#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

Iron Acquisition in : The Roles of IlsA and Bacillibactin in Exogenous Ferritin Iron Mobilization


In host-pathogen interactions, the struggle for iron may have major consequences on the outcome of the disease. To overcome the low solubility and bio-availability of iron, bacteria have evolved multiple systems to acquire iron from various sources such as heme, hemoglobin and ferritin. The molecular basis of iron acquisition from heme and hemoglobin have been extensively studied; however, very little is known about iron acquisition from host ferritin, a 24-mer nanocage protein able to store thousands of iron atoms within its cavity. In the human opportunistic pathogen Bacillus cereus, a surface protein named IlsA (Iron-regulated leucine rich surface protein type A) binds heme, hemoglobin and ferritin in vitro and is involved in virulence. Here, we demonstrate that IlsA acts as a ferritin receptor causing ferritin aggregation on the bacterial surface. Isothermal titration calorimetry data indicate that IlsA binds several types of ferritins through direct interaction with the shell subunits. UV-vis kinetic data show a significant enhancement of iron release from ferritin in the presence of IlsA indicating for the first time that a bacterial protein might alter the stability of the ferritin iron core. Disruption of the siderophore bacillibactin production drastically reduces the ability of B. cereus to utilize ferritin for growth and results in attenuated bacterial virulence in insects. We propose a new model of iron acquisition in B. cereus that involves the binding of IlsA to host ferritin followed by siderophore assisted iron uptake. Our results highlight a possible interplay between a surface protein and a siderophore and provide new insights into host adaptation of B. cereus and general bacterial pathogenesis.


Vyšlo v časopise: Iron Acquisition in : The Roles of IlsA and Bacillibactin in Exogenous Ferritin Iron Mobilization. PLoS Pathog 10(2): e32767. doi:10.1371/journal.ppat.1003935
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.ppat.1003935

Souhrn

In host-pathogen interactions, the struggle for iron may have major consequences on the outcome of the disease. To overcome the low solubility and bio-availability of iron, bacteria have evolved multiple systems to acquire iron from various sources such as heme, hemoglobin and ferritin. The molecular basis of iron acquisition from heme and hemoglobin have been extensively studied; however, very little is known about iron acquisition from host ferritin, a 24-mer nanocage protein able to store thousands of iron atoms within its cavity. In the human opportunistic pathogen Bacillus cereus, a surface protein named IlsA (Iron-regulated leucine rich surface protein type A) binds heme, hemoglobin and ferritin in vitro and is involved in virulence. Here, we demonstrate that IlsA acts as a ferritin receptor causing ferritin aggregation on the bacterial surface. Isothermal titration calorimetry data indicate that IlsA binds several types of ferritins through direct interaction with the shell subunits. UV-vis kinetic data show a significant enhancement of iron release from ferritin in the presence of IlsA indicating for the first time that a bacterial protein might alter the stability of the ferritin iron core. Disruption of the siderophore bacillibactin production drastically reduces the ability of B. cereus to utilize ferritin for growth and results in attenuated bacterial virulence in insects. We propose a new model of iron acquisition in B. cereus that involves the binding of IlsA to host ferritin followed by siderophore assisted iron uptake. Our results highlight a possible interplay between a surface protein and a siderophore and provide new insights into host adaptation of B. cereus and general bacterial pathogenesis.


Zdroje

1. PierreJL, FontecaveM (1999) Iron and activated oxygen species in biology: the basic chemistry. Biometals 12: 195–199.

2. SchaibleUE, KaufmannSH (2004) Iron and microbial infection. Nat Rev Microbiol 2: 946–953.

3. MiethkeM, MarahielMA (2007) Siderophore-based iron acquisition and pathogen control. Microbiol Mol Biol Rev 71: 413–451.

4. OngST, HoJZ, HoB, DingJL (2006) Iron-withholding strategy in innate immunity. Immunobiology 211: 295–314.

5. SkaarEP (2010) The battle for iron between bacterial pathogens and their vertebrate hosts. PLoS Pathog 6: e1000949.

6. BullenJJ, RogersHJ, SpaldingPB, WardCG (2005) Iron and infection: the heart of the matter. FEMS Immunol Med Microbiol 43: 325–330.

