Disease | influenza |
Symptom | |infection |
Sentences | 1183 |
PubMedID- 26038484 | The asymptomatic infection of poultry with these pathogenic influenza viruses that have acquired human receptor specificity in live poultry markets facilitates the transmission of these pathogenic reassortant influenza viruses to humans.39 there is a link between human highly pathogenic h5n1 avian influenza virus (hph5n1) infection and live poultry markets in china.40 influenza infection of ostrich and emu can lead to the selection of pb2-e627k and pb2-d701n mutants,41 and ratite-origin isolates of low pathogenicity can easily be converted to highly pathogenic avian influenza viruses in chickens.42,43,44 the mixing of new birds with unsold birds in live poultry markets sustains the circulation of these reassortant viruses. |
PubMedID- 26237589 | infection with influenza a virus is responsible for considerable morbidity and mortality in children worldwide. |
PubMedID- 24073006 | infection with influenza a viruses is still a major health issue, and the treatment options are limited. |
PubMedID- 23525089 | We demonstrate that nod2(-/-) and ripk2(-/-) mice are hypersusceptible to infection with influenza a virus. |
PubMedID- 22516350 | However, infection or outbreaks of avian influenza a virus in gray seals have not been reported, probably because virus attachment is required but is not sufficient for infection. |
PubMedID- 24564491 | This study was conducted using agilent's whole mouse genome microarray 4x44k and recorded gene expression changes in mouse lungs after a non-lethal infection with influenza a virus over a period of 60 days. |
PubMedID- 23977434 | infection with influenza results in a respiratory illness that for most individuals is self limiting. |
PubMedID- 22739232 | infection with influenza virus causes a high degree of morbidity and mortality3. |
PubMedID- 24465206 | Furthermore, using a model of co-infection with influenza a followed subsequently by staphylococcus aureus inoculation, data from the same laboratory indicates a novel mechanism by which influenza a-induced type i ifns inhibit th17 immunity and increase susceptibility to secondary bacterial pneumonia . |
PubMedID- 26035023 | As shown in figure 2, esa-2 strongly inhibited infection caused by all of the influenza virus strains except for an earlier laboratory-adapted strain, a/pr8/34 (h1n1). |
PubMedID- 24507376 | Funding: emergency research project on human infection with avian influenza h7n9 virus, the national basic research program of china, and the national mega-projects for infectious diseases. |
PubMedID- 22241979 | Although virus was not detected in the nasal wash on day 8 post-infection, a low level of aerosol particles containing influenza viral rna was observed. |
PubMedID- 24624130 | Following infection with influenza virus, elevated levels of type 1 ifns have been shown to leave mice more susceptible to infection with s. pneumoniae (61). |
PubMedID- 21629679 | Screening of migrants may be enhanced or introduced in situations of international public health concern such as was observed in sars , human infection with avian influenza, and the h1n1 (2009) influenza pandemic . |
PubMedID- 21252579 | Conclusion: this case report shows that neurological complications can occur after respiratory tract infection with pandemic influenza a (h1n1) 2009 virus. |
PubMedID- 21561668 | Furthermore, we have conducted the first examination of the regulated expression of porcine alveolar macrophage tlr3 during in vivo co-infection with influenza virus and bordetella bronchiseptica. |
PubMedID- 22405508 | Objectives: these studies characterize mucosal antiviral antibody production in children during lower respiratory infection (lri) with h1n1 influenza versus other viral lri and examine the relationship between mucosal antiviral antibodies and protection against severe disease. |
PubMedID- 22025201 | Knock-out of cd200 or cd200r1 leads to mφ hyperactivity and autoimmune disease in vivo , and recent studies have shown that deleting or inhibiting the cd200-cd200r1 interaction renders mice more susceptible to lung inflammation during infection with influenza virus . |
PubMedID- 23803487 | Human infection with avian influenza a h7n9 virus: an assessment of clinical severity. |
PubMedID- 23569641 | Much of the work in abm to date has focussed on the simulation of contact-based infection spread associated with influenza-like illnesses and other respiratory infections, including coarse-scale community, country, and global models to finer-scale community and institutional models ,. |
PubMedID- 20537158 | This shows likely exposure to and infection with 2009 influenza a (h1n1), and the subsequent development of antibodies which may be protective, without increasing transmission. |
PubMedID- 23908874 | The first laboratory-confirmed cases of infection with pandemic influenza a(h1n1) 2009 in the western pacific region were reported on 28 april 2009. |
PubMedID- 21668688 | Conclusions: we identified significant differences in the physiological responses of male and female mice to infection with influenza a, which occurred in the absence of variation in viral titre and cellular inflammation. |
PubMedID- 24569108 | Probable longer incubation period for human infection with avian influenza a(h7n9) virus in jiangsu province, china, 2013. |
PubMedID- 22992381 | Immunized dba/2j mice did not lose body weight and survived lethal infection with mouse-adapted h1n1 influenza a virus. |
