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pmid:31521183

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

Conor E Fogarty · Min Zhao · Donald P McManus · Mary G Duke · Scott F Cummins · Tianfang Wang

Parasites & vectors · 2019 doi:10.1186/s13071-019-3708-0

Paper

complete

Experiment

partial

Data

partial

Analysis

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
id
pmid:31521183
kind
science-record
content_hash
sha256:2a74cdebbe2655b84391e587db2138e1ecf0427542f1ddd7280a9dc637579edf
schema
https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json
created_at
2026-11-01T15:40:49Z
updated_at
2026-11-01T22:44:11Z
generator object · 2 fields
name
corpus-assay-engine
run_id
reading-sci-2026-11-01
paper object · 10 fields
state
complete
title
Comparative study of excretory-secretory proteins released by Schistosoma mansoni-resistant, susceptible and naïve Biomphalaria glabrata.
doi
10.1186/s13071-019-3708-0
pmid
31521183
authors array · 6 items
[0]
Conor E Fogarty
[1]
Min Zhao
[2]
Donald P McManus
[3]
Mary G Duke
[4]
Scott F Cummins
[5]
Tianfang Wang
journal
Parasites & vectors
year
2019
abstract
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.
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A two-way ANOVA test was used to calculate P-values and evaluate the significance of behavioural modifications in response to pH-neutral water, susceptible and F1 resistant SCW.
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null
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sections[5] "Schistosoma mansoni miracidia isolation and behavioural bioassay" paragraph 4
quote
A two-way ANOVA test was used to calculate P-values and evaluate the significance of behavioural modifications in response to pH-neutral water, susceptible and F1 resistant SCW.
state
complete
[1] object · 6 fields
id
claim-data-access
statement
The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE [41] partner repository with the dataset identifier PXD015129. Other datasets analysed in this study are included in this published article and its additional files.
kind
methodological
target
null
evidence array · 1 item
[0] object · 3 fields
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sections[24] "Availability of data and materials" paragraph 2
quote
The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE [41] partner repository with the dataset identifier PXD015129. Other datasets analysed in this study are included in this published article and its additional files.
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The claim, method and evidence span published with the source article.
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the published estimate and its evidence
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the source data with its repository provenance
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https://doi.org/10.1186/s13071-019-3708-0
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10.1186/s13071-019-3708-0
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PMC6744689
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High confidence non-redundant ESPs ([− 10lgP] > 30) with putative anti-pathogen function identified in resistant B. glabrata SCW. Details of coverage, peptide match number and BLAST confidence (e-value) are shown
structure object · 5 fields
pmcid
PMC6744689
section_index
14
section_title
Biomphalaria glabrata ESP annotation and gene ontology analysis
row_count
12
column_count
8
table object · 8 fields
label
Table 1
caption
High confidence non-redundant ESPs ([− 10lgP] > 30) with putative anti-pathogen function identified in resistant B. glabrata SCW. Details of coverage, peptide match number and BLAST confidence (e-value) are shown
rows array · 12 items
[0] array · 8 items
[0]
Description
[1]
− 10lgP
[2]
Coverage (%)a
[3]
No. of peptides
[4]
No. uniqueb
[5]
Avg. mass
[6]
BLASTp e-value
[7]
Accession No.
[1] array · 8 items
[0]
Leukocyte elastase inhibitor-like
[1]
