Transcription factor regulation and cytokine expression following in vitro infection of primary chicken cell culture with low pathogenic avian influenza virus
© Jiang et al.; licensee BioMed Central Ltd. 2013
Received: 16 July 2013
Accepted: 14 November 2013
Published: 19 November 2013
Avian influenza virus (AIV) induced proinflammatory cytokine expression is believed to contribute to the disease pathogenesis following infection of poultry. However, there is limited information on the avian immune response to infection with low pathogenic avian influenza virus (LPAIV).
To gain a better understanding of the early viral-host interactions of LPAIV in chickens, primary chicken embryo hepatocytes (CEH) were infected with four different LPAIVs of U.S. origin. Kinetics of virus replication, transcription factor (c-Jun, p50 and IRF-3) activation and immune response gene (IL-6, IL-1beta, IFN-alpha and Mx) expression were studied at four different time points (6, 12, 24 and 48 hours) post infection and compared to non-infected controls.
CEH can support growth of the tested LPAIVs when with trypsin supplementation. All four immune response genes tested were upregulated following infection as were transcription factors c-Jun, p50 and IRF-3. Amplification of these genes was dependant on virus replication (e.g. inclusion of trypsin), such that immune response genes and transcription factors were upregulated as viral titers increased.
The results of these studies demonstrate the requirement of virus replication for innate immune regulation and broaden our understanding of transcription factor responses related to LPAIV infection in chickens.
KeywordsAvian influenza virus Chicken Cytokine Transcription factor
Avian influenza (AI) infection in poultry can result in high morbidity and mortality, and negatively affect international trade . AIV can be categorized into 16 different hemagglutinin (HA) subtypes (H1–H16) and 9 different neuraminidases (N1–N9) subtypes which can occur in many combinations . During the past decade, low pathogenic (LP) AIV has caused considerable economic loss due to decreased production, increased morbidity and increase the cost of vaccination in poultry industry . LPAI viruses have the potential to evolve into highly pathogenic (HP) AIV and this has been documented in many poultry outbreaks. However, only the H5 and H7 subtypes, have been associated with HPAI mutation [4, 5]. This has led to a new proposed definition of avian influenza to extend all infections caused by H5 and H7 viruses regardless of their virulence as notifiable avian influenza (NAI) . The H9N2 subtype was first reported to infect turkeys in the United States in 1966 and has seriously affected the poultry industry of the Asia and Middle East since the mid-1990s [7–9]. This subtype is considered one of the most likely candidates to cause a new influenza pandemic in humans . In 1999 and 2003, the reports of H9N2 AIV infections of humans in Hong Kong dramatically attracted the attention of the scientific community [11, 12].
The innate immune system response is the first line of defense and limits early virus replication . Cytokines are important immune mediators of innate and acquired immunity responsible for initiating, amplifying and regulating inflammation in response to pathogenic infection [14, 15]. Knowledge of the innate immune recognition of AIV is crucial to understanding the viral pathogenesis in birds. Recognition of pathogen-associated molecular patterns (PAMPs) by host pattern recognition receptors (PRRs) represents a critical step in innate immune responses . Proper communication between host cells and pathogen via PAMPs and PRRs initiates signal transduction pathways which in turn induces the expression of cytokines aimed at controlling pathogens .
Recognition of the virus through PRRs, such as retinoic-acid inducible gene I (RIG-I), melanoma differentiation-associated gene 5 (MDA-5) and toll-like receptors (TLRs) induces activation and translocation of transcription factors to nucleus, including activator protein-1 (AP-1), interferon regulatory (IRF) factor 3 (IRF-3) and nuclear factor-kappa β (NF-κβ), which collaborate to induce transcription of various cytokines such as alpha/beta interferon, leading to clearance of the infectious pathogens . Understanding the mechanisms that regulate innate immune responses to AIV is of key importance to develop novel virus-based therapeutic strategies. In mammals, studies have been carried out to examine the transcription factors signaling pathways after infection with influenza virus, however, in chicken very little is known . Although no commercial kit exists to examine chicken cellular transcription factors, previous reports have confirmed the cross-reactivity between birds and mammals in c-Jun, IRF-3 and p50 [20–24].
Lesions and viral antigen distribution are frequently observed in chicken liver infected with AIV [25–27]. Primary chicken embryo hepatocytes (CEHs) have been used for virus propagation, detection, and subsequent vaccine production [28–30]. Here we used primary CEHs which are readily used to study AIV infections because of their high susceptibility, thus are suitable to detect changes in gene expression early in the course of infection under controlled conditions. In this study, we compared viral replication, virus-induced cytokine gene expression and activation of cellular transcription factors associated with low pathogenic H5N3, H5N9, H7N2 and H9N2 viruses infection of CEH. The objective was to understand the early immune and cellular responses to broaden our understanding of the molecular mechanisms related to LPAIV infection in chicken.
