Transmission of Imported Vaccine-Derived Poliovirus in an Undervaccinated Community in Minnesota

Background.Oral poliovirus vaccine (OPV) has not been used in the United States since 2000. Type 1 vaccinederived poliovirus (VDPV) was identified in September 2005, from an unvaccinated Amish infant hospitalized in Minnesota with severe combined immunodeficiency. An investigation was conducted to d...

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Veröffentlicht in:The Journal of infectious diseases 2009-02, Vol.199 (3), p.391-397
Hauptverfasser: Alexander, James P., Ehresmann, Kristen, Seward, Jane, Wax, Gary, Harriman, Kathleen, Fuller, Susan, Cebelinski, Elizabeth A., Chen, Qi, Kew, Olen M., Pallansch, Mark A., Oberste, M. Steven, Schleiss, Mark, Davis, Jeffrey P., Warshasky, Bryna, Squires, Susan, Hull, Harry F.
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container_end_page 397
container_issue 3
container_start_page 391
container_title The Journal of infectious diseases
container_volume 199
creator Alexander, James P.
Ehresmann, Kristen
Seward, Jane
Wax, Gary
Harriman, Kathleen
Fuller, Susan
Cebelinski, Elizabeth A.
Chen, Qi
Kew, Olen M.
Pallansch, Mark A.
Oberste, M. Steven
Schleiss, Mark
Davis, Jeffrey P.
Warshasky, Bryna
Squires, Susan
Hull, Harry F.
description Background.Oral poliovirus vaccine (OPV) has not been used in the United States since 2000. Type 1 vaccinederived poliovirus (VDPV) was identified in September 2005, from an unvaccinated Amish infant hospitalized in Minnesota with severe combined immunodeficiency. An investigation was conducted to determine the source of the virus and its means of transmission. Methods. The infant was tested serially for poliovirus excretion. Investigations were conducted to detect poliovirus infections or paralytic poliomyelitis in Amish communities in Minnesota, neighboring states, and Ontario, Canada. Genomic sequences of poliovirus isolates were determined for phylogenetic analysis. Results. No source for the VDPV could be identified. In the index community, 8 (35%) of 23 children tested, including the infant, had evidence of type 1 poliovirus or VDPV infection. Phylogenetic analysis suggested that the VDPV circulated in the community for ∼2 months before the infant's infection was detected and that the initiating OPV dose had been given before her birth. No paralytic disease was found in the community, and no poliovirus infections were found in other Amish communities investigated. Conclusions. This is the first demonstrated transmission of VDPV in an undervaccinated community in a developed country. Continued vigilance is needed in all countries to identify poliovirus infections in communities at high risk of poliovirus transmission.
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Steven ; Schleiss, Mark ; Davis, Jeffrey P. ; Warshasky, Bryna ; Squires, Susan ; Hull, Harry F.</creator><creatorcontrib>Alexander, James P. ; Ehresmann, Kristen ; Seward, Jane ; Wax, Gary ; Harriman, Kathleen ; Fuller, Susan ; Cebelinski, Elizabeth A. ; Chen, Qi ; Kew, Olen M. ; Pallansch, Mark A. ; Oberste, M. Steven ; Schleiss, Mark ; Davis, Jeffrey P. ; Warshasky, Bryna ; Squires, Susan ; Hull, Harry F. ; Vaccine-Derived Poliovirus Investigations Group ; Vaccine‐Derived Poliovirus Investigations Group</creatorcontrib><description>Background.Oral poliovirus vaccine (OPV) has not been used in the United States since 2000. Type 1 vaccinederived poliovirus (VDPV) was identified in September 2005, from an unvaccinated Amish infant hospitalized in Minnesota with severe combined immunodeficiency. An investigation was conducted to determine the source of the virus and its means of transmission. Methods. The infant was tested serially for poliovirus excretion. Investigations were conducted to detect poliovirus infections or paralytic poliomyelitis in Amish communities in Minnesota, neighboring states, and Ontario, Canada. Genomic sequences of poliovirus isolates were determined for phylogenetic analysis. Results. No source for the VDPV could be identified. In the index community, 8 (35%) of 23 children tested, including the infant, had evidence of type 1 poliovirus or VDPV infection. Phylogenetic analysis suggested that the VDPV circulated in the community for ∼2 months before the infant's infection was detected and that the initiating OPV dose had been given before her birth. No paralytic disease was found in the community, and no poliovirus infections were found in other Amish communities investigated. Conclusions. This is the first demonstrated transmission of VDPV in an undervaccinated community in a developed country. Continued vigilance is needed in all countries to identify poliovirus infections in communities at high risk of poliovirus transmission.