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. 2011 Jun;49(6):2138-42.
doi: 10.1128/JCM.00327-11. Epub 2011 Apr 20.

Evaluation and clinical validation of an alcohol-based transport medium for preservation and inactivation of respiratory viruses

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Evaluation and clinical validation of an alcohol-based transport medium for preservation and inactivation of respiratory viruses

Kathy Luinstra et al. J Clin Microbiol. 2011 Jun.

Abstract

The clinical and public health importance of influenza and other respiratory viruses has accelerated the development of highly sensitive molecular diagnostics, but data are limited regarding preanalytical stages of diagnostic testing. We evaluated CyMol, an alcohol-based transport medium, for its ability to maintain specimen integrity for up to 21 days of storage at various temperatures; for its ability to inactivate virus; and for its compatibility with antigen- or nucleic acid-based diagnostics for respiratory viruses in clinical samples. In mock-infected samples, both universal transport medium (UTM-RT) and CyMol maintained equivalent viral quantities for at least 14 days at room temperature or colder, whereas a dry swab collection maintained viral quantities only if refrigerated or frozen. CyMol inactivated influenza virus within 5 min of sample immersion. UTM-RT- and CyMol-collected nasal swab specimens from 73 symptomatic students attending a campus health clinic were positive for a respiratory virus in 56.2% of subjects by multiplex PCR testing, including influenza A and B viruses, rhinovirus/enteroviruses, coronaviruses, respiratory syncytial virus, parainfluenza viruses, metapneumovirus, and adenovirus. Detection by PCR was equivalent in UTM-RT- and CyMol-collected specimens and in self- and staff-collected swabs. Direct fluorescent antibody (DFA) testing was substantially less sensitive (23.3%) than multiplex PCR, and DFA testing from UTM-RT-collected swabs was more sensitive than that from CyMol-collected swabs. These data indicate that an alcohol-based transport medium such as CyMol preserves respiratory virus integrity, rapidly inactivates viruses, and is compatible with PCR-based respiratory diagnostics.

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Figures

Fig. 1.
Fig. 1.
Modeled effects of temperature and days of storage on influenza A quantitation for three collection methods: universal transport medium from Copan Italia SpA (UTM-RT; left), CyMol from Copan Italia (center), or dry swab without transport medium (right). The horizontal line at 4.7 indicates a 0.5-log difference from baseline values. Statistics were calculated using a main-effect generalized linear model (SPSS version 18.0).

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