Therapies against Virulence Products of Staphylococcus aureus and Pseudomonas aeruginosa

被引:18
作者
Wiener-Kronish, Jeanine P. [1 ]
Pittet, Jean-Francois [2 ,3 ,4 ]
机构
[1] Massachusetts Gen Hosp, Dept Anesthesia & Crit Care, Boston, MA 02114 USA
[2] Univ Alabama Birmingham, Dept Anesthesiol, Crit Care Div, Birmingham, AL USA
[3] Univ Alabama Birmingham, Dept Surg, Birmingham, AL 35294 USA
[4] Univ Alabama Birmingham, Dept Cell Biol, Birmingham, AL 35294 USA
关键词
Methicillin-resistant S. aureus; Pseudomonas aeruginosa; virulence; antibiotic resistance; Panton-Valentine leukocidin (PVL) gene; toxins; exotoxins; PANTON-VALENTINE LEUKOCIDIN; VENTILATOR-ASSOCIATED PNEUMONIA; METHICILLIN-RESISTANT; III SECRETION; DETERMINANTS; EPIDEMIOLOGY; INFECTIONS; IDENTIFICATION; PROTECTS; SYSTEM;
D O I
10.1055/s-0031-1275535
中图分类号
R4 [临床医学];
学科分类号
100218 [急诊医学];
摘要
Methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa are key pathogens in hospitals (particularly intensive care units), in long-term care facilities, and in outpatients with specific comorbidities and risk factors. Both MRSA and P. aeruginosa display resistance to a wide array of antibiotics. Further, both bacteria contain a variety of virulence products or systems that make it difficult to treat associated infections. Within the past several years, community-acquired MRSA containing virulence factors [particularly the Panton-Valentine leukocidin (PVL) gene] has emerged globally. Given the limited number of novel antibiotics to treat antibiotic-resistant organisms, there is growing interest in treating bacterial infections by targeting specific virulence products or systems. This article reviews potential therapeutic targets in the virulence systems of these two bacteria that are responsible for a large number of serious infections in critically ill patients.
引用
收藏
页码:228 / 235
页数:8
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