Mitochondrial somatic mutations and the lack of viral genomic variation in recurrent respiratory papillomatosis.
Yuhan HaoRyan RuizLiying YangAntonio Galvao NetoMilan R AminDervla KellyStratos AchlatisScott RoofRenjie BingKasthuri KannanStuart M BrownZhiheng PeiRyan C BranskiPublished in: Scientific reports (2019)
Recurrent Respiratory Papillomatosis (RRP) is a rare disease of the aerodigestive tract caused by the Human Papilloma Virus (HPV) that manifests as profoundly altered phonatory and upper respiratory anatomy. Current therapies are primarily symptomatic; enhanced insight regarding disease-specific biology of RRP is critical to improved therapeutics for this challenging population. Multiplex PCR was performed on oral rinses collected from twenty-three patients with adult-onset RRP every three months for one year. Twenty-two (95.6%) subjects had an initial HPV positive oral rinse. Of those subjects, 77.2% had an additional positive oral rinse over 12 months. A subset of rinses were then compared to tissue samples in the same patient employing HPViewer to determine HPV subtype concordance. Multiple HPV copies (60-787 per human cell) were detected in RRP tissue in each patient, but a single dominant HPV was found in individual samples. These data confirm persistent oral HPV infection in the majority of patients with RRP. In addition, three novel HPV6 isolates were found and identical HPV strains, at very low levels, were identified in oral rinses in two patients suggesting potential HPV subtype concordance. Finally, somatic heteroplasmic mtDNA mutations were observed in RRP tissue with 1.8 mutations per sample and two nonsynonymous variants. These data provide foundational insight into both the underlying pathophysiology of RRP, but also potential targets for intervention in this challenging patient cohort.
Keyphrases
- high grade
- cervical cancer screening
- endothelial cells
- copy number
- case report
- escherichia coli
- end stage renal disease
- sars cov
- stem cells
- bone marrow
- oxidative stress
- ejection fraction
- mitochondrial dna
- respiratory tract
- induced pluripotent stem cells
- dna methylation
- cell therapy
- peritoneal dialysis
- real time pcr
- genome wide
- pluripotent stem cells