Logo image
Comparative study of excretory-secretory proteins released by Schistosoma mansoni-resistant, susceptible and naive Biomphalaria glabrata
Journal article   Open access   Peer reviewed

Comparative study of excretory-secretory proteins released by Schistosoma mansoni-resistant, susceptible and naive Biomphalaria glabrata

Conor E Fogarty, Min Zhao, Donald P McManus, Mary G Duke, Scott F Cummins and Tianfang Wang
Parasites & Vectors, Vol.12, pp.1-17
2019
pdf
PDF - Published Version (Open Access)5.61 MBDownloadView
Published VersionCC BY V4.0 Open Access
pdf
Correction to original article2.90 MBDownloadView
CorrectionCC BY V4.0 Open Access
url
https://doi.org/10.1186/s13071-019-3708-0View
Published Version
url
https://doi.org/10.1186/s13071-022-05439-9View
Correction

Abstract

Schistosoma mansoni Biomphalaria glabrata Miracidia excretory-secretory proteins proteomics PPI
Background: Schistosomiasis is a harmful neglected tropical disease caused by infection with Schistosoma spp., such as Schistosoma mansoni. Schistosoma must transition within a molluscan host to survive. Chemical analyses of schistosome-molluscan interactions indicate that host identification involves chemosensation, including naïve host preference. Proteomic technique advances enable sophisticated comparative analyses between infected and naïve snail host proteins. This study aimed to compare resistant, susceptible and naïve Biomphalaria glabrata snail-conditioned water (SCW) to identify potential attractants and deterrents. Methods: Behavioural bioassays were performed on S. mansoni miracidia to compare the effects of susceptible, F1 resistant and naïve B. glabrata SCW. The F1 resistant and susceptible B. glabrata SCW excretory-secretory proteins (ESPs) were fractionated using SDS-PAGE, identified with LC-MS/MS and compared to naïve snail ESPs. Protein-protein interaction (PPI) analyses based on published studies (including experiments, co-expression, text-mining and gene fusion) identified S. mansoni and B. glabrata protein interaction. Data are available via ProteomeXchange with identifier PXD015129. Results: A total of 291, 410 and 597 ESPs were detected in the susceptible, F1 resistant and naïve SCW, respectively. Less overlap in ESPs was identified between susceptible and naïve snails than F1 resistant and naïve snails. F1 resistant B. glabrata ESPs were predominately associated with anti-pathogen activity and detoxification, such as leukocyte elastase and peroxiredoxin. Susceptible B. glabrata several proteins correlated with immunity and anti-inflammation, such as glutathione S-transferase and zinc metalloproteinase, and S. mansoni sporocyst presence. PPI analyses found that uncharacterised S. mansoni protein Smp_142140.1 potentially interacts with numerous B. glabrata proteins. Conclusions: This study identified ESPs released by F1 resistant, susceptible and naïve B. glabrata to explain S. mansoni miracidia interplay. Susceptible B. glabrata ESPs shed light on potential S. mansoni miracidia deterrents. Further targeted research on specific ESPs identified in this study could help inhibit B. glabrata and S. mansoni interactions and stop human schistosomiasis.

Details

Metrics

10 File views/ downloads
102 Record Views

InCites Highlights

These are selected metrics from InCites Benchmarking & Analytics tool, related to this output

Collaboration types
Domestic collaboration
Web Of Science research areas
Parasitology
Tropical Medicine

UN Sustainable Development Goals (SDGs)

This output has contributed to the advancement of the following goals:

#3 Good Health and Well-Being

Source: InCites

Logo image