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The research paper discusses the process of preparing lyophilized (freeze-dried) combinations of equine antisera for identifying different enteroviruses. Antisera from 42 specific enteroviruses are pooled together and rehydrated when needed to test for the presence of these viruses in field isolates.
The main focus of the research paper is the method used for preparing eight distinct pools of antisera, each containing sera from 10 to 11 different enteroviruses. These pools, identified as A to H, are prepared by lyophilizing, or freeze-drying, the antisera. The process involves:
The study further documents the procedures for rehydrating and using these antisera pools, and offers guidance on interpreting the results from serum neutralization tests. The steps include:
This research and its innovative strategy of preparing, storing, and using equine antisera could have several key applications and implications:
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