influenza A virus

• A型インフルエンザウイルス、インフルエンザAウイルス

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swine influenza virus

WordNet

1. a harmful or corrupting agency; "bigotry is a virus that must not be allowed to spread"; "the virus of jealousy is latent in everyone"
2. (virology) ultramicroscopic infectious agent that replicates itself only within cells of living hosts; many are pathogenic; a piece of nucleic acid (DNA or RNA) wrapped in a thin coat of protein
3. a software program capable of reproducing itself and usually capable of causing great harm to files or other programs on the same computer; "a true virus cannot spread to another computer without human assistance" (同)computer virus
4. the 1st letter of the Roman alphabet (同)a
5. the blood group whose red cells carry the A antigen (同)type_A, group A
6. an acute febrile highly contagious viral disease (同)flu, grippe

PrepTutorEJDIC

1. ビールス,ろ過性病原体
2. answer / ampere
3. インフルエンザ,流行性感冒
4. arsenicの化学記号

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2012/11/28 11:02:56」(JST)

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Orthomyxoviridae
Electron micrograph of influenza A viruses
Virus classification
Group:	Group V ((-)ssRNA)
Family:	Orthomyxoviridae
Genera
Influenzavirus A Influenzavirus B Influenzavirus C Isavirus Thogotovirus

Influenza A virus causes influenza in birds and some mammals, and is the only species of influenzavirus A. Influenzavirus A is a genus of the Orthomyxoviridae family of viruses. Strains of all subtypes of influenza A virus have been isolated from wild birds, although disease is uncommon. Some isolates of influenza A virus cause severe disease both in domestic poultry and, rarely, in humans. Occasionally, viruses are transmitted from wild aquatic birds to domestic poultry, and this may cause an outbreak or give rise to human influenza pandemics.

Influenza A viruses are negative-sense, single-stranded, segmented RNA viruses. The several subtypes are labeled according to an H number (for the type of hemagglutinin) and an N number (for the type of neuraminidase). There are 17 different H antigens (H1 to H17) and nine different N antigens (N1 to N9). The newest H antigen type, identified as H17 by researchers, was isolated from fruit bats in 2012.

Each virus subtype has mutated into a variety of strains with differing pathogenic profiles; some are pathogenic to one species but not others, some are pathogenic to multiple species.

A filtered and purified influenza A vaccine for humans has been developed, and many countries have stockpiled it to allow a quick administration to the population in the event of an avian influenza pandemic. Avian influenza is sometimes called avian flu, and colloquially, bird flu. In 2011, researchers reported the discovery of an antibody effective against all types of the influenza A virus.

Variants and subtypes

Influenza (Flu)
Types
Avian (A/H5N1 subtype) Canine Equine Swine (A/H1N1 subtype)
Vaccines
2009 pandemic (Pandemrix) ACAM-FLU-A Fluzone Influvac Live attenuated (FluMist) Optaflu
Treatment
Amantadine Arbidol Laninamivir Oseltamivir Peramivir Rimantadine Vitamin D Zanamivir
Pandemics
2009 Swine 1968–1969 Hong Kong 1918
Outbreaks
2008 West Bengal 2007 Bernard Matthews H5N1 2007 Australian equine 2006 H5N1 India 1976 swine flu
See also
Flu season Influenza evolution Influenza research Influenza-like illness Historical annual reformulations of the influenza vaccine

H5N1

Influenza A virus subtype H5N1 Genetic structure Infection Human mortality Global spread in 2004 in 2005 in 2006 in 2007 Social impact Pandemic Vaccine

Influenza type A viruses are categorized into subtypes based on the type of two proteins on the surface of the viral envelope:

H = hemagglutinin, a protein that causes red blood cells to agglutinate.

N = neuraminidase, an enzyme that cleaves the glycosidic bonds of the monosaccharide, neuraminic acid

Different influenza viruses encode for different hemagglutinin and neuraminidase proteins. For example, the H5N1 virus designates an influenza A subtype that has a type 5 hemagglutinin (H) protein and a type 1 neuraminidase (N) protein. There are 17 known types of hemagglutinin and 9 known types of neuraminidase, so, in theory, 153 different combinations of these proteins are possible.

