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  1. Article: Triacylglycerols and Polar Lipids in Cow and Goat Milk are Differentially Affected by Various Lipid Supplemented Diets

    Fougère, Hélène / Delavaud, Carole / Le Faouder, Pauline / Bertrand‐Michel, Justine / Bernard, Laurence

    European journal of lipid science and technology. 2021 Oct., v. 123, no. 10

    2021  

    Abstract: This study characterizes milk triacylglycerol (TAG) and polar lipid (PL) fractions from cows and goats fed various lipid supplements modulating milk fat content. Twelve Holstein cows and 12 Alpine goats, at 86 ± 24.9 and 61 ± 1.8 days in milk, ... ...

    Abstract This study characterizes milk triacylglycerol (TAG) and polar lipid (PL) fractions from cows and goats fed various lipid supplements modulating milk fat content. Twelve Holstein cows and 12 Alpine goats, at 86 ± 24.9 and 61 ± 1.8 days in milk, respectively, are allocated to one of 4 groups to receive diets supplemented with either corn oil [5% dry matter intake (DMI)] plus wheat starch (COS), marine algae powder (MAP; 1.5% DMI) or hydrogenated palm oil (HPO; 3% DMI), or a no‐added‐lipid control diet (CTL), according to a 4 × 4 Latin square design with 28 d experimental periods. Milk TAG and PL contents are determined by liquid chromatography‐mass spectrometry (LC‐MS). Multivariate analysis and ANOVA demonstrate major between‐species differences in diet effects. In cows, COS specifically increases TAG 54:3 and 54:4 associated with milk fat depression (MFD), and increases the sum of phosphatidylcholines (PC) and phosphatidylinositols (PI). In addition to causing a MFD, MAP diet increases long‐chain polyunsaturated TAG in both species, with higher magnitude in cows than in goats, and decreases the sum of PI in goats. HPO increases TAG 52:1 and the sum of PI in cows, but not in goats. Practical applications: Feed strategies can quickly and efficiently modulate the ruminant milk fat production and composition to improve nutritional quality for consumers. Certain starch‐rich diets supplemented with polyunsaturated fatty acids (PUFA)‐rich vegetable oils and diets supplemented with marine products (long‐chain PUFA) reduce milk fat secretion and modify the milk fatty acid (FA) profile in cows, but not—or less so—in goats. Advanced analysis of both the TAG and PL fractions of milk fat is required to unravel these differences in lipid metabolism between cows and goats fed various lipid‐supplemented diets. This study brings new insight on using nutritional strategies to control milk lipid composition according to ruminant species.
    Keywords Holstein ; corn oil ; cows ; dry matter intake ; goat milk ; lipid content ; lipid metabolism ; liquid chromatography ; mass spectrometry ; milk ; milk fat yield ; milk fatty acids ; multivariate analysis ; nutritive value ; palm oils ; phosphatidylcholines ; phosphatidylinositols ; secretion ; technology ; triacylglycerols ; vegetables ; wheat starch
    Language English
    Dates of publication 2021-10
    Publishing place John Wiley & Sons, Ltd
    Document type Article
    Note JOURNAL ARTICLE
    ZDB-ID 2003265-1
    ISSN 1438-7697
    ISSN 1438-7697
    DOI 10.1002/ejlt.202100009
    Database NAL-Catalogue (AGRICOLA)

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  2. Article ; Online: Enriched PUFA environment of Leishmania infantum promastigotes promotes the accumulation of lipid mediators and favors parasite infectivity towards J774 murine macrophages

    Leroux, Marine / Bouazizi‐Ben Messaoud, Hana / Luquain‐Costaz, Céline / Jordheim, Lars P. / Le Faouder, Pauline / Gustin, Marie‐Paule / Aoun, Karim / Lawton, Philippe / Azzouz‐Maache, Samira / Delton, Isabelle

    Lipids. 2023 Mar., v. 58, no. 2 p.81-92

    2023  

    Abstract: Leishmania parasites are the causative agents of visceral or cutaneous leishmaniasis in humans and of canine leishmaniosis. The macrophage is the predilected host cell of Leishmania in which the promastigote stage is transformed into amastigote. We ... ...

