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pmid:31649645

Francisella tularensis subsp. holarctica Releases Differentially Loaded Outer Membrane Vesicles Under Various Stress Conditions.

Jana Klimentova · Ivona Pavkova · Lenka Horcickova · Jan Bavlovic · Olga Kofronova · Oldrich Benada · Jiri Stulik

Frontiers in microbiology · 2019 doi:10.3389/fmicb.2019.02304

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

Execution

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
id
pmid:31649645
kind
science-record
content_hash
sha256:4303dbc4d3930e2c7bf0312cb5643492b11f066ee921e31b17636d07fde33815
schema
https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json
created_at
2026-11-01T15:40:51Z
updated_at
2026-11-01T22:44:17Z
generator object · 2 fields
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corpus-assay-engine
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reading-sci-2026-11-01
paper object · 10 fields
state
complete
title
Francisella tularensis subsp. holarctica Releases Differentially Loaded Outer Membrane Vesicles Under Various Stress Conditions.
doi
10.3389/fmicb.2019.02304
pmid
31649645
authors array · 7 items
[0]
Jana Klimentova
[1]
Ivona Pavkova
[2]
Lenka Horcickova
[3]
Jan Bavlovic
[4]
Olga Kofronova
[5]
Oldrich Benada
[6]
Jiri Stulik
journal
Frontiers in microbiology
year
2019
abstract
Francisella tularensis is a Gram-negative, facultative intracellular bacterium, causing a severe disease called tularemia. It secretes unusually shaped nanotubular outer membrane vesicles (OMV) loaded with a number of virulence factors and immunoreactive proteins. In the present study, the vesicles were purified from a clinical isolate of subsp. holarctica strain FSC200. We here provide a comprehensive proteomic characterization of OMV using a novel approach in which a comparison of OMV and membrane fraction is performed in order to find proteins selectively enriched in OMV vs. membrane. Only these proteins were further considered to be really involved in the OMV function and/or their exceptional structure. OMV were also isolated from bacteria cultured under various cultivation conditions simulating the diverse environments of F. tularensis life cycle. These included conditions mimicking the milieu inside the mammalian host during inflammation: oxidative stress, low pH, and high temperature (42°C); and in contrast, low temperature (25°C). We observed several-fold increase in vesiculation rate and significant protein cargo changes for high temperature and low pH. Further proteomic characterization of stress-derived OMV gave us an insight how the bacterium responds to the hostile environment of a mammalian host through the release of differentially loaded OMV. Among the proteins preferentially and selectively packed into OMV during stressful cultivations, the previously described virulence factors connected to the unique intracellular trafficking of Francisella were detected. Considerable changes were also observed in a number of proteins involved in the biosynthesis and metabolism of the bacterial envelope components like O-antigen, lipid A, phospholipids, and fatty acids. Data are available via ProteomeXchange with identifier PXD013074.
claims array · 2 items
[0] object · 6 fields
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claim-method
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Multiple sample test (ANOVA) was used to compare the differences among all cultivation conditions. The MS proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE (Perez-Riverol et al., 2019) partner repository with the dataset identifier PXD013074.
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methodological
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null
evidence array · 2 items
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source:pmid:31649645
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sections[21] "Protein Cargo of OMV in Different Stress Conditions" paragraph 2
quote
Multiple sample test (ANOVA) was used to compare the differences among all cultivation conditions.
[1] object · 3 fields
asset
source:pmid:31649645
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sections[12] "Proteomic Analysis" paragraph 3
quote
The MS proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE (Perez-Riverol et al., 2019) partner repository with the dataset identifier PXD013074.
state
complete
[1] object · 6 fields
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claim-data-access
statement
The datasets generated for this study can be found in the ProteomeXchange, PXD013074.
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methodological
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null
evidence array · 1 item
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sections[23] "Data Availability Statement" paragraph 2
quote
The datasets generated for this study can be found in the ProteomeXchange, PXD013074.