73.93
[2]
15
[3]
2
[4]
1
[5]
15593
[6]
1.01E−98
[7]
BGLB007529-PB
[2] array · 8 items
[0]
Haemoglobin type 1
[1]
69.56
[2]
12
[3]
4
[4]
1
[5]
20380
[6]
4.65E−130
[7]
BGLB026333-PA
[3] array · 8 items
[0]
Superoxide dismutase [Cu-Zn]
[1]
59.07
[2]
14
[3]
2
[4]
2
[5]
16447
[6]
4.39E−104
[7]
BGLB000035-PA
[4] array · 8 items
[0]
Adenosine deaminase CECR1
[1]
58.36
[2]
8
[3]
2
[4]
2
[5]
25076
[6]
3.34E−159
[7]
BGLB033953-PA
[5] array · 8 items
[0]
Glutathione peroxidase-like
[1]
50.23
[2]
12
[3]
2
[4]
2
[5]
22859
[6]
1.85E−151
[7]
BGLB008980-PC
[6] array · 8 items
[0]
Heat-shock 70 kDa protein cognate 4
[1]
45.56
[2]
5
[3]
4
[4]
4
[5]
71177
[6]
0
[7]
BGLB007783-PB
[7] array · 8 items
[0]
Enolase-phosphatase E1
[1]
42.13
[2]
13
[3]
2
[4]
2
[5]
19313
[6]
4.05E−119
[7]
BGLB029757-PA
[8] array · 8 items
[0]
Peroxiredoxin 1
[1]
39.55
[2]
4
[3]
1
[4]
1
[5]
27567
[6]
0
[7]
BGLB000120-PA
[9] array · 8 items
[0]
Rho GDP-dissociation inhibitor 1
[1]
32.87
[2]
4
[3]
1
[4]
1
[5]
23176
[6]
2.75E−143
[7]
BGLB011409-PB
[10] array · 8 items
[0]
Carboxypeptidase B
[1]
32.85
[2]
12
[3]
1
[4]
1
[5]
12298
[6]
2.51E−73
[7]
BGLB037596-PA
[11] array · 8 items
[0]
Putative tyrosinase-like protein tyr-1
[1]
31.61
[2]
2
[3]
1
[4]
1
[5]
67700
[6]
0
[7]
BGLB030046-PA
locator
section[14]/table-wrap[1]#Tab1
[2] object · 16 fields
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asset:table:pmid:31521183:2
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sha256:ade14208a1415dc843274206ff4b2cb0fc0643e0eeb91bc4741c0e321e8206c3
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section[14]/table-wrap[2]#Tab2
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null
note
High confidence non-redundant ESPs (-10lgP > 30) identified in the susceptible B. glabrata SCW. Details of coverage, peptide match number and BLAST confidence (e-value) are shown
structure object · 5 fields
pmcid
PMC6744689
section_index
14
section_title
Biomphalaria glabrata ESP annotation and gene ontology analysis
row_count
17
column_count
8
table object · 8 fields
label
Table 2
caption
High confidence non-redundant ESPs (-10lgP > 30) identified in the susceptible B. glabrata SCW. Details of coverage, peptide match number and BLAST confidence (e-value) are shown
rows array · 17 items
[0] array · 8 items
[0]
Description
[1]
− 10lgP
[2]
Coverage (%)a
[3]
No. of peptides
[4]
No. uniqueb
[5]
Avg. mass
[6]
BLASTp e-value
[7]
Accession No.
[1] array · 8 items
[0]
Zinc metalloproteinase/disintegrin-like
[1]
178.26
[2]
42
[3]
21
[4]
20
[5]
51345
[6]
0
[7]
BGLB040280-PA
[2] array · 8 items
[0]
Endothelin-converting enzyme 1-like isoform X2
[1]
111.23
[2]
11
[3]
6
[4]
6
[5]
56937
[6]
0
[7]
BGLB029484-PA
[3] array · 8 items
[0]
DUF4347 domain-containing protein
[1]
105.24
[2]
34
[3]
4
[4]
4
[5]
24685
[6]
9.89E−168
[7]
BGLB031575-PA
[4] array · 8 items
[0]
Solute carrier family 35-member E4
[1]
99.19
[2]
26
[3]
3
[4]
3
[5]
14320
[6]
8.17E−89
[7]
BGLB032352-PA
[5] array · 8 items
[0]
Proactivator polypeptide-like
[1]
91.36
[2]
8
[3]
6
[4]
5
[5]
68048
[6]
0
[7]
BGLB024213-PA
[6] array · 8 items
[0]
Probable serine carboxypeptidase CPVL
[1]
84.31
[2]
9
[3]
4
[4]
4
[5]
51401
[6]
0
[7]
BGLB030391-PA
[7] array · 8 items
[0]
Phospholipase B1, membrane-associated-like
[1]
79.92
[2]
8
[3]
3
[4]
3
[5]
44658
[6]
0
[7]
BGLB030448-PB
[8] array · 8 items
[0]
Chitinase-like protein PB1E7.04c
[1]
78
[2]
4
[3]
4
[4]
2
[5]
117976
[6]
0
[7]
BGLB017725-PA
[9] array · 8 items
[0]
Endothelin-converting enzyme 2-like
[1]
73.3
[2]
13
[3]
2
[4]
2
[5]
17072
[6]
5.67E−106
[7]
BGLB034604-PA
[10] array · 8 items
[0]
Cathepsin L1-like
[1]
39.16
[2]
7
[3]
2
[4]
2
[5]
26721
[6]
0
[7]
BGLB006210-PB
[11] array · 8 items
[0]
Collagen alpha-3(VI) chain-like isoform X1
[1]
35.7
[2]
3
[3]
1
[4]
1
[5]
34307
[6]
0
[7]
BGLB016458-PA
[12] array · 8 items
[0]
Probable glutathione S-transferase 7
[1]
35.27
[2]
8
[3]
2
[4]
2
[5]
23436
[6]
9.5E−150
[7]
BGLB004187-PC
[13] array · 8 items
[0]
Mucin-like protein
[1]
34.76
[2]
0
[3]
1
[4]
1
[5]
200228
[6]