PubMedID- 23940654 | Similarly, the translocation of mir-484 was also observed after infection with a human influenza virus (a/wsn/33), in the a549 cells (figure s5a) and in cell lines, mdck (figures s5b–c) and hela (data not shown). |
PubMedID- 21998693 | As shown in figure 7, splenocytes from all mouse strains (wild-type and knockouts) expressed high levels of cd69 on cd19+ cells following infection with live influenza virus. |
PubMedID- 20876312 | In support of this view and in contrast to infection with influenza virus, primary tcd8+ cell responses to opvs do not require tcd4+ cell help and can occur in the absence of cd28 costimulation (fang and sigal, 2006). |
PubMedID- 25126178 | Background: human infection with avian influenza a h7n9 has emerged in china since february, 2013. |
PubMedID- 23844161 | For example it was observed that experimental infection (aerosol) with pig influenza type a subtype h1n2 (large white/german landrace crossbreds, described in ) led to a small, positive pig agp serum response (unpublished). |
PubMedID- 21124892 | By constraining one cell population to the specific parameter values defined in for in-host human infection with influenza a (h1n1), we explore the dynamics of the model in the parameter space of the secondary cell population. |
PubMedID- 24722424 | infection with influenza virus (a/brisbane/59/2007) was performed in an infection medium consisting of dmem supplemented with glutamine (2 mm), hepes (25 mm), bovine serum albumin (0.2%; a7888; sigma), and tpck-trypsin (1 μg/ml; t1426; sigma). |
PubMedID- 20145532 | Rapidly progressive lethal infection with novel influenza a (h1n1) 2009 virus in a kidney recipient: a cautionary tale. |
PubMedID- 21173107 | Upon infection with influenza a virus, mouse lungs develop large numbers of inducible bronchus-associated lymphoid tissues (ibalts) that promote local immunity and memory to the virus (moyron-quiroz et al., 2004, 2006). |
PubMedID- 24421115 | Evaluation of heterosubtypic cross-protection against highly pathogenic h5n1 by active infection with human seasonal influenza a virus or trivalent inactivated vaccine immunization in ferret models. |
PubMedID- 21880755 | infection with seasonal influenza a viruses induces immunity to potentially pandemic influenza a viruses of other subtypes (heterosubtypic immunity). |
PubMedID- 26030884 | Moreover, very recently, puma protein levels were shown to be increased after infection with influenza a virus . |
PubMedID- 22238617 | After infection with either influenza virus or viral-like particles (vlps), mdck and mdbk cells were grown in l-15 medium containing 15 mm hepes, ph7.5, nonessential amino acids, 0.75 g of nahco3 per liter, and 0.125% (w/v) of bovine serum albumin. |
PubMedID- 23734994 | Agent interactions in both tissue (left) and lymph node (right) as a result of infection with the influenza a virus. |
PubMedID- 25168591 | Methods: here we inhibited nxf1 and crm1 nuclear export prior to infection with influenza a/udorn/307/1972(h3n2) virus and analyzed influenza intron-less mrnas using cellular fractionation and reverse transcription-quantitative polymerase chain reaction (rt-qpcr). |
PubMedID- 22969304 | infection with seasonal influenza can cause serious morbidity and mortality in hospitalized patients.1 the reported effectiveness of the modern trivalent influenza vaccine ranges from 74%2 to 89.4%,3 depending upon the population and study type. |
PubMedID- 24204140 | In addition, intranasal agnp administration in mice significantly enhanced survival after infection with the h3n2 influenza virus. |
PubMedID- 24312008 | In fact, infection with live influenza virus induced changes analogous to those provoked by the lps and polyi:c challenges (jurgens et al., 2012), and a recent study by ji et al. |
PubMedID- 24122799 | infection with influenza c virus was detected in 38 of 892 young men during their service. |
PubMedID- 24576842 | Correlation between reported human infection with avian influenza a h7n9 virus and cyber user awareness: what can we learn from digital epidemiology. |
PubMedID- 24518691 | We report the detection of one case of co-infection with influenza a(h1n1)pdm09 and b, occurred during the 2012-2013 influenza season in sicily. |
PubMedID- 20438121 | This study presents the proteomics analysis on the change of proteins to h5n1 avian influenza virus with neurovirulence infection in chicken brain tissue. |
PubMedID- 24027503 | The effects of specific pathogens have been modeled in animals by prenatal infection with the influenza virus (shi et al., 2003, 2005) and by adult infection with the toxoplasma parasite (vyas et al., 2007). |
PubMedID- 21994612 | The recent findings by shen and colleagues indicating that p53 levels are upregulated upon infection with influenza a virus, leading to irf9 and bax upregulation , are consistent with previous studies that demonstrated that p53 is important for influenza-induced apoptosis, and thus, cells retaining wt p53 have an enhanced apoptotic response to influenza a infection, which results in impaired viral replication 7. |
PubMedID- 23936461 | In mouse studies of infectious disease, antigen specific cd8 t cell responses were compromised in the absence of ox40 after infection with influenza virus, cytomegalovirus, vaccinia virus, listeria monocytogenes (lm), or lymphocytic choriomeningitis virus (lcmv) . |