BK Polyomavirus Diversity After Hematopoietic Stem Cell Transplantation

Author:

Odegard Elizabeth A1ORCID,Meeds Heidi L1,Kleiboeker Steven B2,Ziady Assem34,Sabulski Anthony54,Jodele Sonata34,Seif Alix E67,Davies Stella M34,Laskin Benjamin L68,Blackard Jason T1ORCID

Affiliation:

1. Division of Digestive Diseases, University of Cincinnati College of Medicine , Ohio

2. Eurofins Viracor Laboratories , Lenexa, Kansas

3. Department of Pediatrics, University of Cincinnati College of Medicine , Ohio

4. Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center , Ohio

5. Department of Pediatrics, University of Cincinnati College of Medicine, Ohio

6. Perelman School of Medicine, University of Pennsylvania , Pennsylvania

7. Division of Oncology, The Children's Hospital of Philadelphia , Pennsylvania

8. Division of Nephrology, The Children's Hospital of Philadelphia , Pennsylvania

Abstract

Abstract BK polyomavirus (BKPyV) infection is common after hematopoietic stem cell transplantation (HSCT) and is associated with the development of hemorrhagic cystitis (HC). The role that BKPyV plays in the pathogenesis of HC is not well characterized. We investigated the impact of BKPyV diversity on the development of HC using a previously established cohort of pediatric HSCT patients. There were 147 urine samples with quantifiable BKPyV at month 1 after HSCT; 137 (93.2%) were amplified using our in-house polymerase chain reaction approach and sent for next-generation sequencing. Subtype Ia was most frequent (61.3%), followed by subtype Ib1 (31.4%). The median viral load of subtype Ia samples was higher than for subtype Ib1 at month 1. Across the protein coding regions, APOBEC-induced mutations and signature patterns associated with HC were identified. This is the largest sequencing study of a single cohort of HSCT patients, providing a vast resource of sequence data for future analyses.

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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