<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-13T00:08:50Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:20.500.12327/876" metadataPrefix="marc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:20.500.12327/876</identifier><datestamp>2025-10-22T11:18:56Z</datestamp><setSpec>com_2072_4428</setSpec><setSpec>com_2072_4427</setSpec><setSpec>col_2072_487898</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Parés, Sílvia</subfield>
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      <subfield code="a">Fàbregas, Francesc</subfield>
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      <subfield code="a">Bach, Àlex</subfield>
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      <subfield code="a">Garcia-Fruitos, Elena</subfield>
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      <subfield code="a">de Prado, Ana</subfield>
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      <subfield code="a">Alomar, Oscar</subfield>
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      <subfield code="c">2020-02-11</subfield>
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      <subfield code="a">Mammary serum amyloid A3 (M-SAA3) has shown potential in stimulating innate immunity during intramammary infections, at calving and at dryoff. In this study, we produced recombinant caprine M-SAA3 to test its ability to reduce intramammary infections with Staphylococcus aureus, Streptococcus uberis, Streptococcus dysgalactiae, and Escherichia coli, which are all common mastitis-producing pathogens. Recombinant production of M-SAA3 (followed by lipopolysaccharide removal to avoid lipopolysaccharide-nonspecific stimulation of the immune system) was successfully achieved. Mammary serum amyloid A3 stimulated the expression of IL-8 in a dose-dependent manner in primary mammary cultures. Although a direct killing effect on Staph. aureus by M-SAA3 was not detected, this acute phase protein was able to reduce Staph. aureus, Strep. uberis, and Strep. dysgalactiae infections by up to 50% and induced a reduction in E. coli counts of 67%. In general, the best concentration of caprine M-SAA3 for inhibiting infections was the lowest concentration tested (10 μg/mL), although higher concentrations (up to 160 μg/mL) increased its antimicrobial potential against some pathogens.</subfield>
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      <subfield code="a">Parés, Sílvia, Francesc Fàbregas, Àlex Bach, Elena Garcia-Fruitós, Ana de Prado, and Anna Arís. 2020. "Short Communication: Recombinant Mammary Serum Amyloid A3 As A Potential Strategy For Preventing Intramammary Infections In Dairy Cows At Dryoff". Journal Of Dairy Science 103 (4): 3615-3621. doi:10.3168/jds.2019-17276.</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12327/876</subfield>
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      <subfield code="a">https://doi.org/10.3168/jds.2019-17276</subfield>
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      <subfield code="a">Short communication: Recombinant mammary serum amyloid A3 as a potential strategy for preventing intramammary infections in dairy cows at dryoff</subfield>
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