</description><identifier>ISSN: 0022-1899</identifier><identifier>EISSN: 1537-6613</identifier><identifier>DOI: 10.1086/596052</identifier><identifier>PMID: 19090774</identifier><identifier>CODEN: JIDIAQ</identifier><language>eng</language><publisher>Oxford: The University of Chicago Press</publisher><subject>Adolescent ; Amino Acid Sequence ; Antigens, Viral - chemistry ; Antigens, Viral - genetics ; Applied microbiology ; Biological and medical sciences ; Bone Marrow Transplantation ; Child, Preschool ; Communities ; Epidemiology ; Feces - virology ; Female ; Fundamental and applied biological sciences. Psychology ; Humans ; Immunoglobulins, Intravenous - therapeutic use ; Infant ; Infants ; Infections ; Infectious diseases ; Medical sciences ; Microbiology ; Minnesota ; Miscellaneous ; Oral poliovirus vaccine ; Phylogeny ; Polio ; Poliomyelitis - prevention &amp; control ; Poliomyelitis - transmission ; Poliomyelitis - virology ; Poliovirus ; Poliovirus - classification ; Poliovirus - genetics ; Poliovirus - isolation &amp; purification ; Poliovirus Vaccines - administration &amp; dosage ; Poliovirus Vaccines - immunology ; Preventive medicine ; Severe Combined Immunodeficiency - complications ; Severe Combined Immunodeficiency - therapy ; Time Factors ; Vaccination ; Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects) ; Virology ; Viruses</subject><ispartof>The Journal of infectious diseases, 2009-02, Vol.199 (3), p.391-397</ispartof><rights>Copyright 2008 Infectious Diseases Society of America</rights><rights>2009 by the Infectious Diseases Society of America 2009</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c393t-8a9a2148a1dbc5c59e8d819bebc5c3a6245cdef88c9698005476b87f93e452743</citedby><cites>FETCH-LOGICAL-c393t-8a9a2148a1dbc5c59e8d819bebc5c3a6245cdef88c9698005476b87f93e452743</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/40254431$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/40254431$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,799,27903,27904,57995,58228</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=21050849$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19090774$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Alexander, James P.</creatorcontrib><creatorcontrib>Ehresmann, Kristen</creatorcontrib><creatorcontrib>Seward, Jane</creatorcontrib><creatorcontrib>Wax, Gary</creatorcontrib><creatorcontrib>Harriman, Kathleen</creatorcontrib><creatorcontrib>Fuller, Susan</creatorcontrib><creatorcontrib>Cebelinski, Elizabeth A.</creatorcontrib><creatorcontrib>Chen, Qi</creatorcontrib><creatorcontrib>Kew, Olen M.</creatorcontrib><creatorcontrib>Pallansch, Mark A.</creatorcontrib><creatorcontrib>Oberste, M. Steven</creatorcontrib><creatorcontrib>Schleiss, Mark</creatorcontrib><creatorcontrib>Davis, Jeffrey P.</creatorcontrib><creatorcontrib>Warshasky, Bryna</creatorcontrib><creatorcontrib>Squires, Susan</creatorcontrib><creatorcontrib>Hull, Harry F.</creatorcontrib><creatorcontrib>Vaccine-Derived Poliovirus Investigations Group</creatorcontrib><creatorcontrib>Vaccine‐Derived Poliovirus Investigations Group</creatorcontrib><title>Transmission of Imported Vaccine-Derived Poliovirus in an Undervaccinated Community in Minnesota</title><title>The Journal of infectious diseases</title><addtitle>The Journal of Infectious Diseases</addtitle><addtitle>The Journal of Infectious Diseases</addtitle><description>Background.Oral poliovirus vaccine (OPV) has not been used in the United States since 2000. Type 1 vaccinederived poliovirus (VDPV) was identified in September 2005, from an unvaccinated Amish infant hospitalized in Minnesota with severe combined immunodeficiency. An investigation was conducted to determine the source of the virus and its means of transmission. Methods. The infant was tested serially for poliovirus excretion. Investigations were conducted to detect poliovirus infections or paralytic poliomyelitis in Amish communities in Minnesota, neighboring states, and Ontario, Canada. Genomic sequences of poliovirus isolates were determined for phylogenetic analysis. Results. No source for the VDPV could be identified. In the index community, 8 (35%) of 23 children tested, including the infant, had evidence of type 1 poliovirus or VDPV infection. Phylogenetic analysis suggested that the VDPV circulated in the community for ∼2 months before the infant's infection was detected and that the initiating OPV dose had been given before her birth. No paralytic disease was found in the community, and no poliovirus infections were found in other Amish communities investigated. Conclusions. 