全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Ixodes scapularis Tick Saliva Proteins Sequentially Secreted Every 24 h during Blood Feeding

DOI: 10.1371/journal.pntd.0004323

Full-Text   Cite this paper   Add to My Lib

Abstract:

Ixodes scapularis is the most medically important tick species and transmits five of the 14 reportable human tick borne disease (TBD) agents in the USA. This study describes LC-MS/MS identification of 582 tick- and 83 rabbit proteins in saliva of I. scapularis ticks that fed for 24, 48, 72, 96, and 120 h, as well as engorged but not detached (BD), and spontaneously detached (SD). The 582 tick proteins include proteases (5.7%), protease inhibitors (7.4%), unknown function proteins (22%), immunity/antimicrobial (2.6%), lipocalin (3.1%), heme/iron binding (2.6%), extracellular matrix/ cell adhesion (2.2%), oxidant metabolism/ detoxification (6%), transporter/ receptor related (3.2%), cytoskeletal (5.5%), and housekeeping-like (39.7%). Notable observations include: (i) tick saliva proteins of unknown function accounting for >33% of total protein content, (ii) 79% of proteases are metalloproteases, (iii) 13% (76/582) of proteins in this study were found in saliva of other tick species and, (iv) ticks apparently selectively inject functionally similar but unique proteins every 24 h, which we speculate is the tick's antigenic variation equivalent strategy to protect important tick feeding functions from host immune system. The host immune responses to proteins present in 24 h I. scapularis saliva will not be effective at later feeding stages. Rabbit proteins identified in our study suggest the tick's strategic use of host proteins to modulate the feeding site. Notably fibrinogen, which is central to blood clotting and wound healing, was detected in high abundance in BD and SD saliva, when the tick is preparing to terminate feeding and detach from the host. A remarkable tick adaptation is that the feeding lesion is completely healed when the tick detaches from the host. Does the tick concentrate fibrinogen at the feeding site to aide in promoting healing of the feeding lesion? Overall, these data provide broad insight into molecular mechanisms regulating different tick feeding phases. These data set the foundation for in depth I. scapularis tick feeding physiology and TBD transmission studies.

References

[1]  Sonenshine DE, Roe RM. (2014) Biology of ticks volume 1. Oxford, United Kingdom: Oxford University Press. 370 p.
[2]  Jongejan F, Uilenberg G. (1994) Ticks and control methods. Rev Sci Tech 13(4): 1201–1226. pmid:7711310
[3]  Grisi L, Leite RC, Martins JR, Barros AT, Andreotti R, et al. (2014) Reassessment of the potential economic impact of cattle parasites in Brazil. Rev Bras Parasitol Vet 23(2): 150–156. S1984-29612014000200150 [pii]. pmid:25054492 doi: 10.1590/s1984-29612014042
[4]  Jongejan F, Uilenberg G. (2004) The global importance of ticks. Parasitology 129 Suppl: S3–14. pmid:15938502 doi: 10.1017/s0031182004005967
[5]  Dantas-Torres F, Chomel BB, Otranto D. (2012) Ticks and tick-borne diseases: A one health perspective. Trends Parasitol 28(10): 437–446. doi: 10.1016/j.pt.2012.07.003. pmid:22902521
[6]  Burgdorfer W, Barbour AG, Hayes SF, Benach JL, Grunwaldt E, et al. (1982) Lyme disease-a tick-borne spirochetosis? Science 216(4552): 1317–1319. pmid:7043737 doi: 10.1126/science.7043737
[7]  Levin ML, Ross DE. (2004) Acquisition of different isolates of Anaplasma phagocytophilum by Ixodes scapularis from a model animal. Vector Borne Zoonotic Dis 4(1): 53–59. pmid:15018773 doi: 10.1089/153036604773082997
[8]  Crowder CD, Carolan HE, Rounds MA, Honig V, Mothes B, et al. (2014) Prevalence of Borrelia miyamotoi in Ixodes ticks in Europe and the United States. Emerg Infect Dis 20(10): 1678–1682. doi: 10.3201/eid2010.131583. pmid:25280366
[9]  Prusinski MA, Kokas JE, Hukey KT, Kogut SJ, Lee J, et al. (2014) Prevalence of Borrelia burgdorferi (spirochaetales: Spirochaetaceae), anaplasma phagocytophilum (Rickettsiales: Anaplasmataceae), and Babesia microti (Piroplasmida: Babesiidae) in Ixodes scapularis (Acari: Ixodidae) collected from recreational lands in the hudson valley region, new york state. J Med Entomol 51(1): 226–236. pmid:24605473 doi: 10.1603/me13101
[10]  Dupuis AP 2nd, Peters RJ, Prusinski MA, Falco RC, Ostfeld RS, et al. (2013) Isolation of deer tick virus (Powassan virus, lineage II) from Ixodes scapularis and detection of antibody in vertebrate hosts sampled in the Hudson Valley, New York state. Parasit Vectors 6: 185-3305-6-185. doi: 10.1186/1756-3305-6-185
[11]  Rizzoli A, Rosa R, Mantelli B, Pecchioli E, Hauffe H, et al. (2004) Ixodes ricinus, transmitted diseases and reservoirs. Parassitologia 46(1–2): 119–122. pmid:15305699
[12]  Fraser CM, Casjens S, Huang WM, Sutton GG, Clayton R, et al. (1997) Genomic sequence of a lyme disease spirochaete, Borrelia burgdorferi. Nature 390(6660): 580–586. pmid:9403685
[13]  Hill CA, Kafatos FC, Stansfield SK, Collins FH. (2005) Arthropod-borne diseases: Vector control in the genomics era. Nat Rev Microbiol 3(3): 262–268. nrmicro1101 [pii]. pmid:15703759 doi: 10.1038/nrmicro1101
[14]  Hoen AG, Rollend LG, Papero MA, Carroll JF, Daniels TJ, et al. (2009) Effects of tick control by acaricide self-treatment of white-tailed deer on host-seeking tick infection prevalence and entomologic risk for Ixodes scapularis-borne pathogens. Vector Borne Zoonotic Dis 9(4): 431–438. doi: 10.1089/vbz.2008.0155. pmid:19650738
[15]  Piesman J, Eisen L. (2008) Prevention of tick-borne diseases. Annu Rev Entomol 53: 323–343. pmid:17877457 doi: 10.1146/annurev.ento.53.103106.093429
[16]  Willadsen P. (2006) Vaccination against ectoparasites. Parasitology 133 Suppl: S9–S25. pmid:17274852 doi: 10.1017/s0031182006001788
[17]  George JE, Pound JM, Davey RB. (2004) Chemical control of ticks on cattle and the resistance of these parasites to acaricides. Parasitology 129 Suppl: S353–66. pmid:15938518 doi: 10.1017/s0031182003004682
