Low-cost gelling agents for tissue culture propagation of plantain

2021 ◽  
pp. 341-348
Author(s):  
S. Hegele ◽  
M. Hegele ◽  
J.N. Wünsche
1994 ◽  
Vol 37 (1) ◽  
pp. 15-23 ◽  
Author(s):  
Parthasarathi Bhattacharya ◽  
Satyahari Dey ◽  
Bimal Chandra Bhattacharyya

2001 ◽  
pp. 453-456 ◽  
Author(s):  
P.A. Sansberro ◽  
H.Y. Rey ◽  
C.V. Luna ◽  
L.A. Mroginski

In Vitro ◽  
1976 ◽  
Vol 12 (12) ◽  
pp. 797-813 ◽  
Author(s):  
Lynn R. Miller ◽  
Toshio Murashige

mSphere ◽  
2021 ◽  
Vol 6 (3) ◽  
Author(s):  
Ryohei Hirose ◽  
Naoto Watanabe ◽  
Risa Bandou ◽  
Takuma Yoshida ◽  
Tomo Daidoji ◽  
...  

ABSTRACT Human coronavirus (HCoV)-OC43 rarely shows a cytopathic effect (CPE) after infection of various cell lines, and the indirect immunoperoxidase assay (IPA), a relatively complex procedure, has long been used as an alternative assay. Because HCoV-OC43 uses cell-surface transmembrane protease serine 2 (TMPRSS2) for cell entry, VeroE6 cells expressing TMPRSS2 may show a clear CPE after HCoV-OC43 infection. The aim of this study was to construct a 50% tissue culture infectious dose (TCID50) assay for HCoV-OC43 based on CPE evaluation using VeroE6/TMPRSS2 cells. VeroE6/TMPRSS2 cells showed clear CPEs 3 to 4 days after low-titer HCoV-OC43 infection. Evaluation of viral kinetics indicated that the viral titer in the culture supernatant of VeroE6/TMPRSS2 cells in the early stages of infection was higher than that of other cells. In comparison, between the CPE-based and the IPA-based (i.e., the reference titer) methods, the titer measured with CPE evaluation 4 to 5 days after infection using VeroE6/TMPRSS2 cells showed a much smaller difference from the reference titer than that measured using other cells. Thus, the TCID50 assay using CPE evaluation with VeroE6/TMPRSS2 cells provides the correct titer value and will greatly contribute to future research on HCoV-OC43. IMPORTANCE HCoV-OC43 rarely shows a cytopathic effect (CPE) in infected cell lines, and thus the plaque and TCID50 assays by CPE observation are not applicable for titration; the indirect immunoperoxidase assay (IPA) is used instead. However, the IPA is relatively complex, time-consuming, costly, and not suitable for simultaneous titration of many samples. We developed a TCID50 assay using CPE evaluation with TMPRSS2-expressing VeroE6/TMPRSS2 cells that provides the same accuracy as the conventional IPA-based viral titration and does not require any staining procedures using antibodies or substrates. This titration method will greatly contribute to future research on HCoV-OC43 by allowing simple, low-cost, and accurate titration of this virus.


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