7. RatledgeC, DoverLG (2000) Iron metabolism in pathogenic bacteria. Annu Rev Microbiol 54: 881–941.

8. LitwinCM, CalderwoodSB (1993) Role of iron in regulation of virulence genes. Clin Microbiol Rev 6: 137–149.

9. ChuBC, Garcia-HerreroA, JohansonTH, KrewulakKD, LauCK, et al. (2010) Siderophore uptake in bacteria and the battle for iron with the host; a bird's eye view. Biometals 23: 601–611.

10. WandersmanC, DelepelaireP (2012) Haemophore functions revisited. Mol Microbiol 85: 618–631.

11. MazmanianSK, SkaarEP, GasparAH, HumayunM, GornickiP, et al. (2003) Passage of heme-iron across the envelope of Staphylococcus aureus. Science 299: 906–909.

12. NoblesCL, MaressoAW (2011) The theft of host heme by Gram-positive pathogenic bacteria. Metallomics 3: 788–796.

13. AlmeidaRS, BrunkeS, AlbrechtA, ThewesS, LaueM, et al. (2008) the hyphal-associated adhesin and invasin Als3 of Candida albicans mediates iron acquisition from host ferritin. PLoS Pathog 4: e1000217.

14. DaouN, BuissonC, GoharM, VidicJ, BierneH, et al. (2009) IlsA, a unique surface protein of Bacillus cereus required for iron acquisition from heme, hemoglobin and ferritin. PLoS Pathog 5: e1000675.

15. GobinJ, HorwitzMA (1996) Exochelins of Mycobacterium tuberculosis remove iron from human iron-binding proteins and donate iron to mycobactins in the M. tuberculosis cell wall. J Exp Med 183: 1527–1532.

16. JinB, NewtonSM, ShaoY, JiangX, CharbitA, et al. (2006) Iron acquisition systems for ferric hydroxamates, haemin and haemoglobin in Listeria monocytogenes. Mol Microbiol 59: 1185–1198.

17. LarsonJA, HowieHL, SoM (2004) Neisseria meningitidis accelerates ferritin degradation in host epithelial cells to yield an essential iron source. Mol Microbiol 53: 807–820.

18. SikkemaDJ, BrubakerRR (1989) Outer membrane peptides of Yersinia pestis mediating siderophore-independent assimilation of iron. Biol Met 2: 174–184.

19. WhitbyPW, VanwagonerTM, SpringerJM, MortonDJ, SealeTW, et al. (2006) Burkholderia cenocepacia utilizes ferritin as an iron source. J Med Microbiol 55: 661–668.

20. Bou-AbdallahF (2010) The iron redox and hydrolysis chemistry of the ferritins. Biochim Biophys Acta 1800: 719–731.

21. WattRK (2011) The many faces of the octahedral ferritin protein. Biometals 24: 489–500.

22. DeneerHG, HealeyV, BoychukI (1995) Reduction of exogenous ferric iron by a surface-associated ferric reductase of Listeria spp. Microbiology 141 (Pt 8) 1985–1992.

23. BottoneEJ (2010) Bacillus cereus, a volatile human pathogen. Clin Microbiol Rev 23: 382–398.

24. Vilas-BoasGT, PerucaAP, ArantesOM (2007) Biology and taxonomy of Bacillus cereus, Bacillus anthracis, and Bacillus thuringiensis. Can J Microbiol 53: 673–687.

25. RaymondB, JohnstonPR, Nielsen-LeRouxC, LereclusD, CrickmoreN (2010) Bacillus thuringiensis: an impotent pathogen? Trends Microbiol 18: 189–194.

26. FukushimaT, SiaAK, AllredBE, NichiporukR, ZhouZ, et al. (2012) Bacillus cereus iron uptake protein fishes out an unstable ferric citrate trimer. Proc Natl Acad Sci U S A 109: 16829–16834.

27. HarvieDR, EllarDJ (2005) A ferric dicitrate uptake system is required for the full virulence of Bacillus cereus. Curr Microbiol 50: 246–250.

28. ParkRY, ChoiMH, SunHY, ShinSH (2005) Production of catechol-siderophore and utilization of transferrin-bound iron in Bacillus cereus. Biol Pharm Bull 28: 1132–1135.

29. SatoN, IkedaS, MikamiT, MatsumotoT (1999) Bacillus cereus dissociates hemoglobin and uses released heme as an iron source. Biol Pharm Bull 22: 1118–1121.

