Complexity of Human Cytomegalovirus Infection in South African HIV-Exposed Infants with Pneumonia.
Kerusha GovenderRaveen ParboosingSalvatore CamioloPetr HubáčekIrene GoerzerElisabeth Puchhammer-StöcklNicolás M SuárezPublished in: Viruses (2022)
Human cytomegalovirus (HCMV) can cause significant end-organ diseases such as pneumonia in HIV-exposed infants. Complex viral factors may influence pathogenesis including: a large genome with a sizeable coding capacity, numerous gene regions of hypervariability, multiple-strain infections, and tissue compartmentalization of strains. We used a whole genome sequencing approach to assess the complexity of infection by comparing high-throughput sequencing data obtained from respiratory and blood specimens of HIV-exposed infants with severe HCMV pneumonia with those of lung transplant recipients and patients with hematological disorders. There were significantly more specimens from HIV-exposed infants showing multiple HCMV strain infection. Some genotypes, such as UL73 G4B and UL74 G4, were significantly more prevalent in HIV-exposed infants with severe HCMV pneumonia. Some genotypes were predominant in the respiratory specimens of several patients. However, the predominance was not statistically significant, precluding firm conclusions on anatomical compartmentalization in the lung.
Keyphrases
- antiretroviral therapy
- hiv positive
- hiv infected
- hiv testing
- human immunodeficiency virus
- hiv aids
- hepatitis c virus
- men who have sex with men
- endothelial cells
- escherichia coli
- newly diagnosed
- sars cov
- ejection fraction
- genome wide
- gene expression
- epstein barr virus
- intensive care unit
- chronic kidney disease
- dna methylation
- respiratory tract
- community acquired pneumonia
- transcription factor
- patient reported outcomes
- drug induced
- diffuse large b cell lymphoma
- genome wide analysis