013: 441–445.
- Church D et al. Burn Wound Infections. Clinical Microbiology Reviews. 13(4); (2000): 534–546.
- Singh V. Antimicrobial resistance: In Microbial Pathogens and Strategies for Combating Them: Science, Technology and Education. Formatex Research Center. 2013, vol. 1: pp. 291–296.
- Wright GD. Bacterial resistance to antibiotics: enzymatic degradation and modification. Advanced Drug Delivery Reviews. 57(10); 2005: 1451-1470.
- Alekshun MN and Levy SB. Molecular Mechanisms of Antibacterial Multidrug Resistance. Cell. 128(6); 2007: 1037-1050.
- Wilson DN. Ribosome-targeting antibiotics and mechanisms of bacterial resistance. Nature Reviews Microbiology. 12(1); 2014: 35-48.
- Alanis AJ. Resistance to Antibiotics: Are We in the Post-Antibiotic Era? Archives of Medical Research. 36(6); 2005: 697-705.
- Magiorakos AP et al. Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clinical Microbiology and Infection. 18(3); 2012: 268-281.
- Nikaido H. Multidrug resistance in bacteria. Annual Review of Biochemistry 78; 2009: 119–146.
- Washington W Jr et al. Koneman's color atlas and textbook of diagnostic microbiology. Philadelphia: Lippincott Williams and Wilkins. 2005; 6thed.
- Clinical and Laboratory Standards Institute. Performance standards for antimicrobial susceptibility testing, 17th informational supplement. CLSI Document M100-S23. Wayne, USA, 2013.
- Clinical and Laboratory Standards Institute. Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically: Approvated standard, CLSI Document M07-A9. Wayne, USA, 2012.
- Adler JL et al. Proteus infections in a general hospital. II. Some clinical and epidemiologic characteristic. With an analysis of 71 cases of Proteus bacteremia. Annals of InternalMediine. 75; 1971:531-536
- Grahnquist L, Lundberg B and Tullus K. Neonatal Proteusmeningoencephalitis. Case report. ActaPathologicaMicrobiologicaEtImmunologicaScandinavica100; 1992:734-36.
- Lu CH et al. Gram-negative bacillary meningitis in adult post-neurosurgical patients. Surgical Neurology. 52; 1999:438-443
- Mordi RM and Momoh MI. Incidence of Proteus species in wound infections and their sensitivity pattern in the University of Benin Teaching Hospital. African Journal of Bacteriology.8(5); 2009: 725-30.
- Manikandan C and Amsath I. Antibiotic susceptibility of bacterial strains isolated from wound infection patients in Pattukkottai, Tamilnadu, India. International Journal of Current Microbiology and Applied Scienes.2(6); 2013: 195-203.
- Al-Ali KY. Microbial Profile of Burn Wound Infections in Burn Patients, Taif, Saudi Arabia.Archives of Clinical Microbiology. 7(2); 2016:15.
- El-Tahawy AT. Bacteriology of diabetic foot Infections. Saudi Medical Journal.21 (4); 2000: 344-347.
- Cunha MA et al. Antibiotic resistance patterns of urinary tract infections in a northeastern Brazilian capital. Revista do Instituto de Sao Medicina Tropical de Paulo. 58; 2016:2
- Xavier W et al. Emergence of multi drug resistant bacteria in diabetic patients with lower limb wounds. Indian Journal of MedicalReserach. 140(3); 2014: 435–437.
- Song CT. Burns infection profile of Singapore: prevalence of multidrug-resistant Acinetobacterbaumannii and the role of blood cultures. Burns and Trauma. 4; 2016:13