Диссертация (1140384), страница 26
Текст из файла (страница 26)
Maseda, K.Saito, A. Nakajima, T. Nakae // FEMS Microbiology Letters – 2000. – Vol. 192, №1. – P. 107–112.147.Maseda, H. Enhancement of the mexAB-oprM efflux pump expression by aquorum-sensing autoinducer and its cancellation by a regulator, MexT, of themexEF-oprN efflux pump operon in Pseudomonas aeruginosa / H. Maseda, I.Sawada, K. Saito, H. Uchiyama, T. Nakae, N. Nomura // Antimicrobial agents andchemotherapy. – 2004. – Vol. 48, № 4. – P.
1320–1328.148.Masuda, N. Substrate specificities of MexAB-OprM, MexCD-OprJ, andMexXY-OprM efflux pumps in Pseudomonas aeruginosa // N. Masuda, E.Sakagawa, S. Ohya, N. Gotoh, H. Tsujimoto, T. Nishino // Antimicrobial Agentsand Chemotherapy. – 2000. – Vol. 44, № 12. – P.
3322–3327.149.Mathew, A. The use of analytical isoelectric focusing for detection andidentification of beta-lactamases / A. Mathew, A.M. Harris, M.J. Marshall, G.W.Ross // Journal of General Microbiol. – 1975. – Vol. 88, № 1. – P. 169–178.150.Mayr, F.B. Epidemiology of severe sepsis / F.B. Mayr, S. Yende, D.C. Angus //Virulence. – 2014. – Vol. 5, № 1. – P. 4–11.151.McCoy, L.S. Polymyxins and analogues bind to ribosomal RNA and interferewith eukaryotic translation in vitro / L.S. McCoy, K.D. Roberts, R.L. Nation, P.E.Thompson, T. Velkov, J.
Li, Y. Tor // European journal of chemical biology. – 2013.– № 14. – P. 2083–2086.152.McDaniel, C. A putative ABC transporter permease is necessary for resistanceto acidified nitrite and EDTA in Pseudomonas aeruginosa under aerobic andanaerobic planktonic and biofilm conditions / C. McDaniel, S. Su, W. Panmanee,164G.W. Lau, T. Browne, K.
Cox, A.T. Paul, S.H. Ko, J.E. Mortensen, J.S. Lam, D.A.Muruve, D.J. Hassett // Frontiers in Microbiology. – 2016. – V. 1, №7. – P. 291.153.McPhee, J.B. Cationic antimicrobial peptides activate a two-componentregulatory system, PmrA-PmrB, that regulates resistance to polymyxin B andcationic antimicrobial peptides in Pseudomonas aeruginosa / J.B. McPhee, S.Lewenza, R.E. Hancock // Molecular Microbiology. – 2003. – № 50. – P. 205–217.154.Meisenberg, G.
Principles of medical biochemistry / G. Meisenberg, W.H.Simmons. - Chicago: Elsevier, 2017. – P. 134.155.Meyer, J.M. Exogenous siderophore-mediated iron uptake in Pseudomonasaeruginosa: possible involvement of porin OprF in iron translocation / J.M. Meyer //Journal of General Microbiology. – 1992. – Vol. 138, № 5. – P.
951–958.156.Mine, T. Expression in Escherichia coli of a new multidrug efflux pump,MexXY, from Pseudomonas aeruginosa / T. Mine, Y. Morita, A. Kataoka, T.Mizushima, T. Tsuchiya // Antimicrobial Agents and Chemotherapy. – 1999. – Vol.43, № 2. – P.
415–417.157.Mirande, C. Rapid detection of carbapenemase activity: benefits and weaknessesof MALDI-TOF MS / C. Mirande, I. Canard, S. Buffet Croix Blanche, J.P. Charrier,A. van Belkum, M. Welker, S. Chatellier // European Journal of ClinicalMicrobiology and Infectious Diseases. – 2015. – Vol. 34, № 11. – P. 2225–2234.158.Mogi, T. Polymyxin B identified as an inhibitor of alternative NADHdehydrogenase and malate: Quinone oxidoreductase from the Gram-positivebacterium Mycobacterium smegmatis / T.
