Identification and characterization of a sialidase released by the salivary gland of the hematophagous insect Triatoma infestans

被引:24
作者
Amino, R
Porto, RM
Chammas, R
Egami, MI
Schenkman, S
机构
[1] Univ Fed Sao Paulo, Escola Paulista Med, Dept Microbiol Imunol & Parasitol, BR-04023062 Sao Paulo, Brazil
[2] Univ Fed Sao Paulo, Escola Paulista Med, Dept Histol, BR-04023062 Sao Paulo, Brazil
[3] Ludwig Inst Canc Res, BR-01509010 Sao Paulo, Brazil
关键词
D O I
10.1074/jbc.273.38.24575
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sialidases (EC 3.2.1.18) are commonly found in viruses, bacteria, fungi, protozoa, and vertebrates, but not in invertebrates. We have previously reported the presence of a new siaIidase activity in the gut of exclusively hematophagous insects of the Triatoma genus, which transmit Chagas' disease (Amino, R., Acosta, A, Morita, O. M., Chioccola, V. L. P., and Schenkman, S. (1995) Glycobiology 5, 625-631). Here we show that this sialidase is present in the salivary gland of Triatoma infestans, and it is released with the saliva during the insect bite. The sialidase was purified to homogeneity (>5000 times) to a specific activity of more than 20 units/mg. It elutes from a gel filtration column with a volume corresponding to the size of 33 kDa, and it migrates as a single 26-kDa band in SDS-polyacrylamide gel electrophoresis, which is unusually smaller when compared with other known sialidases. T. infestans sialidase hydrolyzes preferentially alpha 2-->3-linked sialic acids at pH 4-8, with maximaI activity between pH 5.5 and 6.5, which is compatible with the optimal pH of secreted sialidases. The sialidase is competitively inhibited by 2-deoxy-2,3-dehydro-N-acetyl-neuraminic acid (K-i = 0.075 mM) and differently from many sialidases, with exception of Salmonella typhimurium sialidase, it is inhibited competitively by HEPES (K-i = 15 mM). The fact that T. infestans sialidase is released with the saliva and can hydrolyze sialyl-Lewis(x) blood groups, which are the ligands for selectins, suggests that it might have a role in the blood feeding.
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页码:24575 / 24582
页数:8
相关论文
共 40 条
[1]   A SIALIDASE ACTIVITY IN THE MIDGUT OF THE INSECT TRIATOMA-INFESTANS IS RESPONSIBLE FOR THE LOW-LEVELS OF SIALIC-ACID IN TRYPANOSOMA-CRUZI GROWING IN THE INSECT VECTOR [J].
AMINO, R ;
SERRANO, AA ;
MORITA, OM ;
PEREIRACHIOCCOLA, VL ;
SCHENKMAN, S .
GLYCOBIOLOGY, 1995, 5 (06) :625-631
[2]  
ANSORGE W, 1983, ELECTROPHORESIS, V82, P235
[3]   SELECTINS [J].
BEVILACQUA, MP ;
NELSON, RM .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (02) :379-387
[4]   TRANS-SIALIDASE AND SIALIC-ACID ACCEPTERS FROM INSECT TO MAMMALIAN STAGES OF TRYPANOSOMA-CRUZI [J].
BRIONES, MRS ;
EGIMA, CM ;
ACOSTA, A ;
SCHENKMAN, S .
EXPERIMENTAL PARASITOLOGY, 1994, 79 (02) :211-214
[5]  
BRIONES MRS, 1995, J MOL EVOL, V41, P120, DOI 10.1007/BF00170663
[6]   TRYPANOSOMA-CRUZI TRANS-SIALIDASE GENE LACKING C-TERMINAL REPEATS AND EXPRESSED IN EPIMASTIGOTE FORMS [J].
BRIONES, MRS ;
EGIMA, CM ;
SCHENKMAN, S .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1995, 70 (1-2) :9-17
[7]  
CHOU MY, 1994, J BIOL CHEM, V269, P18821
[8]   A SIALIDASE FROM THE HEPATOPANCREAS OF THE SHRIMP PENAEUS-JAPONICUS (CRUSTACEA, DECAPODA) - REVERSIBLE BINDING WITH THE ACIDIC BETA-GALACTOSIDASE [J].
CHUANG, NN ;
YANG, BC .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-PHARMACOLOGY TOXICOLOGY & ENDOCRINOLOGY, 1990, 97 (02) :353-356
[9]   Inhibitory effect of neuraminidase on SP-induced histamine release and TNF-alpha mRNA in rat mast cells: Evidence of a receptor-independent mechanism [J].
Cocchiara, R ;
Bongiovanni, A ;
Albeggiani, G ;
Azzolina, A ;
Lampiasi, N ;
DiBlasi, F ;
Geraci, D .
JOURNAL OF NEUROIMMUNOLOGY, 1997, 75 (1-2) :9-18
[10]   BACTERIAL SIALIDASES - ROLES IN PATHOGENICITY AND NUTRITION [J].
CORFIELD, T .
GLYCOBIOLOGY, 1992, 2 (06) :509-521