    Abstract Leishmania parasites are the causative agents of visceral or cutaneous leishmaniasis in humans and of canine leishmaniosis. The macrophage is the predilected host cell of Leishmania in which the promastigote stage is transformed into amastigote. We previously showed changes in the fatty acid composition (FA) of lipids in two strains of Leishmania donovani upon differentiation of promastigote to amastigote, including increased proportions of arachidonic acid (AA) and to a less extent of docosahexaenoic acid (DHA). Here, we carried out supplementation with AA or DHA on two Leishmania infantum strains, a visceral (MON‐1) and a cutaneous (MON‐24), to evaluate the role of these FA in parasite/macrophage interactions. The proportions of AA or DHA in total lipids were significantly increased in promastigotes cultured in AA‐ or DHA‐supplemented media compared to controls. The content of FA‐derived oxygenated metabolites was enhanced in supplemented strains, generating especially epoxyeicosatrienoic acids (11,12‐ and 14,15‐EET) and hydroxyeicosatetraenoic acids (5‐ and 8‐ HETE) from AA, and hydroxydocosahexaenoic acids (14‐ and 17‐HDoHE) from DHA. For both MON‐1 and MON‐24, AA‐supplemented promastigotes showed higher infectivity towards J774 macrophages as evidenced by higher intracellular amastigote numbers. Higher infectivity was observed after DHA supplementation for MON‐24 but not MON‐1 strain. ROS production by macrophages increased upon parasite infection, but only minor change was observed between control and supplemented parasites. We propose that under high AA or DHA environment that is associated with AA or DHA enrichment of promastigote lipids, FA derivatives can accumulate in the parasite, thereby modulating parasite infectivity towards host macrophages.
    Keywords Leishmania donovani ; Leishmania infantum ; arachidonic acid ; cutaneous leishmaniasis ; docosahexaenoic acid ; dogs ; fatty acid composition ; macrophages ; metabolites ; mice ; parasites ; pathogenicity ; promastigotes
    Language English
    Dates of publication 2023-03
    Size p. 81-92.
    Publishing place John Wiley & Sons, Inc.
    Document type Article ; Online
    Note JOURNAL ARTICLE
    ZDB-ID 241539-2
    ISSN 1558-9307 ; 0024-4201
    ISSN (online) 1558-9307
    ISSN 0024-4201
    DOI 10.1002/lipd.12365
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  3. Article ; Online: Dysosmobacter welbionis effects on glucose, lipid, and energy metabolism are associated with specific bioactive lipids.

    Moens de Hase, Emilie / Petitfils, Camille / Alhouayek, Mireille / Depommier, Clara / Le Faouder, Pauline / Delzenne, Nathalie M / Van Hul, Matthias / Muccioli, Giulio G / Cenac, Nicolas / Cani, Patrice D

    Journal of lipid research

    2023  Volume 64, Issue 10, Page(s) 100437

    Abstract: The newly identified bacterium Dysosmobacter welbionis ... ...

    Abstract The newly identified bacterium Dysosmobacter welbionis J115
    Language English
    Publishing date 2023-08-28
    Publishing country United States
    Document type Journal Article
    ZDB-ID 80154-9
    ISSN 1539-7262 ; 0022-2275
    ISSN (online) 1539-7262
    ISSN 0022-2275
    DOI 10.1016/j.jlr.2023.100437
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  4. Article ; Online: Integrated analysis of whole blood oxylipin and cytokine responses after bacterial, viral, and T cell stimulation reveals new immune networks.