30. SatoN, KurotakiH, IkedaS, DaioR, NishinomeN, et al. (1999) Lactoferrin inhibits Bacillus cereus growth and heme analogs recover its growth. Biol Pharm Bull 22: 197–199.

31. SatoN, KurotakiH, WatanabeT, MikamiT, MatsumotoT (1998) Use of hemoglobin as an iron source by Bacillus cereus. Biol Pharm Bull 21: 311–314.

32. SinevaE, ShadrinA, RodikovaEA, Andreeva-KovalevskayaZI, ProtsenkoAS, et al. (2012) Iron regulates expression of Bacillus cereus hemolysin II via global regulator Fur. J Bacteriol 194: 3327–3335.

33. FedhilaS, DaouN, LereclusD, Nielsen-LeRouxC (2006) Identification of Bacillus cereus internalin and other candidate virulence genes specifically induced during oral infection in insects. Mol Microbiol 62: 339–355.

34. Bou-AbdallahF, ArosioP, LeviS, Janus-ChandlerC, ChasteenND (2003) Defining metal ion inhibitor interactions with recombinant human H- and L-chain ferritins and site-directed variants: an isothermal titration calorimetry study. J Biol Inorg Chem 8: 489–497.

35. Bou-AbdallahF, ArosioP, SantambrogioP, YangX, Janus-ChandlerC, et al. (2002) Ferrous ion binding to recombinant human H-chain ferritin. An isothermal titration calorimetry study. Biochemistry 41: 11184–11191.

36. Bou-AbdallahF, McNallyJ, LiuXX, MelmanA (2011) Oxygen catalyzed mobilization of iron from ferritin by iron(III) chelate ligands. Chem Commun (Camb) 47: 731–733.

37. CrichtonRR, RomanF, RolandF (1980) Iron mobilization from ferritin by chelating agents. J Inorg Biochem 13: 305–316.

38. JohnsonJ, KenealeyJ, HiltonRJ, BrosnahanD, WattRK, et al. (2011) Non-reductive iron release from horse spleen ferritin using desferoxamine chelation. J Inorg Biochem 105: 202–207.

39. KoppischAT, DhunganaS, HillKK, BoukhalfaH, HeineHS, et al. (2008) Petrobactin is produced by both pathogenic and non-pathogenic isolates of the Bacillus cereus group of bacteria. Biometals 21: 581–589.

40. WilsonMK, AbergelRJ, RaymondKN, ArceneauxJE, ByersBR (2006) Siderophores of Bacillus anthracis, Bacillus cereus, and Bacillus thuringiensis. Biochem Biophys Res Commun 348: 320–325.

41. ArnowLE (1937) Proposed Chemical Mechanisms for the Production of Skin Erythema and Pigmentation by Radiant Energy. Science 86: 176.

42. TidmarshGF, KlebbaPE, RosenbergLT (1983) Rapid release of iron from ferritin by siderophores. J Inorg Biochem 18: 161–168.

43. ZawadzkaAM, AbergelRJ, NichiporukR, AndersenUN, RaymondKN (2009) Siderophore-mediated iron acquisition systems in Bacillus cereus: Identification of receptors for anthrax virulence-associated petrobactin. Biochemistry 48: 3645–3657.

44. CendrowskiS, MacArthurW, HannaP (2004) Bacillus anthracis requires siderophore biosynthesis for growth in macrophages and mouse virulence. Mol Microbiol 51: 407–417.

45. KoppischAT, BrowderCC, MoeAL, ShelleyJT, KinkelBA, et al. (2005) Petrobactin is the primary siderophore synthesized by Bacillus anthracis str. Sterne under conditions of iron starvation. Biometals 18: 577–585.

46. LeeJY, PassalacquaKD, HannaPC, ShermanDH (2011) Regulation of petrobactin and bacillibactin biosynthesis in Bacillus anthracis under iron and oxygen variation. PLoS One 6: e20777.

47. WilsonMK, AbergelRJ, ArceneauxJE, RaymondKN, ByersBR (2010) Temporal production of the two Bacillus anthracis siderophores, petrobactin and bacillibactin. Biometals 23: 129–134.

48. PhamDQ, WinzerlingJJ (2010) Insect ferritins: Typical or atypical? Biochim Biophys Acta 1800: 824–833.

49. KimBS, LeeCS, YunCY, YeoSM, ParkWM, et al. (2001) Characterization and immunological analysis of ferritin from the hemolymph of Galleria mellonella. Comp Biochem Physiol A Mol Integr Physiol 129: 501–509.