0
[7]
BGLB016329-PA
[14] array · 8 items
[0]
Bypass of stop codon protein 1-like
[1]
34.45
[2]
7
[3]
1
[4]
1
[5]
16031
[6]
8.96E−99
[7]
BGLB034270-PA
[15] array · 8 items
[0]
ADAM family mig-17-like
[1]
32.27
[2]
2
[3]
1
[4]
1
[5]
51159
[6]
0
[7]
BGLB040281-PA
[16] array · 8 items
[0]
Glyceraldehyde-3-phosphate dehydrogenasec
[1]
27.37
[2]
3
[3]
1
[4]
1
[5]
25914
[6]
1.03E−176
[7]
BGLB010592-PB
locator
section[14]/table-wrap[2]#Tab2
[3] object · 16 fields
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asset:table:pmid:31521183:3
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section[15]/table-wrap[1]#Tab3
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null
note
A list of non-redundant S. mansoni ESPs identified in susceptible SCW. Details of sequence coverage, average mass, number of peptides and unique peptides and accession names are shown
structure object · 5 fields
pmcid
PMC6744689
section_index
15
section_title
Schistosoma mansoni proteins identified from susceptible SCW of B. glabrata
row_count
14
column_count
8
table object · 8 fields
label
Table 3
caption
A list of non-redundant S. mansoni ESPs identified in susceptible SCW. Details of sequence coverage, average mass, number of peptides and unique peptides and accession names are shown
rows array · 14 items
[0] array · 8 items
[0]
Description
[1]
− 10lgP
[2]
Coveragea (%)
[3]
No. of peptides
[4]
No. uniqueb
[5]
Avg. mass
[6]
BLASTp e-value
[7]
Accession No.
[1] array · 8 items
[0]
Uncharacterised protein
[1]
66.61
[2]
8
[3]
3
[4]
3
[5]
31951
[6]
0
[7]
Smp_179420.1
[2] array · 8 items
[0]
Egg protein CP391B-like
[1]
54.01
[2]
6
[3]
1
[4]
1
[5]
25520
[6]
4.00E−157
[7]
Smp_193380.1
[3] array · 8 items
[0]
Glyceraldehyde-3-phosphate dehydrogenase
[1]
44.08
[2]
7
[3]
3
[4]
1
[5]
33808
[6]
0
[7]
Smp_056970.4
[4] array · 8 items
[0]
Putative zinc finger protein
[1]
37.91
[2]
1
[3]
3
[4]
1
[5]
286355
[6]
0
[7]
Smp_132000.1
[5] array · 8 items
[0]
Uncharacterised protein
[1]
28.51
[2]
19
[3]
2
[4]
2
[5]
7535
[6]
3.00E−41
[7]
Smp_202190.1
[6] array · 8 items
[0]
Uncharacterised protein
[1]
21.49
[2]
1
[3]
1
[4]
1
[5]
228220
[6]
0
[7]
Smp_198230.1
[7] array · 8 items
[0]
Uncharacterised protein
[1]
21.43
[2]
2
[3]
1
[4]
1
[5]
48135
[6]
0
[7]
Smp_137420.1
[8] array · 8 items
[0]
Putative nicotinate phosphoribosyltransferase
[1]
20.87
[2]
1
[3]
1
[4]
1
[5]
60943
[6]
0
[7]
Smp_035460.1
[9] array · 8 items
[0]
Tfiif-alpha
[1]
20.19
[2]
1
[3]
1
[4]
1
[5]
92315
[6]
0
[7]
Smp_088460.1
[10] array · 8 items
[0]
Uncharacterised protein
[1]
20.01
[2]
4
[3]
1
[4]
1
[5]
28284
[6]
0
[7]
Smp_093980.1
[11] array · 8 items
[0]
Uncharacterised protein
[1]
19.55
[2]
2
[3]
1
[4]
1
[5]
47835
[6]
0
[7]
Smp_130330.1
[12] array · 8 items
[0]
Proline–serine–threonine phosphatase interacting protein
[1]
19.54
[2]
1
[3]
1
[4]
1
[5]
141331
[6]
0
[7]
Smp_028140.1
[13] array · 8 items
[0]
Uncharacterised protein
[1]
18.4
[2]
1
[3]
1
[4]
1
[5]
83862
[6]
0
[7]
Smp_142140.1
locator
section[15]/table-wrap[1]#Tab3
gaps array · 0 items
analysis object · 4 fields
state
complete
methods array · 2 items
[0] object · 10 fields
id
method-1
family
group_comparison
specific
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Group comparison
dsl_operations array · 4 items
[0]
group_summary
[1]
welch_t
[2]
bootstrap_mean_difference
[3]
group_comparison_anova
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
two_or_more_groups_continuous
evidence object · 3 fields
score
1
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verbatim
quote
A two-way ANOVA test was used to calculate P-values and evaluate the significance of behavioural modifications in response to pH-neutral water, susceptible and F1 resistant SCW.
[1] object · 10 fields
id
method-2
family
network_analysis
specific
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label
Network / pathway analysis
dsl_operations array · 3 items
[0]
build_graph
[1]
centrality_scores
[2]
pathway_enrich
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
edge_list