[18]  Mulenga A, Sugino M, Nakajim M, Sugimoto C, Onuma M. (2001) Tick-encoded serine proteinase inhibitors (serpins); potential target antigens for tick vaccine development. J Vet Med Sci 63(10): 1063–1069. pmid:11714020 doi: 10.1292/jvms.63.1063
[19]  Ribeiro JM. (1987) Role of saliva in blood-feeding by arthropods. Annu Rev Entomol 32: 463–478. pmid:2880553 doi: 10.1146/annurev.en.32.010187.002335
[20]  Ribeiro JM. (1995) Blood-feeding arthropods: Live syringes or invertebrate pharmacologists? Infect Agents Dis 4(3): 143–152. pmid:8548192
[21]  Richter D, Matuschka FR, Spielman A, Mahadevan L. (2013) How ticks get under your skin: Insertion mechanics of the feeding apparatus of Ixodes ricinus ticks. Proc Biol Sci 280(1773): 20131758. doi: 10.1098/rspb.2013.1758. pmid:24174106
[22]  Ribeiro JM, Makoul GT, Levine J, Robinson DR, Spielman A. (1985) Antihemostatic, antiinflammatory, and immunosuppressive properties of the saliva of a tick, Ixodes dammini. J Exp Med 161(2): 332–344. pmid:2982989 doi: 10.1084/jem.161.2.332
[23]  Francischetti IM, Sa-Nunes A, Mans BJ, Santos IM, Ribeiro JM. (2009) The role of saliva in tick feeding. Front Biosci (Landmark Ed) 14: 2051–2088. 3363 [pii]. doi: 10.2741/3363
[24]  Oliveira CJ, Sa-Nunes A, Francischetti IM, Carregaro V, Anatriello E, et al. (2011) Deconstructing tick saliva: Non-protein molecules with potent immunomodulatory properties. J Biol Chem 286(13): 10960–10969. doi: 10.1074/jbc.M110.205047. pmid:21270122
[25]  Nuttall PA, Labuda M. (2004) Tick-host interactions: Saliva-activated transmission. Parasitology 129 Suppl: S177–89. pmid:15938511 doi: 10.1017/s0031182004005633
[26]  Bell JF, Stewart SJ, Wikel SK. (1979) Resistance to tick-borne Francisella tularensis by tick-sensitized rabbits: Allergic klendusity. Am J Trop Med Hyg 28(5): 876–880. pmid:484770
[27]  Jones LD, Nuttall PA. (1990) The effect of host resistance to tick infestation on the transmission of Thogoto virus by ticks. J Gen Virol 71 (Pt 5)(Pt 5): 1039–1043. pmid:2345364 doi: 10.1099/0022-1317-71-5-1039
[28]  Nazario S, Das S, de Silva AM, Deponte K, Marcantonio N, et al. (1998) Prevention of Borrelia burgdorferi transmission in guinea pigs by tick immunity. Am J Trop Med Hyg 58(6): 780–785. pmid:9660463
[29]  Burke G, Wikel SK, Spielman A, Telford SR, McKay K, et al. (2005) Hypersensitivity to ticks and Lyme disease risk. Emerg Infect Dis 11(1): 36–41. pmid:15705320
[30]  Francischetti IM, My Pham V, Mans BJ, Andersen JF, Mather TN, et al. (2005) The transcriptome of the salivary glands of the female western black-legged tick Ixodes pacificus (Acari: Ixodidae). Insect Biochem Mol Biol 35(10): 1142–1161. S0965-1748(05)00123-2 [pii]. pmid:16102420 doi: 10.1016/j.ibmb.2005.05.007
[31]  Francischetti IM, Mans BJ, Meng Z, Gudderra N, Veenstra TD, et al. (2008) An insight into the sialome of the soft tick, Ornithodorus parkeri. Insect Biochem Mol Biol 38(1): 1–21. S0965-1748(07)00224-X [pii]. pmid:18070662 doi: 10.1016/j.ibmb.2007.09.009
[32]  Francischetti IM, Meng Z, Mans BJ, Gudderra N, Hall M, et al. (2008) An insight into the salivary transcriptome and proteome of the soft tick and vector of epizootic bovine abortion, Ornithodoros coriaceus. J Proteomics 71(5): 493–512. doi: 10.1016/j.jprot.2008.07.006. pmid:18725333
[33]  Francischetti IM, Anderson JM, Manoukis N, Pham VM, Ribeiro JM. (2011) An insight into the sialotranscriptome and proteome of the coarse bontlegged tick, Hyalomma marginatum rufipes. J Proteomics 74(12): 2892–2908. doi: 10.1016/j.jprot.2011.07.015. pmid:21851864
[34]  Karim S, Singh P, Ribeiro JM. (2011) A deep insight into the sialotranscriptome of the gulf coast tick, Amblyomma maculatum. PLoS One 6(12): e28525. doi: 10.1371/journal.pone.0028525. pmid:22216098
[35]  Karim S, Ribeiro JM. (2015) An insight into the sialome of the lone star tick, Amblyomma americanum, with a glimpse on its time dependent gene expression. PLoS One 10(7): e0131292. doi: 10.1371/journal.pone.0131292. pmid:26131772
[36]  Kotsyfakis M, Schwarz A, Erhart J, Ribeiro JM. (2015) Tissue- and time-dependent transcription in Ixodes ricinus salivary glands and midguts when blood feeding on the vertebrate host. Sci Rep 5: 9103. doi: 10.1038/srep09103. pmid:25765539
[37]  Ribeiro JM, Anderson JM, Manoukis NC, Meng Z, Francischetti IM. (2011) A further insight into the sialome of the tropical bont tick, Amblyomma variegatum. BMC Genomics 12: 136-2164-12-136. doi: 10.1186/1471-2164-12-136
[38]  Ribeiro JM, Labruna MB, Mans BJ, Maruyama SR, Francischetti IM, et al. (2012) The sialotranscriptome of Antricola delacruzi female ticks is compatible with non-hematophagous behavior and an alternative source of food. Insect Biochem Mol Biol 42(5): 332–342. doi: 10.1016/j.ibmb.2012.01.003. pmid:22306723
[39]  Schwarz A, von Reumont BM, Erhart J, Chagas AC, Ribeiro JM, et al. (2013) De novo Ixodes ricinus salivary gland transcriptome analysis using two next-generation sequencing methodologies. FASEB J 27(12): 4745–4756. doi: 10.1096/fj.13-232140. pmid:23964076
[40]  Radulovic ZM, Kim TK, Porter LM, Sze SH, Lewis L, et al. (2014) A 24–48 h fed Amblyomma americanum tick saliva immuno-proteome. BMC Genomics 15: 518-2164-15-518. doi: 10.1186/1471-2164-15-518
[41]  Lewis LA, Radulovic ZM, Kim TK, Porter LM, Mulenga A. (2015) Identification of 24h Ixodes scapularis immunogenic tick saliva proteins. Ticks Tick Borne Dis 6(3): 424–434. doi: 10.1016/j.ttbdis.2015.03.012. pmid:25825233
[42]  Mulenga A, Kim TK, Ibelli AM. (2013) Deorphanization and target validation of cross-tick species conserved novel Amblyomma americanum tick saliva protein. Int J Parasitol 43(6): 439–451. doi: 10.1016/j.ijpara.2012.12.012. pmid:23428900
