1.Enteroviruses isolated in patients with acute respiratory infections
Journal of Preventive Medicine 2005;15(5):10-14
In 2004, 185 specimens of patients with acute respiratory illnesses that were tested negative to influenza viruses were isolated to determine enteroviruses. The results showed that 10.8% were positive with enteroviruses. These isolated enteroviruses consist of 13 Coxsackievirus B, 1 Echovirus, 1 Poliosabin type 1, and 5 untyped Enteroviruses. The result also showed that 8.1% of isolated viruses were Adenoviruses
Respiratory Tract Infections
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Orthomyxoviridae
2.Partial purification and characterization of host celluar protease of chicken embryo infected with influenza virus.
Mee Yoen PARK ; Chul Yong SONG ; Sang In CHUNG
Journal of the Korean Society of Virology 1993;23(1):47-55
No abstract available.
Chickens*
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Embryonic Structures*
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Influenza, Human*
;
Orthomyxoviridae*
3.Comparison of Overt and Inapparent Influenzal Infection in Ferret.
Yonsei Medical Journal 1968;9(1):18-23
In relation rto the size of viral inoculum, influenzal infection in ferrets caused by the inoculation of a mouse-adapted subline of PR 8 strain of type A influenza virus was studied. The results are summarized as follows; 1) When ferrets were inoculated with a highly diluted virus (10-7), a small proportion of them experienced inapparent infections and the rest of them escaped the infection. 2) With the increased size of viral inocula, there was a good correlation between the size of infecting does and the frequency of overt infections in ferrets. 3) Nasal tissues were the main locus of viral multiplication in ferrets at 72 hours after viral inoculation. Viral multiplication in nasal tissues was demonstrated only in a small proportion of ferrets which were inocu1ated with a 10-7 dilution of virus; however, when the size of vira1 inoculum was increased above this level, all ferrets had viral growth in their nasal tissues. 4) The involvement of pulmonary tissues, viral growth in those tissues and the development of gross lung lesions were significantly rare. There was no dear-cut relationship between the size of infecting doses and the frequency of such plumonary involvements in ferrets.
Animal
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Carnivora
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Female
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Influenza/microbiology*
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Orthomyxoviridae*
4.Antiviral Agents Against Influenza Viruses.
Sehee PARK ; Jin Il KIM ; Man Seong PARK
Journal of Bacteriology and Virology 2012;42(4):284-293
In annual epidemics and occasional pandemics, influenza viruses cause acute respiratory illnesses in infected humans. Vaccines and antiviral drugs are two main arsenals available for a fight against influenza viruses. However, vaccines often exhibit a limited efficacy in high risk populations, and antiviral drugs are always concerned for mutations, which confer viral resistance. Here we review current advances and knowledge in relation to the usage of antiviral drugs as a prophylactic or therapeutic and the mechanism of resistant variants mainly against the neuraminidase inhibitors. Comprehensive understanding of the resistant mechanism will pave a road for developing new antivirals and/or finding medical or natural alternatives inducing less frequent resistance, and application of combination therapy using two or three different kinds of antivirals can suggest a useful medical intervention against both of seasonal and highly pathogenic influenza viruses including resistant variants. In this review, we provide insights of antiviral drugs for the control and prevention of influenza viruses.
Antiviral Agents
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Humans
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Influenza, Human
;
Neuraminidase
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Orthomyxoviridae
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Pandemics
;
Seasons
;
Vaccines
5.Application of Diagnostic Microarray Technique in Subtyping and Pathotyping of Avian Influenza Viruses Isolated in Mongolia.
Jung Hoon KWON ; Ji Hoon KIM ; Dong hun LEE ; Hyunseok CHO ; Seung Yong HWANG ; Seong Su YUK ; Tseren Ochir ERDENE-OCHIR ; Jin Yong NOH ; Woo Tack HONG ; Jei Hyun JEONG ; Sol JEONG ; Gyeong Bin GWON ; Sang Won LEE ; In Soo CHOI ; Chang Seon SONG
Journal of Bacteriology and Virology 2016;46(1):22-26
Asian-lineage H5 highly pathogenic avian influenza (HPAI) viruses have caused continuous outbreaks in poultry and wild birds. Development of rapid and accurate diagnostic methods is needed for preventing further spread of the virus and reducing the time required for eradication of the virus. We developed a low-density microarray for the rapid detection and identification of avian influenza virus subtypes H5, H7, and H9 and their pathotypes in a previous study. In the present study, we evaluated previously developed diagnostic microarray using avian influenza viruses isolated in Mongolia, including H5 HPAI viruses. All H5 HPAI viruses isolated in Mongolia were shown as H5-specific and highly pathogenic pattern in the microarray. H2, H3 and H12 viruses isolated in Mongolia used in this study did not show any H5, H7 and H9 patterns. These results indicated that this diagnostic microarray has enormous potential for the rapid subtyping and pathotyping of influenza viruses, including viruses isolated in Mongolia.
Animals
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Birds
;
Disease Outbreaks
;
Influenza in Birds*
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Mongolia*
;
Orthomyxoviridae
;
Poultry
6.Biological characteristics of influenza virus.
Chinese Journal of Pediatrics 2003;41(3):164-167
7.Oseltamivir efficacy, side effects, and safety in children with influenza.
