Infection control by antibody disruption of bacterial quorum sensing signaling

被引:184
作者
Park, Junguk
Jagasia, Reshma
Kaufmann, Gunnar F.
Mathison, John C.
Ruiz, Diana I.
Moss, Jason A.
Meijler, Michael M.
Ulevitch, Richard J.
Janda, Kim D.
机构
[1] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
[3] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
[4] Scripps Res Inst, Worm Inst Res & Med, La Jolla, CA 92037 USA
来源
CHEMISTRY & BIOLOGY | 2007年 / 14卷 / 10期
关键词
D O I
10.1016/j.chembiol.2007.08.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Quorum sensing (QS) is the process through which bacteria communicate utilizing small diffusible molecules termed autoinducers. It has been demonstrated that QS controls a plethora of microbial processes including the expression of virulence factors. Here we report an immunopharmacotherapeutic approach for the attenuation of QS in the Gram-positive human pathogen Staphylococcus aureus. An anti-autoinducer monoclonal antibody, AP4-24H11, was elicited against a rationally designed hapten, and efficiently inhibited QS in vitro through the sequestration of the autoinducing peptide (AIP)-4 produced by S. aureus RN4850. Importantly, AP4-24H11 suppressed S. aureus pathogenicity in an abscess formation mouse model in vivo and provided complete protection against a lethal S. aureus challenge. These findings provide a strong foundation for further investigations of immunopharmacotherapy for the treatment of bacterial infections in which QS controls the expression of virulence factors.
引用
收藏
页码:1119 / 1127
页数:9
相关论文
共 44 条
[1]  
[Anonymous], [No title captured]
[2]   Autoinducer of virulence as a target for vaccine and therapy against Staphylococcus aureus [J].
Balaban, N ;
Goldkorn, T ;
Nhan, RT ;
Dang, LB ;
Scott, S ;
Ridgley, RM ;
Rasooly, A ;
Wright, SC ;
Larrick, JW ;
Rasooly, R ;
Carlson, JR .
SCIENCE, 1998, 280 (5362) :438-440
[3]   α-toxin is a mediator of Staphylococcus aureus-induced cell death and activates caspases via the intrinsic death pathway independently of death receptor signaling [J].
Bantel, H ;
Sinha, B ;
Domschke, W ;
Peters, G ;
Schulze-Osthoff, K ;
Jänicke, RU .
JOURNAL OF CELL BIOLOGY, 2001, 155 (04) :637-647
[4]   Passive antibody therapy for infectious diseases [J].
Casadevall, A ;
Dadachova, E ;
Pirofski, L .
NATURE REVIEWS MICROBIOLOGY, 2004, 2 (09) :695-703
[5]   Virulence regulation and quorum sensing in staphylococcal infections: Competitive AgrC antagonists as quorum sensing inhibitors [J].
Chan, WC ;
Coyle, BJ ;
Williams, P .
JOURNAL OF MEDICINAL CHEMISTRY, 2004, 47 (19) :4633-4641
[6]   Bacterial quorum sensing in pathogenic relationships [J].
de Kievit, TR ;
Iglewski, BH .
INFECTION AND IMMUNITY, 2000, 68 (09) :4839-4849
[7]   Comparison of two standardisation methods in real-time quantitative RT-PCR to follow Staphylococcus aureus genes expression during in vitro growth [J].
Eleaume, H ;
Jabbouri, S .
JOURNAL OF MICROBIOLOGICAL METHODS, 2004, 59 (03) :363-370
[8]   Census and consensus in bacterial ecosystems: The LuxR-LuxI family of quorum-sensing transcriptional regulators [J].
Fuqua, C ;
Winans, SC ;
Greenberg, EP .
ANNUAL REVIEW OF MICROBIOLOGY, 1996, 50 :727-751
[9]   Molecular mechanisms of agr quorum sensing in virulent staphylococci [J].
George, Elizabeth A. ;
Muir, Tom W. .
CHEMBIOCHEM, 2007, 8 (08) :847-855
[10]   Small molecule inhibitors of bacterial quorum sensing and biofilm formation [J].
Geske, GD ;
Wezeman, RJ ;
Siegel, AP ;
Blackwell, HE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (37) :12762-12763