50. Yuk Ji-EunD-HS, Chi-WonCHOI, JikhyonHAN, Hye-KyoungCHOI, Jong-BaePARK, Seock-YeonHWANG2, Sang KyunKOH, Chi-YoungYUN (2005) Characterization of Tissue-Ferritin Purified from Wax Moth, Galleria mellonella. ENTOMOLOGICAL RESEARCH 35: 227–234.

51. RamaraoN, Nielsen-LerouxC, LereclusD (2012) The Insect Galleria mellonella as a Powerful Infection Model to Investigate Bacterial Pathogenesis. J Vis Exp (70) e4392.

52. ChenTT, LiL, ChungDH, AllenCD, TortiSV, et al. (2005) TIM-2 is expressed on B cells and in liver and kidney and is a receptor for H-ferritin endocytosis. J Exp Med 202: 955–965.

53. LiL, FangCJ, RyanJC, NiemiEC, LebronJA, et al. (2010) Binding and uptake of H-ferritin are mediated by human transferrin receptor-1. Proc Natl Acad Sci U S A 107: 3505–3510.

54. LiJY, ParagasN, NedRM, QiuA, ViltardM, et al. (2009) Scara5 is a ferritin receptor mediating non-transferrin iron delivery. Dev Cell 16: 35–46.

55. KobeB, KajavaAV (2001) The leucine-rich repeat as a protein recognition motif. Curr Opin Struct Biol 11: 725–732.

56. TaylorJM, HeinrichsDE (2002) Transferrin binding in Staphylococcus aureus: involvement of a cell wall-anchored protein. Mol Microbiol 43: 1603–1614.

57. BalderasMA, NoblesCL, HonsaES, AlickiER, MaressoAW (2012) Hal Is a Bacillus anthracis heme acquisition protein. J Bacteriol 194: 5513–5521.

58. CarlsonPEJr, CarrKA, JanesBK, AndersonEC, HannaPC (2009) Transcriptional profiling of Bacillus anthracis Sterne (34F2) during iron starvation. PLoS One 4: e6988.

59. FisherM, HuangYS, LiX, McIverKS, ToukokiC, et al. (2008) Shr is a broad-spectrum surface receptor that contributes to adherence and virulence in group A streptococcus. Infect Immun 76: 5006–5015.

60. OuattaraM, CunhaEB, LiX, HuangYS, DixonD, et al. (2010) Shr of group A streptococcus is a new type of composite NEAT protein involved in sequestering haem from methaemoglobin. Mol Microbiol 78: 739–756.

61. KernJW, SchneewindO (2008) BslA, a pXO1-encoded adhesin of Bacillus anthracis. Mol Microbiol 68: 504–515.

62. TarlovskyY, FabianM, SolomahaE, HonsaE, OlsonJS, et al. (2010) A Bacillus anthracis S-layer homology protein that binds heme and mediates heme delivery to IsdC. J Bacteriol 192: 3503–3511.

63. WattRK, HiltonRJ, GraffDM (2010) Oxido-reduction is not the only mechanism allowing ions to traverse the ferritin protein shell. Biochim Biophys Acta 1800: 745–759.

64. TheilEC, LiuXS, ToshaT (2008) Gated Pores in the Ferritin Protein Nanocage. Inorganica Chim Acta 361: 868–874.

65. JinW, TakagiH, PancorboB, TheilEC (2001) “Opening” the ferritin pore for iron release by mutation of conserved amino acids at interhelix and loop sites. Biochemistry 40: 7525–7532.

66. LiuX, JinW, TheilEC (2003) Opening protein pores with chaotropes enhances Fe reduction and chelation of Fe from the ferritin biomineral. Proc Natl Acad Sci U S A 100: 3653–3658.

67. LiuXS, PattersonLD, MillerMJ, TheilEC (2007) Peptides selected for the protein nanocage pores change the rate of iron recovery from the ferritin mineral. J Biol Chem 282: 31821–31825.

68. GalvezN, RuizB, CuestaR, ColacioE, Dominguez-VeraJM (2005) Release of iron from ferritin by aceto- and benzohydroxamic acids. Inorg Chem 44: 2706–2709.

69. SanchezP, GalvezN, ColacioE, MinonesE, Dominguez-VeraJM (2005) Catechol releases iron(III) from ferritin by direct chelation without iron(II) production. Dalton Trans 811–813.

