Norovirus dose-response : are currently available data informative enough to determine how susceptible humans are to infection from a single virus?

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      <subfield code="a">Schmidt, Philip J.</subfield>
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      <subfield code="a">Norovirus dose-response</subfield>
      <subfield code="b">: are currently available data informative enough to determine how susceptible humans are to infection from a single virus?</subfield>
      <subfield code="c">Philip J. Schmidt</subfield>
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      <subfield code="a">Two forms of single-hit infection dose-response models have previously been developed to assess available data from human feeding trials and estimate the norovirus dose-response relationship. The mechanistic interpretations of these models include strong assumptions that warrant reconsideration: the first study includes an implicit assumption that there is no immunity to Norwalk virus among the specific study population, while the recent second study includes assumptions that such immunity could exist and that the nonimmune have no defensive barriers to prevent infection from exposure to just one virus. Both models addressed unmeasured virus aggregation in administered doses. In this work, the available data are reanalyzed using a generalization of the first model to explore these previous assumptions. It was hypothesized that concurrent estimation of an unmeasured degree of virus aggregation and important dose-response parameters could lead to structural nonidentifiability of the model (i.e., that a diverse range of alternative mechanistic interpretations yield the same optimal fit), and this is demonstrated using the profile likelihood approach and by algebraic proof. It is also demonstrated that omission of an immunity parameter can artificially inflate the estimated degree of aggregation and falsely suggest high susceptibility among the nonimmune. The currently available data support the assumption of immunity within the specific study population, but provide only weak information about the degree of aggregation and susceptibility among the nonimmune. The probability of infection at low and moderate doses may be much lower than previously asserted, but more data from strategically designed dose-response experiments are needed to provide adequate information.</subfield>
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      <subfield code="w">MAP20077000345</subfield>
      <subfield code="t">Risk analysis : an international journal</subfield>
      <subfield code="d">McLean, Virginia : Society for Risk Analysis, 1987-2015</subfield>
      <subfield code="x">0272-4332</subfield>
      <subfield code="g">01/07/2015 Volumen 35 Número 7 - julio 2015 </subfield>
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