Abstract
In 1903 de Schweinitz and Dorset (1) described the serial transmission of hog cholera (HC) using body fluids of diseased pigs. The fluids had been filtrated through ‘finest porcelain filters’, thus indicating that the causative agent of hog cholera was a filtrable substance rather than the ‘hog cholera bacillus’. These first attempts to characterize hog cholera virus (HCV) particles were followed by experiments using more advanced filtration techniques, electron microscopy, electrophoresis, and ultracentrifugation. Probably due to technical difficulties early results were inconsistent. Table 1 summarizes the attempts to assess the size of HCV particles (2–24). Kernkamp (2) calculated a size of smaller than 35 nm after filtration of the virus through collodion membranes. An even smaller size of 15–25 nm was determined by Pehl and Gralheer (4). However, in more recent filtration studies (6, 9, 11) particle sizes varied from approximately 29 nm to 50 nm. In experiments by Kubin (9), e.g., pigs only seroconverted after being inoculated with filtrates from membranes with a pore size of 35–100 nm.
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Moennig, V. (1988). Characteristics of the Virus. In: Liess, B. (eds) Classical Swine Fever and Related Viral Infections. Developments in Veterinary Virology, vol 5. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-2083-8_3
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