[43]  Ibelli AM, Kim TK, Hill CC, Lewis LA, Bakshi M, et al. (2014) A blood meal-induced Ixodes scapularis tick saliva serpin inhibits trypsin and thrombin, and interferes with platelet aggregation and blood clotting. Int J Parasitol 44(6): 369–379. doi: 10.1016/j.ijpara.2014.01.010. pmid:24583183
[44]  Chalaire KC, Kim TK, Garcia-Rodriguez H, Mulenga A. (2011) Amblyomma americanum (L.) (Acari: Ixodidae) tick salivary gland serine protease inhibitor (serpin) 6 is secreted into tick saliva during tick feeding. J Exp Biol 214(Pt 4): 665–673. doi: 10.1242/jeb.052076. pmid:21270316
[45]  Horn F, dos Santos PC, Termignoni C. (2000) Boophilus microplus anticoagulant protein: An antithrombin inhibitor isolated from the cattle tick saliva. Arch Biochem Biophys 384(1): 68–73. S0003986100920769 [pii]. pmid:11147837 doi: 10.1006/abbi.2000.2076
[46]  Pichu S, Ribeiro JM, Mather TN. (2009) Purification and characterization of a novel salivary antimicrobial peptide from the tick, Ixodes scapularis. Biochem Biophys Res Commun 390(3): 511–515. doi: 10.1016/j.bbrc.2009.09.127. pmid:19852941
[47]  Pichu S, Ribeiro JM, Mather TN, Francischetti IM. (2014) Purification of a serine protease and evidence for a protein C activator from the saliva of the tick, Ixodes scapularis. Toxicon 77: 32–39. doi: 10.1016/j.toxicon.2013.10.025. pmid:24184517
[48]  Valenzuela JG, Francischetti IM, Pham VM, Garfield MK, Mather TN, et al. (2002) Exploring the sialome of the tick Ixodes scapularis. J Exp Biol 205(Pt 18): 2843–2864. pmid:12177149
[49]  Oliveira CJ, Anatriello E, de Miranda-Santos IK, Francischetti IM, Sa-Nunes A, et al. (2013) Proteome of Rhipicephalus sanguineus tick saliva induced by the secretagogues pilocarpine and dopamine. Ticks Tick Borne Dis 4(6): 469–477. doi: 10.1016/j.ttbdis.2013.05.001. pmid:24029695
[50]  Tirloni L, Reck J, Terra RM, Martins JR, Mulenga A, et al. (2014) Proteomic analysis of cattle tick Rhipicephalus (Boophilus) microplus saliva: A comparison between partially and fully engorged females. PLoS One 9(4): e94831. doi: 10.1371/journal.pone.0094831. pmid:24762651
[51]  Mudenda L, Pierle SA, Turse JE, Scoles GA, Purvine SO, et al. (2014) Proteomics informed by transcriptomics identifies novel secreted proteins in Dermacentor andersoni saliva. Int J Parasitol 44(13): 1029–1037. doi: 10.1016/j.ijpara.2014.07.003. pmid:25110293
[52]  Tirloni L, Islam MS, Kim TK, Diedrich JK, Yates JR 3rd, et al. (2015) Saliva from nymph and adult females of Haemaphysalis longicornis: A proteomic study. Parasit Vectors 8(1): 338. doi: 10.1186/s13071-015-0918-y
[53]  Diaz-Martin V, Manzano-Roman R, Valero L, Oleaga A, Encinas-Grandes A, et al. (2013) An insight into the proteome of the saliva of the argasid tick Ornithodoros moubata reveals important differences in saliva protein composition between the sexes. J Proteomics 80: 216–235. doi: 10.1016/j.jprot.2013.01.015. pmid:23416086
[54]  Vizcaino JA, Deutsch EW, Wang R, Csordas A, Reisinger F, et al. (2014) ProteomeXchange provides globally coordinated proteomics data submission and dissemination. Nat Biotechnol 32(3): 223–226. doi: 10.1038/nbt.2839. pmid:24727771
[55]  McDonald WH, Tabb DL, Sadygov RG, MacCoss MJ, Venable J, et al. (2004) MS1, MS2, and SQT-three unified, compact, and easily parsed file formats for the storage of shotgun proteomic spectra and identifications. Rapid Commun Mass Spectrom 18(18): 2162–2168. pmid:15317041 doi: 10.1002/rcm.1603
[56]  Xu T, Park SK, Venable JD, Wohlschlegel JA, Diedrich JK, et al. (2015) ProLuCID: An improved SEQUEST-like algorithm with enhanced sensitivity and specificity. J Proteomics. S1874-3919(15)30059-2 [pii]. doi: 10.1016/j.jprot.2015.07.001
[57]  Carvalho PC, Yates Iii JR, Barbosa VC. (2010) Analyzing shotgun proteomic data with PatternLab for proteomics. Curr Protoc Bioinformatics Chapter 13: Unit 13.13.1–15. doi: 10.1002/0471250953.bi1313s30
[58]  Ashburner M, Ball CA, Blake JA, Botstein D, Butler H, et al. (2000) Gene ontology: Tool for the unification of biology. the gene ontology consortium. Nat Genet 25(1): 25–29. pmid:10802651 doi: 10.1038/75556
[59]  Rawlings ND, Barrett AJ, Bateman A. (2012) MEROPS: The database of proteolytic enzymes, their substrates and inhibitors. Nucleic Acids Res 40(Database issue): D343–50. doi: 10.1093/nar/gkr987. pmid:22086950
[60]  Marchler-Bauer A, Derbyshire MK, Gonzales NR, Lu S, Chitsaz F, et al. (2015) CDD: NCBI's conserved domain database. Nucleic Acids Res 43(Database issue): D222–6. doi: 10.1093/nar/gku1221. pmid:25414356
[61]  Tatusov RL, Fedorova ND, Jackson JD, Jacobs AR, Kiryutin B, et al. (2003) The COG database: An updated version includes eukaryotes. BMC Bioinformatics 4: 41. pmid:12969510
[62]  Bateman A, Birney E, Cerruti L, Durbin R, Etwiller L, et al. (2002) The pfam protein families database. Nucleic Acids Res 30(1): 276–280. pmid:11752314 doi: 10.1093/nar/30.1.276
[63]  Schultz J, Copley RR, Doerks T, Ponting CP, Bork P. (2000) SMART: A web-based tool for the study of genetically mobile domains. Nucleic Acids Res 28(1): 231–234. gkd062 [pii]. pmid:10592234 doi: 10.1093/nar/28.1.231
[64]  Florens L, Carozza MJ, Swanson SK, Fournier M, Coleman MK, et al. (2006) Analyzing chromatin remodeling complexes using shotgun proteomics and normalized spectral abundance factors. Methods 40(4): 303–311. S1046-2023(06)00207-6 [pii]. pmid:17101441 doi: 10.1016/j.ymeth.2006.07.028
[65]  Paoletti AC, Parmely TJ, Tomomori-Sato C, Sato S, Zhu D, et al. (2006) Quantitative proteomic analysis of distinct mammalian mediator complexes using normalized spectral abundance factors. Proc Natl Acad Sci U S A 103(50): 18928–18933. 0606379103 [pii]. pmid:17138671 doi: 10.1073/pnas.0606379103
[66]  Zhu W, Smith JW, Huang CM. (2010) Mass spectrometry-based label-free quantitative proteomics. J Biomed Biotechnol 2010: 840518. doi: 10.1155/2010/840518. pmid:19911078
[67]  Warnes GR, Bolker B, Bonebakker L, Gentleman R, Huber W, et al. (2013) Various R programming tools for plotting data. The comprehensive R archive network. .
