Abstract

BackgroundRespiratory syncytial virus (RSV) is a common respiratory pathogen that can cause severe pneumonia. In vivo studies of RSV can be difficult due to variation in viral infection and disease severity in some animal models. Factors that may contribute to the variation are decreases in viral titer due to preparation and storage and method of virus administration. Nebulization is one method of RSV administration that provides even distribution of virus to all lung lobes; however, the exact quantity of the virus killed by nebulization is not defined. To test the hypothesis that sucrose enhances RSV stability and infectivity, a series of in vitro experiments were conducted with RSV strain Memphis 37 stored at varying concentrations (0%, 3%, 5%, 8%, 10%, 15%, and 20%) of sucrose as a possible cryo- and nebulization protectant. The optimal in vitro concentration was then assessed in vivo in a lamb model.MethodsPrior to titering the virus on HEp-2 cells, the various virus solutions were subjected to one freeze-thaw cycle and one nebulization cycle. Forty-eight hours after viral plating, infectious foci were detected and counted using immunofluorescent imaging. Titers were determined after freeze-thaw and after freeze-thaw followed by nebulization, then compared to the stock titers (before freezing) as well as to one another to determine the loss of infectivity. To further test this in vivo, lambs 2 to 3-days-old were infected via nebulization with RSV using inoculate containing either 20% sucrose or no sucrose followed by assessments of infection severity.ResultsNebulization of virus in 0% sucrose resulted in a 0.580 log reduction in infectivity while virus in 20% sucrose exhibited a 0.297 log reduction. In vivo studies demonstrated that 20% sucrose enhanced RSV lesions and antigen distribution.ConclusionsThe data suggests that both nebulization and freeze-thawing of RSV in the absence of sucrose cause unacceptable losses in viral infectivity and that sucrose acts as a RSV protectant in both regards.

Highlights

  • Respiratory syncytial virus (RSV) is a common respiratory pathogen that can cause severe pneumonia

  • respiratory syncytial virus (RSV) in 3% sucrose concentration showed no log drop (0.00% loss) due to freeze-thawing and a 0.831 log drop (85.25% loss) due to nebulization representing an overall log drop of 0.694 (79.75% loss) (Figure 1)

  • RSV in 8% sucrose concentration showed no log drop (0.00% loss) due to freeze-thawing and a 0.477 log drop (66.67% loss) due to nebulization suggesting an overall log drop of 0.448 (64.38% loss) (Figure 1)

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Summary

Introduction

Respiratory syncytial virus (RSV) is a common respiratory pathogen that can cause severe pneumonia. In vivo studies of RSV can be difficult due to variation in viral infection and disease severity in some animal models. Nebulization is one method of RSV administration that provides even distribution of virus to all lung lobes; the exact quantity of the virus killed by nebulization is not defined. Respiratory syncytial virus (RSV) is estimated to cause 64 million cases of respiratory disease annually with the majority of cases occurring in children under the age of 5 and approximately 160,000 cases resulting in death [1,2,3,4,5,6,7]. While each method has its advantages and disadvantages, nebulization results in a uniform distribution of virus throughout all lung lobes; the extent to which nebulization damages or disrupts RSV has not yet been explored

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