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Steven</au><au>Schleiss, Mark</au><au>Davis, Jeffrey P.</au><au>Warshasky, Bryna</au><au>Squires, Susan</au><au>Hull, Harry F.</au><aucorp>Vaccine-Derived Poliovirus Investigations Group</aucorp><aucorp>Vaccine‐Derived Poliovirus Investigations Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transmission of Imported Vaccine-Derived Poliovirus in an Undervaccinated Community in Minnesota</atitle><jtitle>The Journal of infectious diseases</jtitle><stitle>The Journal of Infectious Diseases</stitle><addtitle>The Journal of Infectious Diseases</addtitle><date>2009-02-01</date><risdate>2009</risdate><volume>199</volume><issue>3</issue><spage>391</spage><epage>397</epage><pages>391-397</pages><issn>0022-1899</issn><eissn>1537-6613</eissn><coden>JIDIAQ</coden><abstract>Background.Oral poliovirus vaccine (OPV) has not been used in the United States since 2000. Type 1 vaccinederived poliovirus (VDPV) was identified in September 2005, from an unvaccinated Amish infant hospitalized in Minnesota with severe combined immunodeficiency. An investigation was conducted to determine the source of the virus and its means of transmission. Methods. The infant was tested serially for poliovirus excretion. Investigations were conducted to detect poliovirus infections or paralytic poliomyelitis in Amish communities in Minnesota, neighboring states, and Ontario, Canada. Genomic sequences of poliovirus isolates were determined for phylogenetic analysis. Results. No source for the VDPV could be identified. In the index community, 8 (35%) of 23 children tested, including the infant, had evidence of type 1 poliovirus or VDPV infection. Phylogenetic analysis suggested that the VDPV circulated in the community for ∼2 months before the infant's infection was detected and that the initiating OPV dose had been given before her birth. No paralytic disease was found in the community, and no poliovirus infections were found in other Amish communities investigated. Conclusions. This is the first demonstrated transmission of VDPV in an undervaccinated community in a developed country. Continued vigilance is needed in all countries to identify poliovirus infections in communities at high risk of poliovirus transmission.</abstract><cop>Oxford</cop><pub>The University of Chicago Press</pub><pmid>19090774</pmid><doi>10.1086/596052</doi><tpages>7</tpages></addata></record>
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source Jstor Complete Legacy; Oxford University Press Journals All Titles (1996-Current); MEDLINE; Alma/SFX Local Collection
subjects Adolescent
Amino Acid Sequence
Antigens, Viral - chemistry
Antigens, Viral - genetics
Applied microbiology
Biological and medical sciences
Bone Marrow Transplantation
Child, Preschool
Communities
Epidemiology
Feces - virology
Female
Fundamental and applied biological sciences. Psychology
Humans
Immunoglobulins, Intravenous - therapeutic use
Infant
Infants
Infections
Infectious diseases
Medical sciences
Microbiology
Minnesota
Miscellaneous
Oral poliovirus vaccine
Phylogeny
Polio
Poliomyelitis - prevention & control
Poliomyelitis - transmission
Poliomyelitis - virology
Poliovirus
Poliovirus - classification
Poliovirus - genetics
Poliovirus - isolation & purification
Poliovirus Vaccines - administration & dosage
Poliovirus Vaccines - immunology
Preventive medicine
Severe Combined Immunodeficiency - complications
Severe Combined Immunodeficiency - therapy
Time Factors
Vaccination
Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects)
Virology
Viruses
title Transmission of Imported Vaccine-Derived Poliovirus in an Undervaccinated Community in Minnesota
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