In the current study, five novel avian β-defensins (AvBDs) were identified and characterized in tissues from Peking ducks (Anas platyrhynchos). The nucleotide sequences of these cDNAs comprised 198 bp, 182 bp, 201 bp, 204 bp, and 168 bp, and encoded 65, 60, 66, 67, and 55 amino acids, respectively. Homology, characterization and comparison of these genes with AvBD from other avian species confirmed that they were Apl_AvBD1, 3, 5, 6, and 16. Recombinant AvBDs were produced and purified by expressing these genes in Escherichia coli. In addition, peptides were synthesized according to the respective AvBD sequences. Investigation of the antibacterial activity of the Apl_AvBDs showed that all of them exhibited antibacterial activity against all 12 bacteria investigated (P<0.05 or P<0.01). In addition, the antibacterial activity of all of the AvBDs against M. tetragenus and P. multocida decreased significantly in the presence of 150 mM NaCl (P<0.01). None of the AvBDs showed hemolytic activity. Consistent with their broad-spectrum antibacterial activity, the five novel Apl_AvBDs inhibited replication of duck hepatitis virus (DHV) in vitro significantly (P<0.05). The mRNA expression of all five Apl_AvBD in most tissues, including immune organs and the liver, was upregulated in response to DHV infection at different time points. These findings provide evidence that these defensins activate the immune response to combat microbial infection.
References
[1]
Rodrigue DC, Tauxe RV, Rowe B (1990) International increase in Salmonella enteritidis: a new pandemic? Epidemiol Infect 105: 21–27.
[2]
White DG, Zhao S, Sudler R, Ayers S, Fredman S, et al. (2001) The isolation of antibiotic-resistant salmonella from retail groud meats. N Engl J Med 345: 1147–1154.
[3]
Zasloff M (2002) Antimicrobial peptides of multicellular organisms. Nature 415: 389–395.
[4]
Brogden KA, Ackermann M, McCray Jr PB, Tack BF (2003) Antimicrobial peptides in animals and their role in host defences. Int J Antimicrob Agents 22: 465–478.
[5]
Ganz T (2005) Defensins and other antimicrobial peptides: a historical perspective and an update. Comb Chem High Throughput Screening 8: 209–217.
[6]
Lynn DJ, Higgs R, Gaines S, Tierney J, James T, et al. (2004) Bioinformatic discovery and initial characterisation of nine novel antimicrobial peptide genes in the chicken. Immunogenetics 56: 170–177.
[7]
Lynn DJ, Higgs R, Lloyd AT, O’Farrell y C, Hervé-Grépinet V, et al. (2007) Avian beta-defensin nomenclature: a community proposed update. Immunol Lett 110: 86–89.
[8]
Ma DY, Liu SW, Han ZX, Li YJ, Shan AS (2008) Expression and characterization of recombinant gallinacin-9 and gallinacin-8 in Escherichia coli. Protein Expr Puri. 58: 284–291.
[9]
Ma DY, Liao WY, Wang RQ, Han ZX, Liu SW (2009) Two novel duck antibacterial peptides, avian beta-defensins 9 and 10, with antimicrobial activity. J Microbiol Biotechnol 19: 1447–1455.
[10]
Ma DY, Wang RQ, Liao WY, Han ZX, Liu SW (2009) Identification and characterization of a novel antibacterial peptide, avian beta-defensin 2 from ducks. J Microbiol 47: 610–618.
[11]
Wang RQ, Ma DY, Lin LJ, Zhou CY, Han ZX, et al. (2010) Identification and characterization of an avian β-defensin orthologue, avian β-defensin 9, from quails. Appl Microbiol Biotechnol 87: 1395–1405.
[12]
Ma DY, Lin LJ, Zhang KX, Han ZX, Shao YH, et al. (2011) Three novel Anas platyrhynchos avian β-defensins, upregulated by duck hepatitis virus, with antibacterial and antiviral activities. Molecular Immunology 49: 84–96.
[13]
Ma DY, Lin LJ, Zhang KX, Han ZX, Shao YH, et al. (2012) Discovery and characterization of Coturnix chinensis avian β-defensin 10, with broad antibacterial activity. Journal of peptide science 18: 224–232.
[14]
Ma DY, Zhou CY, Zhang MY, Han ZX, Shao YH, et al. (2012) Functional analysis and induction of four novel goose (Anser cygnoides) avian β-defensins in response to salmonella enteritidis infection. Comp Immunol Microbiol Infect Dis 35: 197–207.
[15]
van Dijk A, Veldhuizen EJ, Haagsman HP (2008) Avian defensins. Vet Immunol Immunopathol 124: 1–18.
[16]
Olsen B, Munster VJ, Wallensten A, Waldenstrom J, Osterhaus AD, et al. (2006) Global patterns of influenza A virus in wild birds. Science 312: 384–388.