Growth kinetics of viruses on CEH
Pro-inflammatory IL-6/IL-1β expression following virus growth on CEH
IL-1β expression was similar in CEH with trypsin supplementation with a peak at 24 hpi and decreased at 48 hpi. H7N2 also demonstrated the highest level of expression (8.8-fold) at 24 hpi. Interestingly, the IL-6 and IL-1β expression in CEH without trypsin after infection were far lower compared to expression observed with trypsin.
Interferon-α and Myxovirus (Mx) expression following virus growth on CEH
Activation of c-Jun, p50 and IRF-3 by LPAIVs
In these studies we compared the effects of different LPAIV on transcription factor activation and immune response gene expression in primary CEH. For the first time we demonstrate that chicken cells increase activation of c-Jun, IRF-3 and p50 transcription factors after AIV infection, which correlated with increased cytokine expression. Transcription factor activation and immune response gene induction also correlated with virus growth.
Early after infection, viruses are capable of triggering a series of intracellular events which may be accompanied by changes in host gene expression and activation of a variety of intracellular signaling pathways that are in part exploited by the virus to ensure efficient replication . In mammals, influenza virus infection and replication result in the production of multiple proinflammatory, chemotactic and antiviral cytokines [32, 33]. Cytokine gene expression are associated with the activation of a series of signal transducing molecules, such as AP-1 , STAT  and IRF , in influenza virus infected cells. However, our understanding of which transcription factors are involved in the cytokine gene expression mounted by the chicken cells to AIV is unknown.
When CEHs were infected with LPAIVs in the presence of trypsin, viral titers were increased, especially the H7N2 virus. This result suggests that LPAIV cannot replicate very well in CEH without exogenous trypsin. This is consistent with previous reports that report a need for trypsin-like proteases to cleave the hemagglutinin protein into the HA1 and HA2 subunits, which is required for the virus to be infectious [37, 38].
Infection with HPAI in birds and mammals is associated with severe pathology and increased mortality. One possible hypothesis for the cause of death in mammals due to HPAI infection is the acute induction of high levels of inflammatory cytokines, a so called cytokine storm [39–41]. The results of our study also demonstrate increased expression of pro-inflammation cytokines, IL-6, IL-1β and IFN-α, following LPAIV infection in vitro. These results correlate with previous studies which have also demonstrated increased pro-inflammatory cytokines expression following LPAIV infection [42, 43].
Interferon regulatory factors are a family of DNA-binding proteins involved in mediating the cellular immune response following viral infection. In mammals influenza virus infection induces activation of IRF-3 signaling [44–46], however its role in chicken immunity remains in question. It has been reported that chicken IRF-3 is activated by type I and type II IFN and its binding specificity has been demonstrated [47, 48]. More recently, Liniger reported that chicken IRF-3 was required for virus-mediated type I IFN induction in DF-1 cells . In our study, we also demonstrate increased IRF-3 production after infection with all isolates of LPAIV tested.
The transcription factor NF-κβ is known as a major regulator of the inflammatory response [50, 51]; however, its role in avian influenza virus replication and virus-induced immune response is ill-defined. In recent studies, NF-κB subunit p50 knockout cells demonstrated that activation of p50 is obsolete for production of interferon stimulated genes (ISG) upon virus infection  and that p50 is the predominant negative regulator of ISGs in the context of influenza virus infection . In our studies, we observed that infection with LPAIV induced an increase in p50 DNA binding after infection. Furthermore, the increased activation of p50 correlated with a resulting increase of proinflammatory cytokines. A previous study has reported that treatment of chicken heterophils with either flagellin or lipopolysaccharide induced a significant increase in DNA binding by the NF-κB family member p50 . These results demonstrate the significant role of p50 activation in inducing the expression of pro-inflammatory cytokines in chicken following infection.
In mammals, influenza virus infection induces transcription factor c-Jun and AP-1 activation and signaling, and helps to generate many of the biological effects of IFN production [34, 44–46, 55–59]. However in gallinaceous birds very little was known about the signaling pathways after infection with AIV. We observed an increase in c-Jun activation after infection of CEH with LPAIV. The increased transcription factor activation correlated with increased proinflammatory response, these sequential processes suggest that c-Jun and IRF-3 likely mediate the induction of IL-6, IL-1β and IFN-α gene expression. Similar timing of transcription factor activation and cytokine gene expression was found in mammalian cells [34, 45]. To our knowledge these findings confirm for the first time, that similar to mammal cells, infection of chicken cells with LPAIV increases protein expression of host DNA-binding transcription factors.
Our results demonstrate CEH can efficiently support growth of the LPAIV with trypsin supplementation in the medium after infection, especially the H7N2 virus. After infection all immune response genes tested were upregulated and the transcription factors, c-Jun, IRF-3 and p50, were also increased compared to sham-infected controls. These data will broaden our understanding the avian immune response to infection with LPAIV and has implications for strategies that target the innate immune system for improving resistance to avian influenza.
Materials and methods
Cells isolation and culture
Primary CEHs were isolated from 14-day-old white leghorn chicken embryos of Specific Pathogen Free (SPF) eggs as previously described  and were cultured at 37°C and 5% CO2 in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% fetal bovine serum (Invitrogen, CA,USA), 2 mM glutamine and antibiotics (final concentration: penicillin, 100 U/ml; streptomycin, 100 μg/ml). Cell viability was assessed by the Trypan Blue exclusion test and was not less than 90% for each preparation. Contamination by non-hepatocyte cells was minimal by microscopic examination. The cells were counted and suspensions were diluted to 2 × 106 viable (dye-excluding) cells per ml. The cells were distributed into 60 × 15 mm culture dishes (Becton Dickinson, NJ, USA) for virus growth kinetics and RNA extraction or nuclear extraction, respectively. For each experiment, cells were prepared on the same day and under the same conditions.
Virus and cell culture infection
A/turkey/Wisconsin/68 (H5N9), A/chicken/Texas/167280-4/02 (H5N3), A/turkey/Virginia/158512/02 (H7N2) and A/chicken/NJ/12220/97 (H9N2) LPAI viruses were propagated in allantoic cavities of 9–11 day of embryonation SPF chicken eggs. Viral titers were determined as previously described . All experiments using infectious virus were conducted in bio-safety level 2 (BSL-2) facilities at the Southeast Poultry Research Laboratory (SEPRL), Agricultural Research Service, United States Department of Agriculture (USDA).
Virus growth curves
The growth curves of the viruses were determined by virus titration of cell culture supernatants at different time points after infection of primary CEH. Briefly, cells were infected with each virus at a multiplicity of infection (MOI) of one in DMEM, negative control cells were set up identically but without the addition of virus. Culture dishes were gently rocked every 15 min for 1 h at 37°C, non-adsorbed viruses were removed and the cells were washed with sterile phosphate buffered saline (PBS). DMEM supplemented with 2% FBS or 1 μg/mL TPCK trypsin (Sigma–Aldrich, St. Louis, MO) for CEHs were added per dish and the dishes were incubated at 37°C and 5% CO2. At 6, 12, 24, and 48 hours post-infection (hpi), supernatants were collected and stored at -80°C until used for titrations in SPF embryos. Virus titers were determined using the method of Reed and Muench and expressed as 50% egg infectious dose (EID50) .
Isolation of RNA and quantification of cytokine gene expression
Total RNA was isolated from infected and control cells at each time point using the RNeasy mini kit (Qiagen) in accordance with the manufacturer’s instructions, and treated with RNase-free DNase I (Invitrogen) to remove genomic DNA. All RNA samples were checked by using a Nanodrop spectrophotometer (Nanodrop Technologies, Wilmington, DE). Relative cytokine mRNA expression in the abovementioned cells were examined by quantitative RT-PCR. Interleukin (IL)-1β, IL-6, IFN-α, and Mx expression were determined as previously described [15, 63]. Briefly, quantitative PCR was performed for each sample in triplicate in a total volume of 25 μl, consisting of 12.5 μl iQ SYBR Green supermix (Bio-Rad Laboratories, CA, USA) with 1 μl of each primer at concentration of 10 pmol/μl, 0.5 μl iScript reverse transcriptase, 5 μl RNase/DNase-free water, and 5 μl diluted RNA. PCR conditions were the same for each targeted gene and are as follows: 10 min at 50°C, 95°C for 5 min, followed by 45 cycles of 95°C for 10 s and 58°C for 30 s. For each reaction, melting curves were analyzed to determine the specificity of each gene. Primers were derived from previously published sequence and synthesized by Integrated DNA Technologies . Sequences are as follows (forward, reverse): IL-6 (5’-GCGAGAACAGCATGGAGATG-3’, 5’-CTGTTCGCCTTTCAGACCTAC-3’); IL-1β (5’-ACATGTCGTGTGTGATGA-3’, 5’-GCTTCATCTTCTACCGCCTG-3’); IFN-α (5’-GACAGCCAACGCCAAAGC-3’, 5’-AATGCTTGAGCAGCAGCGAC-3’); Mx (5’-CAGGACATCAACGACAATCT-3’, 5’-TTGCCAGATGAGGGATAGTA-3’) and 28S (5’-GGCGAAGCCAGAGGAAACT-3’, 5’-GACGACCGATTTGCACGTC-3’). RNA from individual cell samples was normalized using 28S house-keeping gene. For each gene, amplification was verified using four 10-fold serial dilutions of standard spleen cell RNA in the same PCR run. Expression was determined by the standard curve method . Data are expressed as fold change in cytokine messenger RNA (mRNA) levels in infected groups compared with those from uninfected groups.
c-Jun, IRF-3 and p50 activation analysis
The ELISA-based Trans-Am transcription factor kits (Active Motif, Carlsbad, CA, USA) were used to detect and quantify c-Jun, IRF-3 and p50 activation as previously described . The 96-well plates are contain immobilized oligonucleotides containing transcription response elements for c-Jun (5′-TGAGTCA-3′), NF-κβ p50 consensus binding site (5′-GGGACTTTCC-3′) or IRF consensus binding site (5′-GAAACTGAAACT-3′). The active forms of the subunits for c-Jun or p50 or IRF-3 in nuclear extracts can be detected using specific antibodies for epitopes that are accessible only when the nuclear factors are activated and bound to their target DNA. Preparation of nuclear extract was done according to the manufacturer’s instructions. The specificity of the assays was checked by measuring the ability of soluble wild type or mutated c-Jun, p50 and IRF-3 oligonucleotides to inhibit binding. The results are expressed as specific binding (absorbance measured in the presence of the mutated oligonucleotides minus that measured in the presence of the wild-type oligonucleotides) according to the manufacturer’s instructions.
Data are expressed as the mean ± standard deviation. Statistical differences were analyzed with Tukey one-way ANOVA using Prism 5 (GraphPad Co., San Diego, CA).
The authors wish to thank Cam Greene and Aniko Zsak for expert technical help. This research was supported by USDA, ARS, CRIS project 6612-32000-062.
Author disclosure statement
The authors declare that they have no competing interests.
- Kapczynski DR, Liljebjelke K, Kulkarni G, Hunt H, Jiang HJ, Petkov D: Cross reactive cellular immune responses in chickens previously exposed to low pathogenic avian influenza. BMC Proc 2011,5(4):S13.PubMedPubMed CentralView ArticleGoogle Scholar
- Swayne DE, Kapczynski D: Strategies and challenges for eliciting immunity against avian influenza virus in birds. Immunol Rev 2008, 225: 314-331. 10.1111/j.1600-065X.2008.00668.xPubMedView ArticleGoogle Scholar
- Kapczynski DR, Swayne DE: Influenza vaccines for avian species. Curr Top Microbiol Immunol 2009, 333: 133-152.PubMedGoogle Scholar
- Veits J, Weber S, Stech O, Breithaupt A, Graber M, Gohrbandt S, Bogs J, Hundt J, Teifke JP, Mettenleiter TC, Stech J: Avian influenza virus hemagglutinins H2, H4, H8, and H14 support a highly pathogenic phenotype. Proc Natl Acad Sci USA 2012, 109: 2579-2584. 10.1073/pnas.1109397109PubMedPubMed CentralView ArticleGoogle Scholar
- Capua I, Alexander DJ: Avian influenza infections in birds–a moving target. Influenza Other Respi Viruses 2007, 1: 11-18.View ArticleGoogle Scholar
- Capua I, Alexander DJ: Avian influenza: recent developments. Avian Pathol 2004, 33: 393-404. 10.1080/03079450410001724085PubMedView ArticleGoogle Scholar
- Fusaro A, Monne I, Salviato A, Valastro V, Schivo A, Amarin NM, Gonzalez C, Ismail MM, Al-Ankari AR, Al-Blowi MH, et al.: Phylogeography and evolutionary history of reassortant H9N2 viruses with potential human health implications. J Virol 2011, 85: 8413-8421. 10.1128/JVI.00219-11PubMedPubMed CentralView ArticleGoogle Scholar
- Homme PJ, Easterday BC: Avian influenza virus infections: I: Characteristics of influenza A-turkey-Wisconsin-1966 virus. Avian Dis 1970, 14: 66-74. 10.2307/1588557PubMedView ArticleGoogle Scholar
- Soda K, Asakura S, Okamatsu M, Sakoda Y, Kida H: H9N2 influenza virus acquires intravenous pathogenicity on the introduction of a pair of di-basic amino acid residues at the cleavage site of the hemagglutinin and consecutive passages in chickens. Virol J 2011, 8: 64. 10.1186/1743-422X-8-64PubMedPubMed CentralView ArticleGoogle Scholar
- Qiao C, Liu Q, Bawa B, Shen H, Qi W, Chen Y, Mok CK, Garcia-Sastre A, Richt JA, Ma W: Pathogenicity and transmissibility of reassortant H9 influenza viruses with genes from pandemic H1N1 virus. J Gen Virol 2012, 93: 2337-2345. 10.1099/vir.0.044040-0PubMedPubMed CentralView ArticleGoogle Scholar
- Butt KM, Smith GJ, Chen H, Zhang LJ, Leung YH, Xu KM, Lim W, Webster RG, Yuen KY, Peiris JS, Guan Y: Human infection with an avian H9N2 influenza A virus in Hong Kong in 2003. J Clin Microbiol 2005, 43: 5760-5767. 10.1128/JCM.43.11.5760-5767.2005PubMedPubMed CentralView ArticleGoogle Scholar
- Saito T, Lim W, Suzuki T, Suzuki Y, Kida H, Nishimura SI, Tashiro M: Characterization of a human H9N2 influenza virus isolated in Hong Kong. Vaccine 2001, 20: 125-133. 10.1016/S0264-410X(01)00279-1PubMedView ArticleGoogle Scholar
- Maecker H, Varfolomeev E, Kischkel F, Lawrence D, LeBlanc H, Lee W, Hurst S, Danilenko D, Li J, Filvaroff E, et al.: TWEAK attenuates the transition from innate to adaptive immunity. Cell 2005, 123: 931-944. 10.1016/j.cell.2005.09.022PubMedView ArticleGoogle Scholar
- Lowenthal JW, Lambrecht B, van den Berg TP, Andrew ME, Strom AD, Bean AG: Avian cytokines - the natural approach to therapeutics. Dev Comp Immunol 2000, 24: 355-365. 10.1016/S0145-305X(99)00083-XPubMedView ArticleGoogle Scholar
- Jiang H, Yang H, Kapczynski DR: Chicken interferon alpha pretreatment reduces virus replication of pandemic H1N1 and H5N9 avian influenza viruses in lung cell cultures from different avian species. Virol J 2011, 8: 447. 10.1186/1743-422X-8-447PubMedPubMed CentralView ArticleGoogle Scholar
- Meylan E, Tschopp J, Karin M: Intracellular pattern recognition receptors in the host response. Nature 2006, 442: 39-44. 10.1038/nature04946PubMedView ArticleGoogle Scholar
- Janeway CA Jr, Medzhitov R: Innate immune recognition. Annu Rev Immunol 2002, 20: 197-216. 10.1146/annurev.immunol.20.083001.084359PubMedView ArticleGoogle Scholar
- Zhong B, Tien P, Shu HB: Innate immune responses: crosstalk of signaling and regulation of gene transcription. Virology 2006, 352: 14-21. 10.1016/j.virol.2006.04.029PubMedView ArticleGoogle Scholar
- Bowie AG, Unterholzner L: Viral evasion and subversion of pattern-recognition receptor signalling. Nat Rev Immunol 2008, 8: 911-922. 10.1038/nri2436PubMedView ArticleGoogle Scholar
- Bos TJ, Monteclaro FS, Mitsunobu F, Ball AR Jr, Chang CH, Nishimura T, Vogt PK: Efficient transformation of chicken embryo fibroblasts by c-Jun requires structural modification in coding and noncoding sequences. Genes Dev 1990, 4: 1677-1687. 10.1101/gad.4.10.1677PubMedView ArticleGoogle Scholar
- Capobianco AJ, Chang D, Mosialos G, Gilmore TD: p105, the NF-kappa B p50 precursor protein, is one of the cellular proteins complexed with the v-Rel oncoprotein in transformed chicken spleen cells. J Virol 1992, 66: 3758-3767.PubMedPubMed CentralGoogle Scholar
- Grant CE, Vasa MZ, Deeley RG: cIRF-3, a new member of the interferon regulatory factor (IRF) family that is rapidly and transiently induced by dsRNA. Nucleic Acids Res 1995, 23: 2137-2146. 10.1093/nar/23.12.2137PubMedPubMed CentralView ArticleGoogle Scholar
- Saitoh T, Tun-Kyi A, Ryo A, Yamamoto M, Finn G, Fujita T, Akira S, Yamamoto N, Lu KP, Yamaoka S: Negative regulation of interferon-regulatory factor 3-dependent innate antiviral response by the prolyl isomerase Pin1. Nat Immunol 2006, 7: 598-605. 10.1038/ni1347PubMedView ArticleGoogle Scholar
- Takahasi K, Suzuki NN, Horiuchi M, Mori M, Suhara W, Okabe Y, Fukuhara Y, Terasawa H, Akira S, Fujita T, Inagaki F: X-ray crystal structure of IRF-3 and its functional implications. Nat Struct Biol 2003, 10: 922-927. 10.1038/nsb1001PubMedView ArticleGoogle Scholar
- Kapczynski DR, Pantin-Jackwood M, Guzman SG, Ricardez Y, Spackman E, Bertran K, Suarez DL, Swayne DE: Characterization of the 2012 highly pathogenic avian influenza H7N3 virus isolated from poultry in an outbreak in Mexico: pathobiology and vaccine protection. J Virol 2013, 87: 9086-9096. 10.1128/JVI.00666-13PubMedPubMed CentralView ArticleGoogle Scholar
- Post J, de Geus ED, Vervelde L, Cornelissen JB, Rebel JM: Systemic distribution of different low pathogenic avian influenza (LPAI) viruses in chicken. Virol J 2013, 10: 23. 10.1186/1743-422X-10-23PubMedPubMed CentralView ArticleGoogle Scholar
- van Riel D, van den Brand JM, Munster VJ, Besteboer TM, Fouchier RA, Osterhaus AD, Kuiken T: Pathology and virus distribution in chickens naturally infected with highly pathogenic avian influenza A virus (H7N7) During the 2003 outbreak in The Netherlands. Vet Pathol 2009, 46: 971-976. 10.1354/vp.08-VP-0215-K-BCPubMedView ArticleGoogle Scholar
- Lee J, Foster DN, Bottje WG, Jang HM, Chandra YG, Gentles LE, Kong BW: Establishment of an immortal chicken embryo liver-derived cell line. Poult Sci 2013, 92: 1604-1612. 10.3382/ps.2012-02582PubMedView ArticleGoogle Scholar
- Lukert PD: Immunofluorescence of avian infectious bronchitis virus in primary chicken embryo kidney, liver, lung, and fibroblast cell cultures. Arch Gesamte Virusforsch 1966, 19: 265-272. 10.1007/BF01241849PubMedView ArticleGoogle Scholar
- Allan GM, McNulty MS: A direct immunofluorescence test for the rapid detection of avian influenza virus antigen in tissue impression smears. Avian Pathol 1985, 14: 449-460. 10.1080/03079458508436248PubMedView ArticleGoogle Scholar
- Julkunen I, Sareneva T, Pirhonen J, Ronni T, Melen K, Matikainen S: Molecular pathogenesis of influenza A virus infection and virus-induced regulation of cytokine gene expression. Cytokine Growth Factor Rev 2001, 12: 171-180. 10.1016/S1359-6101(00)00026-5PubMedView ArticleGoogle Scholar
- Kaufmann A, Salentin R, Meyer RG, Bussfeld D, Pauligk C, Fesq H, Hofmann P, Nain M, Gemsa D, Sprenger H: Defense against influenza A virus infection: essential role of the chemokine system. Immunobiology 2001, 204: 603-613. 10.1078/0171-2985-00099PubMedView ArticleGoogle Scholar
- Ma W, Belisle SE, Mosier D, Li X, Stigger-Rosser E, Liu Q, Qiao C, Elder J, Webby R, Katze MG, Richt JA: 2009 pandemic H1N1 influenza virus causes disease and upregulation of genes related to inflammatory and immune responses, cell death, and lipid metabolism in pigs. J Virol 2011, 85: 11626-11637. 10.1128/JVI.05705-11PubMedPubMed CentralView ArticleGoogle Scholar
- Ludwig S, Ehrhardt C, Neumeier ER, Kracht M, Rapp UR, Pleschka S: Influenza virus-induced AP-1-dependent gene expression requires activation of the JNK signaling pathway. J Biol Chem 2001, 276: 10990-10998. 10.1074/jbc.M009902200View ArticleGoogle Scholar
- Bot A, Rodrigo E, Wolfe T, Bot S, Von Herrath MG: Infection-triggered regulatory mechanisms override the role of STAT 4 in control of the immune response to influenza virus antigens. J Virol 2003, 77: 5794-5800. 10.1128/JVI.77.10.5794-5800.2003PubMedPubMed CentralView ArticleGoogle Scholar
- Ronni T, Sareneva T, Pirhonen J, Julkunen I: Activation of IFN-alpha, IFN-gamma, MxA, and IFN regulatory factor 1 genes in influenza A virus-infected human peripheral blood mononuclear cells. J Immunol 1995, 154: 2764-2774.PubMedGoogle Scholar
- Chen J, Lee KH, Steinhauer DA, Stevens DJ, Skehel JJ, Wiley DC: Structure of the hemagglutinin precursor cleavage site, a determinant of influenza pathogenicity and the origin of the labile conformation. Cell 1998, 95: 409-417. 10.1016/S0092-8674(00)81771-7PubMedView ArticleGoogle Scholar
- Steinhauer DA: Role of hemagglutinin cleavage for the pathogenicity of influenza virus. Virology 1999, 258: 1-20. 10.1006/viro.1999.9716PubMedView ArticleGoogle Scholar
- Salomon R, Hoffmann E, Webster RG: Inhibition of the cytokine response does not protect against lethal H5N1 influenza infection. Proc Natl Acad Sci USA 2007, 104: 12479-12481. 10.1073/pnas.0705289104PubMedPubMed CentralView ArticleGoogle Scholar
- Cameron CM, Cameron MJ, Bermejo-Martin JF, Ran L, Xu L, Turner PV, Ran R, Danesh A, Fang Y, Chan PK, et al.: Gene expression analysis of host innate immune responses during Lethal H5N1 infection in ferrets. J Virol 2008, 82: 11308-11317. 10.1128/JVI.00691-08PubMedPubMed CentralView ArticleGoogle Scholar
- Zheng BJ, Chan KW, Lin YP, Zhao GY, Chan C, Zhang HJ, Chen HL, Wong SS, Lau SK, Woo PC, et al.: Delayed antiviral plus immunomodulator treatment still reduces mortality in mice infected by high inoculum of influenza A/H5N1 virus. Proc Natl Acad Sci USA 2008, 105: 8091-8096. 10.1073/pnas.0711942105PubMedPubMed CentralView ArticleGoogle Scholar
- Adams SC, Xing Z, Li J, Cardona CJ: Immune-related gene expression in response to H11N9 low pathogenic avian influenza virus infection in chicken and Pekin duck peripheral blood mononuclear cells. Mol Immunol 2009, 46: 1744-1749. 10.1016/j.molimm.2009.01.025PubMedView ArticleGoogle Scholar
- Xing Z, Cardona CJ, Li J, Dao N, Tran T, Andrada J: Modulation of the immune responses in chickens by low-pathogenicity avian influenza virus H9N2. J Gen Virol 2008, 89: 1288-1299. 10.1099/vir.0.83362-0PubMedView ArticleGoogle Scholar
- Fitzgerald KA, McWhirter SM, Faia KL, Rowe DC, Latz E, Golenbock DT, Coyle AJ, Liao SM, Maniatis T: IKKepsilon and TBK1 are essential components of the IRF3 signaling pathway. Nat Immunol 2003, 4: 491-496. 10.1038/ni921PubMedView ArticleGoogle Scholar
- Kim MJ, Latham AG, Krug RM: Human influenza viruses activate an interferon-independent transcription of cellular antiviral genes: outcome with influenza A virus is unique. Proc Natl Acad Sci USA 2002, 99: 10096-10101. 10.1073/pnas.152327499PubMedPubMed CentralView ArticleGoogle Scholar
- Zhang B, Li M, Chen L, Yang K, Shan Y, Zhu L, Sun S, Li L, Wang C: The TAK1-JNK cascade is required for IRF3 function in the innate immune response. Cell Res 2009, 19: 412-428. 10.1038/cr.2009.8PubMedView ArticleGoogle Scholar
- Grant CE, May DL, Deeley RG: DNA binding and transcription activation by chicken interferon regulatory factor-3 (chIRF-3). Nucleic Acids Res 2000, 28: 4790-4799. 10.1093/nar/28.23.4790PubMedPubMed CentralView ArticleGoogle Scholar
- May DL, Grant CE, Deeley RG: Cloning and promoter analysis of the chicken interferon regulatory factor-3 gene. DNA Cell Biol 2000, 19: 555-566. 10.1089/104454900439782PubMedView ArticleGoogle Scholar
- Liniger M, Summerfield A, Zimmer G, McCullough KC, Ruggli N: Chicken cells sense influenza A virus infection through MDA5 and CARDIF signaling involving LGP2. J Virol 2012, 86: 705-717. 10.1128/JVI.00742-11PubMedPubMed CentralView ArticleGoogle Scholar
- Flory E, Kunz M, Scheller C, Jassoy C, Stauber R, Rapp UR, Ludwig S: Influenza virus-induced NF-kappaB-dependent gene expression is mediated by overexpression of viral proteins and involves oxidative radicals and activation of IkappaB kinase. J Biol Chem 2000, 275: 8307-8314. 10.1074/jbc.275.12.8307PubMedView ArticleGoogle Scholar
- Pahl HL, Baeuerle PA: Expression of influenza virus hemagglutinin activates transcription factor NF-kappa B. J Virol 1995, 69: 1480-1484.PubMedPubMed CentralGoogle Scholar
- Wang X, Hussain S, Wang EJ, Li MO, Garcia-Sastre A, Beg AA: Lack of essential role of NF-kappa B p50, RelA, and cRel subunits in virus-induced type 1 IFN expression. J Immunol 2007, 178: 6770-6776.PubMedView ArticleGoogle Scholar
- Wei L, Sandbulte MR, Thomas PG, Webby RJ, Homayouni R, Pfeffer LM: NFkappaB negatively regulates interferon-induced gene expression and anti-influenza activity. J Biol Chem 2006, 281: 11678-11684. 10.1074/jbc.M513286200PubMedPubMed CentralView ArticleGoogle Scholar
- Kogut MH, Genovese KJ, He H, Kaiser P: Flagellin and lipopolysaccharide up-regulation of IL-6 and CXCLi2 gene expression in chicken heterophils is mediated by ERK1/2-dependent activation of AP-1 and NF-kappaB signaling pathways. Innate Immun 2008, 14: 213-222. 10.1177/1753425908094416PubMedView ArticleGoogle Scholar
- Kawai T, Akira S: Toll-like receptor and RIG-I-like receptor signaling. Ann N Y Acad Sci 2008, 1143: 1-20. 10.1196/annals.1443.020PubMedView ArticleGoogle Scholar
- Kim TK, Maniatis T: The mechanism of transcriptional synergy of an in vitro assembled interferon-beta enhanceosome. Mol Cell 1997, 1: 119-129. 10.1016/S1097-2765(00)80013-1PubMedView ArticleGoogle Scholar
- Kujime K, Hashimoto S, Gon Y, Shimizu K, Horie T: p38 mitogen-activated protein kinase and c-jun-NH2-terminal kinase regulate RANTES production by influenza virus-infected human bronchial epithelial cells. J Immunol 2000, 164: 3222-3228.PubMedView ArticleGoogle Scholar
- Takeuchi O, Akira S: MDA5/RIG-I and virus recognition. Curr Opin Immunol 2008, 20: 17-22. 10.1016/j.coi.2008.01.002PubMedView ArticleGoogle Scholar
- Saito T, Owen DM, Jiang F, Marcotrigiano J, Gale M Jr: Innate immunity induced by composition-dependent RIG-I recognition of hepatitis C virus RNA. Nature 2008, 454: 523-527. 10.1038/nature07106PubMedPubMed CentralView ArticleGoogle Scholar
- McNulty MS, Allan GM, Todd D, McFerran JB, McKillop ER, Collins DS, McCracken RM: Isolation of rotaviruses from turkeys and chickens: demonstration of distinct serotypes and RNA electropherotypes. Avian Pathol 1980, 9: 363-375. 10.1080/03079458008418420PubMedView ArticleGoogle Scholar
- Lavrentieva IN, Medvedeva TE, Golubev DB: Characterization of the reproduction of influenza A epidemic viruses in cell cultures. Acta Virol 1986, 30: 137-142.PubMedGoogle Scholar
- Reed LJ, Muench H: A simple method for estimating fifty percent endpoints. American Journal of Hygiene 1938, 27: 493-497.Google Scholar
- Kapczynski DR, Kogut MH: Measurement of avian cytokines with real-time RT-PCR following infection with the avian influenza virus. Methods Mol Biol 2008, 436: 127-134.PubMedGoogle Scholar
- Rue CA, Susta L, Cornax I, Brown CC, Kapczynski DR, Suarez DL, King DJ, Miller PJ, Afonso CL: Virulent Newcastle disease virus elicits a strong innate immune response in chickens. J Gen Virol 2011, 92: 931-939. 10.1099/vir.0.025486-0PubMedView ArticleGoogle Scholar
- Morrison TB, Weis JJ, Wittwer CT: Quantification of low-copy transcripts by continuous SYBR Green I monitoring during amplification. Biotechniques 1998, 24: 954-958. 960, 962PubMedGoogle Scholar
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