Mogi, Y. Murase, M. Mori, K. Shiomi, S.Omura, M.P. Paranagama, K. Kita // The Journal of Biochemistry. – 2009. – № 146.– P. 491–499.159.Monteferrante, C.G. Evaluation of different pretreatment protocols to detectaccurately clinical carbapenemase-producing Enterobacteriaceae by MALDI-TOF /C.G. Monteferrante, S. Sultan, M.T. Ten Kate, L.J. Dekker, K.
Sparbier, M. Peer,M. Kostzrewa, T.M. Luider, W.H. Goessens, P.C. Burgers // Journal ofAntimicrobial Chemotherapy. – 2016. – Vol. 71, № 10. – P. 2856–2867.165160.Mortimer, P.G. A comparison of methods used for measuring the accumulationof quinolones by Enterobacteriaceae, Pseudomonas aeruginosa and Staphylococcusaureus / P.G. Mortimer, L.J. Piddock // Journal of Antimicrobial Chemotherapy. –1991. –Vol. 28, № 5. – P. 639–653.161.Moskowitz, S.M. PmrB mutations promote polymyxin resistance ofPseudomonas aeruginosa isolated from colistin-treated cystic fibrosis patients /S.M.
Moskowitz, M.K. Brannon, N. Dasgupta, M. Pier, N. Sgambati, A.K. Miller,S.E. Selgrade, S.I. Miller, M. Denton, S.P. Conway, H.K. Johansen, N. Hoiby //Antimicrobial Agents and Chemotherapy. – 2012. – Vol. 56, № 2. – P. 1019-1030.162.Moubareck, C. GES-11, a novel integron-associated GES variant inAcinetobacter baumannii / C. Moubareck, S. Bremont, M.C.
Conroy, P. Courvalin,T. Lambert // Antimicrobial Agents and Chemotherapy. – 2009. - Vol. 53, № 8. – P.3579–3581.163.Muller, C. A two-component regulatory system interconnects resistance topolymyxins, aminoglycosides, fluoroquinolones, and β-Lactams in Pseudomonasaeruginosa / C.A. Muller, P. Plesiat, K. Jeannot // Antimicrobial Agents andChemotherapy. – 2010.
– № 55. – P. 1211–1221.164.National Center for Biotechnology Information [электронный ресурс] // URL:https://www.ncbi.nlm.nih.gov/pubmed (дата обращения: 20.12.2017).165.Nichols, W.W. Inhibition of tobramycin diffusion by binding to alginate / W.W.Nichols, S.M. Dorrington, M.P. Slack, H.L. Walmsley // Antimicrobial agents andchemotherapy. – 1988. – Vol. 32, № 4. – P.
518-523.166.Nishino, K. EvgA of the two-component signal transduction system modulatesproduction of the YhiUV multidrug transporter in Escherichia coli / K. Nishino, A.Yamaguchi // Journal of Bacteriology. – 2002. – Vol. 184, № 8. – P. 2319–2323.167.Nordmann, P. Strategies for identification of carbapenemase-producingEnterobacteriaceae / P. Nordmann, L. Poirel // Journal of AntimicrobialChemotherapy. – 2013. – Vol. 68, № 3.
– P. 487–489.166168.Notomi, T. Loop-mediated isothermal amplification of DNA / T. Notomi, H.Okayama, H. Masubuchi, T. Yonekawa, K. Watanabe, N. Amino, T. Hase // NucleicAcids Research. – 2000. – Vol. 28, №12. – P. E63.169.Ocampo-Sosa, A.A. Alterations of OprD in carbapenem-intermediate and -susceptible strains of Pseudomonas aeruginosa isolated from patients withbacteremia in a Spanish Multicenter Study / A.A.
Ocampo-Sosa, G. Cabot, C.Rodriguez, E. Roman, F. Tubau, M. Macia, B. Moya, L. Zamorano, C. Suarez, C.Pena, M.A. Dominguez; G. Moncalian, A. Oliver, L. Martinez-Martinez //Antimicrobial Agents and Chemotherapy. – 2012. – Vol. 56, № 4. – P. 1703–1713.170.Ochs, M.M. Amino acid-mediated induction of the basic amino acid-specificouter membrane porin OprD from Pseudomonas aeruginosa / M.M.
