Schistosoma mansoni: Immunodiagnosis Is Improved by Sodium Metaperiodate Which Reduces Cross-reactivity Due to Glycosylated Epitopes of Soluble Egg Antigen

2000 ◽  
Vol 95 (2) ◽  
pp. 106-112 ◽  
Author(s):  
B. Alarcón de Noya ◽  
C. Colmenares ◽  
H. Lanz ◽  
M.A. Caracciolo ◽  
S. Losada ◽  
...  
Keyword(s):  
Schistosoma Mansoni ◽  
Cross Reactivity ◽  
Sodium Metaperiodate ◽  
Egg Antigen

scholarly journals Do intestinal parasites interfere with the seroepidemiologic surveillance of Schistosoma mansoni infection?

1996 ◽  
Vol 116 (3) ◽  
pp. 323-329 ◽  
Author(s):  
B. Alarcón De Noya ◽  
C. Colmenares ◽  
S. Losada ◽  
Z. Fermin ◽  
G. Masroua ◽  
...  
Keyword(s):  
Schistosoma Mansoni ◽  
False Positive ◽  
Total Population ◽  
Intestinal Parasites ◽  
Field Work ◽  
Cross Reactivity ◽  
Cross Reaction ◽  
Protein Fractions ◽  
Egg Antigen ◽  
Immunoenzymatic Assay

SUMMARYIn view of the known cross-reactivity of sera from patients with intestinal parasites to some Schistosoma mansoni antigens, field work was conducted in an area of Venezuela non-endemic for schistosomiasis using the routine immunoenzymatic assay (ELISA) with soluble egg antigen (SEA). False positive reactions represented 15·3% of the total population as determined by SEA–ELISA. SEA-immunoblotting of the false positive sera indicated that protein fractions of 91 and 80 kDa appear to be responsible for cross-reactivity. Sera from hookworm infected individuals produced a higher frequency and intensity of cross-reaction than other sera. SEA-fractions of 105, 54, 46, 42, 32, 25 and 15 kDa were the most specific.

ATP diphosphohydrolase from Schistosoma mansoni egg: characterization and immunocytochemical localization of a new antigen

Parasitology ◽  
2004 ◽  
Vol 129 (1) ◽  
pp. 51-57 ◽  
Author(s):  
P. FARIA-PINTO ◽  
M. N. L. MEIRELLES ◽  
H. L. LENZI ◽  
E. M. MOTA ◽  
M. L. O. PENIDO ◽  
...  
Keyword(s):  
Schistosoma Mansoni ◽  
Polyacrylamide Gel Electrophoresis ◽  
Cross Reactivity ◽  
Outer Side ◽  
Western Blots ◽  
Atp Diphosphohydrolase ◽  
Antigenic Properties ◽  
Egg Shell ◽  
Net Charges ◽  
Egg Antigen

The fact that the Schistosoma mansoni egg has two ATP diphosphohydrolase (EC 3.6.1.5) isoforms with different net charges and an identical molecular weight of 63000, identified by non-denaturing polyacrylamide gel electrophoresis and immunological cross-reactivity with potato apyrase antibodies, is shown. In soluble egg antigen (SEA), only the isoform with the lower net negative charge was detected and seemed to be the predominant species in this preparation. By confocal fluorescence microscopy, using anti-potato apyrase antibodies, the S. mansoni egg ATP diphosphohydrolase was detected on the external surface of miracidium and in von Lichtenberg's envelope. Intense fluorescence was also seen in the outer side of the egg-shell, entrapped by the surface microspines, suggesting that a soluble isoform is secreted. ATP diphosphohydrolase antigenicity was tested using the vegetable protein as antigen. The purified potato apyrase was recognized in Western blots by antibodies present in sera from experimentally S. mansoni-infected mice. In addition, high levels of IgG anti-ATP diphosphohydrolase antibodies were detected by ELISA in the same sera. This work represents the first demonstration of antigenic properties of S. mansoni ATP diphosphohydrolase and immunological cross-reactivity between potato apyrase and sera from infected individuals.

