Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 2013 Feb;108(1):36-40.
doi: 10.1590/s0074-02762013000100006.

Detection of replication-defective hepatitis A virus based on the correlation between real-time polymerase chain reaction and ELISA in situ results

Affiliations
Comparative Study

Detection of replication-defective hepatitis A virus based on the correlation between real-time polymerase chain reaction and ELISA in situ results

Alyne Moraes Costa et al. Mem Inst Oswaldo Cruz. 2013 Feb.

Abstract

ELISA in situ can be used to titrate hepatitis A virus (HAV) particles and real-time polymerase chain reaction (RT-PCR) has been shown to be a fast method to quantify the HAV genome. Precise quantification of viral concentration is necessary to distinguish between infectious and non-infectious particles. The purpose of this study was to compare cell culture and RT-PCR quantification results and determine whether HAV genome quantification can be correlated with infectivity. For this purpose, three stocks of undiluted, five-fold diluted and 10-fold diluted HAV were prepared to inoculate cells in a 96-well plate. Monolayers were then incubated for seven, 10 and 14 days and the correlation between the ELISA in situ and RT-PCR results was evaluated. At 10 days post-incubation, the highest viral load was observed in all stocks of HAV via RT-PCR (10(5) copies/mL) (p = 0.0002), while ELISA revealed the highest quantity of particles after 14 days (optical density = 0.24, p < 0.001). At seven days post-infection, there was a significant statistical correlation between the results of the two methods, indicating equivalents titres of particles and HAV genome during this period of infection. The results reported here indicate that the duration of growth of HAV in cell culture must be taken into account to correlate genome quantification with infectivity.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1. comparison between the numbers of viral particles analyzed by ELISA in situ and the number of amplified copies of the genome of hepa titis A virus analyzed by real-time (RT) polymerase chain reaction according to the days of incubation. dpi: days post-infection; EIA: ensyme immunoassay; OD: optical density; *: analysis of variance of RT values; **: ELISA values.
Fig. 2
Fig. 2. correlation of the amounts of hepatitis A virus particles and RNA, estimated by tissue culture infective dose (TCID50) and cycle threshold (Ct) values of real-time polymerase chain reaction. dpi: days post-infection.

Similar articles

Cited by

References

    1. de Paula VS, Diniz-Mendes L, Villar LM, Luz SL, Silva LA, Jesus MS, da Silva NM, Gaspar AM. Hepatitis A virus in environmental water samples from the Amazon Basin. Water Res. 2007;41:1169–1176. - PubMed
    1. de Paula VS, Perse AS, Amado LA, de Morais LM, de Lima SM, Tourinho RS, Gaspar AM, Pinto MA. Kinetics of hepatitis A virus replication in vivo and in vitro using negative-strand quantitative PCR. Eur J Clin Microbiol Infect Dis. 2009;28:1167–1176. - PubMed
    1. Donia D, Bonanni E, Diaco L, Divizia M. Statistical correlation between enterovirus genome copy numbers and infectious viral particles in wastewater samples. Lett Appl Microbiol. 2009;50:237–240. - PubMed
    1. Dudek T, Knipe DM. Replication-defective viruses as vaccines and vaccine vectors. Virology. 2006;344:230–239. - PubMed
    1. Forcic D, Kosutic-Gulija T, Santak M, Jug R, Ivancic-Jelecki J, Markusic M, Mazuran R. Comparisons of mumps virus potency estimates obtained by 50% cell culture infective dose assay and plaque assay. Vaccine. 2009;28:1887–1892. - PubMed

Publication types