    Villain, Etienne / Chanson, Aurélie / Mainka, Malwina / Kampschulte, Nadja / Le Faouder, Pauline / Bertrand-Michel, Justine / Brandolini-Bulon, Marion / Charbit, Bruno / Musvosvi, Munyaradzi / Bilek, Nicole / Scriba, Thomas J / Quintana-Murci, Lluis / Schebb, Nils Helge / Duffy, Darragh / Gladine, Cécile

    iScience

    2023  Volume 26, Issue 8, Page(s) 107422

    Abstract: Oxylipins are major immunomodulating mediators, yet studies of inflammation focus mainly on cytokines. Here, using a standardized whole-blood stimulation system, we characterized the oxylipin-driven inflammatory responses to various stimuli and their ... ...

    Abstract Oxylipins are major immunomodulating mediators, yet studies of inflammation focus mainly on cytokines. Here, using a standardized whole-blood stimulation system, we characterized the oxylipin-driven inflammatory responses to various stimuli and their relationships with cytokine responses. We performed a pilot study in 25 healthy individuals using 6 different stimuli: 2 bacterial stimuli (LPS and live BCG), 2 viral stimuli (vaccine-grade poly I:C and live H1N1 attenuated influenza), an enterotoxin superantigen and a Null control. All stimuli induced a strong production of oxylipins but most importantly, bacterial, viral, and T cell immune responses show distinct oxylipin signatures. Integration of the oxylipin and cytokine responses for each condition revealed new immune networks improving our understanding of inflammation regulation. Finally, the oxylipin responses and oxylipin-cytokine networks were compared in patients with active tuberculosis or with latent infection. This revealed different responses to BCG but not LPS stimulation highlighting new regulatory pathways for further investigations.
    Language English
    Publishing date 2023-07-18
    Publishing country United States
    Document type Journal Article
    ISSN 2589-0042
    ISSN (online) 2589-0042
    DOI 10.1016/j.isci.2023.107422
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Enriched PUFA environment of Leishmania infantum promastigotes promotes the accumulation of lipid mediators and favors parasite infectivity towards J774 murine macrophages.

    Leroux, Marine / Bouazizi-Ben Messaoud, Hana / Luquain-Costaz, Céline / Jordheim, Lars P / Le Faouder, Pauline / Gustin, Marie-Paule / Aoun, Karim / Lawton, Philippe / Azzouz-Maache, Samira / Delton, Isabelle

    Lipids

    2022  Volume 58, Issue 2, Page(s) 81–92

    Abstract: Leishmania parasites are the causative agents of visceral or cutaneous leishmaniasis in humans and of canine leishmaniosis. The macrophage is the predilected host cell of Leishmania in which the promastigote stage is transformed into amastigote. We ... ...

    Abstract Leishmania parasites are the causative agents of visceral or cutaneous leishmaniasis in humans and of canine leishmaniosis. The macrophage is the predilected host cell of Leishmania in which the promastigote stage is transformed into amastigote. We previously showed changes in the fatty acid composition (FA) of lipids in two strains of Leishmania donovani upon differentiation of promastigote to amastigote, including increased proportions of arachidonic acid (AA) and to a less extent of docosahexaenoic acid (DHA). Here, we carried out supplementation with AA or DHA on two Leishmania infantum strains, a visceral (MON-1) and a cutaneous (MON-24), to evaluate the role of these FA in parasite/macrophage interactions. The proportions of AA or DHA in total lipids were significantly increased in promastigotes cultured in AA- or DHA-supplemented media compared to controls. The content of FA-derived oxygenated metabolites was enhanced in supplemented strains, generating especially epoxyeicosatrienoic acids (11,12- and 14,15-EET) and hydroxyeicosatetraenoic acids (5- and 8- HETE) from AA, and hydroxydocosahexaenoic acids (14- and 17-HDoHE) from DHA. For both MON-1 and MON-24, AA-supplemented promastigotes showed higher infectivity towards J774 macrophages as evidenced by higher intracellular amastigote numbers. Higher infectivity was observed after DHA supplementation for MON-24 but not MON-1 strain. ROS production by macrophages increased upon parasite infection, but only minor change was observed between control and supplemented parasites. We propose that under high AA or DHA environment that is associated with AA or DHA enrichment of promastigote lipids, FA derivatives can accumulate in the parasite, thereby modulating parasite infectivity towards host macrophages.
    MeSH term(s) Humans ; Mice ; Animals ; Dogs ; Leishmania infantum/metabolism ; Parasites ; Macrophages/parasitology ; Leishmaniasis, Cutaneous/parasitology ; Arachidonic Acid/pharmacology ; Arachidonic Acid/metabolism ; Leishmaniasis, Visceral/parasitology ; Mice, Inbred BALB C
    Chemical Substances Arachidonic Acid (27YG812J1I)
    Language English
    Publishing date 2022-12-21
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 241539-2
    ISSN 1558-9307 ; 0024-4201
    ISSN (online) 1558-9307
    ISSN 0024-4201
    DOI 10.1002/lipd.12365
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  6. Article: Untargeted Lipidomic Profiling of Dry Blood Spots Using SFC-HRMS.