Some variants are identified and named according to the isolate they resemble, thus are presumed to share lineage (example Fujian flu virus-like); according to their typical host (example human flu virus); according to their subtype (example H3N2); and according to their deadliness (example LP, low pathogenic). So a flu from a virus similar to the isolate A/Fujian/411/2002(H3N2) is called Fujian flu, human flu, and H3N2 flu.

Variants are sometimes named according to the species (host) in which the strain is endemic or to which it is adapted. The main variants named using this convention are:

• Bird flu
• Human flu
• Swine influenza
• Equine influenza
• Canine influenza

Variants have also sometimes been named according to their deadliness in poultry, especially chickens:

• Low pathogenic avian influenza (LPAI)
• Highly pathogenic avian influenza (HPAI), also called deadly flu or death flu

Most known strains are extinct strains. For example, the annual flu subtype H3N2 no longer contains the strain that caused the Hong Kong flu.

Annual flu

Main article: Flu season

The annual flu (also called "seasonal flu" or "human flu") in the U.S. "results in approximately 36,000 deaths and more than 200,000 hospitalizations each year. In addition to this human toll, influenza is annually responsible for a total cost of over $10 billion in the U.S."

The annually updated, trivalent influenza vaccine consists of hemagglutinin (HA) surface glycoprotein components from influenza H3N2, H1N1, and B influenza viruses.

Measured resistance to the standard antiviral drugs amantadine and rimantadine in H3N2 has increased from 1% in 1994 to 12% in 2003 to 91% in 2005.

"Contemporary human H3N2 influenza viruses are now endemic in pigs in southern China and can reassort with avian H5N1 viruses in this intermediate host."

F16 antibody

F16, an antibody that targets the hemagglutinin protein, was recently discovered, and is the only known antibody effective against all 16 subtypes of the influenza A virus.

Structure and genetics

See also: H5N1 genetic structure

"The physical structure of all influenza A viruses is similar. The virions or virus particles are enveloped and can be either spherical or filamentous in form. In clinical isolates that have undergone limited passages in eggs or tissue culture, there are more filamentous than spherical particles, whereas passaged laboratory strains consist mainly of spherical virions."

The Influenza A virus genome is contained on eight single (non-paired) RNA strands that code for eleven proteins (HA, NA, NP, M1, M2, NS1, NEP, PA, PB1, PB1-F2, PB2). The total genome size is 13,588 bases. The segmented nature of the genome allows for the exchange of entire genes between different viral strains during cellular cohabitation. The eight RNA segments are:

• HA encodes hemagglutinin (about 500 molecules of hemagglutinin are needed to make one virion) "The extent of infection into host organism is determined by HA. Influenza viruses bud from the apical surface of polarized epithelial cells (e.g. bronchial epithelial cells) into lumen of lungs and are therefore usually pneumotropic. The reason is that HA is cleaved by tryptase clara which is restricted to lungs. However HAs of H5 and H7 pantropic avian viruses subtypes can be cleaved by furin and subtilisin-type enzymes, allowing the virus to grow in other organs than lungs."
• NA encodes neuraminidase (about 100 molecules of neuraminidase are needed to make one virion).
• NP encodes nucleoprotein.
• M encodes two matrix proteins (the M1 and the M2) by using different reading frames from the same RNA segment (about 3000 matrix protein molecules are needed to make one virion).
• NS encodes two distinct non-structural proteins (NS1 and NEP) by using different reading frames from the same RNA segment.
• PA encodes an RNA polymerase.
• PB1 encodes an RNA polymerase and PB1-F2 protein (induces apoptosis) by using different reading frames from the same RNA segment.
• PB2 encodes an RNA polymerase.

