Transmission of Imported Vaccine-Derived Poliovirus in an Undervaccinated Community in Minnesota
MAJOR ARTICLE
Transmission of Imported Vaccine-Derived
Poliovirus in an Undervaccinated Community in
Minnesota
James P. Alexander,1 Kristen Ehresmann,2 Jane Seward,1 Gary Wax,2,a Kathleen Harriman,2,a Susan Fuller,2
Elizabeth A. Cebelinski,2 Qi Chen,1 Jaume Jorba,1 Olen M. Kew,1 Mark A. Pallansch,1 M. Steven Oberste,1
Mark Schleiss,3 Jeffrey P. Davis,4 Bryna Warshawsky,5 Susan Squires,6 and Harry F. Hull,2,a for the Vaccine-Derived
Poliovirus Investigations Groupb
1
National Center for Immunizations and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia; 2Minnesota
Department of Health, St. Paul, and 3University of Minnesota School of Medicine, Minneapolis; 4Division of Public Health, Wisconsin Department
of Health and Family Services, Madison; 5Middlesex–London Health Unit, London, and 6Public Health Agency of Canada, Ottawa, Ontario, Canada
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.
Because of successful vaccination programs, endemic
poliomyelitis was eliminated from the United States by
the mid-1970s. In 1979, after importation of wild poliovirus, the last US polio outbreak occurred in unvaccinated Amish communities, involving 13 cases of paraReceived 17 July 2008; accepted 27 August 2008; electronically published 17
December 2008.
Potential conflicts of interest: none reported.
Presented in part: National Vaccine Advisory Committee, Washington, DC, 8
February 2006; National Immunization Conference, Atlanta, 7 March 2006.
Financial support: none reported.
a Present affiliations: California Department of Public Health, Immunization
Branch, Epidemiology and Surveillance Section, Richmond (K.H.); HF Hull Associates, St. Paul, Minnesota (H.F.H.); HealthEast Care System, St. Joseph’s Hospital,
St. Paul, Minnesota (G.W.).
b Study group members are listed after the text.
Reprints or correspondence: Dr. James Alexander, 1600 Clifton Rd. NE, Mail
Stop E-05, Atlanta, GA 30333 ().
The Journal of Infectious Diseases 2009; 199:391–7
© 2008 by the Infectious Diseases Society of America. All rights reserved.
0022-1899/2009/19903-0014$15.00
DOI: 10.1086/596052
lytic disease in 3 states and subclinical infections in 3
other states as well as 2 cases of paralytic disease in Ontario, Canada [1, 2]. From 1980 to 1997, a mean of 9
reported paralytic poliomyelitis cases occurred annually
in the United States [3, 4]. Nearly all were vaccineassociated paralytic polio (VAPP), underscoring the ongoing risk associated with oral poliovirus vaccine
(OPV), estimated to be 1 case of VAPP per 2.9 million
doses distributed [4]. As the occurrence of wild poliovirus importations declined to only 5 in the 1980s and to 2
in the 1990s [3, 4], the risk-benefit equation changed in
favor of using inactivated poliovirus vaccine (IPV) routinely. From 1997 to 2000, the transition in vaccination
policy from an all-OPV to an all-IPV schedule eliminated VAPP in the United States; the last endemically
acquired case of VAPP occurred in 1999 [4 – 6].
In addition to causing VAPP, OPV use is also associated with the rare occurrence of genetically drifted
Vaccine-Derived Poliovirus Type 1 in the US
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vaccine-derived polioviruses (VDPVs) that can circulate in undervaccinated populations (circulating VDPVs [cVDPVs]) or
cause persistent infections in immunodeficient individuals (immunodeficiency-related VDPVs [iVDPVs]) [7–9]. In September
2005, a poliovirus infection in an unvaccinated Amish infant was
identified by the Minnesota Department of Health and reported
to the Centers for Disease Control and Prevention. The virus was
identified as type 1 VDPV. The present report describes the epidemiologic and laboratory investigations and control efforts regarding the first VDPV with community transmission detected
in the United States.
METHODS
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Alexander et al.
Index patient investigation. We reviewed the infant’s medical, family, and social history to identify potential sources for
exposure to polioviruses. We confirmed the infant’s VDPV infection and monitored her for ongoing excretion of VDPVs during treatment of the underlying immunodeficiency, using approximately weekly testing (from late September 2005 through
January 2006) of serum samples for neutralizing antibody to
polioviruses and of stool specimens for VDPVs.
Hospital and health care investigations and interventions. In October 2005, we conducted investigations at the
4 hospitals (hospitals 1– 4) to which the infant had been admitted, to determine whether she had been infected in the health
care setting or whether her infection had been transmitted to
others. Hospital staff offered IPV to health care workers and
patients with recent or ongoing exposure who were not current
for polio vaccination [6]. At hospitals 1–3, where the infant had
been admitted during July–August 2005, hospital infection control staff reviewed health care worker and patient records to
identify contacts. We surveyed contact health care workers and
infection control staff reviewed contact patient records regarding relevant recent illness and immunologic status. At hospital 4,
where the infant remained hospitalized in October 2005, we surveyed staff who reported exposure to the infant or her environment without the use of contact precautions regarding polio vaccination status, immunologic status, and recent illnesses in
themselves or family members. Hospital staff collected stool
specimens from potentially exposed staff and from patients who
were located in the same medical units as the infant.
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