

@article {13685,
	title = {{Norwalk virus: how infectious is it?}},
	journal = {Journal of Medical Virology},
	volume = {80},
	number = {8},
	year = {2008},
	pages = {1468{\textendash}1476},
	abstract = {Noroviruses are major agents of viral gastroenteritis worldwide. The infectivity of Norwalk virus, the prototype norovirus, has been studied in susceptible human volunteers. A new variant of the hit theory model of microbial infection was developed to estimate the variation in Norwalk virus infectivity, as well as the degree of virus aggregation, consistent with independent (electron microscopic) observations. Explicit modeling of viral aggregation allows us to express virus infectivity per single infectious unit (particle). Comparison of a primary and a secondary inoculum showed that passage through a human host does not change Norwalk virus infectivity. We estimate the average probability of infection for a single Norwalk virus particle to be close to 0.5, exceeding that reported for any other virus studied to date. Infected subjects had a dose-dependent probability of becoming ill, ranging from 0.1 (at a dose of 10(3) NV genomes) to 0.7 (at 10(8) virus genomes). A norovirus dose response model is important for understanding its transmission and essential for development of a quantitative risk model. Norwalk virus is a valuable model system to study virulence because genetic factors are known for both complete and partial protection; the latter can be quantitatively described as heterogeneity in dose response models.},
	keywords = {Biological, Caliciviridae Infections, Caliciviridae Infections: genetics, Caliciviridae Infections: physiopathology, Caliciviridae Infections: transmission, Caliciviridae Infections: virology, Electron, Gastroenteritis, Gastroenteritis: genetics, Gastroenteritis: physiopathology, Gastroenteritis: virology, Humans, Microscopy, Models, Monte Carlo Method, Norovirus, Norwalk virus, Norwalk virus: genetics, Norwalk virus: isolation {\&} purification, Norwalk virus: pathogenicity, Norwalk virus: ultrastructure, QMRA, Reverse Transcriptase Polymerase Chain Reaction, Risk Assessment, RNA, Viral, Viral: analysis},
	author = {Peter FM Teunis and Moe, Christine L and Liu, Pengbo and Miller, Sara E and Lindesmith, Lisa and Baric, Ralph S and Le Pendu, Jacques and Calderon, Rebecca L}
}