[68]  Mulenga A, Erikson K. (2011) A snapshot of the Ixodes scapularis degradome. Gene 482(1–2): 78–93. doi: 10.1016/j.gene.2011.04.008. pmid:21596113
[69]  Francischetti IM, Mather TN, Ribeiro JM. (2003) Cloning of a salivary gland metalloprotease and characterization of gelatinase and fibrin(ogen)lytic activities in the saliva of the Lyme disease tick vector Ixodes scapularis. Biochem Biophys Res Commun 305(4): 869–875. S0006291X0300857X [pii]. pmid:12767911 doi: 10.1016/s0006-291x(03)00857-x
[70]  Decrem Y, Mariller M, Lahaye K, Blasioli V, Beaufays J, et al. (2008) The impact of gene knock-down and vaccination against salivary metalloproteases on blood feeding and egg laying by Ixodes ricinus. Int J Parasitol 38(5): 549–560. pmid:17959179 doi: 10.1016/j.ijpara.2007.09.003
[71]  Weldon CL, Mackessy SP. (2012) Alsophinase, a new P-III metalloproteinase with alpha-fibrinogenolytic and hemorrhagic activity from the venom of the rear-fanged puerto rican racer Alsophis portoricensis (Serpentes: Dipsadidae). Biochimie 94(5): 1189–1198. doi: 10.1016/j.biochi.2012.02.006. pmid:22349739
[72]  Zhang P, Shi J, Shen B, Li X, Gao Y, et al. (2009) Stejnihagin, a novel snake metalloproteinase from Trimeresurus stejnegeri venom, inhibited L-type Ca2+ channels. Toxicon 53(2): 309–315. doi: 10.1016/j.toxicon.2008.12.006. pmid:19114053
[73]  Fox JW, Serrano SM. (2005) Structural considerations of the snake venom metalloproteinases, key members of the M12 reprolysin family of metalloproteinases. Toxicon 45(8): 969–985. S0041-0101(05)00064-4 [pii]. pmid:15922769 doi: 10.1016/j.toxicon.2005.02.012
[74]  Mulenga A, Sugimoto C, Onuma M. (2000) Issues in tick vaccine development: Identification and characterization of potential candidate vaccine antigens. Microbes Infect 2(11): 1353–1361. pmid:11018452 doi: 10.1016/s1286-4579(00)01289-2
[75]  Mulenga A, Tsuda A, Sugimoto C, Onuma M. (2002) Blood meal acquisition by ticks; molecular advances and implications for vaccine development. Jpn J Vet Res 49(4): 261–272. pmid:11949474
[76]  Prevot PP, Couvreur B, Denis V, Brossard M, Vanhamme L, et al. (2007) Protective immunity against Ixodes ricinus induced by a salivary serpin. Vaccine 25(17): 3284–3292. S0264-410X(07)00012-6 [pii]. pmid:17270322 doi: 10.1016/j.vaccine.2007.01.008
[77]  Maritz-Olivier C, Stutzer C, Jongejan F, Neitz AW, Gaspar AR. (2007) Tick anti-hemostatics: Targets for future vaccines and therapeutics. Trends Parasitol 23(9): 397–407. S1471-4922(07)00173-0 [pii]. pmid:17656153 doi: 10.1016/j.pt.2007.07.005
[78]  Palenikova J, Lieskovska J, Langhansova H, Kotsyfakis M, Chmelar J, et al. (2015) Ixodes ricinus salivary serpin IRS-2 affects Th17 differentiation via inhibition of the interleukin-6/STAT-3 signaling pathway. Infect Immun 83(5): 1949–1956. doi: 10.1128/IAI.03065-14. pmid:25712932
[79]  Kovarova Z, Chmelar J, Sanda M, Brynda J, Mares M, et al. (2010) Crystallization and diffraction analysis of the serpin IRS-2 from the hard tick Ixodes ricinus. Acta Crystallogr Sect F Struct Biol Cryst Commun 66(Pt 11): 1453–1457. doi: 10.1107/S1744309110032343. pmid:21045293
[80]  Chmelar J, Oliveira CJ, Rezacova P, Francischetti IM, Kovarova Z, et al. (2011) A tick salivary protein targets cathepsin G and chymase and inhibits host inflammation and platelet aggregation. Blood 117(2): 736–744. doi: 10.1182/blood-2010-06-293241. pmid:20940421
[81]  Lieskovska J, Palenikova J, Sirmarova J, Elsterova J, Kotsyfakis M, et al. (2015) Tick salivary cystatin sialostatin L2 suppresses IFN responses in mouse dendritic cells. Parasite Immunol 37(2): 70–78. doi: 10.1111/pim.12162. pmid:25408129
[82]  Horka H, Staudt V, Klein M, Taube C, Reuter S, et al. (2012) The tick salivary protein sialostatin L inhibits the Th9-derived production of the asthma-promoting cytokine IL-9 and is effective in the prevention of experimental asthma. J Immunol 188(6): 2669–2676. doi: 10.4049/jimmunol.1100529. pmid:22327077
[83]  Sa-Nunes A, Bafica A, Antonelli LR, Choi EY, Francischetti IM, et al. (2009) The immunomodulatory action of sialostatin L on dendritic cells reveals its potential to interfere with autoimmunity. J Immunol 182(12): 7422–7429. doi: 10.4049/jimmunol.0900075. pmid:19494265
[84]  Kotsyfakis M, Karim S, Andersen JF, Mather TN, Ribeiro JM. (2007) Selective cysteine protease inhibition contributes to blood-feeding success of the tick Ixodes scapularis. J Biol Chem 282(40): 29256–29263. M703143200 [pii]. pmid:17698852 doi: 10.1074/jbc.m703143200
[85]  Kotsyfakis M, Sa-Nunes A, Francischetti IM, Mather TN, Andersen JF, et al. (2006) Antiinflammatory and immunosuppressive activity of sialostatin L, a salivary cystatin from the tick Ixodes scapularis. J Biol Chem 281(36): 26298–26307. M513010200 [pii]. pmid:16772304 doi: 10.1074/jbc.m513010200
[86]  Lieskovska J, Palenikova J, Langhansova H, Chagas AC, Calvo E, et al. (2015) Tick sialostatins L and L2 differentially influence dendritic cell responses to Borrelia spirochetes. Parasit Vectors 8: 275-015-0887-1. doi: 10.1186/s13071-015-0887-1
[87]  Flower DR. (1994) The lipocalin protein family: A role in cell regulation. FEBS Lett 354(1): 7–11. 0014-5793(94)01078-1 [pii]. pmid:7957904 doi: 10.1016/0014-5793(94)01078-1
[88]  Flower DR. (1996) The lipocalin protein family: Structure and function. Biochem J 318 (Pt 1)(Pt 1): 1–14. pmid:8761444 doi: 10.1042/bj3180001
[89]  Dartt DA. (2011) Tear lipocalin: Structure and function. Ocul Surf 9(3): 126–138. pmid:21791187 doi: 10.1016/s1542-0124(11)70022-2
[90]  Paesen GC, Adams PL, Harlos K, Nuttall PA, Stuart DI. (1999) Tick histamine-binding proteins: Isolation, cloning, and three-dimensional structure. Mol Cell 3(5): 661–671. S1097-2765(00)80359-7 [pii]. pmid:10360182 doi: 10.1016/s1097-2765(00)80359-7
[91]  Paesen GC, Adams PL, Nuttall PA, Stuart DL. (2000) Tick histamine-binding proteins: Lipocalins with a second binding cavity. Biochim Biophys Acta 1482(1–2): 92–101. S0167-4838(00)00168-0 [pii]. pmid:11058751 doi: 10.1016/s0167-4838(00)00168-0
[92]  Mans BJ. (2005) Tick histamine-binding proteins and related lipocalins: Potential as therapeutic agents. Curr Opin Investig Drugs 6(11): 1131–1135. pmid:16312134
[93]  Smathers RL, Petersen DR. (2011) The human fatty acid-binding protein family: Evolutionary divergences and functions. Hum Genomics 5(3): 170–191. 63W0473601481088 [pii]. pmid:21504868 doi: 10.1186/1479-7364-5-3-170
[94]  Ganfornina MD, Kayser H, Sanchez D. (2000) Lipocalins in arthropoda: Diversification and functional explorations. In: Madame Curie Bioscience Database [Internet] Austin (TX): Landes Bioscience.
