Stephanie M Pouch1, Shalika B Katugaha2, Wun-Ju Shieh3, Pallavi Annambhotla4, William L Walker5,6, Sridhar V Basavaraju4, Jefferson Jones4, Thanhthao Huynh3, Sarah Reagan-Steiner3, Julu Bhatnagar3, Kacie Grimm7, Susan L Stramer7, Julie Gabel8, G Marshall Lyon1, Aneesh K Mehta1, Prem Kandiah9, David C Neujahr10, Jeffrey Javidfar11, Ram M Subramanian12, Samir M Parekh12, Palak Shah13, Lauren Cooper13, Mitchell A Psotka13, Rachel Radcliffe14, Carl Williams15, Sherif R Zaki3, J Erin Staples5, Marc Fischer5, Amanda J Panella5, Robert S Lanciotti5, Janeen J Laven5, Olga Kosoy5, Ingrid B Rabe5, Carolyn V Gould5. 1. Division of Infectious Diseases, Emory University School of Medicine, Atlanta, Georgia. 2. Infectious Diseases Physicians, Inc, Inova Fairfax Hospital Heart and Vascular Institute, Falls Church, Virginia. 3. Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention (CDC), Atlanta, Georgia. 4. Division of Healthcare Quality Promotion, National Center for Emerging and Zoonotic Infectious Diseases (NCEZID), Centers for Disease Control and Prevention (CDC), Atlanta, Georgia. 5. Division of Vector-Borne Diseases, NCEZID, CDC, Fort Collins, Colorado. 6. Epidemic Intelligence Service, Center for Surveillance, Epidemiology and Laboratory Services, CDC, Atlanta, Georgia. 7. American Red Cross, Gaithersburg, Maryland, Emory University School of Medicine, Atlanta, Georgia. 8. Georgia Department of Public Health, Emory University School of Medicine, Atlanta, Georgia. 9. Department of Neurology and Neurosurgery, Emory University School of Medicine, Atlanta, Georgia. 10. Division of Pulmonary Allergy and Critical Care Medicine, Emory University School of Medicine, Atlanta, Georgia. 11. Department of Surgery, Emory University School of Medicine, Atlanta, Georgia. 12. Division of Digestive Diseases, Emory University School of Medicine, Atlanta, Georgia. 13. Department of Heart Failure and Transplantation, Inova Fairfax Hospital Heart and Vascular Institute, Falls Church, Virginia. 14. Division of Acute Disease Epidemiology, South Carolina Department of Health and Environmental Control, Columbia. 15. North Carolina Division of Public Health, Raleigh.
Abstract
BACKGROUND: In fall 2017, 3 solid organ transplant (SOT) recipients from a common donor developed encephalitis within 1 week of transplantation, prompting suspicion of transplant-transmitted infection. Eastern equine encephalitis virus (EEEV) infection was identified during testing of endomyocardial tissue from the heart recipient. METHODS: We reviewed medical records of the organ donor and transplant recipients and tested serum, whole blood, cerebrospinal fluid, and tissue from the donor and recipients for evidence of EEEV infection by multiple assays. We investigated blood transfusion as a possible source of organ donor infection by testing remaining components and serum specimens from blood donors. We reviewed data from the pretransplant organ donor evaluation and local EEEV surveillance. RESULTS: We found laboratory evidence of recent EEEV infection in all organ recipients and the common donor. Serum collected from the organ donor upon hospital admission tested negative, but subsequent samples obtained prior to organ recovery were positive for EEEV RNA. There was no evidence of EEEV infection among donors of the 8 blood products transfused into the organ donor or in products derived from these donations. Veterinary and mosquito surveillance showed recent EEEV activity in counties nearby the organ donor's county of residence. Neuroinvasive EEEV infection directly contributed to the death of 1 organ recipient and likely contributed to death in another. CONCLUSIONS: Our investigation demonstrated EEEV transmission through SOT. Mosquito-borne transmission of EEEV to the organ donor was the likely source of infection. Clinicians should be aware of EEEV as a cause of transplant-associated encephalitis.
BACKGROUND: In fall 2017, 3 solid organ transplant (SOT) recipients from a common donor developed encephalitis within 1 week of transplantation, prompting suspicion of transplant-transmitted infection. Easternequineencephalitis virus (EEEV) infection was identified during testing of endomyocardial tissue from the heart recipient. METHODS: We reviewed medical records of the organ donor and transplant recipients and tested serum, whole blood, cerebrospinal fluid, and tissue from the donor and recipients for evidence of EEEVinfection by multiple assays. We investigated blood transfusion as a possible source of organ donorinfection by testing remaining components and serum specimens from blood donors. We reviewed data from the pretransplant organ donor evaluation and local EEEV surveillance. RESULTS: We found laboratory evidence of recent EEEVinfection in all organ recipients and the common donor. Serum collected from the organ donor upon hospital admission tested negative, but subsequent samples obtained prior to organ recovery were positive for EEEV RNA. There was no evidence of EEEVinfection among donors of the 8 blood products transfused into the organ donor or in products derived from these donations. Veterinary and mosquito surveillance showed recent EEEV activity in counties nearby the organ donor's county of residence. Neuroinvasive EEEV infection directly contributed to the death of 1 organ recipient and likely contributed to death in another. CONCLUSIONS: Our investigation demonstrated EEEV transmission through SOT. Mosquito-borne transmission of EEEV to the organ donor was the likely source of infection. Clinicians should be aware of EEEV as a cause of transplant-associated encephalitis.
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