Ochs, C.D. Lu,R.E. Hancock, A.T. Abdelal // Journal of Bacteriology. – 1999. – Vol. 181, №17. –P. 5426–5432.171.Ochs, M.M. Negative regulation of the Pseudomonas aeruginosa outermembrane porin OprD selective for imipenem and basic amino acids / M.M. Ochs,M.P. McCusker, M. Bains, R.E. Hancock // Antimicrobial Agents andChemotherapy. – 1999.
– № 43. – P. 1085–1090.172.Olaitan, A.O. Mechanisms of polymyxin resistance: acquired and intrinsicresistance in bacteria [Электронный ресурс] / A.O. Olaitan, S. Morand, J.M.Rolain // Frontiers in Microbiology. – 2014. –Vol. 5, № 643. – Режим доступа:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4244539/.173.Ooka, T.
Inference of the impact of insertion sequence (IS) elements on bacterialgenome diversification through analysis of small-size structural polymorphisms inEscherichia coli O157 genomes / T. Ooka, Y. Ogura, M. Asadulghani, M. Ohnishi,K. Nakayama, J. Terajima, H. Watanabe, T. Hayashi // Genome Research.
– 2009. –Vol. 19, №10. – P. 1809–1816.174.Oviano,M.Rapiddirectdetectionofcarbapenemase-producingEnterobacteriaceae in clinical urine samples by MALDI-TOF MS analysis / M.167Oviano, C.L. Ramirez, L.P. Barbeyto, G. Bou // Journal of AntimicrobialChemotherapy. – 2017.
– Vol. 72, № 5. – P. 1350–1354.175.Pasteran, F. Sensitive screening tests for suspected class A carbapenemaseproduction in species of Enterobacteriaceae / F. Pasteran, T. Mendez, L. Guerriero,M. Rapoport, A. Corso // Journal of Clinical Microbiology. – 2009. – Vol. 47, № 6.– P. 1631-1639.176.Paul, D. Occurrence of co-existing bla VIM-2 and bla NDM-1 in clinical isolatesof Pseudomonas aeruginosa from India [Электронный ресурс] / D.
Paul, D. Dhar,A.P. Maurya, S. Mishra, G.D. Sharma, A. Chakravarty, A. Bhattacharjee // Annalsof Clinical Microbiology and Antimicrobials. – 2016. – Vol. 15, № 31. – Режимдоступа: https://www.ncbi.nlm.nih.gov/pubmed/27154587.177.Perez-Perez, F.J. Detection of plasmid-mediated AmpC beta-lactamase genes inclinical isolates by using multiplex PCR / F.J. Perez-Perez, N.D. Hanson // Journalof Clinical Microbiology. – 2002. – Vol. 40, № 6.
– P. 2153–2162.178.Pfeifer, Y. Resistance to cephalosporins and carbapenems in Gram-negativebacterial pathogens / Y. Pfeifer, A. Cullik, W. Witte // International Journal ofMedical Microbiology. – 2010. – Vol. 300, № 6. – P. 371–379.179.Pirnay, J.P. Analysis of the Pseudomonas aeruginosa oprD gene from clinicaland environmental isolates / J.P. Pirnay, D. De Vos, D. Mossialos, A. Vanderkelen,P. Cornelis, M. Zizi // Environmental Microbiology. – 2002. – Vol.
4, № 12. – P.872–882.180.Poirel, L. Multiplex PCR for detection of acquired carbapenemase genes / L.Poirel, T.R. Walsh, V. Cuvillier, P. Nordmann // Diagnostic Microbiology andInfectious Disease. – 2011. – Vol. 70, № 1. – P. 119–123.181.Poole, K. Efflux-mediated resistance to fluoroquinolones in gram-negativebacteria / K. Poole // Antimicrobial Agents and Chemotherapy. – 2000. – Vol. 44, №9.
![](https://s.studizba.com/z.php?f=/templates/si/i/noavatar.png&w=100&h=100&t=1"){kind=avatar}
