Lack of a Major Role of Staphylococcus aureus Panton-Valentine Leukocidin in Lower Respiratory Tract Infection in Nonhuman Primates

被引:37
作者
Olsen, Randall J. [1 ,3 ]
Kobayashi, Scott D. [5 ]
Ayeras, Ara A. [1 ]
Ashraf, Madiha [1 ,4 ]
Graves, Shawna F. [5 ]
Ragasa, Willie [1 ]
Humbird, Tammy [7 ]
Greaver, Jamieson L. [7 ]
Cantu, Constance [1 ]
Swain, Jody L. [6 ]
Jenkins, Leslie [8 ]
Blasdel, Terry [7 ]
Cagle, Philip T. [1 ]
Gardner, Donald J. [2 ]
DeLeo, Frank R. [5 ]
Musser, James M. [1 ,3 ]
机构
[1] Methodist Hosp, Res Inst, Ctr Mol & Translat Human Infect Dis Res, Houston, TX 77030 USA
[2] Methodist Hosp, Res Inst, Comparat Med Program, Houston, TX 77030 USA
[3] Methodist Hosp, Dept Pathol, Houston, TX 77030 USA
[4] Methodist Hosp, Dept Med, Houston, TX 77030 USA
[5] NIAID, Lab Human Bacterial Pathogenesis, Rocky Mt Labs, NIH, Hamilton, MT USA
[6] NIAID, Vet Branch, Rocky Mt Labs, NIH, Hamilton, MT USA
[7] Univ Houston, Div Res, Houston, TX 77004 USA
[8] Baylor Coll Med, Ctr Comparat Med, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
LYMPHOID-TISSUE IBALT; VIRULENCE DETERMINANTS; NECROTIZING PNEUMONIA; SKIN INFECTIONS; HEALTHY-ADULTS; INFLUENZA; DISEASE; EPIDEMIOLOGY; USA300; VIRUS;
D O I
10.2353/ajpath.2010.090960
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Panton-Valentine leukocidin (PVL) is a two-component cytolytic toxin epidemiologically linked to community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) infections, including serious invasive infections caused by the epidemic clone referred to as strain USA300. Although PVL has long been known to be a S. aureus virulence molecule in vitro, the relative contribution of this leukotoxin to invasive CA-MRSA infections such as pneumonia remains controversial. We developed a nonhuman primate model of CA-MRSA pneumonia and used it to test the hypothesis that PVL contributes to lower respiratory tract infections caused by S. aureus strain USA300. The lower respiratory tract disease observed in this monkey model mimicked the clinical and pathological features of early mild to moderate S. aureus pneumonia in humans, including fine-structure histopathology. In this experiment using a large sample of monkeys and multiple time points of examination, no involvement of PVL in virulence could be de-tected. Compared with the wild-type parental USA300 strain, the isogenic PVL deletion-mutant strain caused equivalent lower respiratory tract pathology. We conclude that PVL does not contribute to lower respiratory tract infection in this nonhuman primate model of human CA-MRSA pneumonia. (Am J Pathol 2010, 176:1346-1354; DOI: 10.2353/ajpath.2010.090960)
引用
收藏
页码:1346 / 1354
页数:9
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