Abstract
The isolation of influenza viruses in Madin Darby Canine Kidney (MDCK) cells has shown preferential isolation of a great percentage of Influenza B strains at the first passage than Influenza A strains. During in vitro isolation of Influenza viruses, majority of type A viruses are not confirmed as positive isolates by Hemagglutination (HA) assay despite having higher virulence and pathogenicity versus influenza B viruses. This study investigated the differences in IFN-γ and IL-10 cytokines secreted by MDCK cells upon exposure to the viruses and thus provided possible answers as to why influenza type B can easily be isolated from MDCK cells compared to influenza A. Positive influenza viruses were inoculated onto MDCK cells. IFN-γ and IL-10 cytokines stimulated by the viruses in MDCK cells were measured by indirect ELISA at 1 hour, 12 hours, 48 hours and 72 hours post inoculation (pi). A total of 46 specimens, with 23 specimens from each virus type were analyzed. IFN-γ was significantly higher at 1 hour pi in MDCK cells for influenza type A at p value of 0.024 than type B. No statistical significance was observed in means of cytokine IL-10 between influenza type A and type B. The study may show that IFN-γ is correlated to the preferential isolation of influenza type B over type A viruses. Anti-inflammatory cytokines may not necessarily be playing a role in the preferential growth of influenza type B, a less virulent type over influenza type A in MDCK cells.
Highlights
This study investigated the differences in IFN-γ and Interleukin 10 (IL-10) cytokines secreted by Madin Darby Canine Kidney (MDCK) cells upon exposure to the viruses and provided possible answers as to why influenza type B can be isolated from MDCK cells compared to influenza A
There are 18 HA and 11 NA which can undergo re-assortment or mutations to give rise to new or variant strain among influenza type A viruses. It was in this regard that strains such as the case of influenza B had formed a homogeneous group, which started to diverge antigenically into two distinct lineages, whose first representatives were B/Victoria/2/87 and B/Yamagata/16/88, as the Victoria and Yamagata lineages respectively [3]
Sample size The hypothesis comparing the means of the outcome variable in the two independent populations was considered
Summary
There are 18 HA and 11 NA which can undergo re-assortment or mutations to give rise to new or variant strain among influenza type A viruses It was in this regard that strains such as the case of influenza B had formed a homogeneous group, which started to diverge antigenically into two distinct lineages, whose first representatives were B/Victoria/2/87 and B/Yamagata/16/88, as the Victoria and Yamagata lineages respectively [3]. This nomenclature system was adapted after the World Health Organization (WHO) where B denotes for the type of Influenza virus, Victoria as the place of origin, 2 as the strain serial number and 87 as the year of isolation. A similar nomenclature system exists for influenza A viruses [4]
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have