This paper is only available as a PDF. To read, Please Download here.
Background
HPV genomes can be detected on medical devices following hospital disinfectant procedures.
Recent reports concluded that oncogenic HPVs derived from laboratory tissue-based
models are not susceptible to commonly used high-level disinfectants, intensifying
concerns that medical instruments may provide transmission of nosocomial HPVs infections.
Therefore, we determined the infectious load of HPVs from clinical lesions and investigated
the effectiveness of disinfectants on HPV virions derived from laboratory model systems.
Methods
Infectious HPV virions were isolated from cell culture, organotypic epithelial tissue
cultures, and mouse xenografts. Clinical samples from recurrent respiratory papillomas
(RRPs) and anogenital warts were obtained under IRB approval. The infectivity of HPV
virion stocks was measured by the detection of spliced viral E1^E4 mRNAs in infected
keratinocytes. Infections were validated by time-dependent detection of E1^E4 mRNAs,
resistance to ribonuclease treatment and susceptibility to antibody-mediated neutralization.
Our infectivity assay demonstrated a dynamic range of >3-5 log10. Suspension-based
disinfection assays employed diluted ortho-phthalaldehyde (OPA) and 0.825% hypochlorite.
Results
In contrast to prior reports, we found that validated HPV virions obtained from a
variety of sources were susceptible to a 2.5 to 4 log10 reduction in infectious titer
when exposed as directed to OPA or hypochlorite. Some HPV virion stocks failed to
meet the infectivity criteria of time-dependent detection of E1^E4 mRNAs, resistance
to ribonuclease and susceptibility to antibody-mediated neutralization. Such unvalidated
virus stocks are likely to produce spurious results and lead to confounding conclusions.
Assessment of HPV infectious titers from clinical lesions suggests that compared to
common warts, clinical RRP and anogenital warts have lower levels of virions present
at apical surfaces.
Conclusions
We conclude that laboratory sourced HPVs are susceptible to disinfection by OPA and
hypochlorite. As the levels of infectious virions recovered from HPV-induced lesions
fall below those used in our assays, proper cleaning and disinfection processing is
likely to be effective
To read this article in full you will need to make a payment
Purchase one-time access:
Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online accessOne-time access price info
- For academic or personal research use, select 'Academic and Personal'
- For corporate R&D use, select 'Corporate R&D Professionals'
Subscribe:
Subscribe to American Journal of Infection ControlAlready a print subscriber? Claim online access
Already an online subscriber? Sign in
Register: Create an account
Institutional Access: Sign in to ScienceDirect
Article Info
Identification
Copyright
© 2020 Published by Elsevier Inc.