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Bidirectional transfer of human cytomegalovirus strains in donor and recipient seropositive lung transplant patients.
Külekci, Büsra; Mollik, Madlen; Schwarz, Stefan; Perkmann-Nagele, Nicole; Geleff, Silvana; Jaksch, Peter; Hoetzenecker, Konrad; Lambers, Christopher; Puchhammer-Stöckl, Elisabeth; Goerzer, Irene.
Afiliación
  • Külekci B; Center for Virology, Medical University of Vienna, Vienna, Austria.
  • Mollik M; Center for Virology, Medical University of Vienna, Vienna, Austria.
  • Schwarz S; Department of Thoracic Surgery, Medical University of Vienna, Vienna, Austria.
  • Perkmann-Nagele N; Divison of Clinical Virology, Department of Laboratory Medicine, University of Vienna, Vienna, Austria.
  • Geleff S; Department of Pathology, Medical University of Vienna, Vienna, Austria.
  • Jaksch P; Department of Thoracic Surgery, Medical University of Vienna, Vienna, Austria.
  • Hoetzenecker K; Department of Thoracic Surgery, Medical University of Vienna, Vienna, Austria.
  • Lambers C; Department of Thoracic Surgery, Medical University of Vienna, Vienna, Austria.
  • Puchhammer-Stöckl E; Center for Virology, Medical University of Vienna, Vienna, Austria.
  • Goerzer I; Center for Virology, Medical University of Vienna, Vienna, Austria.
J Med Virol ; 96(7): e29770, 2024 Jul.
Article en En | MEDLINE | ID: mdl-38949200
ABSTRACT
Donor and recipient human cytomegalovirus (HCMV) seropositive (D+R+) lung transplant recipients (LTRs) often harbor multiple strains of HCMV, likely due to transmitted donor (D) strains and reactivated recipient (R) strains. To date, the extent and timely occurrence of each likely source in shaping the post-transplantation (post-Tx) strain population is unknown. Here, we deciphered the D and R origin of the post-Tx HCMV strain composition in blood, bronchoalveolar lavage (BAL), and CD45+ BAL cell subsets. We investigated either D and/or R formalin-fixed paraffin-embedded blocks or fresh D lung tissue from four D+R+ LTRs obtained before transplantation. HCMV strains were characterized by short amplicon deep sequencing. In two LTRs, we show that the transplanted lung is reseeded by R strains within the first 6 months after transplantation, likely by infiltrating CD14+ CD163+/- alveolar macrophages. In three LTRs, we demonstrate both rapid D-strain dissemination and persistence in the transplanted lung for >1 year post-Tx. Broad inter-host diversity contrasts with intra-host genotype sequence stability upon transmission, during follow-up and across compartments. In D+R+ LTRs, HCMV strains of both, D and R origin can emerge first and dominate long-term in subsequent episodes of infection, indicating replication of both sources despite pre-existing immunity.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Donantes de Tejidos / Trasplante de Pulmón / Infecciones por Citomegalovirus / Citomegalovirus / Receptores de Trasplantes Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Med Virol Año: 2024 Tipo del documento: Article País de afiliación: Austria Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Donantes de Tejidos / Trasplante de Pulmón / Infecciones por Citomegalovirus / Citomegalovirus / Receptores de Trasplantes Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Med Virol Año: 2024 Tipo del documento: Article País de afiliación: Austria Pais de publicación: Estados Unidos