[17]
Sch?gger H, von Jagow G (1987) Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa. Anal Biochem 166: 368–379.
[18]
Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72: 248–254.
[19]
Available: http://www.oie.int/eng/publicat/en standards.htm.Accessed 2004 Jun 3.
[20]
Shin SY, Park EJ, Yang ST, Jung HJ, Eom SH, et al. (2001) Structure-activity analysis of SMAP-29, a sheep leukocytes-derived antimicrobial peptide. Biochem Biophys Res Commun 285: 1046–1051.
[21]
Xiao YJ, Cai Y, Bommineni YR, Fernando SC, Prakash O, et al. (2006) Identification and functional characterization of three chicken cathelicidins with potent antimicrobial activity. J Biol Chem 281: 2858–2867.
[22]
Yu K, Park K, Kang SW, Shin SY, Hahm KS, et al. (2002) Solution structure of a cathelicidin-derived antimicrobial peptide, CRAMP as determined by NMR spectroscopy. J Pept Res 60: 1–9.
[23]
Sadeyen JR, Trotereau J, Protais J, Beaumont C, Sellier N, et al. (2006) Salmonella carrier-state in hens: study of host resistance by a gene expression approach. Microbes Infect 8: 1308–1314.
[24]
SAS (1996) Institute. SAS User’s Guide: Statistics, SAS Institute Inc. Cary, NC.
[25]
Lehrer RI, Ganz T (2002) Defensins of vertebrate animals. Curr. Opin. Immunol 14: 96–102.
[26]
Chan DI, Prenner EJ, Vogel HJ (2006) Tryptophan- and arginine-rich antimicrobial peptides: Structures and mechnisms of action. Biochemica Biophysica Acta - Biomembranes 1758: 1184–1202.
[27]
Powers JS, Hancock REW (2003) The relationship between peptide structure and antibacterial activity. Peptides 24: 1681–1691.
[28]
Harwig SSL, Swiderek KM, Kokryakov VN, Tan L, Lee TD, et al. (1994) Gallinacins: cysteine-rich antimicrobial peptides of chicken leukocytes. FEBS Lett 342: 281–285.
[29]
Sugiarto H, Yu PL (2006) Identification of three novel ostricacins: an update on the phylogenetic perspective of β-defensins. Int J Antimicrob Agents 27: 229–235.
[30]
Veldhuizen EJ, Rijnders M, Claassen EA, van Dijk A, Haagsman HP (2008) Porcine beta-defensin 2 displays broad antimicrobial activity against pathogenic intestinal bacteria. Mol Immunol 45: 386–394.
[31]
Ryan LK, Dai JJ, Yin ZW, Megjugorac N, Uhlhorn V, et al. (2011) Modulation of human β-defensin-1 (hBD-1) in plasmacytoid dendritic cells (PDC), monocytes, and epithelial cells by influenza virus, Herpes simplex virus, and Sendai virus and its possible role in innate immunity. Journal of Leukocyte Biology. 90: 343–356.
[32]
Bastian A, Sch?fer H (2001) Human α-defensin 1 (HNP-1) inhibits adenoviral infection in vitro. Regul Pept 101: 157–161.
[33]
Virella-Lowell I, Poirier A, Chesnut KA, Brantly M, Flotte TR (2000) Inhibition of recombinant adeno-associated virus (rAAV) transduction by bronchial secretions from cystic fibrosis patients. Gene Therapy 7: 1783–1789.
Grubor B, Gallup JM, Meyerholz DK, Crouch EC, Evans RB, et al. (2004) Enhanced surfactant protein and defensin mRNA levels and reduced viral replication during parainfluenza virus type 3 pneumonia in neonatal lambs. Clin Vaccine Immunol 11: 599–607.
[36]
Chong KT, Thangavel RR, Tang X (2008) Enhanced expression of murine β-defensins (MBD-1, -2,- 3, and -4) in upper and lower airway mucosa of influenza virus infected mice. Virology 380: 136–143.
[37]
Duits LA, Nibbering PH, van Strijen E, Vos JB, Mannesse-Lazeroms SPG, et al. (2003) Rhinovirus increases human β-defensin-2 and -3 mRNA expression in cultured bronchial epithelial cells. FEMS Immunol Med Microbiol 38: 59–64.
[38]
Proud D, Sanders SP, Wiehler S (2004) Human rhinovirus infection induces airway epithelial cell production of human β-defensin 2 both in vitro and in vivo. J Immunol 172: 4637–4645.
[39]
Chong KT, Xiang L, Wang X, Jun EL, Xi LF, et al. (2006) High level expression of human epithelial β-defensins (hBD-1, 2 and 3) in papillomavirus induced lesions. Virol J 3: 75.