Efficacy of Chemical Treatments Against Murine Norovirus, Feline Calicivirus, and MS2 Bacteriophage

2010 ◽  
Vol 7 (3) ◽  
pp. 319-326 ◽  
Author(s):  
Doris H. D'Souza ◽  
Xiaowei Su
2017 ◽  
Vol 2017 (9) ◽  
pp. 3095-3102
Author(s):  
Joseph G Jacangelo ◽  
Nathan Dunkin ◽  
Shih-Chi Weng ◽  
James McQuarrie ◽  
Kati Bell ◽  
...  

2017 ◽  
Vol 51 (5) ◽  
pp. 2972-2981 ◽  
Author(s):  
Nathan Dunkin ◽  
ShihChi Weng ◽  
Kellogg J. Schwab ◽  
James McQuarrie ◽  
Kati Bell ◽  
...  

2007 ◽  
Vol 74 (2) ◽  
pp. 477-484 ◽  
Author(s):  
Jinhee Bae ◽  
Kellogg J. Schwab

ABSTRACT Human noroviruses (NoVs) are a significant cause of nonbacterial gastroenteritis worldwide, with contaminated drinking water a potential transmission route. The absence of a cell culture infectivity model for NoV necessitates the use of molecular methods and/or viral surrogate models amenable to cell culture to predict NoV inactivation. The NoV surrogates murine NoV (MNV), feline calicivirus (FCV), poliovirus (PV), and male-specific coliphage MS2, in conjunction with Norwalk virus (NV), were spiked into surface water samples (n = 9) and groundwater samples (n = 6). Viral persistence was monitored at 25°C and 4°C by periodically analyzing virus infectivity (for all surrogate viruses) and nucleic acid (NA) for all tested viruses. FCV infectivity reduction rates were significantly higher than those of the other surrogate viruses. Infectivity reduction rates were significantly higher than NA reduction rates at 25°C (0.18 and 0.09 log10/day for FCV, 0.13 and 0.10 log10/day for PV, 0.12 and 0.06 log10/day for MS2, and 0.09 and 0.05 log10/day for MNV) but not significant at 4°C. According to a multiple linear regression model, the NV NA reduction rates (0.04 ± 0.01 log10/day) were not significantly different from the NA reduction rates of MS2 (0.05 ± 0.03 log10/day) and MNV (0.04 ± 0.03 log10/day) and were significantly different from those of FCV (0.08 ± 0.03 log10/day) and PV (0.09 ± 0.03 log10/day) at 25°C. In conclusion, MNV shows great promise as a human NoV surrogate due to its genetic similarity and environmental stability. FCV was much less stable and thus questionable as an adequate surrogate for human NoVs in surface water and groundwater.


Food Control ◽  
2016 ◽  
Vol 60 ◽  
pp. 25-30 ◽  
Author(s):  
Dong Joo Seo ◽  
Su Been Jeon ◽  
Hyejin Oh ◽  
Bog-Hieu Lee ◽  
Sook-Young Lee ◽  
...  

Viruses ◽  
2019 ◽  
Vol 11 (11) ◽  
pp. 996
Author(s):  
Oscar Salvador Barrera-Vázquez ◽  
Clotilde Cancio-Lonches ◽  
Carlos Emilio Miguel-Rodríguez ◽  
Monica Margarita Valdes Pérez ◽  
Ana Lorena Gutiérrez-Escolano

It is known that levels of the anti-apoptotic protein survivin are reduced during Murine norovirus MNV-1 and Feline calicivirus (FCV) infection as part of the apoptosis establishment required for virus release and propagation in the host. Recently, our group has reported that overexpression of survivin causes a reduction of FCV protein synthesis and viral progeny production, suggesting that survivin may affect early steps of the replicative cycle. Using immunofluorescence assays, we observed that overexpression of survivin, resulted in the reduction of FCV infection not only in transfected but also in the neighboring nontransfected CrFK cells, thus suggesting autocrine and paracrine protective effects. Cells treated with the supernatants collected from CrFK cells overexpressing survivin showed a reduction in FCV but not MNV-1 protein production and viral yield, suggesting that FCV binding and/or entry were specifically altered. The reduced ability of FCV to bind to the surface of the cells overexpressing survivin, or treated with the supernatants collected from these cells, correlate with the reduction in the cell surface of the FCV receptor, the feline junctional adhesion molecule (fJAM) 1, while no effect was observed in the cells transfected with the pAm-Cyan vector or in cells treated with the corresponding supernatants. Moreover, the overexpression of survivin affects neither Vaccinia virus (VACV) production in CrFK cells nor MNV-1 virus production in RAW 267.4 cells, indicating that the effect is specific for FCV. All of these results taken together indicate that cells that overexpress survivin, or cell treatment with the conditioned medium from these cells, results in the reduction of the fJAM-1 molecule and, therefore, a specific reduction in FCV entry and infection.


2012 ◽  
Vol 31 (2) ◽  
pp. 210-214 ◽  
Author(s):  
Min Hwa Lee ◽  
Seung-Hee Yoo ◽  
Sang-Do Ha ◽  
Changsun Choi

2011 ◽  
Vol 35 (4) ◽  
pp. 429-435 ◽  
Author(s):  
Min-Hwa Lee ◽  
Bog-Hieu Lee ◽  
Ji-Youn Jung ◽  
Doo-Sung Cheon ◽  
Kyung-Tack Kim ◽  
...  

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