Surface-expressed enolases of Plasmodium and other pathogens

Memorias do Instituto Oswaldo Cruz

Volumn 106, Issue SUPPL. 1, 2011, Pages 85-90

  Ghosh, Anil Kumar ^a   Jacobs Lorena, Marcelo ^a  

^a JOHNS HOPKINS BLOOMBERG SCHOOL OF PUBLIC HEALTH   (United States)

Author keywords

Cell surface enolase; Pathogenicity; Plasmodium

Indexed keywords

EID: 80051755246     PISSN: 00740276     EISSN: 16788060     Source Type: Journal    
DOI: 10.1590/S0074-02762011000900011     Document Type: Article

References (39)

1. Adrian PV, Bogaert D, Oprins M, Rapola S, Lahdenkari M, Kilpi T, de Groot R, Käyhty H, Hermans PW 2004. Development of antibodies against pneumococcal proteins alpha-enolase, immunoglobulin A1 protease, streptococcal lipoprotein rotamase A, and putative proteinase maturation protein A in relation to pneumococcal carriage and otitis media. Vaccine 22: 2737-2742.
2. Avilan L, Calcagno M, Figuera M, Lemus L, Puig J, Rodriguez AM 2000. Interaction of Leishmania mexicana promastigotes with the plasminogen-plasmin system. Mol Biochem Parasitol 110: 183-193.
3. Bergmann S, Rohde M, Preissner KT, Hammerschmidt S 2005. The nine residue plasminogen-binding motif of the pneumococcal enolase is the major cofactor of plasmin-mediated degradation of extracellular matrix, dissolution of fibrin and transmigration. Thromb Haemost 94: 304-311.
4. Bergmann S, Wild D, Diekmann O, Frank R, Bracht D, Chhatwal GS, Hammerschmidt S 2003. Identification of a novel plasmin(ogen)-binding motif in surface displayed alpha-enolase of Streptococcus pneumoniae. Mol Microbiol 49: 411-423.
5. Calcagno M, Avilan L, Colasante C, Berrueta L, Salmen 2002. Interaction of different Leishmania mexicana morphotypes with plasminogen. Parasitol Res 88: 972-980.
6. Carneiro CR, Postol E, Nomizo R, Reis LF, Brentani RR 2004. Identification of enolase as a laminin-binding protein on the surface of Staphylococcus aureus. Microbes Infect 6: 604-608.
7. Cutler JE 1991. Putative virulence factors of Candida albicans. Annu Rev Microbiol 45: 187-218.
8. Derbise A, Song YP, Parikh S, Fischetti VA, Pancholi V 2004. Role of the C-terminal lysine residues of streptococcal surface enolase in Glu- and Lys-plasminogen-binding activities of group A streptococci. Infect Immun 72: 94-105.
9. Dinis M, Tavares D, Veiga-Malta I, Fonseca AJ, Andrade EB, Trigo G, Ribeiro A, Videira A, Cabrita AM, Ferreira P 2009. Oral therapeutic vaccination with Streptococcus sobrinus recombinant enolase confers protection against dental caries in rats. J Infect Dis 199: 116-123.
10. Eberhard T, Kronvall G, Ullberg M 1999. Surface bound plasmin promotes migration of Streptococcus pneumoniae through reconstituted basement membranes. Microb Pathog 26: 175-181.
11. Ehinger S, Schubert WD, Bergmann S, Hammerschmidt S, Heinz DW 2004. Plasmin(ogen)-binding alpha-enolase from Streptococcus pneumonia: crystal structure and evolution of plasmin(ogen)-binding sites. J Mol Biol 343: 997-1005.
12. Ghosh A, Edwards MJ, Jacobs-Lorena M 2000. The journey of malaria parasite in the mosquito: hopes for the new century. Parasitol Today 16: 196-201.
13. Hannaert V, Brinkmann H, Nowitzki U, Lee JA, Albert MA, Sensen CW, Gaasterland T, Müller M, Michels P, Martin W 2000. Enolase from Trypanosoma brucei, from the amitochondriate protist Mastigamoeba balamuthi, and from the chloroplast and cytosol of Euglena gracilis: pieces in the evolutionary puzzle of the eukaryotic glycolytic pathway. Mol Biol Evol 17: 989-1000.
14. Hotez P, Ottesen E, Fenwick A, Molyneux D 2006. The neglected tropical diseases: the ancient afflictions of stigma and poverty and the prospects for their control and elimination. Adv Exp Med Biol 582: 23-33.
15. Jolodar A, Fischer P, Bergmann S, Büttner DW, Hammerschmidt S, Brattig NW 2003. Molecular cloning of an alpha-enolase from the human filarial parasite Onchocerca volvulus that binds human plasminogen. Biochim Biophys Acta 1627: 111-120.
16. Jong AY, Chen SH, Stins MF, Kim KS, Tuan TL, Huang SH 2003. Binding of Candida albicans enolase to plasmin(ogen) results in enhanced invasion of human brain microvascular endothelial cells. J Med Microbiol 52: 615-622.