evidence object · 3 fields
score
0.7
band
medium
quote
Protein-protein interaction
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gaps array · 0 items
capability object · 3 fields
state
complete
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[0] object · 6 fields
capability_id
capability:computational_analysis
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Computational analysis platform
assay_families array · 9 items
[0]
meta_analysis
[1]
machine_learning
[2]
survival_analysis
[3]
statistical_regression
[4]
pca
[5]
molecular_docking
[6]
network_analysis
[7]
differential_expression
[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
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blocked
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R4
blocked_on
data:accession_absent
axes object · 3 fields
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true
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The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: anova.
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R1
capability_id
capability:computational_analysis
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owned
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The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
data object · 6 fields
tier
R4
reachable
false
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The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE [41] partner repository with the dataset identifier PXD015129. Other datasets analysed in this study are included in this published article and its additional files.
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fractionated using SDS-PAGE, identified with LC-MS/MS and compared to naïve snail ESPs. Protein-pr
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thods Availability of data and materials The mass spectrometry proteomics data have been deposited to the P
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of data and materials The mass spectrometry proteomics data have been deposited to the ProteomeXcha
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A two-way ANOVA test was used to calculate P-values and evaluate the significance of behavioural modifications in response to pH-neutral water, susceptible and F1 resistant SCW.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:31521183", "kind": "science-record", "revision": 8, "content_hash": "sha256:2a74cdebbe2655b84391e587db2138e1ecf0427542f1ddd7280a9dc637579edf", "created_at": "2026-11-01T15:40:49Z", "updated_at": "2026-11-01T22:44:11Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Comparative study of excretory-secretory proteins released by Schistosoma mansoni-resistant, susceptible and naïve Biomphalaria glabrata.", "doi": "10.1186/s13071-019-3708-0", "pmid": "31521183", "authors": ["Conor E Fogarty", "Min Zhao", "Donald P McManus", "Mary G Duke", "Scott F Cummins", "Tianfang Wang"], "journal": "Parasites & vectors", "year": 2019, "abstract": "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.\nMETHODS: 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.\nRESULTS: 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.\nCONCLUSIONS: 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.", "claims": [{"id": "claim-method", "statement": "A two-way ANOVA test was used to calculate P-values and evaluate the significance of behavioural modifications in response to pH-neutral water, susceptible and F1 resistant SCW.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:31521183", "locator": "sections[5] \"Schistosoma mansoni miracidia isolation and behavioural bioassay\" paragraph 4", "quote": "A two-way ANOVA test was used to calculate P-values and evaluate the significance of behavioural modifications in response to pH-neutral water, susceptible and F1 resistant SCW."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE [41] partner repository with the dataset identifier PXD015129. 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