    Le Faouder, Pauline / Soullier, Julia / Tremblay-Franco, Marie / Tournadre, Anthony / Martin, Jean-François / Guitton, Yann / Carlé, Caroline / Caspar-Bauguil, Sylvie / Denechaud, Pierre-Damien / Bertrand-Michel, Justine

    Metabolites

    2021  Volume 11, Issue 5

    Abstract: Lipids are essential cellular constituents that have many critical roles in physiological functions. They are notably involved in energy storage and cell signaling as second messengers, and they are major constituents of cell membranes, including lipid ... ...

    Abstract Lipids are essential cellular constituents that have many critical roles in physiological functions. They are notably involved in energy storage and cell signaling as second messengers, and they are major constituents of cell membranes, including lipid rafts. As a consequence, they are implicated in a large number of heterogeneous diseases, such as cancer, diabetes, neurological disorders, and inherited metabolic diseases. Due to the high structural diversity and complexity of lipid species, the presence of isomeric and isobaric lipid species, and their occurrence at a large concentration scale, a complete lipidomic profiling of biological matrices remains challenging, especially in clinical contexts. Using supercritical fluid chromatography coupled with high-resolution mass spectrometry, we have developed and validated an untargeted lipidomic approach to the profiling of plasma and blood. Moreover, we have tested the technique using the Dry Blood Spot (DBS) method and found that it allows for the easy collection of blood for analysis. To develop the method, we performed the optimization of the separation and detection of lipid species on pure standards, reference human plasma (SRM1950), whole blood, and DBS. These analyses allowed an in-house lipid data bank to be built. Using the MS-Dial software, we developed an automatic process for the relative quantification of around 500 lipids species belonging to the 6 main classes of lipids (including phospholipids, sphingolipids, free fatty acids, sterols, and fatty acyl-carnitines). Then, we compared the method using the published data for SRM 1950 and a mouse blood sample, along with another sample of the same blood collected using the DBS method. In this study, we provided a method for blood lipidomic profiling that can be used for the easy sampling of dry blood spots.
    Language English
    Publishing date 2021-05-11
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2662251-8
    ISSN 2218-1989
    ISSN 2218-1989
    DOI 10.3390/metabo11050305
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  7. Article ; Online: Discovery and quantification of lipoamino acids in bacteria.

    Hueber, Amandine / Petitfils, Camille / Le Faouder, Pauline / Langevin, Geoffrey / Guy, Alexandre / Galano, Jean-Marie / Durand, Thierry / Martin, Jean-François / Tabet, Jean-Claude / Cenac, Nicolas / Bertrand-Michel, Justine

    Analytica chimica acta

    2021  Volume 1193, Page(s) 339316

    Abstract: Improving knowledge about metabolites produced by the microbiota is a key point to understand its role in human health and disease. Among them, lipoamino acid (LpAA) containing asparagine and their derivatives are bacterial metabolites which could have ... ...