[95]  Sangamnatdej S, Paesen GC, Slovak M, Nuttall PA. (2002) A high affinity serotonin- and histamine-binding lipocalin from tick saliva. Insect Mol Biol 11(1): 79–86. 311 [pii]. pmid:11841505 doi: 10.1046/j.0962-1075.2001.00311.x
[96]  Keller PM, Waxman L, Arnold BA, Schultz LD, Condra C, et al. (1993) Cloning of the cDNA and expression of moubatin, an inhibitor of platelet aggregation. J Biol Chem 268(8): 5450–5456. pmid:8449907
[97]  Beaufays J, Adam B, Decrem Y, Prevot PP, Santini S, et al. (2008) Ixodes ricinus tick lipocalins: Identification, cloning, phylogenetic analysis and biochemical characterization. PLoS One 3(12): e3941. doi: 10.1371/journal.pone.0003941. pmid:19096708
[98]  Wang J, Bian G, Pan W, Feng T, Dai J. (2015) Molecular characterization of a defensin gene from a hard tick, Dermacentor silvarum. Parasit Vectors 8: 25-014-0625-0. doi: 10.1186/s13071-014-0625-0
[99]  Tonk M, Cabezas-Cruz A, Valdes JJ, Rego RO, Chrudimska T, et al. (2014) Defensins from the tick Ixodes scapularis are effective against phytopathogenic fungi and the human bacterial pathogen Listeria grayi. Parasit Vectors 7: 554-014-0554-y. doi: 10.1186/preaccept-8265353130225079
[100]  Tonk M, Cabezas-Cruz A, Valdes JJ, Rego RO, Rudenko N, et al. (2014) Identification and partial characterisation of new members of the Ixodes ricinus defensin family. Gene 540(2): 146–152. doi: 10.1016/j.gene.2014.03.002. pmid:24607035
[101]  Zheng H, Zhou L, Yang X, Wang D, Liu J. (2012) Cloning and characterization of a male-specific defensin-like antimicrobial peptide from the tick Haemaphysalis longicornis. Dev Comp Immunol 37(1): 207–211. doi: 10.1016/j.dci.2011.10.004. pmid:22033149
[102]  Chrudimska T, Slaninova J, Rudenko N, Ruzek D, Grubhoffer L. (2011) Functional characterization of two defensin isoforms of the hard tick Ixodes ricinus. Parasit Vectors 4: 63-3305-4-63. doi: 10.1186/1756-3305-4-63
[103]  Lu X, Che Q, Lv Y, Wang M, Lu Z, et al. (2010) A novel defensin-like peptide from salivary glands of the hard tick, Haemaphysalis longicornis. Protein Sci 19(3): 392–397. doi: 10.1002/pro.317. pmid:20027626
[104]  Saito Y, Konnai S, Yamada S, Imamura S, Nishikado H, et al. (2009) Identification and characterization of antimicrobial peptide, defensin, in the taiga tick, Ixodes persulcatus. Insect Mol Biol 18(4): 531–539. doi: 10.1111/j.1365-2583.2009.00897.x. pmid:19604312
[105]  Sonenshine DE, Ceraul SM, Hynes WE, Macaluso KR, Azad AF. (2002) Expression of defensin-like peptides in tick hemolymph and midgut in response to challenge with Borrelia burgdorferi, Escherichia coli and Bacillus subtilis. Exp Appl Acarol 28(1–4): 127–134. pmid:14570122 doi: 10.1023/a:1025354326877
[106]  Nakajima Y, van der Goes van Naters-Yasui A, Taylor D, Yamakawa M. (2002) Antibacterial peptide defensin is involved in midgut immunity of the soft tick, Ornithodoros moubata. Insect Mol Biol 11(6): 611–618. 372 [pii]. pmid:12421419 doi: 10.1046/j.1365-2583.2002.00372.x
[107]  Fogaca AC, Lorenzini DM, Kaku LM, Esteves E, Bulet P, et al. (2004) Cysteine-rich antimicrobial peptides of the cattle tick Boophilus microplus: Isolation, structural characterization and tissue expression profile. Dev Comp Immunol 28(3): 191–200. S0145305X03001514 [pii]. pmid:14642886 doi: 10.1016/j.dci.2003.08.001
[108]  Esteves E, Fogaca AC, Maldonado R, Silva FD, Manso PP, et al. (2009) Antimicrobial activity in the tick Rhipicephalus (Boophilus) microplus eggs: Cellular localization and temporal expression of microplusin during oogenesis and embryogenesis. Dev Comp Immunol 33(8): 913–919. doi: 10.1016/j.dci.2009.02.009. pmid:19454333
[109]  Silva FD, Rezende CA, Rossi DC, Esteves E, Dyszy FH, et al. (2009) Structure and mode of action of microplusin, a copper II-chelating antimicrobial peptide from the cattle tick Rhipicephalus (Boophilus) microplus. J Biol Chem 284(50): 34735–34746. doi: 10.1074/jbc.M109.016410. pmid:19828445
[110]  Lai R, Takeuchi H, Lomas LO, Jonczy J, Rigden DJ, et al. (2004) A new type of antimicrobial protein with multiple histidines from the hard tick, Amblyomma hebraeum. FASEB J 18(12): 1447–1449. pmid:15247144 doi: 10.1096/fj.03-1154fje
[111]  Silva FD, Rossi DC, Martinez LR, Frases S, Fonseca FL, et al. (2011) Effects of microplusin, a copper-chelating antimicrobial peptide, against Cryptococcus neoformans. FEMS Microbiol Lett 324(1): 64–72. doi: 10.1111/j.1574-6968.2011.02386.x. pmid:22092765
[112]  Kaufman WR. (2007) Gluttony and sex in female Ixodid ticks: How do they compare to other blood-sucking arthropods? J Insect Physiol 53(3): 264–273. S0022-1910(06)00171-5 [pii]. pmid:17113595 doi: 10.1016/j.jinsphys.2006.10.004
[113]  Ponka P. (1997) Tissue-specific regulation of iron metabolism and heme synthesis: Distinct control mechanisms in erythroid cells. Blood 89(1): 1–25. pmid:8978272
[114]  Ponka P. (1999) Cellular iron metabolism. Kidney Int Suppl 69: S2–11. pmid:10084280 doi: 10.1046/j.1523-1755.1999.055suppl.69002.x
[115]  Toh SQ, Glanfield A, Gobert GN, Jones MK. (2010) Heme and blood-feeding parasites: Friends or foes? Parasit Vectors 3: 108-3305-3-108. doi: 10.1186/1756-3305-3-108
[116]  Citelli M, Lara FA, da Silva Vaz I Jr, Oliveira PL. (2007) Oxidative stress impairs heme detoxification in the midgut of the cattle tick, Rhipicephalus (Boophilus) microplus. Mol Biochem Parasitol 151(1): 81–88. S0166-6851(06)00309-4 [pii]. pmid:17123644 doi: 10.1016/j.molbiopara.2006.10.008
[117]  Graca-Souza AV, Maya-Monteiro C, Paiva-Silva GO, Braz GR, Paes MC, et al. (2006) Adaptations against heme toxicity in blood-feeding arthropods. Insect Biochem Mol Biol 36(4): 322–335. S0965-1748(06)00012-9 [pii]. pmid:16551546
[118]  Lara FA, Lins U, Paiva-Silva G, Almeida IC, Braga CM, et al. (2003) A new intracellular pathway of haem detoxification in the midgut of the cattle tick Boophilus microplus: Aggregation inside a specialized organelle, the hemosome. J Exp Biol 206(Pt 10): 1707–1715. pmid:12682102 doi: 10.1242/jeb.00334
[119]  Galay RL, Umemiya-Shirafuji R, Mochizuki M, Fujisaki K, Tanaka T. (2015) Iron metabolism in hard ticks (Acari: Ixodidae): The antidote to their toxic diet. Parasitol Int 64(2): 182–189. doi: 10.1016/j.parint.2014.12.005. pmid:25527065
[120]  Maya-Monteiro CM, Daffre S, Logullo C, Lara FA, Alves EW, et al. (2000) HeLp, a heme lipoprotein from the hemolymph of the cattle tick, Boophilus microplus. J Biol Chem 275(47): 36584–36589. pmid:10964932 doi: 10.1074/jbc.m007344200
[121]  Maya-Monteiro CM, Alves LR, Pinhal N, Abdalla DS, Oliveira PL. (2004) HeLp, a heme-transporting lipoprotein with an antioxidant role. Insect Biochem Mol Biol 34(1): 81–88. pmid:14976984 doi: 10.1016/j.ibmb.2003.09.005
