Sequence typing of human adenoviruses isolated from Polish patients subjected to allogeneic hematopoietic stem cell transplantation - a single center experience

• Published in: Hematology (Luxembourg) Vol. 23; no. 9; pp. 633 - 638
• Main Authors: Przybylski, Maciej, Rynans, Sylwia, Waszczuk-Gajda, Anna, Bilinski, Jarosław, Basak, Grzegorz W., Jędrzejczak, Wiesław W., Wróblewska, Marta, Młynarczyk, Grażyna, Dzieciątkowski, Tomasz
• Format: Journal Article
• Language: English
• Published: England Taylor & Francis 21.10.2018
• Subjects: Adenoviridae - classification; Adenoviridae - genetics; Adenoviridae - isolation & purification; Adenoviridae - metabolism; Adenoviridae Infections - blood; Adenoviridae Infections - genetics; Adult; Allografts; Antibodies, Viral - blood; Female; Graft vs Host Disease - blood; Graft vs Host Disease - genetics; Graft vs Host Disease - virology; HAdV type; Hematopoietic Stem Cell Transplantation; Humans; Immunoglobulin G - blood; Male; Middle Aged; Poland; post-transplant infections; sequence-based typing; hematopoietic stem cell transplantation; sequence-based typing; HAdV type; post-transplant infections
• ISSN: 1607-8454; 1607-8454
• DOI: 10.1080/10245332.2018.1457308

Purpose: Human adenoviruses (HAdV) from species A, B and C are commonly recognized as pathogens causing severe morbidity and mortality in hematopoietic stem cell transplant (HSCT) recipients. The purpose of the present study was to determine HAdV types responsible for viremia in HSCT recipients at a large tertiary hospital in Poland. Methods: Analysis of partial nucleotide sequences of HAdV hexon gene was used to type 40 clinical isolates of HAdV obtained from 40 HSCT recipients. Results: We identified six different HAdV serotypes belonging to species B, C and E. We demonstrated high variability in sequences of detected HAdV types, and patients infected with the same HAdV types were not hospitalized at the same time, which suggests the low possibility of cross-infection. In almost all patients, anti-HAdV antibodies in IgG class were detected, which indicates a history of HAdV infection in the past. Clinical symptoms accompanying HAdV viremia were in 89%, and in 61.5% of individuals, HAdV was a sole pathogen detected. There were no cases with high-level HAdV viremia and severe systemic or organ infections. Graft-versus-host disease (GvHD) was present in patients infected with species B and C, but grade II of GvHD was observed only in patients infected with HAdV-B. Conclusions: The predominance of HAdV-C and common presence of anti-HAdV antibodies in IgG class may strongly suggest that most infections in the present study were reactivations of HAdV persisting into the patient's mucosa-associated lymphoid tissues. Variability of HAdV sequences suggests that cross-infections between patients were very rare. ABBREVIATIONS: GvHD: graft-versus-host disease; HAdV: human adenoviruses; HSCT: hematopoietic stem cell transplantation