Eun Sun SEO ; Geun Hwa PARK ; Sung Mi KIM ; Sung Won KIM ; Woo Sik JUNG ; Kyung Soon CHO ; Yeon Gyeong PARK ; Chang Kyu LEE ; Chun KANG ; Joo Yeon LEE ; Woo Young CHOI
Korean Journal of Pediatrics 2010;53(1):56-66
PURPOSE: Although oseltamivir is widely used for treatment of influenza, few clinical studies of its efficacy and resistance have been performed in Korea. We evaluated the safety, side effects, and efficacy of oseltamivir treatment in Korean pediatric patients. METHODS: We analyzed 321 children diagnosed with influenza at Busan St. Mary's Medical Center, Korea, between January 2008 and June 2008 (first study period) and November 2008 and January 2009 (second study period). Patients were divided into two groups: those receiving oseltamivir treatment for 5 days and those receiving only symptomatic treatment. We investigated clinical symptoms, side effects, and resistance to oseltamivir. We also identified influenza strains and evaluated resistance to oseltamivir using an influenza virus culture. RESULTS: One hundred eighty-six patients were assigned to the treatment group, and 135 were assigned to the control group. The treatment group showed shorter admission duration (4.4 days) compared with controls (5.0 days) (P=0.000) and had fewer lower respiratory tract complications compared with controls (P<0.05). No significant statistical difference in the virus antigenic type was observed between the groups. In the first study period, virus culture showed influenza B (41.7% vs. 49.6%), A/H3N2 (7.9% vs. 8.4%), and A/H1N1 (9.4% vs. 6.5%). In the second study period, only A/H1N1 (55.3% vs. 50.0%) was isolated, except for one case of A (H3N2) in the treatment group. No differences in short- and long-term side effects, including neuropsychologic side effects, were noted between groups. There was no resistance to oseltamivir before or after treatment in the first study period. CONCLUSION: Based on our results, we suggest that osetalmivir therapy in pediatric patients is effective.
Child
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Humans
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Influenza, Human
;
Korea
;
Orthomyxoviridae
;
Oseltamivir
;
Respiratory System
;
Viruses
8.Neuraminidase Inhibitors from the Fruiting Body of Phellinus igniarius.
Ji Yul KIM ; Dae Won KIM ; Byung Soon HWANG ; E Eum WOO ; Yoon Ju LEE ; Kyeong Woon JEONG ; In Kyoung LEE ; Bong Sik YUN
Mycobiology 2016;44(2):117-120
During our ongoing investigation of neuraminidase inhibitors from medicinal fungi, we found that the fruiting bodies of Phellinus igniarius exhibited significant inhibitory activity against neuraminidase from recombinant H3N2 influenza viruses. Two active compounds were isolated from the methanolic extract of P. igniarius through solvent partitioning and Sephadex LH-20 column chromatography. The active compounds were identified as phelligridins E and G on proton nuclear magnetic resonance (¹H NMR) and electrospray ionization mass measurements. These compounds inhibited neuraminidases from recombinant rvH1N1, H3N2, and H5N1 influenza viruses, with IC₅₀ values in the range of 0.7~8.1 µM.
Chromatography
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Fruit*
;
Fungi
;
Magnetic Resonance Spectroscopy
;
Methanol
;
Neuraminidase*
;
Orthomyxoviridae
;
Protons
9.Review on the etiological property of the swine influenza virus.
Ning DU ; Xiao-Xing YANG ; Min WANG ; Yu LAN ; Lei YANG ; Yan-Hui CHENG ; Li-Qi LIU ; Yong-Kun CHEN ; Yuan-Ji GUO ; De-Xin LI ; Yue-Long SHU
Chinese Journal of Virology 2009;25 Suppl():39-47
10.Innate and adaptive T cells in influenza disease.
Simone NÜSSING ; Sneha SANT ; Marios KOUTSAKOS ; Kanta SUBBARAO ; Thi H O NGUYEN ; Katherine KEDZIERSKA
Frontiers of Medicine 2018;12(1):34-47
Influenza is a major global health problem, causing infections of the respiratory tract, often leading to acute pneumonia, life-threatening complications and even deaths. Over the last seven decades, vaccination strategies have been utilized to protect people from complications of influenza, especially groups at high risk of severe disease. While current vaccination regimens elicit strain-specific antibody responses, they fail to generate cross-protection against seasonal, pandemic and avian viruses. Moreover, vaccines designed to generate influenza-specific T-cell responses are yet to be optimized. During natural infection, viral replication is initially controlled by innate immunity before adaptive immune responses (T cells and antibody-producing B cells) achieve viral clearance and host recovery. Adaptive T and B cells maintain immunological memory and provide protection against subsequent infections with related influenza viruses. Recent studies also shed light on the role of innate T-cells (MAIT cells, γδ cells, and NKT cells) in controlling influenza and linking innate and adaptive immune mechanisms, thus making them attractive targets for vaccination strategies. We summarize the current knowledge on influenza-specific innate MAIT and γδ T cells as well as adaptive CD8 and CD4 T cells, and discuss how these responses can be harnessed by novel vaccine strategies to elicit cross-protective immunity against different influenza strains and subtypes.
Adaptive Immunity
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Animals
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Cross Protection
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Humans
;
Immunity, Innate
;
Influenza Vaccines
;
therapeutic use
;
Influenza, Human
;
immunology
;
Orthomyxoviridae
;
immunology
;
Orthomyxoviridae Infections
;
immunology
;
T-Lymphocytes
;
immunology
;
Vaccination