[122]  Gudderra NP, Neese PA, Sonenshine DE, Apperson CS, Roe RM. (2001) Developmental profile, isolation, and biochemical characterization of a novel lipoglycoheme-carrier protein from the american dog tick, Dermacentor variabilis (Acari: Ixodidae) and observations on a similar protein in the soft tick, Ornithodoros parkeri (Acari: Argasidae). Insect Biochem Mol Biol 31(4–5): 299–311. S0965174800001223 [pii]. pmid:11222939 doi: 10.1016/s0965-1748(00)00122-3
[123]  Graca-Souza AV, Arruda MA, de Freitas MS, Barja-Fidalgo C, Oliveira PL. (2002) Neutrophil activation by heme: Implications for inflammatory processes. Blood 99(11): 4160–4165. pmid:12010821 doi: 10.1182/blood.v99.11.4160
[124]  Dutra FF, Bozza MT. (2014) Heme on innate immunity and inflammation. Front Pharmacol 5: 115. doi: 10.3389/fphar.2014.00115. pmid:24904418
[125]  Cornelis P. (2010) Iron uptake and metabolism in pseudomonads. Appl Microbiol Biotechnol 86(6): 1637–1645. doi: 10.1007/s00253-010-2550-2. pmid:20352420
[126]  Cornelis P, Wei Q, Andrews SC, Vinckx T. (2011) Iron homeostasis and management of oxidative stress response in bacteria. Metallomics 3(6): 540–549. doi: 10.1039/c1mt00022e. pmid:21566833
[127]  Dumas Z, Ross-Gillespie A, Kummerli R. (2013) Switching between apparently redundant iron-uptake mechanisms benefits bacteria in changeable environments. Proc Biol Sci 280(1764): 20131055. doi: 10.1098/rspb.2013.1055. pmid:23760867
[128]  Ballouche M, Cornelis P, Baysse C. (2009) Iron metabolism: A promising target for antibacterial strategies. Recent Pat Antiinfect Drug Discov 4(3): 190–205. Abstract 02 for E.Pub [pii]. pmid:19594436 doi: 10.2174/157489109789318514
[129]  Posey JE, Gherardini FC. (2000) Lack of a role for iron in the Lyme disease pathogen. Science 288(5471): 1651–1653. 8561 [pii]. pmid:10834845 doi: 10.1126/science.288.5471.1651
[130]  Rojkind M, Dominguez-Rosales JA, Nieto N, Greenwel P. (2002) Role of hydrogen peroxide and oxidative stress in healing responses. Cell Mol Life Sci 59(11): 1872–1891. pmid:12530519 doi: 10.1007/pl00012511
[131]  Narasimhan S, Sukumaran B, Bozdogan U, Thomas V, Liang X, et al. (2007) A tick antioxidant facilitates the Lyme disease agent's successful migration from the mammalian host to the arthropod vector. Cell Host Microbe 2(1): 7–18. S1931-3128(07)00127-8 [pii]. pmid:18005713 doi: 10.1016/j.chom.2007.06.001
[132]  Das S, Banerjee G, DePonte K, Marcantonio N, Kantor FS, et al. (2001) Salp25D, an Ixodes scapularis antioxidant, is 1 of 14 immunodominant antigens in engorged tick salivary glands. J Infect Dis 184(8): 1056–1064. JID010466 [pii]. pmid:11574922 doi: 10.1086/323351
[133]  Rudenko N, Golovchenko M, Edwards MJ, Grubhoffer L. (2005) Differential expression of Ixodes ricinus tick genes induced by blood feeding or Borrelia burgdorferi infection. J Med Entomol 42(1): 36–41. pmid:15691006 doi: 10.1093/jmedent/42.1.36
[134]  Mulenga A, Khumthong R, Blandon MA. (2007) Molecular and expression analysis of a family of the Amblyomma americanum tick lospins. J Exp Biol 210(Pt 18): 3188–3198. doi: 10.1242/jeb.006494. pmid:17766296
[135]  Xu XL, Cheng TY, Yang H, Yan F, Yang Y. (2015) De novo sequencing, assembly and analysis of salivary gland transcriptome of Haemaphysalis flava and identification of sialoprotein genes. Infect Genet Evol 32: 135–142. doi: 10.1016/j.meegid.2015.03.010. pmid:25784566
[136]  Ribeiro JM, Alarcon-Chaidez F, Francischetti IM, Mans BJ, Mather TN, et al. (2006) An annotated catalog of salivary gland transcripts from Ixodes scapularis ticks. Insect Biochem Mol Biol 36(2): 111–129. doi: 10.1016/j.ibmb.2005.11.005. pmid:16431279
[137]  Chmelar J, Anderson JM, Mu J, Jochim RC, Valenzuela JG, et al. (2008) Insight into the sialome of the castor bean tick, Ixodes ricinus. BMC Genomics 9: 233-2164-9-233. doi: 10.1186/1471-2164-9-233
[138]  Schwarz A, Tenzer S, Hackenberg M, Erhart J, Gerhold-Ay A, et al. (2014) A systems level analysis reveals transcriptomic and proteomic complexity in Ixodes ricinus midgut and salivary glands during early attachment and feeding. Mol Cell Proteomics 13(10): 2725–2735. doi: 10.1074/mcp.M114.039289. pmid:25048707
[139]  Kemp DH, Stone BF, Binnington KC. (1982) Tick attachment and feeding: Role of the mouthparts, feeding apparatus, salivary gland secretions and the host response. In: Obenchain F, Galun R, editors. Physiology of Ticks. Oxford, UK: Pergamon Press Ltd. pp. 138–139.
[140]  Sauer JR, McSwain JL, Bowman AS, Essenberg RC. (1995) Tick salivary gland physiology. Annu Rev Entomol 40: 245–267. doi: 10.1146/annurev.en.40.010195.001333. pmid:7810988
[141]  Mulenga A, Khumthong R. (2010) Silencing of three Amblyomma americanum (L.) insulin-like growth factor binding protein-related proteins prevents ticks from feeding to repletion. J Exp Biol 213(Pt 7): 1153–1161. doi: 10.1242/jeb.035204. pmid:20228352
[142]  Heemskerk JW, Bevers EM, Lindhout T. (2002) Platelet activation and blood coagulation. Thromb Haemost 88(2): 186–193. pmid:12195687
[143]  Moriarty R, McManus CA, Lambert M, Tilley T, Devocelle M, et al. (2015) A novel role for the fibrinogen asn-gly-arg (NGR) motif in platelet function. Thromb Haemost 113(2): 290–304. doi: 10.1160/TH14-04-0366. pmid:25413489
[144]  Merzendorfer H, Zimoch L. (2003) Chitin metabolism in insects: Structure, function and regulation of chitin synthases and chitinases. J Exp Biol 206(Pt 24): 4393–4412. pmid:14610026 doi: 10.1242/jeb.00709
[145]  Arakane Y, Muthukrishnan S. (2010) Insect chitinase and chitinase-like proteins. Cell Mol Life Sci 67(2): 201–216. doi: 10.1007/s00018-009-0161-9. pmid:19816755
[146]  Kim TK, Curran J, Mulenga A. (2014) Dual silencing of long and short Amblyomma americanum acidic chitinase forms weakens the tick cement cone stability. J Exp Biol 217(Pt 19): 3493–3503. doi: 10.1242/jeb.107979. pmid:25189365
[147]  Freitas DR, Rosa RM, Moura DJ, Seitz AL, Colodel EM, et al. (2007) Cell death during preoviposition period in Boophilus microplus tick. Vet Parasitol 144(3–4): 321–327. S0304-4017(06)00612-1 [pii]. pmid:17157985 doi: 10.1016/j.vetpar.2006.10.017
[148]  Doillon CJ, Hembry RM, Ehrlich HP, Burke JF. (1987) Actin filaments in normal dermis and during wound healing. Am J Pathol 126(1): 164–170. pmid:3544851
[149]  Martin P, Lewis J. (1992) Actin cables and epidermal movement in embryonic wound healing. Nature 360(6400): 179–183. pmid:1436096 doi: 10.1038/360179a0
[150]  Cowin AJ. (2006) Role of the actin cytoskeleton in wound healing and scar formation. Primary Intention 14(1): 39–42.