70. DertzEA, XuJ, StintziA, RaymondKN (2006) Bacillibactin-mediated iron transport in Bacillus subtilis. J Am Chem Soc 128: 22–23.

71. AbergelRJ, ZawadzkaAM, RaymondKN (2008) Petrobactin-mediated iron transport in pathogenic bacteria: coordination chemistry of an unusual 3,4-catecholate/citrate siderophore. J Am Chem Soc 130: 2124–2125.

72. AbergelRJ, WilsonMK, ArceneauxJE, HoetteTM, StrongRK, et al. (2006) Anthrax pathogen evades the mammalian immune system through stealth siderophore production. Proc Natl Acad Sci U S A 103: 18499–18503.

73. GhigoJM, LetoffeS, WandersmanC (1997) A new type of hemophore-dependent heme acquisition system of Serratia marcescens reconstituted in Escherichia coli. J Bacteriol 179: 3572–3579.

74. DowerWJ, MillerJF, RagsdaleCW (1988) High efficiency transformation of E. coli by high voltage electroporation. Nucleic Acids Res 16: 6127–6145.

75. LereclusD, ArantesO, ChaufauxJ, LecadetM (1989) Transformation and expression of a cloned delta-endotoxin gene in Bacillus thuringiensis. FEMS Microbiol Lett 51: 211–217.

76. LeviS, LuzzagoA, CesareniG, CozziA, FranceschinelliF, et al. (1988) Mechanism of ferritin iron uptake: activity of the H-chain and deletion mapping of the ferro-oxidase site. A study of iron uptake and ferro-oxidase activity of human liver, recombinant H-chain ferritins, and of two H-chain deletion mutants. J Biol Chem 263: 18086–18092.

77. LeviS, SalfeldJ, FranceschinelliF, CozziA, DornerMH, et al. (1989) Expression and structural and functional properties of human ferritin L-chain from Escherichia coli. Biochemistry 28: 5179–5184.

78. ArnaudM, ChastanetA, DebarbouilleM (2004) New vector for efficient allelic replacement in naturally nontransformable, low-GC-content, gram-positive bacteria. Appl Environ Microbiol 70: 6887–6891.

79. LereclusD, ValladeM, ChaufauxJ, ArantesO, RambaudS (1992) Expansion of insecticidal host range of Bacillus thuringiensis by in vivo genetic recombination. Biotechnology (N Y) 10: 418–421.

80. ArantesO, LereclusD (1991) Construction of cloning vectors for Bacillus thuringiensis. Gene 108: 115–119.

81. SanchisV, AgaisseH, ChaufauxJ, LereclusD (1996) Construction of new insecticidal Bacillus thuringiensis recombinant strains by using the sporulation non-dependent expression system of cryIIIA and a site specific recombination vector. J Biotechnol 48: 81–96.

82. Guerout-FleuryAM, ShazandK, FrandsenN, StragierP (1995) Antibiotic-resistance cassettes for Bacillus subtilis. Gene 167: 335–336.

83. VillafaneR, BechhoferDH, NarayananCS, DubnauD (1987) Replication control genes of plasmid pE194. J Bacteriol 169: 4822–4829.

84. BouillautL, RamaraoN, BuissonC, GiloisN, GoharM, et al. (2005) FlhA influences Bacillus thuringiensis PlcR-regulated gene transcription, protein production, and virulence. Appl Environ Microbiol 71: 8903–8910.

Štítky
Hygiena a epidemiológia Infekčné lekárstvo Laboratórium

Článok vyšiel v časopise

PLOS Pathogens


2014 Číslo 2
Najčítanejšie tento týždeň
Najčítanejšie v tomto čísle
Kurzy

Zvýšte si kvalifikáciu online z pohodlia domova

Získaná hemofilie - Povědomí o nemoci a její diagnostika
nový kurz

Eozinofilní granulomatóza s polyangiitidou
Autori: doc. MUDr. Martina Doubková, Ph.D.

Všetky kurzy
Prihlásenie
Zabudnuté heslo

Zadajte e-mailovú adresu, s ktorou ste vytvárali účet. Budú Vám na ňu zasielané informácie k nastaveniu nového hesla.

Prihlásenie

Nemáte účet?  Registrujte sa

#ADS_BOTTOM_SCRIPTS#