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complete
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experiment object · 8 fields
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complete
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null
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read_published_estimate
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1
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Read the published estimate from the source
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null
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The claim, method and evidence span published with the source article.
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[0]
source:pmid:31649645
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the published estimate and its evidence
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obtain_source_data
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Obtain the source data from the named repository
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The GEO series accession resolves and its sample accessions are listed. This lane did not download the dataset or read its licence.
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data:geo:PXD013074
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the source data with its repository provenance
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Run the published analysis
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Apply the paper's statistical method to the resolved series and compare the result with the published target.
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data:geo:PXD013074
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the replicated result and its comparison
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source:pmid:31649645
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https://doi.org/10.3389/fmicb.2019.02304
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10.3389/fmicb.2019.02304
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Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.
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PMC6795709
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europe_pmc_fulltext
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whole_body_without_references
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data:geo:PXD013074
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=PXD013074
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The datasets generated for this study can be found in the ProteomeXchange, PXD013074.
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GEO
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GEO accession URL
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The datasets generated for this study can be found in the ProteomeXchange, PXD013074.
access_statement_kind
data_availability_statement
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sample_count
null
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null
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null
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title
Proteomic characterization and label-free comparison of outer membrane vesicles from Francisella tularensis subsp. holarctica strain FSC200 isolated from different cultivation conditions
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2026-10-31T18:35:55Z
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identifier_resolution_only_no_download_no_licence_read
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Cultivation conditions and stress treatments summary.
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pmcid
PMC6795709
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5
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Temperature and pH Stress
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TABLE 1
caption
Cultivation conditions and stress treatments summary.
rows array · 14 items
[0] array · 6 items
[0]
Condition
[1]
Time of harvest (h)
[2]
OMV quantification
[3]
OMV isolation for TEM
[4]
SEM of bacteria
[5]
Proteomic comparison
[1] array · 7 items
[0]
Untreateda
[1]
37°C, pH 6.8
[2]
16
[3]
Yes
[4]
Yes
[5]
Yes
[6]
Yes
[2] array · 7 items
[0]
High temperature
[1]
42°C
[2]
16
[3]
Yes
[4]
Yes
[5]
Yes
[6]
Yes
[3] array · 7 items
[0]
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[1]
25°C
[2]
16/40
[3]
Yes/yes
[4]
Yes/no
[5]
Yes/no
[6]
Yes/no
[4] array · 7 items
[0]
pH
[1]
7.4
[2]
16
[3]
Yes
[4]
No
[5]
No
[6]
No
[5] array · 7 items
[0]
[1]
6.3
[2]
16
[3]
Yes
[4]
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[5]
No
[6]
No
[6] array · 7 items
[0]
[1]
5.8
[2]
16
[3]
Yes
[4]
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[5]
No
[6]
No
[7] array · 7 items
[0]
[1]
5.3
[2]
16/40b
[3]
Yes/yes
[4]
Yes/no
[5]
Yes/no
[6]
Yes/no
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[0]
[1]
4.8
[2]
16
[3]
No
[4]
No
[5]
No
[6]
No
[9] array · 7 items
[0]
[1]
4.3
[2]
16
[3]
No
[4]
No
[5]
No
[6]
No
[10] array · 7 items
[0]
Oxidative stress
[1]
5 mM H2O2
[2]
12 h of standard cultivation, 4 h of treatment
[3]
Yes
[4]
No
[5]
No
[6]
No
[11] array · 7 items
[0]
[1]
10mM H2O2
[2]
[3]
Yes
[4]
Yes
[5]
Yes
[6]
Yes
[12] array · 7 items
[0]
[1]
50mM H2O2
[2]
[3]
Noc
[4]
No
[5]
No
[6]
No
[13] array · 7 items
[0]
Agar plate
[1]
McLeod
[2]
24
[3]
No
[4]
Yes
[5]
Yes
[6]
Yes
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section[5]/table-wrap[1]#T1
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Proteins enriched in OMV in comparison with the membrane fraction, only proteins with enrichment factor >20 are shown.