The genome segments have common terminal sequences, and the ends of the RNA strands are partially complementary, allowing them to bond to each other by hydrogen bonds. After transcription from negative-sense to positive-sense RNA the +RNA strands get the cellular 5' cap added by cap snatching, which involves the viral protein NS1 binding to the cellular pre-mRNAs. The cap is then cleaved from the cellular pre-mRNA using a second viral protein, PA. The short oligo cap is then added to the influenza +RNA strands, allowing its processing as messenger RNA by ribosomes. The +RNA strands also serve for synthesis of -RNA strands for new virions.

The RNA synthesis and its assembly with the nucleoprotein takes place in the cell nucleus, the synthesis of proteins takes place in the cytoplasm. The assembled virion cores leave the nucleus and migrate towards the cell membrane, with patches of viral transmembrane proteins (hemagglutinin, neuraminidase and M2 proteins) and an underlying layer of the M1 protein, and bud through these patches, releasing finished enveloped viruses into the extracellular fluid.

Evidence has been found for the presence of RNA structure in Influenza A virus. Structured RNA appears to be favored in the +RNA, and is clustered near regions with functional importance. Two pseudoknot RNA structures were predicted that include the 3' splice site in Segments 7 and 8, which are both alternatively spliced to produce the M2 and NEP proteins respectively. Towards the 5' splice sites of these mRNAs, hairpin loop and multibranch loop structures were predicted. As well as these structures near splice sites, a pseudoknot was proposed in Segment 2, which encompasses the start codon for an internally transcribed open reading frame for a small polypeptide product (PB1-F2).

In Non-humans

See H5N1 for the current epizootic (an epidemic in nonhumans) and panzootic (a disease affecting animals of many species especially over a wide area) of H5N1 influenza

Avian influenza

Main article: Avian influenza

Fowl act as natural asymptomatic carriers of influenza A viruses. Prior to the current H5N1 epizootic, strains of influenza A virus had been demonstrated to be transmitted from wild fowl to only birds, pigs, horses, seals, whales and humans; and only between humans and pigs and between humans and domestic fowl; and not other pathways such as domestic fowl to horse.

Wild aquatic birds are the natural hosts for a large variety of influenza A viruses. Occasionally, viruses are transmitted from these birds to other species and may then cause devastating outbreaks in domestic poultry or give rise to human influenza pandemics.

H5N1 has been shown to be transmitted to tigers, leopards, and domestic cats that were fed uncooked domestic fowl (chickens) with the virus. H3N8 viruses from horses have crossed over and caused outbreaks in dogs. Laboratory mice have been infected successfully with a variety of avian flu genotypes.

Influenza A viruses spread in the air and in manure, and survives longer in cold weather. It can also be transmitted by contaminated feed, water, equipment and clothing; however, there is no evidence the virus can survive in well-cooked meat. Symptoms in animals vary, but virulent strains can cause death within a few days.

"Highly pathogenic avian influenza virus is on every top ten list available for potential agricultural bioweapon agents".

Avian influenza viruses that the OIE and others test for to control poultry disease include: H5N1, H7N2, H1N7, H7N3, H13N6, H5N9, H11N6, H3N8, H9N2, H5N2, H4N8, H10N7, H2N2, H8N4, H14N5, H6N5, H12N5 and others.

Known outbreaks of highly pathogenic flu in poultry 1959–2003

Year	Area	Affected	Subtype
1959	Scotland	chicken	H5N1
1963	England	turkey	H7N3
1966	Ontario (Canada)	turkey	H5N9
1976	Victoria (Australia)	chicken	H7N7
1979	Germany	chicken	H7N7
1979	England	turkey	H7N7
1983	Pennsylvania (USA)*	chicken, turkey	H5N2
1983	Ireland	turkey	H5N8
1985	Victoria (Australia)	chicken	H7N7
1991	England	turkey	H5N1
1992	Victoria (Australia)	chicken	H7N3
1994	Queensland (Australia)	chicken	H7N3
1994	Mexico*	chicken	H5N2
1994	Pakistan*	chicken	H7N3
1997	New South Wales (Australia)	chicken	H7N4
1997	Hong Kong (China)*	chicken	H5N1
1997	Italy	chicken	H5N2
1999	Italy*	turkey	H7N1
2002	Hong Kong (China)	chicken	H5N1
2002	Chile	chicken	H7N3
2003	Netherlands*	chicken	H7N7
*Outbreaks with significant spread to numerous farms, resulting in great economic losses. Most other outbreaks involved little or no spread from the initially infected farms.

