The protective effects of intranasal administration of IL-12 given before influenza virus infection and the negative effects of IL-12 treatment given after viral infection

2016 ◽  
Vol 88 (9) ◽  
pp. 1487-1496 ◽  
Author(s):  
Hiroki Ishikawa ◽  
Satoshi Ino ◽  
Hiraku Sasaki ◽  
Toshie Fukui ◽  
Chikara Kohda ◽  
...  
2003 ◽  
Vol 31 (3) ◽  
pp. 244-246 ◽  
Author(s):  
K Kusaka ◽  
J Yamakawa ◽  
K Kawaura ◽  
T Itoh ◽  
T Takahashi ◽  
...  

We describe a 32-year-old man with electrocardiographic (ECG) changes consistent with Brugada syndrome and influenza virus infection. The ECG pattern changed after 1 week to one of early repolarization in V1 and V2. This case suggests an association between Brugada syndrome and viral infection.


2010 ◽  
Vol 10 (9) ◽  
pp. 1101-1106 ◽  
Author(s):  
Takayuki Izumo ◽  
Toshihiro Maekawa ◽  
Masayuki Ida ◽  
Akane Noguchi ◽  
Yoshinori Kitagawa ◽  
...  

2010 ◽  
Vol 155 (4) ◽  
pp. 535-544 ◽  
Author(s):  
Zhiwei Sui ◽  
Quanjiao Chen ◽  
Rui Wu ◽  
Hongbo Zhang ◽  
Mei Zheng ◽  
...  

Nutrients ◽  
2020 ◽  
Vol 12 (10) ◽  
pp. 2925
Author(s):  
Shohei Satomi ◽  
Sofia Khanum ◽  
Poppy Miller ◽  
Shigenori Suzuki ◽  
Hiroyuki Suganuma ◽  
...  

Influenza virus type A (IAV) is a seasonal acute respiratory disease virus with severe symptoms, and an effective preventive measure is required. Despite many reports describing the potentially protective effects of lactic acid bacteria, few studies have investigated the effects of nutritional supplement combinations. This study reports the effect of the combined intake of heat-killed Lactobacillus brevis KB290 (KB290) and vitamin A (VA) on mice challenged with a sublethal dose of IAV. For 2 weeks, five groups of mice were fed either placebo, KB290, VA, or a combination of KB290 and VA (KB290+VA). After subsequent IAV challenge, bodyweight and general health were monitored for up to 2 weeks. Viral titres were determined in the lungs of animal subgroups euthanised at days 3, 7, and 14 after IAV challenge. A significant loss was observed in the bodyweights of IAV-infected animals from day 1 post-IAV challenge, whereas the mice fed KB290+VA did not lose any weight after IAV infection, indicating successful protection from the infection. Additionally, mice in the KB290+VA group showed the highest reduction in lung viral titres. In conclusion, the combination of KB290 and VA could be a useful food supplement relevant for protection against seasonal influenza virus infection in humans.


Vaccine ◽  
2003 ◽  
Vol 21 (31) ◽  
pp. 4532-4538 ◽  
Author(s):  
Izumi Watanabe ◽  
Ted M. Ross ◽  
Shin-ichi Tamura ◽  
Takeshi Ichinohe ◽  
Satoshi Ito ◽  
...  

1987 ◽  
Vol 61 (11) ◽  
pp. 1248-1251 ◽  
Author(s):  
Nobuko SUGIMOTO ◽  
Yukie SUMI ◽  
Takako FUJITA ◽  
Yasuko KAWATA ◽  
Keiko KATO ◽  
...  

Author(s):  
Marta De Angelis ◽  
Donatella Amatore ◽  
Paola Checconi ◽  
Alessandra Zevini ◽  
Alessandra Fraternale ◽  
...  

Influenza virus infection induces oxidative stress in host cells by decreasing the intracellular content of glutathione (GSH) and increasing reactive oxygen species (ROS) level. Glucose-6-phosphate dehydrogenase (G6PD) is responsible for the production of reducing equivalents of nicotinamide adenine dinucleotide phosphate (NADPH) that is used to regenerate the reduced form of GSH, thus restoring redox homeostasis. Cells deficient in G6PD display elevated levels of ROS and an increased susceptibility to viral infection, although the consequences of G6PD modulation during viral infection remain to be elucidated. In this study, we demonstrated that influenza virus infection decreases G6PD expression and activity, resulting in an increase in oxidative stress and virus replication. Moreover, the down regulation of G6PD correlated with a decrease in the expression of nuclear factor erythroid 2-related factor 2 (NRF2), a key transcription factor that regulates the expression of the antioxidant response gene network. Also down-regulated in influenza virus infected cells was sirtuin 2 (SIRT2), a NADPH-dependent deacetylase involved in the regulation of G6PD activity. Acetylation of G6PD increased during influenza virus infection in a manner that was strictly dependent on SIRT2 expression. Furthermore, the use of a pharmacological activator of SIRT2 rescued GSH production and NRF2 expression, leading to decreased influenza virus replication. Overall, these data identify a novel strategy used by influenza virus to induce oxidative stress and to favor its replication in host cells. These observations furthermore suggest that manipulation of metabolic and oxidative stress pathways could define new therapeutic strategies to interfere with influenza virus infection.


eLife ◽  
2018 ◽  
Vol 7 ◽  
Author(s):  
Alistair B Russell ◽  
Cole Trapnell ◽  
Jesse D Bloom

Viral infection can dramatically alter a cell’s transcriptome. However, these changes have mostly been studied by bulk measurements on many cells. Here we use single-cell mRNA sequencing to examine the transcriptional consequences of influenza virus infection. We find extremely wide cell-to-cell variation in the productivity of viral transcription – viral transcripts comprise less than a percent of total mRNA in many infected cells, but a few cells derive over half their mRNA from virus. Some infected cells fail to express at least one viral gene, but this gene absence only partially explains variation in viral transcriptional load. Despite variation in viral load, the relative abundances of viral mRNAs are fairly consistent across infected cells. Activation of innate immune pathways is rare, but some cellular genes co-vary in abundance with the amount of viral mRNA. Overall, our results highlight the complexity of viral infection at the level of single cells.


2011 ◽  
Vol 32 (2) ◽  
pp. 256-267 ◽  
Author(s):  
Hiroki Ishikawa ◽  
Hiraku Sasaki ◽  
Toshie Fukui ◽  
Koji Fujita ◽  
Etsuko Kutsukake ◽  
...  

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