17. Keeling PJ 2004. Polymorphic insertions and deletions in parabasalian enolase genes. J Mol Evol 58: 550-556.
18. Kolberg J, Aase A, Bergmann S, Herstad TK, Rødal G, Frank R, Rohde M, Hammerschmidt S 2006. Streptococcus pneumoniae enolase is important for plasminogen binding despite low abundance of enolase protein on the bacterial cell surface. Microbiology 152: 1307-1317.
19. López-Villar E, Monteoliva L, Larsen MR, Sachon E, Shabaz M, Pardo M, Pla J, Gil C, Roepstorff P, Nombela C 2006. Genetic and proteomic evidences support the localization of yeast enolase in the cell surface. Proteomics 6 (Suppl. 1): S107-118.
20. Lottenberg R, Minning-Wenz D, Boyle MD 1994. Capturing host plasmin(ogen): a common mechanism for invasive pathogens? Trends Microbiol 2: 20-24.
21. Maldonado J, Marina C, Puig J, Maizo Z, Avlin L 2006. A study of cutaneous lesions caused by Leishmania mexicana in plasminogen-deficient mice. Exp Mol Pathol 80: 289-294.
22. Molyneux DH 2006. Control of human parasitic diseases: context and overview. Adv Parasitol 61: 1-45.
23. Pal-Bhowmick I, Mehta M, Coppens I, Sharma S, Jarori GK 2007. Protective properties and surface localization of Plasmodium falciparum enolase. Infect Immun 75: 5500-5508.
24. Pancholi V, Fischetti VA 1998. Alpha-enolase, a novel strong plasmin(ogen) binding protein on the surface of pathogenic streptococci. J Biol Chem 273: 14503-14515.
25. Pizarro-Cerdá J, Cossart P 2006. Bacterial adhesion and entry into host cells. Cell 124: 715-727.
26. Ponting CP, Marshall JM, Cederholm-Williams SA 1992. Plasminogen: a structural review. Blood Coagul Fibrinolysis 3: 605-614.
27. Quiñones W, Peña P, Domingo-Sananes M, Cáceres A, Michels PA, Avilan L, Concepción JL 2007. Leishmania mexicana: molecular cloning and characterization of enolase. Exp Parasitol 116: 241-251.
28. Read M, Hicks KE, Sims PF, Hyde JE 1994. Molecular characterisation of the enolase gene from the human malaria parasite Plasmodium falciparum. Evidence for ancestry within a photosynthetic lineage. Eur J Biochem 220: 513-520.
29. Roth EF Jr, Calvin MC, Max-Audit I, Rosa J, Rosa R 1988. The enzymes of the glycolytic pathway in erythrocytes infected with Plasmodium falciparum malaria parasites. Blood 72: 1922-1925.
30. Rugemalila JB, Ogundahunsi OA, Stedman TT, Kilama WL 2007. Multilateral initiative on malaria: justification, evolution, achievements, challenges, opportunities, and future plans. Am J Trop Med Hyg 77 (Suppl. 6): 296-302.
31. Sato K, Kano S, Matsumoto Y, Glanarongran R, Krudsood S, Looareesuwan S, Aikawa M, Suzuki M 2000. Application of yeast enolase as antigen for immunodiagnosis of malaria. Southeast Asian J Trop Med Public Health 31 (Suppl. 1): 79-84.
32. Shao L, Devenport M, Jacobs-Lorena M 2001. The peritrophic matrix of hematophagous insects. Arch Insect Biochem Physiol 47: 119-125.
33. Snow RW, Guerra CA, Noor AM, Myint HY, Hay SI 2005. The global distribution of clinical episodes of Plasmodium falciparum malaria. Nature 434: 214-217.
34. Trottier S, Higgins R, Brochu G, Gottschalk M 1991. A case of human endocarditis due to Streptococcus suis in North-America. Rev Infect Dis 13: 1251-1252.
35. Virkola R, Lähteenmäki K, Eberhard T, Kuusela P, van Alphen L, Ullberg M, Korhonen TK 1996. Interaction of Haemophilus influenzae with the mammalian extracellular matrix. J Infect Dis 173: 1137-1147.
36. Vora HK, Shaik FR, Pal-Bhowmick I, Mout R, Jarori GK 2009. Effect of deletion of a plant like pentapeptide insert on kinetic, structural and immunological properties of enolase from Plasmodium falciparum. Arch Biochem Biophys 485: 128-138.
37. Wheat LJ, White AC, Norden C 1985. Serological diagnosis of Sta-phylococcus aureus osteomyelitis. J Clin Microbiol 21: 764-767.
38. Zhang A, Chen B, Mu X, Li R, Zheng P, Zhao Y, Chen H, Jin M 2009. Identification and characterization of a novel protective antigen, enolase of Streptococcus suis serotype 2. Vaccine 27: 1348-1353.
39. Zieler H, Garon CF, Fischer ER, Shahabuddin M 2000. A tubular network associated with the brush-border surface of the Aedes aegypti midgut: implications for pathogen transmission by mosquitoes. J Exp Biol 203: 1599-1611.