1979: "More than 400 harbor seals, most of them immature, died along the New England coast between December 1979 and October 1980 of acute pneumonia associated with influenza virus, A/Seal/Mass/1/180 (H7N7)."

1995: "[V]accinated birds can develop asymptomatic infections that allow virus to spread, mutate, and recombine (ProMED-mail, 2004j). Intensive surveillance is required to detect these “silent epidemics” in time to curtail them. In Mexico, for example, mass vaccination of chickens against epidemic H5N2 influenza in 1995 has had to continue in order to control a persistent and evolving virus (Lee et al., 2004)."

1997: "Influenza A viruses normally seen in one species sometimes can cross over and cause illness in another species. For example, until 1997, only H1N1 viruses circulated widely in the U.S. pig population. However, in 1997, H3N2 viruses from humans were introduced into the pig population and caused widespread disease among pigs. Most recently, H3N8 viruses from horses have crossed over and caused outbreaks in dogs."

2000: "In California, poultry producers kept their knowledge of a recent H6N2 avian influenza outbreak to themselves due to their fear of public rejection of poultry products; meanwhile, the disease spread across the western United States and has since become endemic."

2003: In Netherlands H7N7 influenza virus infection broke out in poultry on several farms.

2004: In North America, the presence of avian influenza strain H7N3 was confirmed at several poultry farms in British Columbia in February 2004. As of April 2004, 18 farms had been quarantined to halt the spread of the virus.

2005: Tens of millions of birds died of H5N1 influenza and hundreds of millions of birds were culled to protect humans from H5N1. H5N1 is endemic in birds in southeast Asia and represents a long-term pandemic threat.

2006: H5N1 spreads across the globe, killing hundreds of millions of birds and over 100 people, and causing a significant H5N1 impact from both actual deaths and predicted possible deaths.

Swine flu

Main article: Swine influenza

Swine influenza (or "pig influenza") refers to a subset of Orthomyxoviridae that create influenza and are endemic in pigs. The species of Orthomyxoviridae that can cause flu in pigs are influenza A virus and influenza C virus, but not all genotypes of these two species infect pigs. The known subtypes of influenza A virus that create influenza and are endemic in pigs are H1N1, H1N2, H3N1 and H3N2.

Horse flu

Main article: Equine influenza

Horse flu (or "equine influenza") refers to varieties of influenza A virus that affect horses. Horse flu viruses were only isolated in 1956. The two main types of virus are called equine-1 (H7N7), which commonly affects horse heart muscle, and equine-2 (H3N8), which is usually more severe.

Dog flu

Main article: Canine influenza

Dog flu (or "canine influenza") refers to varieties of influenza A virus that affect dogs. The equine influenza virus H3N8 was found to infect and kill – with respiratory illness – greyhound race dogs at a Florida racetrack in January 2004.

H3N8

Main article: Influenza A virus subtype H3N8

H3N8 is now endemic in birds, horses and dogs.

Human influenza virus

"Human influenza virus" usually refers to those subtypes that spread widely among humans. H1N1, H1N2, and H3N2 are the only known influenza A virus subtypes currently circulating among humans.

Genetic factors in distinguishing between "human flu viruses" and "avian influenza viruses" include:

PB2: (RNA polymerase): Amino acid (or residue) position 627 in the PB2 protein encoded by the PB2 RNA gene. Until H5N1, all known avian influenza viruses had a Glu at position 627, while all human influenza viruses had a lysine.

HA: (hemagglutinin): Avian influenza HA binds alpha 2–3 sialic acid receptors, while human influenza HA binds alpha 2–6 sialic acid receptors. Swine influenza viruses have the ability to bind both types of sialic acid receptors.