[151]  Strudwick XL, Cowin AJ. (2012) Cytoskeletal regulation of dermal regeneration. Cells 1(4): 1313–1327. doi: 10.3390/cells1041313. pmid:24710556
[152]  Rockey DC, Weymouth N, Shi Z. (2013) Smooth muscle alpha actin (Acta2) and myofibroblast function during hepatic wound healing. PLoS One 8(10): e77166. doi: 10.1371/journal.pone.0077166. pmid:24204762
[153]  Brock AR, Wang Y, Berger S, Renkawitz-Pohl R, Han VC, et al. (2012) Transcriptional regulation of profilin during wound closure in Drosophila larvae. J Cell Sci 125(Pt 23): 5667–5676. doi: 10.1242/jcs.107490. pmid:22976306
[154]  Ho S, Marcal H, Foster LJ. (2014) Towards scarless wound healing: A comparison of protein expression between human, adult and foetal fibroblasts. Biomed Res Int 2014: 676493. doi: 10.1155/2014/676493. pmid:24605334
[155]  Daimon E, Shibukawa Y, Wada Y. (2013) Calponin 3 regulates stress fiber formation in dermal fibroblasts during wound healing. Arch Dermatol Res 305(7): 571–584. doi: 10.1007/s00403-013-1343-8. pmid:23545751
[156]  Appel S, Allen PG, Vetterkind S, Jin JP, Morgan KG. (2010) H3/acidic calponin: An actin-binding protein that controls extracellular signal-regulated kinase 1/2 activity in nonmuscle cells. Mol Biol Cell 21(8): 1409–1422. doi: 10.1091/mbc.E09-06-0451. pmid:20181831
[157]  Bement WM, Forscher P, Mooseker MS. (1993) A novel cytoskeletal structure involved in purse string wound closure and cell polarity maintenance. J Cell Biol 121(3): 565–578. pmid:8486737 doi: 10.1083/jcb.121.3.565
[158]  Bond JE, Ho TQ, Selim MA, Hunter CL, Bowers EV, et al. (2011) Temporal spatial expression and function of non-muscle myosin II isoforms IIA and IIB in scar remodeling. Lab Invest 91(4): 499–508. doi: 10.1038/labinvest.2010.181. pmid:21102503
[159]  Kim S, Kwon J. (2015) Thymosin beta4 has a major role in dermal burn wound healing that involves actin cytoskeletal remodelling via heat-shock protein 70. J Tissue Eng Regen Med. doi: 10.1002/term.2028
[160]  Lees JG, Ching YW, Adams DH, Bach CT, Samuel MS, et al. (2013) Tropomyosin regulates cell migration during skin wound healing. J Invest Dermatol 133(5): 1330–1339. doi: 10.1038/jid.2012.489. pmid:23303457
[161]  Tossi A, Scocchi M, Skerlavaj B, Gennaro R. (1994) Identification and characterization of a primary antibacterial domain in CAP18, a lipopolysaccharide binding protein from rabbit leukocytes. FEBS Lett 339(1–2): 108–112. 0014-5793(94)80395-1 [pii]. pmid:8313956 doi: 10.1016/0014-5793(94)80395-1
[162]  Larrick JW, Hirata M, Balint RF, Lee J, Zhong J, et al. (1995) Human CAP18: A novel antimicrobial lipopolysaccharide-binding protein. Infect Immun 63(4): 1291–1297. pmid:7890387 doi: 10.1097/00024382-199703001-00022
[163]  Miethke M, Skerra A. (2010) Neutrophil gelatinase-associated lipocalin expresses antimicrobial activity by interfering with L-norepinephrine-mediated bacterial iron acquisition. Antimicrob Agents Chemother 54(4): 1580–1589. doi: 10.1128/AAC.01158-09. pmid:20086155
[164]  Nasioudis D, Witkin SS. (2015) Neutrophil gelatinase-associated lipocalin and innate immune responses to bacterial infections. Med Microbiol Immunol. doi: 10.1007/s00430-015-0394-1
[165]  Levy O. (2000) Antimicrobial proteins and peptides of blood: Templates for novel antimicrobial agents. Blood 96(8): 2664–2672. pmid:11023496
[166]  Brinkmann V, Reichard U, Goosmann C, Fauler B, Uhlemann Y, et al. (2004) Neutrophil extracellular traps kill bacteria. Science 303(5663): 1532–1535. pmid:15001782 doi: 10.1126/science.1092385
[167]  Borregaard N, Sorensen OE, Theilgaard-Monch K. (2007) Neutrophil granules: A library of innate immunity proteins. Trends Immunol 28(8): 340–345. S1471-4906(07)00156-1 [pii]. pmid:17627888 doi: 10.1016/j.it.2007.06.002
[168]  Santamaria-Kisiel L, Rintala-Dempsey AC, Shaw GS. (2006) Calcium-dependent and -independent interactions of the S100 protein family. Biochem J 396(2): 201–214. BJ20060195 [pii]. pmid:16683912 doi: 10.1042/bj20060195
[169]  Laible NJ, Germaine GR. (1985) Bactericidal activity of human lysozyme, muramidase-inactive lysozyme, and cationic polypeptides against Streptococcus sanguis and Streptococcus faecalis: Inhibition by chitin oligosaccharides. Infect Immun 48(3): 720–728. pmid:3922894
[170]  Ibrahim HR, Matsuzaki T, Aoki T. (2001) Genetic evidence that antibacterial activity of lysozyme is independent of its catalytic function. FEBS Lett 506(1): 27–32. S0014-5793(01)02872-1 [pii]. pmid:11591365 doi: 10.1016/s0014-5793(01)02872-1
[171]  Du R, Ho B, Ding JL. (2010) Rapid reprogramming of haemoglobin structure-function exposes multiple dual-antimicrobial potencies. EMBO J 29(3): 632–642. doi: 10.1038/emboj.2009.380. pmid:20019665
[172]  Lee SK, Ding JL. (2013) A perspective on the role of extracellular hemoglobin on the innate immune system. DNA Cell Biol 32(2): 36–40. doi: 10.1089/dna.2012.1897. pmid:23249270
[173]  Fogaca AC, da Silva PI Jr, Miranda MT, Bianchi AG, Miranda A, et al. (1999) Antimicrobial activity of a bovine hemoglobin fragment in the tick Boophilus microplus. J Biol Chem 274(36): 25330–25334. pmid:10464258 doi: 10.1074/jbc.274.36.25330
[174]  Belmonte R, Cruz CE, Pires JR, Daffre S. (2012) Purification and characterization of hb 98–114: A novel hemoglobin-derived antimicrobial peptide from the midgut of Rhipicephalus (Boophilus) microplus. Peptides 37(1): 120–127. doi: 10.1016/j.peptides.2012.05.017. pmid:22749988
[175]  Nakajima Y, Ogihara K, Taylor D, Yamakawa M. (2003) Antibacterial hemoglobin fragments from the midgut of the soft tick, Ornithodoros moubata (Acari: Argasidae). J Med Entomol 40(1): 78–81. pmid:12597657 doi: 10.1603/0022-2585-40.1.78
[176]  Sforca ML, Machado A, Figueredo RC, Oyama S Jr, Silva FD, et al. (2005) The micelle-bound structure of an antimicrobial peptide derived from the alpha-chain of bovine hemoglobin isolated from the tick Boophilus microplus. Biochemistry 44(17): 6440–6451. pmid:15850378 doi: 10.1021/bi0475323
