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Journal ArticleDOI

Characterization and localization of saposin-like protein-2 (SAP-2) in Fasciola gigantica

TLDR
Cloned and expressed FgSAP-2 and produced the antibody against this recombinant protein indicated that SAP-2 is a unique protein that is expressed only in late juvenile and adult F. gigantica, and it could be considered for immunodiagnostic and as a vaccine candidate for fasciolosis.
Abstract
Fasciola gigantica saposin-like protein-2 (FgSAP-2) belongs to a family of lipid-interacting proteins that are involved in the cytolysis of target cells. In this study, we have cloned and expressed FgSAP-2 and produced the antibody against this recombinant protein. Rabbit antiserum against rFgSAP-2 reacted with a similar native protein in the whole body extracts of the 4-week-old juvenile and adult stage, as well as a protein in their excretion–secretion, but not in the tegument. In situ hybridization and immunofluorescence detection revealed the presence of SAP-2 mRNA transcripts and proteins in the cecal epithelial cells of 4-week-old juvenile and adult parasites, but not in the metacercariae and newly excysted juveniles. Moreover, SAP-2 is present only in the cecal epithelial cells lining the distal part of the digestive tract, but not in the tegumental-type epithelium lining the proximal part of the digestive tract. The rFgSAP-2 reacted with antisera from rabbits infected with F. gigantica metacercariae collected at 5 weeks, but not at 2 weeks after infection. Anti-rFgSAP-2 did not exhibit any cross-reactivity with the other parasites' antigens, including Opisthorchis viverrini, Eurytrema pancreaticum, Cotylophoron cotylophorum, Fischoederius cobboldi, Gigantocotyle explanatum, Paramphistomum cervi, Setaria labiato-papillosa, and Haemonchus placei. This finding indicated that SAP-2 is a unique protein that is expressed only in late juvenile and adult F. gigantica, and it could be considered for immunodiagnostic and as a vaccine candidate for fasciolosis.

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Citations
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Journal ArticleDOI

Vaccine potential of recombinant saposin-like protein 2 against Fasciolosis gigantica in mice.

TL;DR: It was found that both Th1 and Th2 humoral immune response were significantly increased in rFgSAP-2 immunized group compared with the control groups, with higher levels of Th2 (IgG1) than Th1 (IGG2a).
Journal ArticleDOI

Molecular cloning and characterization of leucine aminopeptidase from Fasciola gigantica.

TL;DR: The full length of cDNA encoding Fasciola gigantica LAP was cloned from adult parasites and revealed that the FgLAP was closely related and grouped with F. hepatica LAP (FhLAP).
Journal ArticleDOI

Production and characterization of a monoclonal antibody against recombinant saposin-like protein 2 of Fasciola gigantica.

TL;DR: The finding indicated that FgSAP-2 is an abundantly expressed parasite protein that is released into the ES, hence SAP-2 and its MoAb may be used for immunodiagnosis of ruminant and human fasciolosis.
Journal ArticleDOI

Protection against Fasciola gigantica infection in mice by vaccination with recombinant juvenile-specific cathepsin L.

TL;DR: The levels of IgG 1 and IgG2a in the immune sera were shown to be strongly correlated with the numbers of worm recovery, and the correlation coefficient was higher for IgG1.
Journal ArticleDOI

Cytosolic superoxide dismutase can provide protection against Fasciola gigantica.

TL;DR: Anti-rFgSOD exhibited cross reactivity with the other parasites' antigens, including Eurytrema pancreaticum, Cotylophoron cotylophorum, Fischoederius cobboldi, Gastrothylax crumenifer, Paramphistomum cervi, and Setaria labiato papillosa.
References
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Journal ArticleDOI

A short guided tour through functional and structural features of saposin-like proteins.

TL;DR: This review summarizes phylogenetic relations, function and structural features of the members of the APLIPs family, a diverse family of lipid-interacting proteins that have various and only partly understood, but nevertheless essential, cellular functions.
Journal ArticleDOI

Molecular cloning and analysis of stage and tissue-specific expression of cathepsin B encoding genes from Fasciola gigantica.

TL;DR: The switching off of the cat-B2 andCat-B3 genes during the maturation of the parasites implicates that these enzymes may be involved in digesting host tissues during penetration and migration to the liver, whereas cat- B1 present in all stages may perform general digestive function.
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Molecular cloning of a member of the Fasciola hepatica saposin-like protein family.

TL;DR: Using enzyme-linked immunosorbent assay it was found that rFhSAP-2 is highly reactive with sera from rabbits infected with F. hepatica for 2–14 wk as well as withSera from humans with chronic fascioliasis, suggesting that cell lysis could be 1 of the biological functions of this protein.
Journal ArticleDOI

Surfactant protein B propeptide contains a saposin-like protein domain with antimicrobial activity at low pH.

TL;DR: The hypothesis that SP-BN contributes to innate host defense of the lung by supplementing the nonoxidant antimicrobial defenses of alveolar macrophages is supported.
Journal ArticleDOI

A Novel Fasciola hepatica Saposinlike Recombinant Protein with Immunoprophylactic Potential

TL;DR: The hypothesis that this novel rFhSAP-2 protein has immunoprophylactic potential against fascioliasis in rabbits including antifecundity and antipathology effects is supported.
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