Periodate-sensitive immunological cross-reactivity between keyhole limpet haemocyanin (KLH) and serodiagnostic Schistosoma mansoni egg antigens

Parasitology ◽  
1999 ◽  
Vol 118 (1) ◽  
pp. 83-89 ◽  
Author(s):  
J. V. HAMILTON ◽  
P. L. CHIODINI ◽  
P. G. FALLON ◽  
M. J. DOENHOFF
Keyword(s):  
Schistosoma Mansoni ◽  
Sodium Periodate ◽  
Cross Reactivity ◽  
Enzyme Linked Immunosorbent Assay ◽  
Western Immunoblotting ◽  
Diagnostic Efficacy ◽  
Keyhole Limpet Haemocyanin ◽  
Human Schistosomiasis ◽  
High Degree ◽  
Egg Antigen

Both CEF6, a cation-exchange fraction of soluble Schistosoma mansoni egg antigens (SEA), composed of the 2 antigens, alpha-1 and omega-1, and haemocyanin from the keyhole limpet, Megathura crenulata, have shown potential for immunodiagnosis of human schistosomiasis. Possible cross-reactivity between antigens in SEA and keyhole limpet haemocyanin (KLH) was explored by Western immunoblotting and enzyme-linked immunosorbent assay (ELISA) using sera from rabbits immunized with KLH, SEA, CEF6, alpha-1, omega-1, or egg antigen k5. Both immunoassays revealed a high degree of serological cross-reactivity between the schistosome egg antigens and KLH, much of it due to sodium periodate- sensitive epitopes. Cross-reactivity with schistosome antigens with proven diagnostic efficacy may thus, in part, explain the usefulness of KLH for the diagnosis of human schistosomiasis mansoni.

Immunohistochemical and ultrastructural localization of Schistosoma mansoni soluble egg antigens processed by the infected host

Parasitology ◽  
1996 ◽  
Vol 112 (6) ◽  
pp. 537-543 ◽  
Author(s):  
J. J. P. M. Bogers ◽  
H. A. M. Nibbeling ◽  
A. M. Deelder ◽  
E. A. E. Van Marck
Keyword(s):  
Schistosoma Mansoni ◽  
Indirect Evidence ◽  
Ultrastructural Localization ◽  
Carbohydrate Epitopes ◽  
Eosinophilic Granulocytes ◽  
Antigenic Material ◽  
Egg Shells ◽  
Secondary Lysosomes ◽  
Antigen Antibody ◽  
Egg Antigen

SUMMARYThe detection of egg-derived antigens in the serum and urine of Schistosoma mansoni-infected individuals and experimental animals would provide an alternative method to assess the tissue egg burden. The detected levels are, however, not only a function of the amounts of antigen produced, but also of the processing or clearance by the host. In the present study the immunolocalization pattern of antigens using 2 recently described monoclonal antibodies to repetitive carbohydrate epitopes of S. mansoni soluble egg antigen (114–5B1–A and 114–4D12–A) in various organs of the host was investigated. In the liver strong immunoreactivity could be detected around the entrapped eggs and in egg-shells, as well as in Kupffer cells accumulating both antigen and schistosomal pigment. In the spleen, immunohistochemistry revealed antigen in the plasma as well as in secondary lysosomes of macrophages. Strong labelling was found in the vesicles of the eosinophilic granulocytes: indirect evidence perhaps for the presence of antigen–antibody complexes. In conclusion, the secreted egg antigens were sequestered in the reticulo-endothelial macrophages of the liver and the spleen as already partly described for worm-derived antigens. The presence of large quantities of antigenic material in the spleen could suggest an important role of this organ in the clearance of antigen and might even provide an additional explanation for the hepatosplenomegaly mainly present in S. mansoni-infected children.

Immunocytochemical demonstration of a SALMFamide-like neuropeptide in the nervous system of adult and larval stages of the human blood fluke, Schistosoma mansoni

Parasitology ◽  
1995 ◽  
Vol 110 (2) ◽  
pp. 143-153 ◽  
Author(s):  
D. J. A. Brownlee ◽  
I. Fairweather ◽  
C. F. Johnston ◽  
M. C. Thorndyke ◽  
P. J. Skuce
Keyword(s):  
Nervous System ◽  
Schistosoma Mansoni ◽  
Cross Reactivity ◽  
Confocal Scanning Laser Microscopy ◽  
Male Worm ◽  
Male And Female ◽  
Larval Stages ◽  
Confocal Scanning ◽  
Confocal Scanning Laser ◽  
Nerve Cords

SUMMARYThe localization and distribution of SALMFamide immunoreactivity (IR), SI(GFNSALMFamide), in the nervous system of both the adult and larval stages of the trematode Schistosoma mansoni has been determined by an indirect immunofluorescent technique in conjunction with confocal scanning laser microscopy (CSLM). Immunostaining was widespread in the nervous system of adult male and female S. mansoni. In the central nervous system (CNS), IR was evident in nerve cells and fibres in the anterior ganglia, cerebral commissure and dorsal and ventral nerve cords. In the peripheral nervous system (PNS), IR was apparent in nerve plexuses associated with the subtegmental musculature, oral and ventral suckers, the lining of the gynaecophoric canal, and in fine nerve fibres innervating the dorsal tubercles of the male worm. In the reproductive system of male and female worms, Sl-IR was only observed around the ootype/Mehlis' gland complex in the female. Immunostaining was also evident in the nervous system of both miracidium and cercarial larval stages. A post-embedding, IgG-conjugated colloidal gold immunostaining technique was employed to examine the subcellular distribution of SALMFamide-IR in the CNS of S. mansoni. Gold labelling of peptide was localized over dense-cored vesicles within nerve cell bodies and fibres constituting the neuropile of the anterior ganglia, cerebral commissure and nerve cords of the CNS. Antigen pre-absorption studies indicated that the results obtained do suggest S1-like immunostaining and not cross-reactivity with other peptides, in particular FMRFamide.

