Rationale and Prospects of Targeting Bacterial Two-component Systems for Antibacterial Treatment of Cystic Fibrosis Patients

被引:1
作者
Velikova, Nadya [1 ]
Wells, Jerry M. [1 ]
机构
[1] Wageningen Univ, Dept Anim Sci, Host Microbe Interact Grp, Wageningen, Netherlands
基金
欧盟地平线“2020”;
关键词
Bacterial infections; cystic fibrosis; two-component systems; antibacterial treatment; respiratory infection; pathogen; BURKHOLDERIA-CEPACIA COMPLEX; NONTYPABLE HAEMOPHILUS-INFLUENZAE; PSEUDOMONAS-AERUGINOSA INFECTION; ENTERICA SEROVAR TYPHIMURIUM; SIGNAL-TRANSDUCTION SYSTEMS; OPRM EFFLUX PUMP; STAPHYLOCOCCUS-AUREUS; REGULATORY SYSTEM; SENSOR KINASE; MUCOID PSEUDOMONAS;
D O I
10.2174/1389450117666160208145934
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Bacterial respiratory infections are the main reason of morbidity and mortality among cystic fibrosis (CF) patients. In early childhood, the respiratory infections are due to Staphylococcus aureus and Haemophilus influenzae. In older CF patients, pathogenic Gram-negative bacteria like Achromobacter xylosoxidans, Burkholderia cepacia complex and especially Pseudomonas aeruginosa are more frequently seen. P. aeruginosa is a turning point in the respiratory disease in CF and its predominance increases with age. Bacteria use a variety of two-component systems (TCS) to differentially express virulence factors involved in both acute and chronic infections. Here, we review bacterial TCS as targets for antibacterial treatment for CF patients.
引用
收藏
页码:687 / 695
页数:9
相关论文
共 115 条
[1]   A single amino acid substitution in PmrB is associated with polymyxin B resistance in clinical isolate of Pseudomonas aeruginosa [J].
Abraham, Neethu ;
Kwon, Dong H. .
FEMS MICROBIOLOGY LETTERS, 2009, 298 (02) :249-254
[2]   Environmental Burkholderia cepacia complex isolates in human infections [J].
Baldwin, Adam ;
Mahenthiralingam, Eshwar ;
Drevinek, Pavel ;
Vandamme, Peter ;
Govan, John R. ;
Waine, David J. ;
LiPuma, John J. ;
Chiarini, Luigi ;
Dalmastri, Claudia ;
Henry, Deborah A. ;
Speert, David P. ;
Honeybourne, David ;
Maiden, Martin C. J. ;
Dowson, Chris G. .
EMERGING INFECTIOUS DISEASES, 2007, 13 (03) :458-461
[3]   Alterations in Two-Component Regulatory Systems of phoPQ and pmrAB Are Associated with Polymyxin B Resistance in Clinical Isolates of Pseudomonas aeruginosa [J].
Barrow, Kaddy ;
Kwon, Dong H. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2009, 53 (12) :5150-5154
[4]   The role of the QseC quorum-sensing sensor kinase in colonization and norepinephrine-enhanced motility of Salmonella enterica serovar Typhimurium [J].
Bearson, Bradley L. ;
Bearson, Shawn M. D. .
MICROBIAL PATHOGENESIS, 2008, 44 (04) :271-278
[5]   Bacterial Histidine Kinases as Novel Antibacterial Drug Targets [J].
Bem, Agnieszka E. ;
Velikova, Nadya ;
Teresa Pellicer, M. ;
van Baarlen, Peter ;
Marina, Alberto ;
Wells, Jerry M. .
ACS CHEMICAL BIOLOGY, 2015, 10 (01) :213-224
[6]   Evidence of transmission of Burkholderia cepacia, Burkholderia multivorans and Burkholderia dolosa among persons with cystic fibrosis [J].
Biddick, R ;
Spilker, T ;
Martin, A ;
LiPuma, JJ .
FEMS MICROBIOLOGY LETTERS, 2003, 228 (01) :57-62
[7]   Pseudomonas aeruginosa Twitching Motility: Type IV Pili in Action [J].
Burrows, Lori L. .
ANNUAL REVIEW OF MICROBIOLOGY, VOL 66, 2012, 66 :493-520
[8]   The Effect of the Potential PhoQ Histidine Kinase Inhibitors on Shigella flexneri Virulence [J].
Cai, Xia ;
Zhang, Jian ;
Chen, Mingliang ;
Wu, Yang ;
Wang, Xueqing ;
Chen, Jiayu ;
Zhang, Junqin ;
Shen, Xu ;
Qu, Di ;
Jiang, Hualiang .
PLOS ONE, 2011, 6 (08)
[9]   A copper-activated two-component system interacts with zinc and imipenem resistance in Pseudomonas aeruginosa [J].
Caille, Olivier ;
Rossier, Claude ;
Perron, Karl .
JOURNAL OF BACTERIOLOGY, 2007, 189 (13) :4561-4568
[10]   Transmission of Burkholderia cepacia complex:: Evidence for new epidemic clones infecting cystic fibrosis patients in Italy [J].
Campana, S ;
Taccetti, G ;
Ravenni, N ;
Favari, F ;
Cariani, L ;
Sciacca, A ;
Savoia, D ;
Collura, A ;
Fiscarelli, E ;
De Intinis, G ;
Busetti, A ;
Cipolloni, A ;
d'Aprile, A ;
Provenzano, E ;
Collebrusco, I ;
Frontini, P ;
Stassi, G ;
Trancassini, M ;
Tovagliari, D ;
Lavitola, A ;
Doherty, CJ ;
Coenye, T ;
Govan, JRW ;
Vandamme, P .
JOURNAL OF CLINICAL MICROBIOLOGY, 2005, 43 (10) :5136-5142