"About 52 key genetic changes distinguish avian influenza strains from those that spread easily among people, according to researchers in Taiwan, who analyzed the genes of more than 400 A type flu viruses." "How many mutations would make an avian virus capable of infecting humans efficiently, or how many mutations would render an influenza virus a pandemic strain, is difficult to predict. We have examined sequences from the 1918 strain, which is the only pandemic influenza virus that could be entirely derived from avian strains. Of the 52 species-associated positions, 16 have residues typical for human strains; the others remained as avian signatures. The result supports the hypothesis that the 1918 pandemic virus is more closely related to the avian influenza A virus than are other human influenza viruses."

Human flu symptoms usually include fever, cough, sore throat, muscle aches, conjunctivitis and, in severe cases, severe breathing problems and pneumonia that may be fatal. The severity of the infection will depend in large part on the state of the infected person's immune system and if the victim has been exposed to the strain before, and is therefore partially immune.

Highly pathogenic H5N1 avian influenza in a human is far worse, killing 50% of humans that catch it. In one case, a boy with H5N1 experienced diarrhea followed rapidly by a coma without developing respiratory or flu-like symptoms.

The influenza A virus subtypes that have been confirmed in humans, ordered by the number of known human pandemic deaths, are:

• H1N1 caused "Spanish flu" and the 2009 swine flu outbreak
• H2N2 caused "Asian flu" in the late 1950s
• H3N2 caused "Hong Kong flu" in the late 1960s
• H5N1 considered a global influenza pandemic threat through its spread in the mid-2000s
• H7N7 has unusual zoonotic potential
• H1N2 is currently endemic in humans and pigs
• H9N2, H7N2, H7N3, H5N2, and H10N7.

H1N1

Main article: Influenza A virus subtype H1N1

H1N1 is currently pandemic in both human and pig populations. A variant of H1N1 was responsible for the Spanish flu pandemic that killed some 50 million to 100 million people worldwide over about a year in 1918 and 1919. Another variant was named a pandemic threat in the 2009 flu pandemic. Controversy arose in October, 2005, after the H1N1 genome was published in the journal, Science, because of fears that this information could be used for bioterrorism.^{[citation needed]}

H2N2

Main article: Influenza A virus subtype H2N2

The Asian flu, a pandemic outbreak of H2N2 avian influenza, originated in China in 1957, spread worldwide that same year during which a influenza vaccine was developed, lasted until 1958 and caused between one and four million deaths.

H3N2

Main article: Influenza A virus subtype H3N2

H3N2 is currently endemic in both human and pig populations. It evolved from H2N2 by antigenic shift and caused the Hong Kong flu pandemic of 1968 and 1969 that killed up to 750,000. "An early-onset, severe form of influenza A H3N2 made headlines when it claimed the lives of several children in the United States in late 2003."

The dominant strain of annual flu in January 2006 was H3N2. Measured resistance to the standard antiviral drugs amantadine and rimantadine in H3N2 increased from 1% in 1994 to 12% in 2003 to 91% in 2005.

"[C]ontemporary human H3N2 influenza viruses are now endemic in pigs in southern China and can reassort with avian H5N1 viruses in this intermediate host."

H5N1

Main article: Influenza A virus subtype H5N1

H5N1 is the world's major influenza pandemic threat.

"When he compared the 1918 virus with today's human flu viruses, Dr. Taubenberger noticed that it had alterations in just 25 to 30 of the virus's 4,400 amino acids. Those few changes turned a bird virus into a killer that could spread from person to person."

H7N7

Main article: Influenza A virus subtype H7N7

H7N7 has unusual zoonotic potential. In 2003 in Netherlands, 89 people were confirmed to have H7N7 influenza virus infection following an outbreak in poultry on several farms. One death was recorded.

H1N2

Main article: Influenza A virus subtype H1N2

H1N2 is currently endemic in both human and pig populations. The new H1N2 strain appears to have resulted from the reassortment of the genes of the currently circulating influenza H1N1 and H3N2 subtypes. The hemagglutinin protein of the H1N2 virus is similar to that of the currently circulating H1N1 viruses, and the neuraminidase protein is similar to that of the current H3N2 viruses.