    Abstract Improving knowledge about metabolites produced by the microbiota is a key point to understand its role in human health and disease. Among them, lipoamino acid (LpAA) containing asparagine and their derivatives are bacterial metabolites which could have an impact on the host. In this study, our aim was to extend the characterization of this family. We developed a semi-targeted workflow to identify and quantify new candidates. First, the sample preparation and analytical conditions using liquid chromatography (LC) coupled to high resolution mass spectrometry (HRMS) were optimized. Using a theoretical homemade database, HRMS raw data were manually queried. This strategy allowed us to find 25 new LpAA conjugated to Asn, Gln, Asp, Glu, His, Leu, Ile, Lys, Phe, Trp and Val amino acids. These metabolites were then fully characterized by MS
    MeSH term(s) Amino Acid Sequence ; Escherichia coli ; Humans ; Mass Spectrometry ; Peptide Fragments ; Trypsin
    Chemical Substances Peptide Fragments ; Trypsin (EC 3.4.21.4)
    Language English
    Publishing date 2021-11-24
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 1483436-4
    ISSN 1873-4324 ; 0003-2670
    ISSN (online) 1873-4324
    ISSN 0003-2670
    DOI 10.1016/j.aca.2021.339316
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  8. Article ; Online: Heteroleptic Ruthenium(II) Complexes with Bathophenanthroline and Bathophenanthroline Disulfonate Disodium Salt as Fluorescent Dyes for In-Gel Protein Staining.

    Babak, Maria V / Le Faouder, Pauline / Trivelli, Xavier / Venkatesan, Gopalakrishnan / Bezzubov, Stanislav I / Kajjout, Mohammed / Gushchin, Artem L / Hanif, Muhammad / Poizat, Olivier / Vezin, Hervé / Rolando, Christian

    Inorganic chemistry

    2020  Volume 59, Issue 7, Page(s) 4527–4535

    Abstract: The in-gel detection of proteins for various proteomic experiments is commonly done with the fluorescent ... ...

    Abstract The in-gel detection of proteins for various proteomic experiments is commonly done with the fluorescent Ru
    MeSH term(s) Cell Line, Tumor ; Coordination Complexes/chemical synthesis ; Coordination Complexes/chemistry ; Electrophoresis, Polyacrylamide Gel/methods ; Fluorescent Dyes/chemical synthesis ; Fluorescent Dyes/chemistry ; Humans ; Phenanthrolines/chemical synthesis ; Phenanthrolines/chemistry ; Proteins/analysis ; Proteins/chemistry ; Ruthenium/chemistry ; Staining and Labeling/methods
    Chemical Substances Coordination Complexes ; Fluorescent Dyes ; Phenanthrolines ; Proteins ; bathophenanthroline disulfonic acid (28061-20-3) ; bathophenanthroline (4A2B091F0G) ; Ruthenium (7UI0TKC3U5)
    Language English
    Publishing date 2020-03-17
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1484438-2
    ISSN 1520-510X ; 0020-1669
    ISSN (online) 1520-510X
    ISSN 0020-1669
    DOI 10.1021/acs.inorgchem.9b03679
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  9. Article ; Online: Uropathogenic E. coli induces DNA damage in the bladder.

    Chagneau, Camille V / Massip, Clémence / Bossuet-Greif, Nadège / Fremez, Christophe / Motta, Jean-Paul / Shima, Ayaka / Besson, Céline / Le Faouder, Pauline / Cénac, Nicolas / Roth, Marie-Paule / Coppin, Hélène / Fontanié, Maxime / Martin, Patricia / Nougayrède, Jean-Philippe / Oswald, Eric

    PLoS pathogens

    2021  Volume 17, Issue 2, Page(s) e1009310

    Abstract: Urinary tract infections (UTIs) are among the most common outpatient infections, with a lifetime incidence of around 60% in women. We analysed urine samples from 223 patients with community-acquired UTIs and report the presence of the cleavage product ... ...

    Abstract Urinary tract infections (UTIs) are among the most common outpatient infections, with a lifetime incidence of around 60% in women. We analysed urine samples from 223 patients with community-acquired UTIs and report the presence of the cleavage product released during the synthesis of colibactin, a bacterial genotoxin, in 55 of the samples examined. Uropathogenic Escherichia coli strains isolated from these patients, as well as the archetypal E. coli strain UTI89, were found to produce colibactin. In a murine model of UTI, the machinery producing colibactin was expressed during the early hours of the infection, when intracellular bacterial communities form. We observed extensive DNA damage both in umbrella and bladder progenitor cells. To the best of our knowledge this is the first report of colibactin production in UTIs in humans and its genotoxicity in bladder cells.
    MeSH term(s) Aged ; Animals ; DNA Damage ; Escherichia coli Infections/genetics ; Escherichia coli Infections/microbiology ; Escherichia coli Infections/pathology ; Female ; Humans ; Male ; Mice ; Mice, Inbred C3H ; Mutagens/metabolism ; Peptides/metabolism ; Polyketides/metabolism ; Urinary Bladder/metabolism ; Urinary Bladder/microbiology ; Urinary Bladder/pathology ; Urinary Tract Infections/genetics ; Urinary Tract Infections/microbiology ; Urinary Tract Infections/pathology ; Uropathogenic Escherichia coli/isolation & purification
    Chemical Substances Mutagens ; Peptides ; Polyketides ; colibactin
    Language English
    Publishing date 2021-02-25
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2205412-1
    ISSN 1553-7374 ; 1553-7374
    ISSN (online) 1553-7374
    ISSN 1553-7374
    DOI 10.1371/journal.ppat.1009310
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: A novel jaspine B-ceramide hybrid modulates sphingolipid metabolism.

    Garcia, Virginie / Le Faouder, Pauline / Dupuy, Aude / Levade, Thierry / Ballereau, Stéphanie / Génisson, Yves

    Chemistry & biodiversity

    2015  Volume 12, Issue 7, Page(s) 1115–1125

    Abstract: A new sphingolipid hybrid molecule was designed to assemble, within a tail-to-tail double-chain structure, the ceramide hydrophilic moiety and the tetrahydrofuran pharmacophore of jaspine B, a natural product known to interfere with sphingolipid ... ...

    Abstract A new sphingolipid hybrid molecule was designed to assemble, within a tail-to-tail double-chain structure, the ceramide hydrophilic moiety and the tetrahydrofuran pharmacophore of jaspine B, a natural product known to interfere with sphingolipid metabolism. This compound was prepared through acylation of sphingosine with a jaspine B derivative bearing a COOH group in the terminal position of the aliphatic backbone. This new hybrid molecule was evaluated for its capacities to affect melanoma cell viability and sphingolipid metabolism. While retaining the cytotoxicity of ceramide itself, this compound was shown to lower the sphingomyelin cellular levels and significantly enhance the production of sphingosine-1-phosphate, thus representing a novel sphingolipid metabolism modulator.
    MeSH term(s) Animals ; Biological Products/chemistry ; Biological Products/metabolism ; Biological Products/pharmacology ; Cell Line, Tumor ; Cell Survival/drug effects ; Ceramides/chemistry ; Ceramides/metabolism ; Ceramides/pharmacology ; Dose-Response Relationship, Drug ; Humans ; Mice ; Molecular Conformation ; Sphingolipids/chemistry ; Sphingolipids/metabolism ; Sphingosine/analogs & derivatives ; Sphingosine/chemistry ; Sphingosine/metabolism ; Sphingosine/pharmacology ; Structure-Activity Relationship
    Chemical Substances Biological Products ; Ceramides ; Sphingolipids ; pachastrissamine ; Sphingosine (NGZ37HRE42)
    Language English
    Publishing date 2015-07
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2139001-0
    ISSN 1612-1880 ; 1612-1872
    ISSN (online) 1612-1880
    ISSN 1612-1872
    DOI 10.1002/cbdv.201400357
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