structure object · 5 fields
pmcid
PMC6795709
section_index
15
section_title
Protein Characterization of OMV
row_count
29
column_count
6
table object · 8 fields
label
TABLE 2
caption
Proteins enriched in OMV in comparison with the membrane fraction, only proteins with enrichment factor >20 are shown.
rows array · 29 items
[0] array · 6 items
[0]
Protein name
[1]
Gene name
[2]
FTS locus tag
[3]
FTT locus tag
[4]
FTL locus tag
[5]
Enrichmenta
[1] array · 6 items
[0]
Outer membrane protein of unknown function
[1]
[2]
FTS_0008
[3]
FTT_1747
[4]
FTL_0009
[5]
424.2
[2] array · 6 items
[0]
Outer membrane protein OmpH
[1]
ompH
[2]
FTS_0538
[3]
FTT_1572c
[4]
FTL_0536
[5]
254.3
[3] array · 6 items
[0]
Hypothetical protein FTS_1462
[1]
[2]
FTS_1462
[3]
FTT_1334c
[4]
FTL_1494
[5]
246.4
[4] array · 6 items
[0]
Hypothetical protein FTS_1201
[1]
[2]
FTS_1201
[3]
FTT_0975
[4]
FTL_1225
[5]
126.9
[5] array · 6 items
[0]
Hypothetical protein FTS_1538
[1]
[2]
FTS_1538
[3]
FTT_0484
[4]
FTL_1579
[5]
126.5
[6] array · 6 items
[0]
Hypothetical protein FTS_0495
[1]
[2]
FTS_0495
[3]
FTT_0423
[4]
FTL_0493
[5]
102.0
[7] array · 6 items
[0]
Hypothetical protein FTS_0572
[1]
[2]
FTS_0572
[3]
FTT_1538c
[4]
FTL_0573
[5]
101.6
[8] array · 6 items
[0]
Hypothetical protein FTS_0814
[1]
[2]
FTS_0814
[3]
FTT_1137c
[4]
FTL_0822
[5]
73.0
[9] array · 6 items
[0]
Chitinase family 18 protein
[1]
[2]
FTS_1485
[3]
FTT_0715
[4]
FTL_1521
[5]
69.8
[10] array · 6 items
[0]
Hypothetical protein FTS_0402
[1]
[2]
FTS_0402
[3]
FTT_1303c
[4]
FTL_0411
[5]
60.9
[11] array · 6 items
[0]
Peroxidase/catalase
[1]
katG
[2]
FTS_1471
[3]
FTT_0721c
[4]
FTL_1504
[5]
56.7
[12] array · 6 items
[0]
Histidine acid phosphatase
[1]
[2]
FTS_0029
[3]
–
[4]
FTL_0031
[5]
56.5
[13] array · 6 items
[0]
Beta-lactamase class A
[1]
bla
[2]
FTS_0870
[3]
FTT_0611c
[4]
FTL_0879
[5]
48.9
[14] array · 6 items
[0]
Hypothetical protein FTS_1681
[1]
[2]
FTS_1681
[3]
FTT_0165c
[4]
FTL_1724
[5]
44.8
[15] array · 6 items
[0]
Hypothetical protein FTS_0755
[1]
[2]
FTS_0755
[3]
–
[4]
FTL_0755
[5]
38.4
[16] array · 6 items
[0]
Gamma-glutamyltranspeptidase
[1]
ggt
[2]
FTS_0764
[3]
FTT_1181c
[4]
FTL_0766
[5]
37.6
[17] array · 6 items
[0]
Rhodanese-like family protein
[1]
[2]
FTS_0824
[3]
FTT_1127
[4]
FTL_0834
[5]
35.5
[18] array · 6 items
[0]
Pyrrolidone carboxylylate peptidase
[1]
pcp
[2]
FTS_0203
[3]
FTT_0296
[4]
FTL_0207
[5]
35.5
[19] array · 6 items
[0]
Hypothetical protein FTS_1495
[1]
[2]
FTS_1495
[3]
FTT_0704
[4]
FTL_1532
[5]
35.3
[20] array · 6 items
[0]
Hypothetical protein FTS_1272
[1]
[2]
FTS_1272
[3]
FTT_0364c
[4]
FTL_1299
[5]
34.1
[21] array · 6 items
[0]
DNA topoisomerase I
[1]
topA
[2]
FTS_0417
[3]
FTT_0906c
[4]
FTL_0426
[5]
26.7
[22] array · 6 items
[0]
Protein-disulfide isomerase
[1]
[2]
FTS_1514
[3]
FTT_0507
[4]
FTL_1550
[5]
25.2
[23] array · 6 items
[0]