Antibody response to immunization with Schistosoma mansoni egg antigen-antibody complex

1963 ◽  
Vol 13 (2) ◽  
pp. 204-210 ◽  
Author(s):  
Walter Stahl ◽  
José Oliver-González ◽  
Amina Rivera de Sala
Keyword(s):  
Antibody Response ◽  
Schistosoma Mansoni ◽  
Antibody Complex ◽  
Antigen Antibody ◽  
Egg Antigen

Activation of the NLRP3 and AIM2 inflammasomes in a mouse model of Schistosoma mansoni infection

2019 ◽  
Vol 94 ◽  
Author(s):  
T.T.W. Chen ◽  
P.C. Cheng ◽  
K.C. Chang ◽  
J.P. Cao ◽  
J.L. Feng ◽  
...  
Keyword(s):  
Immune Responses ◽  
Schistosoma Mansoni ◽  
Infected Mouse ◽  
Mitochondrial Damage ◽  
Carcinoma Cells ◽  
Inflammasome Activation ◽  
Host Immune Responses ◽  
Significant Release ◽  
The Relationship ◽  
Egg Antigen

Abstract Schistosomiasis is an inflammatory disease that occurs when schistosome species eggs are deposited in the liver, resulting in fibrosis and portal hypertension. Schistosomes can interact with host inflammasomes to elicit host immune responses, leading to mitochondrial damage, generation of high levels of reactive oxygen species (ROS) and activation of apoptosis during inflammation. This study aims to examine whether ROS and NF-κB (p65) expression elicited other types of inflammasome activation in Schistosoma mansoni-infected mouse livers. We examine the relationship between inflammasome activation, mitochondrial damage and ROS production in mouse livers infected with S. mansoni. We demonstrate a significant release of ROS and superoxides and increased NF-κB (p65) in S. mansoni-infected mouse livers. Moreover, activation of the NLRP3 and AIM2 inflammasomes was triggered by S. mansoni infection. Stimulation of HuH-7 hepatocellular carcinoma cells with soluble egg antigen induced activation of the AIM2 inflammasome pathway. In this study, we demonstrate that S. mansoni infection promotes both NLRP3 and AIM2 inflammasome activation.

scholarly journals Evaluation of anti-Schistosoma mansoni igG antibodies in patients with chronic schistosomiasis mansoni before and after specific treatment

2001 ◽  
Vol 43 (3) ◽  
pp. 153-159 ◽  
Author(s):  
Célia Maria V. VENDRAME ◽  
Márcia Dias T. CARVALHO ◽  
Célia Regina F. YAMAMOTO ◽  
Maria Cristina NAKHLE ◽  
Silvino Alves CARVALHO ◽  
...  
Keyword(s):  
Schistosoma Mansoni ◽  
Specific Treatment ◽  
Enzyme Linked Immunosorbent Assay ◽  
Control Group ◽  
Igg Antibodies ◽  
Schistosomiasis Mansoni ◽  
Before And After ◽  
Precipitin Test ◽  
Egg Antigen ◽  
Adult Worm Antigen

The circumoval precipitin test (COPT), enzyme-linked immunosorbent assay (ELISA) and the immunoblotting anti-adult worm antigen (AWA) and soluble egg antigen (SEA) tests were applied to 17 chronically schistosome-infected patients for the detection of anti-Schistosoma mansoni antibodies before and on four occasions after oxamniquine administration over a period of six months. Compared to a control group, schistosomiasis patients showed high levels of IgG antibodies in AWA and SEA-ELISA. A decrease in IgG levels was observed six months after treatment, although negative reactions were not obtained. Significant decreases in IgG1, IgG3 and, mainly, IgG4, but not anti-SEA IgG2 levels were observed six months after treatment, again without negativity. Analysis of anti-AWA IgG antibodies by immunoblotting before treatment showed a 31 kDa strand in 14 patients (82%) which disappeared in three cases up to six months after treatment; furthermore, anti-SEA IgG antibodies showed the same band in nine patients (53%) before treatment, which disappeared in only four cases up to six months after treatment.

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