H9N2

Main article: Influenza A virus subtype H9N2

Low pathogenic avian influenza A (H9N2) infection was confirmed in 1999, in China and Hong Kong in two children, and in 2003 in Hong Kong in one child. All three fully recovered.

H7N2

Main article: Influenza A virus subtype H7N2

One person in New York in 2003 and one person in Virginia in 2002 were found to have serologic evidence of infection with H7N2. Both fully recovered.

H7N3

Main article: Influenza A virus subtype H7N3

In North America, the presence of avian influenza strain H7N3 was confirmed at several poultry farms in British Columbia in February 2004. As of April 2004, 18 farms had been quarantined to halt the spread of the virus. Two cases of humans with avian influenza have been confirmed in that region. "Symptoms included conjunctivitis and mild influenza-like illness." Both fully recovered.

H5N2

Main article: Influenza A virus subtype H5N2

Japan's Health Ministry said January 2006 that poultry farm workers in Ibaraki prefecture may have been exposed to H5N2 in 2005. The H5N2 antibody titers of paired sera of 13 subjects increased fourfold or more.

H10N7

Main article: Influenza A virus subtype H10N7

In 2004 in Egypt, H10N7 was reported for the first time in humans. It caused illness in two infants in Egypt. One child’s father is a poultry merchant.

Evolution

See also: Punctuated equilibrium

Taubenberger says:

"All influenza A pandemics since [the Spanish flu pandemic], and indeed almost all cases of influenza A worldwide (excepting human infections from avian viruses such as H5N1 and H7N7), have been caused by descendants of the 1918 virus, including "drifted" H1N1 viruses and reassorted H2N2 and H3N2 viruses. The latter are composed of key genes from the 1918 virus, updated by subsequently incorporated avian influenza genes that code for novel surface proteins, making the 1918 virus indeed the "mother" of all pandemics.

Researchers from the National Institutes of Health used data from the Influenza Genome Sequencing Project and concluded that during the ten-year period examined, most of the time the hemagglutinin gene in H3N2 showed no significant excess of mutations in the antigenic regions while an increasing variety of strains accumulated. This resulted in one of the variants eventually achieving higher fitness, becoming dominant, and in a brief interval of rapid evolution, rapidly sweeping through the population and eliminating most other variants.

Short-term Evolution In the short-term evolution of influenza A virus, a 2006 study found that stochastic, or random, processes are key factors. Influenza A virus HA antigenic evolution appears to be characterized more by punctuated, sporadic jumps as opposed to a constant rate of antigenic change. Using phylogenetic analysis of 413 complete genomes of human influenza A viruses that were collected throughout the state of New York, the authors of Nelson et al. 2006 were able to show that genetic diversity, and not antigenic drift, shaped the short-term evolution of influenza A via random migration and reassortment. The evolution of these viruses is dominated more by the random importation of genetically different viral strains from other geographic locations and less by natural selection. Within a given season, adaptive evolution is infrequent and had an overall weak effect as evidenced from the data gathered from the 413 genomes. Phylogenetic analysis revealed the different strains were derived from newly imported genetic material as opposed to isolates that had been circulating in New York in previous seasons. Therefore, the gene flow in and out of this population, and not natural selection, was more important in the short term.

See also

• FI6 (antibody)
• Animal virology
• ACAM-FLU-A

Notes

Further reading

Official sources

Further information: H5N1

• Avian influenza and Influenza Pandemics from the Centers for Disease Control and Prevention
• Avian influenza FAQ from the World Health Organization
• Avian influenza information from the Food and Agriculture Organization
• U.S. Government's avian influenza information website
• European Centre for Disease Prevention and Control (ECDC) Stockholm, Sweden

