A Case Report Describing a Persistent SARS-CoV-2 Infection Outcomes and Mutations Associated with B-cell Deficiency

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Authors: Rana Mohamed, Alex Shipe, Andrew J. Lail, Isla E. Emmen, William C. Vuyk, Nicholas R. Minor, Taylor Bradley, Angela Gifford, Nancy A. Wilson, David O’Connor, Jacqueline Garonzik Wang, Jeannina Smith
Cited by: 1
References: 19

Abstract

Abstract Background Immunocompromised (IC) individuals are at increased risk for persistent SARS-CoV-2 infections and can develop new viral mutations and lineages not seen in the community. In this case report, a persistent SARS-CoV-2 infection (330 days) in an IC patient is examined for viral mutations and mutations associated with cryptic lineages. Case Presentation The patient was followed in a longitudinal study examining persistent SARS-CoV-2 in IC patients. The patient provided stool and nasal swab samples biweekly until 28 days post-enrollment, then monthly, and then quarterly after 12 month post enrollment until the participant was no longer positive for SARS-CoV-2. Staff performed RT-qPCR and viral sequencing on the samples. Viral mutations from the XBK lineage were already present in the initial sample. By the end of the infection period, there were 40 fixed consensus changes from XBK of which two mutations were typical for cryptic lineages. Mutations increased steadily over time, with most mutations fixed by day 253, including the cryptic typical mutations. Conclusion This case demonstrates the potential for persistent SARS-CoV-2 infections to develop mutations and lineages in IC patients and highlights the need for continued SARS-CoV-2 monitoring and treatment in this vulnerable population.

Fields of Study & Subjects

Immunodeficiency and Autoimmune Disorders SARS-CoV-2 and COVID-19 Research COVID-19 Clinical Research Studies

Publication details

Journal / source
medRxiv
Publisher
openRxiv
Publication date
17 February 2026
Document type
Preprint