Exodeoxyribonuclease VII large subunit
[1]
xseA
[2]
FTS_0754
[3]
FTT_1190c
[4]
FTL_0754
[5]
24.5
[24] array · 6 items
[0]
Hypothetical protein FTS_0815
[1]
[2]
FTS_0815
[3]
FTT_1136c
[4]
FTL_0823
[5]
23.5
[25] array · 6 items
[0]
Hypothetical protein FTS_0974
[1]
[2]
FTS_0974
[3]
FTT_0540c
[4]
FTL_0994
[5]
23.4
[26] array · 6 items
[0]
Single-strand DNA-binding protein
[1]
ssb
[2]
FTS_0013
[3]
FTT_1752
[4]
FTL_0014
[5]
23.4
[27] array · 6 items
[0]
Outer membrane lipoprotein
[1]
[2]
FTS_1885
[3]
FTT_0211c
[4]
FTL_1939
[5]
21.9
[28] array · 6 items
[0]
Hypothetical protein FTS_0065
[1]
[2]
FTS_0065
[3]
FTT_1676
[4]
FTL_0073
[5]
20.4
locator
section[15]/table-wrap[1]#T2
gaps array · 2 items
[0]
asset:data:geo:PXD013074 not downloaded
[1]
asset:data:geo:PXD013074 licence not read
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state
complete
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method-1
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group_comparison
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[0]
group_summary
[1]
welch_t
[2]
bootstrap_mean_difference
[3]
group_comparison_anova
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[0]
two_or_more_groups_continuous
evidence object · 3 fields
score
1
band
reordered
quote
Multiple sample test (ANOVA) was used to compare the differences among all cultivation conditions. The MS proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE (Perez-Riverol et al., 2019) partner repository with the dataset identifier PXD013074.
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complete
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capability:computational_analysis
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[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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complete
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R1
blocked_on
nothing:replicable_now
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method object · 5 fields
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R1
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true
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[0]
group_summary
[1]
welch_t
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bootstrap_mean_difference
[3]
group_comparison_anova
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basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: anova.
capability object · 4 fields
tier
R1
capability_id
capability:computational_analysis
availability_state
owned
basis
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
R1
reachable
true
accessions array · 1 item
[0]
PXD013074
resolved_accessions array · 1 item
[0]
PXD013074
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[0]
The datasets generated for this study can be found in the ProteomeXchange, PXD013074.