General information

Further information: Flu

• "The Bird Flu and You" Full-color poster provided by the Center for Technology and National Security Policy at the National Defense University, in collaboration with the National Security Health Policy Center
• Influenza Report 2006 Online book. Research level quality information. Highly recommended.
• Special issue on avian flu from Nature
• Nature Reports: Homepage: Avian Flu
• Beigel JH, Farrar J, Han AM, et al. (September 2005). "Avian influenza A (H5N1) infection in humans". N. Engl. J. Med. 353 (13): 1374–85. doi:10.1056/NEJMra052211. PMID 16192482. http://content.nejm.org/cgi/content/full/353/13/1374.
• Pandemic Influenza: Domestic Preparedness Efforts Congressional Research Service Report on Pandemic Preparedness.
• A guide to bird flu and its symptoms from BBC Health
• A Variety of Avian Flu Images and Pictures
• Mahmoud 2005, p. 285 "Highly pathogenic avian influenza virus is on every top ten list available for potential agricultural bioweapon agents"
• Mahmoud, Adel A. F; Institute of Medicine; Knobler, Stacey; Mack, Alison (2005). The Threat of Pandemic Influenza: Are We Ready?: Workshop Summary. Washington, D.C: National Academies Press. ISBN 0-309-09504-2. http://www.nap.edu/openbook.php?record_id=11150&page=R1.
• 'The Threat of Bird Flu': HealthPolitics.com
• Is a Global Flu Pandemic Imminent? from Infection Control Today.
• Bird Flu is a Real Pandemic Threat to Humans by Leonard Crane, author of Ninth Day of Creation.
• Links to Bird Flu pictures (Hardin MD/Univ of Iowa)
• Yoshihiro Kawaoka (2006). Influenza Virology: Current Topics. Caister Academic Pr. ISBN 1-904455-06-9.
• Francisco Sobrino; Thomas Mettenleiter (2008). Animal Viruses: Molecular Biology. Caister Academic Pr. ISBN 1-904455-22-0.

External links

• Influenza Research Database – Database of influenza genomic sequences and related information.
• Health-EU portal European Union response to influenza

UpToDate Contents

全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.

• 1. 成人における季節性インフルエンザの治療 treatment of seasonal influenza in adults
• 2. 小児における季節性インフルエンザ：臨床的特徴および診断 seasonal influenza in children clinical features and diagnosis
• 3. インフルエンザの疫学 epidemiology of influenza
• 4. 成人における季節性インフルエンザの臨床症状 clinical manifestations of seasonal influenza in adults
• 5. 鳥インフルエンザA（H7N9）：疫学、臨床症状、および診断 avian influenza a h7n9 epidemiology clinical manifestations and diagnosis

English Journal

• Multiplexed detection of influenza A virus subtype H5 and H9 via quantum dot-based immunoassay.

• Wu F1, Yuan H2, Zhou C3, Mao M3, Liu Q2, Shen H3, Cen Y2, Qin Z4, Ma L5, Song Li L6.
• Biosensors & bioelectronics.Biosens Bioelectron.2016 Mar 15;77:464-70. doi: 10.1016/j.bios.2015.10.002. Epub 2015 Oct 9.
• A quantum dot-based lateral flow immunoassay system (QD-LFIAS) was developed to simultaneously detect both influenza A virus subtypes H5 and H9. Water-soluble carboxyl-functionalized quantum dots (QDs) were used as fluorescent tags. The QDs were conjugated to specific influenza A virus subtype H5 an
• PMID 26454828

• Photochemical studies and nanomolar photodynamic activities of phthalocyanines functionalized with 1,4,7-trioxanonyl moieties at their non-peripheral positions.

• Sobotta L1, Wierzchowski M2, Mierzwicki M2, Gdaniec Z3, Mielcarek J1, Persoons L4, Goslinski T2, Balzarini J5.
• Journal of inorganic biochemistry.J Inorg Biochem.2016 Feb;155:76-81. doi: 10.1016/j.jinorgbio.2015.11.006. Epub 2015 Nov 14.
• Manganese(III), cobalt(II), copper(II), magnesium(II), zinc(II) and metal-free phthalocyanines, possessing 1,4,7-trioxanonyl substituents, at their non-peripheral positions, were subjected to photochemical, photodynamic and biological activity studies. Demetallated phthalocyanine and its metallated
• PMID 26638008

• Influenza virus infection, myocarditis, "myocarditis", and Takotsubo syndrome: A need for scrutiny.

