Affiliation:
1. Departments of Molecular Genetics and Microbiology and
2. Center for Microbial Pathogenesis, Duke University School of Medicine, Durham, North Carolina
3. Pediatrics and
Abstract
Despite advances in diagnosis and treatment, bacterial sepsis remains a major cause of pediatric morbidity and mortality, particularly among neonates, the critically ill, and the growing immunocompromised patient population. Sepsis is the end point of a complex and dynamic series of events in which both host and microbial factors drive high morbidity and potentially lethal physiologic alterations. In this article we provide a succinct overview of the events that lead to pediatric bloodstream infections (BSIs) and sepsis, with a focus on the molecular mechanisms used by bacteria to subvert host barriers and local immunity to gain access to and persist within the systemic circulation. In the events preceding and during BSI and sepsis, Gram-positive and Gram-negative pathogens use a battery of factors for translocation, inhibition of immunity, molecular mimicry, intracellular survival, and nutrient scavenging. Gaps in understanding the molecular pathogenesis of bacterial BSIs and sepsis are highlighted as opportunities to identify and develop new therapeutics.
Publisher
American Academy of Pediatrics (AAP)
Subject
Pediatrics, Perinatology and Child Health
Reference97 articles.
1. Cellular mechanisms in sepsis;Jean-Baptiste;J Intensive Care Med,2007
2. The epidemiology of severe sepsis in children in the United States;Watson;Am J Respir Crit Care Med,2003
3. Nosocomial bloodstream infections in pediatric patients in United States hospitals: epidemiology, clinical features and susceptibilities;Wisplinghoff;Pediatr Infect Dis J,2003
4. Seventy-five years of neonatal sepsis at Yale: 1928–2003;Bizzarro;Pediatrics,2005
5. Microbiologic spectrum and susceptibility pattern of clinical isolates from the pediatric intensive care unit in a single medical center: 6 years' experience;Lee;J Microbiol Immunol Infect,2009
Cited by
44 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献