Enhanced detection of respiratory viruses using cryopreserved R-Mix ReadyCells
- PMID: 18467164
- DOI: 10.1016/j.jcv.2008.03.015
Enhanced detection of respiratory viruses using cryopreserved R-Mix ReadyCells
Abstract
Background: R-Mix, which contains a fresh mixture of two cell lines, Mv1Lu (mink lung cells) and A549 cells, has shown good sensitivity and specificity for respiratory virus culture. However, it has until recently only been available in North America, in part due to the shipping constraints associated with cell aging and the difficulty in providing these cells to hard to reach regions. Recently, cryopreserved R-Mix ReadyCells for longer storage were developed. These cells, which are shipped on dry ice and have a shelf life as long as 6 months from date of manufacture, can be thawed and used as needed with minimal addition of refeeding media.
Objective: Assess the potential for cryopreserved R-Mix ReadyCells to replace conventional culture.
Study design: Two hundred and twenty-three nasopharyngeal aspirates confirmed as respiratory virus-positive by conventional culture were inoculated into cryopreserved R-Mix ReadyCells and re-inoculated into conventional culture cells simultaneously. After 1 and 3 days of incubation cryopreserved R-Mix ReadyCells and conventional culture cells were screened using a respiratory virus fluorescent antibody pool for the detection of seven major respiratory viruses (influenza A and B viruses, parainfluenza 1, 2 and 3 viruses, respiratory syncytial virus and adenovirus). Positive pool results were further differentiated with specific monoclonal antibodies against the individual viruses.
Results: After 1 day of incubation detection rates for conventional culture were 25%, 39%, 39%, 49%, and 10% for influenza A virus, influenza B virus, parainfluenza viruses, respiratory syncytial virus, and adenovirus, respectively. Corresponding detection rates for cryopreserved R-Mix ReadyCells were 78%, 91%, 72%, 81%, and 65%. Average detection rates of cryopreserved R-Mix ReadyCells for all respiratory viruses were 80% after 1 day incubation and 95% after 3 days incubation, compared to 35% and 70% by conventional culture.
Conclusion: The cryopreserved R-Mix ReadyCells system offers a highly sensitive and rapid method for detection of respiratory viruses that may allow it to replace conventional cell culture systems.
Similar articles
-
Evaluation of R-Mix shell vials for the diagnosis of viral respiratory tract infections.J Clin Virol. 2004 May;30(1):100-5. doi: 10.1016/j.jcv.2003.09.014. J Clin Virol. 2004. PMID: 15072762
-
Optimized detection of respiratory viruses in nasopharyngeal secretions.New Microbiol. 2003 Apr;26(2):133-40. New Microbiol. 2003. PMID: 12737194
-
Comparison of conventional viral cultures with direct fluorescent antibody stains for diagnosis of community-acquired respiratory virus infections in hospitalized children.Pediatr Infect Dis J. 2003 Sep;22(9):789-94. doi: 10.1097/01.inf.0000083823.43526.97. Pediatr Infect Dis J. 2003. PMID: 14506369
-
[Current approaches to the clinical virologic diagnosis of viral respiratory tract infections].Mikrobiyol Bul. 2003 Apr-Jun;37(2-3):195-204. Mikrobiyol Bul. 2003. PMID: 14593903 Review. Turkish.
-
Human bocavirus--a novel parvovirus to infect humans.Intervirology. 2008;51(2):116-22. doi: 10.1159/000137411. Epub 2008 Jun 9. Intervirology. 2008. PMID: 18536522 Review.
Cited by
-
Viral etiologies of lower respiratory tract infections among Egyptian children under five years of age.BMC Infect Dis. 2012 Dec 13;12:350. doi: 10.1186/1471-2334-12-350. BMC Infect Dis. 2012. PMID: 23237512 Free PMC article.
-
Comparison of different cell substrates on the measurement of human influenza virus neutralizing antibodies.PLoS One. 2012;7(12):e52327. doi: 10.1371/journal.pone.0052327. Epub 2012 Dec 20. PLoS One. 2012. PMID: 23284988 Free PMC article.
-
Point: is the era of viral culture over in the clinical microbiology laboratory?J Clin Microbiol. 2013 Jan;51(1):2-4. doi: 10.1128/JCM.02593-12. Epub 2012 Oct 10. J Clin Microbiol. 2013. PMID: 23052302 Free PMC article.
-
Differentiation of Cytopathic Effects (CPE) induced by influenza virus infection using deep Convolutional Neural Networks (CNN).PLoS Comput Biol. 2020 May 13;16(5):e1007883. doi: 10.1371/journal.pcbi.1007883. eCollection 2020 May. PLoS Comput Biol. 2020. PMID: 32401790 Free PMC article.
-
Screening of Fish Cell Lines for Piscine Orthoreovirus-1 (PRV-1) Amplification: Identification of the Non-Supportive PRV-1 Invitrome.Pathogens. 2020 Oct 12;9(10):833. doi: 10.3390/pathogens9100833. Pathogens. 2020. PMID: 33053677 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources