Mechanism of fowl adenovirus serotype 4-induced heart damage and formation of pericardial effusion

Poultry Science - Tập 98 - Trang 1134-1145 - 2019
Yujuan Niu1,2, Qinqin Sun2, Xingpo Liu2, Sidang Liu2
1Institute for Research in Biomedicine, Qingdao University, Qingdao, Shandong Province 266071, China
2College of Animal Science and Technology, Shandong Agricultural University, Tai'an, Shandong Province, 271018, China

Tài liệu tham khảo

Appledorn, 2008, Adenovirus vector-induced innate inflammatory mediators, MAPK signaling, as well as adaptive immune responses are dependent upon both TLR2 and TLR9 in vivo, J. Immunol., 181, 2134, 10.4049/jimmunol.181.3.2134 Cerullo, 2007, Toll-like receptor 9 triggers an innate immune response to helper-dependent adenoviral vectors, Mol. Ther., 15, 378, 10.1038/sj.mt.6300031 Chang, 2017, QSKL protects against myocardial apoptosis on heart failure via PI3K/Akt-p53 signaling pathway, Sci. Rep., 7, 16986, 10.1038/s41598-017-17163-x Choi, 2012, Epidemiological investigation of outbreaks of fowl adenovirus infection in commercial chickens in Korea, Poult. Sci., 91, 2502, 10.3382/ps.2012-02296 Di-Paolo, 2009, Virus binding to a plasma membrane receptor triggers interleukin-1 alpha-mediated proinflammatory macrophage response in vivo, Immunity, 31, 110, 10.1016/j.immuni.2009.04.015 Domanska-Blicharz, 2011, Molecular characterization of fowl adenoviruses isolated from chickens with gizzard erosions, Poult. Sci., 90, 983, 10.3382/ps.2010-01214 Fallach, 2010, Cardiomyocyte Toll-like receptor 4 is involved in heart dysfunction following septic shock or myocardial ischemia, J. Mol. Cell Cardiol., 48, 1236, 10.1016/j.yjmcc.2010.02.020 Foglio, 2017, HMGB1 inhibits apoptosis following MI and induces autophagy via mTORC1 inhibition, J. Cell. Physiol., 232, 1135, 10.1002/jcp.25576 Hafez, 2011, Avian adenoviruses infections with special attention to inclusion body hepatitis/ hydropericardium syndrome and egg drop syndrome, Pak. Vet. J., 31, 85 Harrach B. , Benkö, M., Both, G. W., Brown, M., Davison, A. J., Echavarría, M., 2012. Family—Adenoviridae. Pages 125–141 in Virus Taxonomy (9th ed.). King, A. M. Q., Adams, M. J., Carstens, E. B., Lefkowitz, E. J., eds. Elsevier Academic Press, San Diego. Harrach B. , Kaján, G., 2011. Aviadenovirus. The Springer Index of Viruses. Tidona, C., Darai, G., eds. Springer, New York. Hess, 2000, Detection and differentiation of avian adenoviruses: A review, Avian Pathol., 29, 195, 10.1080/03079450050045440 Iacobelli-Martinez, 2007, Preferential activation of Toll-like receptor nine by CD46-utilizing adenoviruses, J. Virol., 81, 1305, 10.1128/JVI.01926-06 Li, 2016, Fowl adenovirus species C serotype 4 is attributed to the emergence of hepatitis-hydropericardium syndrome in chickens in China, Infect. Genet. Evol., 45, 230, 10.1016/j.meegid.2016.09.006 Li, 2017, Fowl adenovirus serotype 4: Epidemiology, pathogenesis, diagnostic detection, and vaccine strategies, Poult. Sci., 96, 2630, 10.3382/ps/pex087 Lobanov, 2000, Sequence analysis of hexon gene from adenovirus KR95 inducing hydropericardium syndrome in chickens, Mol. Gen. Mikrobiol. Virusol., 1, 30 Maartens, 2014, Inclusion body hepatitis associated with an outbreak of fowl adenovirus type 2 and type 8b in broiler flocks in South Africa, J. S. Afr. Vet. Assoc., 85, e1, 10.4102/jsava.v85i1.1146 Matos, 2016, The outcome of experimentally induced inclusion body hepatitis (IBH) by fowl aviadenoviruses (FAdVs) is crucially influenced by the genetic background of the host, Vet. Res., 47, 69, 10.1186/s13567-016-0350-0 Matos, 2016, Selected clinical chemistry analytes correlate with the pathogenesis of inclusion body hepatitis experimentally induced by fowl aviadenoviruses, Avian Pathol., 45, 520, 10.1080/03079457.2016.1168513 Meng, 2018, Co-infection of fowl adenovirus with different immunosuppressive viruses in a chicken flock, Poult. Sci., 97, 1699, 10.3382/ps/pex414 McMurray, 2012, Eur. Heart J., 33, 1787, 10.1093/eurheartj/ehs104 Mittal, 2014, Characterization of fowl adenoviruses associated with hydropericardium syndrome and inclusion body hepatitis in broiler chickens, Virus Dis., 25, 114, 10.1007/s13337-013-0183-7 Morshed, 2017, Fowl Adenoviruses D and E Cause Inclusion Body Hepatitis Outbreaks in Broiler and Broiler Breeder Pullet Flocks, Avian Dis., 61, 205, 10.1637/11551-120516-Reg.1 Muruve, 2004, The innate immune response to adenovirus vectors, Hum. Gene Ther., 15, 1157, 10.1089/hum.2004.15.1157 Muruve, 2008, The inflammasome recognizes cytosolic microbial and host DNA and triggers an innate immune response, Nature, 452, 103, 10.1038/nature06664 Niu, 2017, Pathogenicity and immunosuppressive potential of fowl adenovirus in specific pathogen free chickens, Poult. Sci., 96, 3885, 10.3382/ps/pex206 Niu, 2016, Hydropericardium syndrome outbreak caused by fowl adenovirus serotype 4 in China in 2015, J. Gen. Virol., 97, 2684, 10.1099/jgv.0.000567 Nociari, 2007, Sensing infection by adenovirus: Toll-like receptor-independent viral DNA recognition signals activation of the interferon regulatory factor 3 master regulator, J. Virol., 81, 4145, 10.1128/JVI.02685-06 Ojkic, 2008, Genotyping of Canadian isolates of fowl adenoviruses, Avian Pathol., 37, 95, 10.1080/03079450701805324 Ookawara, 2014, Method for approximating colloid osmotic pressure in long-term hemodialysis patients, Ther. Apher. Dial., 18, 202, 10.1111/1744-9987.12070 Pan, 2017, Characterization of a hypervirulent fowl adenovirus 4 with the novel genotype newly prevalent in China and establishment of reproduction infection model of hydropericardium syndrome in chickens, Poult. Sci., 96, 1581, 10.3382/ps/pew431 Piek, 2016, The fibrosis-cell death axis in heart failure, Heart Fail. Rev., 21, 199, 10.1007/s10741-016-9536-9 Rathinam, 2012, Regulation of inflammasome signaling, Nat. Immunol., 13, 333, 10.1038/ni.2237 Ruan, 2018, Analysis of pathogenicity and immune efficacy of fowl adenovirus serotype 4 isolates, Poult. Sci., 97, 2647, 10.3382/ps/pey113 Rubartelli, 2012, Redox control of NLRP3 inflammasome activation in health and disease, J. Leukoc. Biol., 92, 951, 10.1189/jlb.0512265 Sandanger, 2013, The NLRP3 inflammasome is up-regulated in cardiac fibroblasts and mediates myocardial ischaemia-reperfusion injury, Cardiovasc. Res., 99, 164, 10.1093/cvr/cvt091 Schachner, 2014, Recombinant FAdV-4 fiber-2 protein protects chickens against hepatitis-hydropericardium syndrome (HHS), Vaccine, 32, 1086, 10.1016/j.vaccine.2013.12.056 Shah, 2017, Fowl adenovirus: history, emergence, biology and development of a vaccine against hydropericardium syndrome, Arch. Virol., 162, 1833, 10.1007/s00705-017-3313-5 Steen, 2004, The heart in systemic sclerosis, Curr. Rheumatol. Rep., 6, 137, 10.1007/s11926-004-0058-4 Tao, 2015, Cardiomyocyte-fibroblast interaction contributes to diabetic cardiomyopathy in mice: Role of HMGB1/TLR4/IL-33 axis, Biochim. Biophys. Acta., 1852, 2075, 10.1016/j.bbadis.2015.07.015 Tibbles, 2002, Activation of p38 and ERK signaling during adenovirus vector cell entry lead to expression of the C-X-C chemokine IP-10, J. Virol., 76, 1559, 10.1128/JVI.76.4.1559-1568.2002 Ulland, 2015, Evasion of inflammasome activation by microbial pathogens, J. Clin. Invest., 125, 469, 10.1172/JCI75254 Wang, 2017, Ghrelin protects the heart against ischemia/reperfusion injury via inhibition of tlr4/nlrp3 inflammasome pathway, Life Sci., 186, 50, 10.1016/j.lfs.2017.08.004 Wu, 2016, MiR-613 suppresses ischemia-reperfusion-induced cardiomyocyte apoptosis by targeting the programmed cell death 10 gene, BST, 10, 251, 10.5582/bst.2016.01122 Yancy, 2013, 2013 ACCF/AHA guideline for the management of heart failure: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines, J. Am. Coll. Cardiol., 16, e147, 10.1016/j.jacc.2013.05.019 Zhang, 2014, Cardiac fibroblasts contribute to myocardial dysfunction in mice with sepsis: the role of NLRP3 inflammasome activation, PLoS One, 9, e107639, 10.1371/journal.pone.0107639 Zhang, 2017, Carbon monoxide releasing molecule-3 improves myocardial function in mice with sepsis by inhibiting NLRP3 inflammasome activation in cardiac fibroblasts, Basic Res. Cardiol., 112, 16, 10.1007/s00395-017-0603-8 Zhu, 2007, Innate immune response to adenoviral vectors is mediated by both toll-like receptor-dependent and -independent pathways, J. Virol., 81, 3170, 10.1128/JVI.02192-06