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Novel poxvirus infection in 2 patients from the United States.
Osadebe, Lynda U; Manthiram, Kalpana; McCollum, Andrea M; Li, Yu; Emerson, Ginny L; Gallardo-Romero, Nadia F; Doty, Jeffrey B; Wilkins, Kimberly; Zhao, Hui; Drew, Clifton P; Metcalfe, Maureen G; Goldsmith, Cynthia S; Muehlenbachs, Atis; Googe, Paul B; Dunn, John; Duenckel, Todd; Henderson, Heather; Carroll, Darin S; Zaki, Sherif R; Denison, Mark R; Reynolds, Mary G; Damon, Inger K.
Afiliación
  • Osadebe LU; Epidemic Intelligence Service, Division of Scientific Education and Professional Development Program Office Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Manthiram K; Division of Pediatric Infectious Disease, Vanderbilt University Medical Center.
  • McCollum AM; Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Li Y; Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Emerson GL; Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Gallardo-Romero NF; Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Doty JB; Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Wilkins K; Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Zhao H; Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Drew CP; Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Metcalfe MG; Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Goldsmith CS; Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Muehlenbachs A; Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Googe PB; Knoxville Dermatopathology Laboratory.
  • Dunn J; Tennessee Department of Health.
  • Duenckel T; Animal and Plant Health Inspection Service, US Department of Agriculture Regional Office, Nashville, Tennessee.
  • Henderson H; Tennessee Department of Health.
  • Carroll DS; Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Zaki SR; Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Denison MR; Knoxville Dermatopathology Laboratory.
  • Reynolds MG; Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Damon IK; Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia.
Clin Infect Dis ; 60(2): 195-202, 2015 Jan 15.
Article en En | MEDLINE | ID: mdl-25301210
ABSTRACT

BACKGROUND:

Some human poxvirus infections can be acquired through zoonotic transmission. We report a previously unknown poxvirus infection in 2 patients, 1 of whom was immunocompromised; both patients had known equine contact.

METHODS:

The patients were interviewed and clinical information was abstracted from the patients' medical files. Biopsies of the skin lesions were collected from both patients for histopathology, immunohistochemistry, and transmission electron microscopy analysis. Oral and skin swabs were collected from animals with frequent contact with the patients, and environmental sampling including rodent trapping was performed on the farm where the immunosuppressed patient was employed. "Pan-pox and high Guanine-cytosine" polymerase chain reaction assays were performed on patient, animal, and environmental isolates. Amplicon sequences of the viral DNA were used for agent identification and phylogenetic analysis.

RESULTS:

Specimens from both human cases revealed a novel poxvirus. The agent shares 88% similarity to viruses in the Parapoxvirus genus and 78% to those in the Molluscipoxvirus genus but is sufficiently divergent to resist classification as either. All animal and environmental specimens were negative for poxvirus and both patients had complete resolution of lesions.

CONCLUSIONS:

This report serves as a reminder that poxviruses should be considered in cutaneous human infections, especially in individuals with known barnyard exposures. The clinical course of the patients was similar to that of parapoxvirus infections, and the source of this virus is currently unknown but is presumed to be zoonotic. This report also demonstrates the importance of a comprehensive approach to diagnosis of human infections caused by previously unknown pathogens.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Poxviridae / Infecciones por Poxviridae Tipo de estudio: Prognostic_studies Límite: Humans País/Región como asunto: America do norte Idioma: En Año: 2015 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Poxviridae / Infecciones por Poxviridae Tipo de estudio: Prognostic_studies Límite: Humans País/Región como asunto: America do norte Idioma: En Año: 2015 Tipo del documento: Article