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Silent circulation of poliovirus in small populations

BACKGROUND: Small populations that have been isolated by conflict make vaccination and surveillance difficult, threatening polio eradication. Silent circulation is caused by asymptomatic infections. It is currently not clear whether the dynamics of waning immunity also influence the risk of silent c...

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Detalles Bibliográficos
Autores principales: Vallejo, Celeste, Keesling, James, Koopman, James, Singer, Burton
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6001964/
https://www.ncbi.nlm.nih.gov/pubmed/30137721
http://dx.doi.org/10.1016/j.idm.2017.11.001
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author Vallejo, Celeste
Keesling, James
Koopman, James
Singer, Burton
author_facet Vallejo, Celeste
Keesling, James
Koopman, James
Singer, Burton
author_sort Vallejo, Celeste
collection PubMed
description BACKGROUND: Small populations that have been isolated by conflict make vaccination and surveillance difficult, threatening polio eradication. Silent circulation is caused by asymptomatic infections. It is currently not clear whether the dynamics of waning immunity also influence the risk of silent circulation in the absence of vaccination. Such circulation can, nevertheless, be present following a declaration of elimination as a result of inadequate acute flaccid paralysis surveillance (AFPS) or environmental surveillance (ES). METHODS: We have constructed a stochastic model to understand how stochastic effects alter the ability of small populations to sustain virus circulation in the absence of vaccination. We analyzed how the stochastic process determinants of the duration of silent circulation that could have been detected by ES were affected by [Formula: see text] , waning dynamics, population size, and AFPS sensitivity in a discrete individual stochastic model with homogeneous contagiousness and random mixing. We measured the duration of silent circulation both by the interval between detected acute flaccid paralysis (AFP) cases and the duration of circulation until elimination. RESULTS: As [Formula: see text] increased and population size increased, the interval between detected AFP cases and the duration of circulation until elimination increased. As AFPS detection rates decreased, the interval between detected AFP cases increased. There was up to a 22 [Formula: see text] chance of silent circulation lasting for more than 3 years with 100 [Formula: see text] AFP detection. The duration of silent circulation was not affected by the waning immunity dynamics. CONCLUSION: We demonstrated that small populations have the potential to sustain prolonged silent circulation. Surveillance in these areas should be intensified before declaring elimination. To further validate these conclusions, it is necessary to realistically relax the simplifying assumptions about mixing and waning.
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spelling pubmed-60019642018-06-20 Silent circulation of poliovirus in small populations Vallejo, Celeste Keesling, James Koopman, James Singer, Burton Infect Dis Model Article BACKGROUND: Small populations that have been isolated by conflict make vaccination and surveillance difficult, threatening polio eradication. Silent circulation is caused by asymptomatic infections. It is currently not clear whether the dynamics of waning immunity also influence the risk of silent circulation in the absence of vaccination. Such circulation can, nevertheless, be present following a declaration of elimination as a result of inadequate acute flaccid paralysis surveillance (AFPS) or environmental surveillance (ES). METHODS: We have constructed a stochastic model to understand how stochastic effects alter the ability of small populations to sustain virus circulation in the absence of vaccination. We analyzed how the stochastic process determinants of the duration of silent circulation that could have been detected by ES were affected by [Formula: see text] , waning dynamics, population size, and AFPS sensitivity in a discrete individual stochastic model with homogeneous contagiousness and random mixing. We measured the duration of silent circulation both by the interval between detected acute flaccid paralysis (AFP) cases and the duration of circulation until elimination. RESULTS: As [Formula: see text] increased and population size increased, the interval between detected AFP cases and the duration of circulation until elimination increased. As AFPS detection rates decreased, the interval between detected AFP cases increased. There was up to a 22 [Formula: see text] chance of silent circulation lasting for more than 3 years with 100 [Formula: see text] AFP detection. The duration of silent circulation was not affected by the waning immunity dynamics. CONCLUSION: We demonstrated that small populations have the potential to sustain prolonged silent circulation. Surveillance in these areas should be intensified before declaring elimination. To further validate these conclusions, it is necessary to realistically relax the simplifying assumptions about mixing and waning. KeAi Publishing 2017-11-08 /pmc/articles/PMC6001964/ /pubmed/30137721 http://dx.doi.org/10.1016/j.idm.2017.11.001 Text en © 2017 The Authors. Production and hosting by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Vallejo, Celeste
Keesling, James
Koopman, James
Singer, Burton
Silent circulation of poliovirus in small populations
title Silent circulation of poliovirus in small populations
title_full Silent circulation of poliovirus in small populations
title_fullStr Silent circulation of poliovirus in small populations
title_full_unstemmed Silent circulation of poliovirus in small populations
title_short Silent circulation of poliovirus in small populations
title_sort silent circulation of poliovirus in small populations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6001964/
https://www.ncbi.nlm.nih.gov/pubmed/30137721
http://dx.doi.org/10.1016/j.idm.2017.11.001
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