basis
The paper names PXD013074 in ProteomeXchange Consortium and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
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[0]
group_summary
[1]
welch_t
[2]
bootstrap_mean_difference
[3]
group_comparison_anova
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[0]
source:pmid:31649645
[1]
data:geo:PXD013074
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asset:table:pmid:31649645:1
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asset:table:pmid:31649645:2
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run_analysis
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data:geo:PXD013074
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MiniMax-M3.1-Flash
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minimax
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minimax
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2026-10-31T18:16:33Z
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single_reader
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extraction
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minimax
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pmid:31649645
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paper
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pmid:31649645
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source:pmid:31649645
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PMID 31649645 full text
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data:geo:PXD013074
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GEO PXD013074
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pmid:31649645
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pmid:31649645
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PMID 31649645 full text
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data:geo:PXD013074
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GEO PXD013074
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agent:corpus-assay-engine
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source:pmid:31649645
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agent:minimax-reader
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activity-resolve-PXD013074
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data:geo:PXD013074
agent
agent:corpus-assay-engine
agents array · 2 items
[0] object · 3 fields
id
agent:corpus-assay-engine
type
software
label
Corpus assay engine
[1] object · 3 fields
id
agent:minimax-reader
type
software
label
MiniMax literature reader
source_run_id
reading-sci-2026-11-01
dsl_catalogue_fingerprint
343fb30756ba6ec3
capability_table_fingerprint
2cb3e42f047d2ecf
snapshot_id
ba34b49490d9bfaf
lineage object · 4 fields
parent_id
pmid:31649645
parent_hash
sha256:c7c439e92911a84dc99a192dc49aa8d13b2b0e3992298b55325b88f7be981ccb
fork_of
null
gaps array · 6 items
[0]
asset:data:geo:PXD013074 licence not read
[1]
asset:data:geo:PXD013074 not downloaded
[2]
execution.not_run
[3]
review.human_critique
[4]
review.independent_reader
[5]
review.machine_critique
assays array · 2 items
[0] object · 11 fields
role
data_generation
definition_version
99e1195c7d6f
required_operations array · 0 items
support_state
partial
source_hashes object · 1 field
assay_lexicon
99e1195c7d6f
confidence
0.85
evidence array · 1 item
[0]
oaded with a number of virulence factors and immunoreactive proteins. In the present study, the vesicles
order_basis
paper_text_order:324
id
assay:1
[1] object · 11 fields
role
analysis
definition_id
group_comparison
definition_version
f2132e96ae6c7a4e
required_operations array · 4 items
[0]
group_summary
[1]
welch_t
[2]
bootstrap_mean_difference
[3]
group_comparison_anova
support_state
supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
Multiple sample test (ANOVA) was used to compare the differences among all cultivation conditions. The MS proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE (Perez-Riverol et al., 2019) partner repository with the dataset identifier PXD013074.
order_basis
consumes_earlier_output
id
assay:2
Complete file
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It secretes unusually shaped nanotubular outer membrane vesicles (OMV) loaded with a number of virulence factors and immunoreactive proteins. In the present study, the vesicles were purified from a clinical isolate of subsp. holarctica strain FSC200. We here provide a comprehensive proteomic characterization of OMV using a novel approach in which a comparison of OMV and membrane fraction is performed in order to find proteins selectively enriched in OMV vs. membrane. Only these proteins were further considered to be really involved in the OMV function and/or their exceptional structure. OMV were also isolated from bacteria cultured under various cultivation conditions simulating the diverse environments of F. tularensis life cycle. These included conditions mimicking the milieu inside the mammalian host during inflammation: oxidative stress, low pH, and high temperature (42°C); and in contrast, low temperature (25°C). We observed several-fold increase in vesiculation rate and significant protein cargo changes for high temperature and low pH. Further proteomic characterization of stress-derived OMV gave us an insight how the bacterium responds to the hostile environment of a mammalian host through the release of differentially loaded OMV. Among the proteins preferentially and selectively packed into OMV during stressful cultivations, the previously described virulence factors connected to the unique intracellular trafficking of Francisella were detected. Considerable changes were also observed in a number of proteins involved in the biosynthesis and metabolism of the bacterial envelope components like O-antigen, lipid A, phospholipids, and fatty acids. Data are available via ProteomeXchange with identifier PXD013074.", "claims": [{"id": "claim-method", "statement": "Multiple sample test (ANOVA) was used to compare the differences among all cultivation conditions. 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