Ring infection. In 2010, Yoong and Pier showed that the administration of antisera, isolated from rabbits immunized with PVL, to S. aureus-infected mice led to worse disease outcomes (209). This study suggested that the proinflammatory activity of PVL on host LIMKI 3MedChemExpress LIMKI 3 immune cells, rather than being detrimental, as described for rabbit pneumonia models, is CBR-5884 site actually beneficial and assists in establishing more productive immune responses and better infection resolution. When PVL is neutralized (or deleted from the S. aureus genome), the overall virulence of S. aureus was actually enhanced rather than diminished (208?210, 233). These studies are in direct opposition to work that was reported the year prior indicating that immunization of mice with PVL led to reduced pathological outcomes in models of necrotizing pneumonia and skin and soft tissue infection (204). Similarly, the administration of anti-PVL antibodies to the eyes of S. aureusinfected mice using a keratitis model demonstrated increased efficacy for the resolution of CA-MRSA (327). An additional study showed that immunization of mice with rationally designed mutants of PVL leads to significantly improved outcomes in a lethal systemic infection model, although the protection observed in this model is likely due to the broadly neutralizing capacity of the sera (lytic factors other than PVL were blocked by sera obtained from PVL-immunized animals) (328). Currently, it is difficult to reconcile the conflicting evidence both in favor of and against leucocidin immunization strategies as viable therapeutic options. As noted above, the majority of PVL-based virulence studies were conducted by using suboptimal murine infection models. PVL is not lytic toward murine leukocytes, although it is capable of eliciting immune-activating properties on murine cells (200, 210). Thus, a major biological function of the toxin is not considered when using murine models to assess virulence features attributed to PVL and the efficacy of antibody-mediated neutralization of the toxin. Studies with human subjects have demonstrated that children can produce remarkably high levels of anti-PVL antibodies at a very young age, yet they still remain susceptible to SSTI caused by S. aureus (329). Such findings suggest that neutralizing antibody alone does not necessarily protect against S. aureus infection. However, it is possible that the presence of PVL antibodies may still have the ability to reduce adverse infection outcomes without necessarily preventing disease. A recent study by Rasigade et al. found that the time to death of patients with necrotizing pneumonia who had previously had PVL infections was significantly longer than that of patients who had not previously had a PVL S. aureus infection (131). However, while the acute onset and pathological outcomes associated with disease were far more rapid in patients who had not experienced PVL S. aureus infections in the past, both patient groups still showed the same number of deaths overall (131). Thus, PVL antibodies may have slowed the progres-June 2014 Volume 78 Numbermmbr.asm.orgAlonzo and Torression of disease but did not prevent the mortality associated with severe S. aureus necrotizing pneumonia. Importantly, both murine and human studies exclusively assessed the therapeutic efficacy of neutralizing the activity of only one leucocidin, PVL. Given the likelihood that any given clinically relevant S. aureus strain will produce at least three bicomponent leuc.Ring infection. In 2010, Yoong and Pier showed that the administration of antisera, isolated from rabbits immunized with PVL, to S. aureus-infected mice led to worse disease outcomes (209). This study suggested that the proinflammatory activity of PVL on host immune cells, rather than being detrimental, as described for rabbit pneumonia models, is actually beneficial and assists in establishing more productive immune responses and better infection resolution. When PVL is neutralized (or deleted from the S. aureus genome), the overall virulence of S. aureus was actually enhanced rather than diminished (208?210, 233). These studies are in direct opposition to work that was reported the year prior indicating that immunization of mice with PVL led to reduced pathological outcomes in models of necrotizing pneumonia and skin and soft tissue infection (204). Similarly, the administration of anti-PVL antibodies to the eyes of S. aureusinfected mice using a keratitis model demonstrated increased efficacy for the resolution of CA-MRSA (327). An additional study showed that immunization of mice with rationally designed mutants of PVL leads to significantly improved outcomes in a lethal systemic infection model, although the protection observed in this model is likely due to the broadly neutralizing capacity of the sera (lytic factors other than PVL were blocked by sera obtained from PVL-immunized animals) (328). Currently, it is difficult to reconcile the conflicting evidence both in favor of and against leucocidin immunization strategies as viable therapeutic options. As noted above, the majority of PVL-based virulence studies were conducted by using suboptimal murine infection models. PVL is not lytic toward murine leukocytes, although it is capable of eliciting immune-activating properties on murine cells (200, 210). Thus, a major biological function of the toxin is not considered when using murine models to assess virulence features attributed to PVL and the efficacy of antibody-mediated neutralization of the toxin. Studies with human subjects have demonstrated that children can produce remarkably high levels of anti-PVL antibodies at a very young age, yet they still remain susceptible to SSTI caused by S. aureus (329). Such findings suggest that neutralizing antibody alone does not necessarily protect against S. aureus infection. However, it is possible that the presence of PVL antibodies may still have the ability to reduce adverse infection outcomes without necessarily preventing disease. A recent study by Rasigade et al. found that the time to death of patients with necrotizing pneumonia who had previously had PVL infections was significantly longer than that of patients who had not previously had a PVL S. aureus infection (131). However, while the acute onset and pathological outcomes associated with disease were far more rapid in patients who had not experienced PVL S. aureus infections in the past, both patient groups still showed the same number of deaths overall (131). Thus, PVL antibodies may have slowed the progres-June 2014 Volume 78 Numbermmbr.asm.orgAlonzo and Torression of disease but did not prevent the mortality associated with severe S. aureus necrotizing pneumonia. Importantly, both murine and human studies exclusively assessed the therapeutic efficacy of neutralizing the activity of only one leucocidin, PVL. Given the likelihood that any given clinically relevant S. aureus strain will produce at least three bicomponent leuc.