• Madias JE1.
• International journal of cardiology.Int J Cardiol.2016 Jan 15;203:1127-8. doi: 10.1016/j.ijcard.2015.09.089. Epub 2015 Nov 21.
• PMID 26608013

Japanese Journal

• インフルエンザウイルスRNAポリメラーゼの構造解析による創薬研究 (AYUMI 構造生物学が推進する医薬基盤とその応用)

• 朴 三用
• 医学のあゆみ 254(8), 551-557, 2015-08-22
• NAID 40020561202

• インフルエンザ : 動物からヒトへ : 新型ウイルス出現への備え (特集 新興・再興感染症と感染症対策)

• 迫田 義博
• 生体の科学 66(4), 301-304, 2015-07
• NAID 40020554774

• 呼吸器感染症におけるPOCTの現状と今後の展開

• 吉田 麻衣子,松田 淳一,栁原 克紀
• 呼吸器内科 = Respiratory medicine 28(1), 63-68, 2015-07
• NAID 40020543948

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Influenza A virusとは？goo Wikipedia (ウィキペディア) 。出典：Wikipedia（ウィキペディア）フリー百科事典。 Influenza A virusとは - goo Wikipedia (ウィキペディア) gooトップ サイトマップ スタートページに設定 RSS ヘルプ メニューへ ...

• Influenza Type A Viruses | Avian Influenza (Flu)

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★リンクテーブル★

リンク元	「A型インフルエンザウイルス」「LLCMK2細胞」「インフルエンザAウイルス」「swine influenza virus」
拡張検索	「influenza A virus infection」「avian influenza A virus」「human influenza A virus」
関連記事	「A」「Ad」「influenza A」「influenza」「virus」

「A型インフルエンザウイルス」

　　[★]

英

influenza A virus

関

A型インフルエンザ

• A型インフルエンザウイルス株の名前

A型/宿主/分離場所/分離材料番号または株名/分離年：（H亜型、N亜型）と表わす。

• 動物の場合

A/swine/Wisconsin/1/84(H1N1)

A型/豚/アメリカのウイスコンシン州/分離材料番号または株名/1984年（H1亜型、N1亜型）

• ヒトの場合

A/Hong Kong/156/97(H5N1)

A型/香港/分離材料番号または株名/1997年（H5亜型、N1亜型）―これは鶏のインフルエンザウイルスに感染して、1997年5月に死亡した香港の3歳の男児から分離されたウイルス株名。ヒトの場合宿主名は省略。

• http://ss.niah.affrc.go.jp/disease/Byouki/Influenza/influenza3.html

「LLCMK2細胞」

　　[★]

英

LLCMK2 cell

• サル腎上皮細胞

• 種：monkey, rhesus
• 組織：kidney

• ウイルス感受性：astrovirus、enterovirus、influenza A virus、influenza B virus、myxovirus、parainfluenza、parainfluenza、parainfluenza、poliovirus、poliovirus、poliovirus、poxvirus、rhinovirus、rotavirus

「インフルエンザAウイルス」

　　[★]

英

influenza A virus

関

A型インフルエンザウイルス

「swine influenza virus」

　　[★]

• ブタインフルエンザウイルス

関

influenza A virus

「influenza A virus infection」

　　[★]

• A型インフルエンザウイルス感染、A型インフルエンザウイルス感染症

「avian influenza A virus」

　　[★]

• トリインフルエンザウイルスA型

「human influenza A virus」

　　[★]

• ヒトインフルエンザA型ウイルス

「A」

　　[★]

• アデニン adenine
• アデノシン adenosine
• アラニン alanine

　 　 　

「Ad」

　　[★]

• アデノウイルス

関

adenoviral、adenovirus

「influenza A」

　　[★]

A型インフルエンザ、インフルエンザA型

「influenza」

　　[★] インフルエンザ

　 　

「virus」

　　[★] ウイルス