[177]  Dobryszycka W. (1997) Biological functions of haptoglobin—new pieces to an old puzzle. Eur J Clin Chem Clin Biochem 35(9): 647–654. pmid:9352226
[178]  Nathan C, Xie QW, Halbwachs-Mecarelli L, Jin WW. (1993) Albumin inhibits neutrophil spreading and hydrogen peroxide release by blocking the shedding of CD43 (sialophorin, leukosialin). J Cell Biol 122(1): 243–256. pmid:8391001 doi: 10.1083/jcb.122.1.243
[179]  Schreiber A, Xiao H, Jennette JC, Schneider W, Luft FC, et al. (2009) C5a receptor mediates neutrophil activation and ANCA-induced glomerulonephritis. J Am Soc Nephrol 20(2): 289–298. doi: 10.1681/ASN.2008050497. pmid:19073822
[180]  Collins HL. (2008) Withholding iron as a cellular defence mechanism—friend or foe? Eur J Immunol 38(7): 1803–1806. doi: 10.1002/eji.200838505. pmid:18546145
[181]  Skaar EP. (2010) The battle for iron between bacterial pathogens and their vertebrate hosts. PLoS Pathog 6(8): e1000949. doi: 10.1371/journal.ppat.1000949. pmid:20711357
[182]  Ganz T. (2009) Iron in innate immunity: Starve the invaders. Curr Opin Immunol 21(1): 63–67. doi: 10.1016/j.coi.2009.01.011. pmid:19231148
[183]  Cassat JE, Skaar EP. (2013) Iron in infection and immunity. Cell Host Microbe 13(5): 509–519. doi: 10.1016/j.chom.2013.04.010. pmid:23684303
[184]  Davie EW, Fujikawa K, Kisiel W. (1991) The coagulation cascade: Initiation, maintenance, and regulation. Biochemistry 30(43): 10363–10370. pmid:1931959 doi: 10.1021/bi00107a001
[185]  Mosesson MW. (2005) Fibrinogen and fibrin structure and functions. J Thromb Haemost 3(8): 1894–1904. JTH1365 [pii]. pmid:16102057 doi: 10.1111/j.1538-7836.2005.01365.x
[186]  Fuchs E, Cleveland DW. (1998) A structural scaffolding of intermediate filaments in health and disease. Science 279(5350): 514–519. pmid:9438837 doi: 10.1126/science.279.5350.514
[187]  Kim S, Coulombe PA. (2007) Intermediate filament scaffolds fulfill mechanical, organizational, and signaling functions in the cytoplasm. Genes Dev 21(13): 1581–1597. 21/13/1581 [pii]. pmid:17606637 doi: 10.1101/gad.1552107
[188]  Schweizer J, Bowden PE, Coulombe PA, Langbein L, Lane EB, et al. (2006) New consensus nomenclature for mammalian keratins. J Cell Biol 174(2): 169–174. jcb.200603161 [pii]. pmid:16831889 doi: 10.1083/jcb.200603161
[189]  Moll R, Divo M, Langbein L. (2008) The human keratins: Biology and pathology. Histochem Cell Biol 129(6): 705–733. doi: 10.1007/s00418-008-0435-6. pmid:18461349
[190]  Katavolos P, Armstrong PM, Dawson JE, Telford SR 3rd. (1998) Duration of tick attachment required for transmission of granulocytic Ehrlichiosis. J Infect Dis 177(5): 1422–1425. pmid:9593039 doi: 10.1086/517829
[191]  des Vignes F, Piesman J, Heffernan R, Schulze TL, Stafford KC 3rd, et al. (2001) Effect of tick removal on transmission of Borrelia burgdorferi and ehrlichia phagocytophila by Ixodes scapularis nymphs. J Infect Dis 183(5): 773–778. JID000708 [pii]. pmid:11181154 doi: 10.1086/318818
[192]  Ebel GD, Kramer LD. (2004) Short report: Duration of tick attachment required for transmission of Powassan virus by deer ticks. Am J Trop Med Hyg 71(3): 268–271. pmid:15381804
[193]  Konnai S, Yamada S, Imamura S, Simuunza M, Chembensof M, et al. (2007) Attachment duration required for Rhipicephalus appendiculatus to transmit Theileria parva to the host. Vector Borne Zoonotic Dis 7(2): 241–248. pmid:17627444 doi: 10.1089/vbz.2006.0616
[194]  Gern L. (2009) Life cycle of Borrelia burgdorferi sensu lato and transmission to humans. Curr Probl Dermatol 37: 18–30. doi: 10.1159/000213068. pmid:19367095
[195]  Turner MJ. (1984) Antigenic variation in parasites. Parasitology 88 (Pt 4)(Pt 4): 613–621. pmid:6387595 doi: 10.1017/s0031182000085528
[196]  Barry JD, McCulloch R. (2001) Antigenic variation in trypanosomes: Enhanced phenotypic variation in a eukaryotic parasite. Adv Parasitol 49: 1–70. pmid:11461029 doi: 10.1016/s0065-308x(01)49037-3
[197]  Horn D. (2014) Antigenic variation in African trypanosomes. Mol Biochem Parasitol 195(2): 123–129. doi: 10.1016/j.molbiopara.2014.05.001. pmid:24859277
[198]  Becker M, Felsberger A, Frenzel A, Shattuck WM, Dyer M, et al. (2015) Application of M13 phage display for identifying immunogenic proteins from tick (Ixodes scapularis) saliva. BMC Biotechnol 15: 43-015-0167-3. doi: 10.1186/s12896-015-0167-3
[199]  Kim TK, Ibelli AM, Mulenga A. (2015) Amblyomma americanum tick calreticulin binds C1q but does not inhibit activation of the classical complement cascade. Ticks Tick Borne Dis 6(1): 91–101. S1877-959X(14)00194-0 [pii]. pmid:25454607 doi: 10.1016/j.ttbdis.2014.10.002
[200]  Schuijt TJ, Narasimhan S, Daffre S, DePonte K, Hovius JW, et al. (2011) Identification and characterization of Ixodes scapularis antigens that elicit tick immunity using yeast surface display. PLoS One 6(1): e15926. doi: 10.1371/journal.pone.0015926. pmid:21246036
[201]  Sanders ML, Glass GE, Nadelman RB, Wormser GP, Scott AL, et al. (1999) Antibody levels to recombinant tick calreticulin increase in humans after exposure to Ixodes scapularis (say) and are correlated with tick engorgement indices. Am J Epidemiol 149(8): 777–784. pmid:10206628 doi: 10.1093/oxfordjournals.aje.a009887
[202]  Buresova V, Hajdusek O, Franta Z, Sojka D, Kopacek P. (2009) IrAM-an alpha2-macroglobulin from the hard tick Ixodes ricinus: Characterization and function in phagocytosis of a potential pathogen Chryseobacterium indologenes. Dev Comp Immunol 33(4): 489–498. doi: 10.1016/j.dci.2008.09.011. pmid:18948134
[203]  Radulovic ZM, Porter LM, Kim TK, Bakshi M, Mulenga A. (2015) Amblyomma americanum tick saliva insulin-like growth factor binding protein-related protein 1 binds insulin but not insulin-like growth factors. Insect Mol Biol 24(5): 539–550. doi: 10.1111/imb.12180. pmid:26108887
[204]  Narasimhan S, Koski RA, Beaulieu B, Anderson JF, Ramamoorthi N, et al. (2002) A novel family of anticoagulants from the saliva of Ixodes scapularis. Insect Mol Biol 11(6): 641–650. 375 [pii]. pmid:12421422 doi: 10.1046/j.1365-2583.2002.00375.x

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133