» Articles » PMID: 15784540

Pyrophosphatase of the Roundworm Ascaris Suum Plays an Essential Role in the Worm's Molting and Development

Overview
Journal Infect Immun
Date 2005 Mar 24
PMID 15784540
Citations 33
Authors
Affiliations
Soon will be listed here.
Abstract

Previous studies indicated that inorganic pyrophosphatase of Ascaris suum (AsPPase) plays an important role in larval survival in the host. Here we describe a precise role for AsPPase in larval molting and development and also describe the potential role of recombinant AsPPase (rAsPPase) in protective immunity to A. suum infection. Using reverse transcriptase PCR analysis, we found that disruption of AsPPase gene function by RNA interference resulted in suppression of AsPPase mRNA levels. RNA interference also caused inhibition of molting of third-stage larvae (31%) and suppression of native protein expression, as demonstrated by a 56% reduction in enzyme activity and quantified by immunoblot and immunofluorescence analyses, suggesting that AsPPase has a role in the molting process. The anatomic location of the AsPPase native enzyme in the hypodermis of larvae along with its elevated expression prior to and during the molting process supports such a role. Anti-rAsPPase immunoglobulin G (IgG) also resulted in 57% inhibition of molting of A. suum lung-stage third-stage larvae to fourth-stage larvae in vitro with developmental arrest. Antigenic epitopes of AsPPase overlapped the enzyme active sites. Mice immunized with rAsPPase exhibited high antigen-specific IgG antibody responses and were protected (>70%) against a challenge A. suum migratory-phase infection. Splenic T cells from rAsPPase-immunized mice produced low levels of T helper 1-type cytokines (gamma interferon and interleukin-2) in vitro but exhibited an elevated interleukin-10 response. A significantly high level of IgG1 subclass antibodies was found in immunized mice. Our results establish that AsPPase has a critical role in the molting and development of Ascaris roundworms and suggest the potential of AsPPase for use as a candidate vaccine against ascariasis.

Citing Articles

A historical and systematic overview of vaccine development.

Gazzinelli-Guimaraes A, Gazzinelli-Guimaraes P, Weatherhead J Parasitology. 2022; 148(14):1795-1805.

PMID: 35586777 PMC: 9109942. DOI: 10.1017/s0031182021001347.


Small RNA pathways in the nematode Ascaris in the absence of piRNAs.

Zagoskin M, Wang J, Neff A, Veronezi G, Davis R Nat Commun. 2022; 13(1):837.

PMID: 35149688 PMC: 8837657. DOI: 10.1038/s41467-022-28482-7.


ASCVac-1, a Multi-Peptide Chimeric Vaccine, Protects Mice Against Infection.

Gazzinelli-Guimaraes A, Nogueira D, Amorim C, Oliveira F, Coqueiro-Dos-Santos A, Carvalho S Front Immunol. 2022; 12:788185.

PMID: 34992603 PMC: 8724438. DOI: 10.3389/fimmu.2021.788185.


Oral vaccination with recombinant Lactobacillus plantarum encoding Trichinella spiralis inorganic pyrophosphatase elicited a protective immunity in BALB/c mice.

Hu C, Xu Y, Hao H, Liu R, Jiang P, Long S PLoS Negl Trop Dis. 2021; 15(10):e0009865.

PMID: 34699522 PMC: 8547688. DOI: 10.1371/journal.pntd.0009865.


Biological properties and roles of a Trichinella spiralis inorganic pyrophosphatase in molting and developmental process of intestinal larval stages.

Hu C, Zeng J, Hao H, Xu Y, Liu F, Liu R Vet Res. 2021; 52(1):6.

PMID: 33413587 PMC: 7791673. DOI: 10.1186/s13567-020-00877-8.


References
1.
Schopf L, Hoffmann K, Cheever A, Urban Jr J, Wynn T . IL-10 is critical for host resistance and survival during gastrointestinal helminth infection. J Immunol. 2002; 168(5):2383-92. DOI: 10.4049/jimmunol.168.5.2383. View

2.
Skelly P, Dadara A, Harn D . Suppression of cathepsin B expression in Schistosoma mansoni by RNA interference. Int J Parasitol. 2003; 33(4):363-9. DOI: 10.1016/s0020-7519(03)00030-4. View

3.
Tsuji N, Isobe T, Yoshihara S . Cloning and characterisation of a peroxiredoxin from the swine roundworm Ascaris suum. Int J Parasitol. 2000; 30(2):125-8. DOI: 10.1016/s0020-7519(99)00180-0. View

4.
Tabara H, Grishok A, Mello C . RNAi in C. elegans: soaking in the genome sequence. Science. 1998; 282(5388):430-1. DOI: 10.1126/science.282.5388.430. View

5.
Garside P, Kennedy M, Wakelin D, Lawrence C . Immunopathology of intestinal helminth infection. Parasite Immunol. 2000; 22(12):605-12. DOI: 10.1046/j.1365-3024.2000.00344.x. View