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Evaluation of circulating immune cells, analytes, and inflammatory markers in sows affected with postpartum dysgalactia syndrome
Postpartum dysgalactia syndrome (PDS) is a condition affecting periparturient sows, characterized by a reduction in milk and colostrum synthesis shortly after farrowing. Insufficient milk production results in substantial economic losses due to increased piglet morbidity/mortality and premature sow...
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Published in: | Journal of animal science 2024-01, Vol.102 |
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creator | Studer, Jamie M Kiefer, Zoë E Koester, Lucas R Johnson, Erika M Schmitz-Esser, Stephan Farkas, Attila Galina Pantoja, Lucina Vonnahme, Kimberly A Greiner, Laura L Keating, Aileen F Baumgard, Lance H Ross, Jason W |
description | Postpartum dysgalactia syndrome (PDS) is a condition affecting periparturient sows, characterized by a reduction in milk and colostrum synthesis shortly after farrowing. Insufficient milk production results in substantial economic losses due to increased piglet morbidity/mortality and premature sow culling. Since PDS develops within a few days following farrowing, the study objectives were to determine if periparturient immune cell profiles and circulating biomarkers differ in sows affected by PDS. We hypothesized differences in immune cells, circulating analytes, and inflammatory markers would exist at farrowing in sows that subsequently developed PDS compared to healthy herd-mates. Thirty-six sows with PDS symptoms were matched by parity and day of lactation with 36 healthy control (CON) sows. Diagnosis of PDS (timepoint 2) occurred on average 9.25 ± 2.67 d after farrowing. Blood samples and litter weights were collected at farrowing (timepoint 1) and at the onset of clinical PDS (timepoint 2). Piglets from PDS sows had lower average daily gain and higher mortality than piglets from CON (P |
doi_str_mv | 10.1093/jas/skae270 |
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Insufficient milk production results in substantial economic losses due to increased piglet morbidity/mortality and premature sow culling. Since PDS develops within a few days following farrowing, the study objectives were to determine if periparturient immune cell profiles and circulating biomarkers differ in sows affected by PDS. We hypothesized differences in immune cells, circulating analytes, and inflammatory markers would exist at farrowing in sows that subsequently developed PDS compared to healthy herd-mates. Thirty-six sows with PDS symptoms were matched by parity and day of lactation with 36 healthy control (CON) sows. Diagnosis of PDS (timepoint 2) occurred on average 9.25 ± 2.67 d after farrowing. Blood samples and litter weights were collected at farrowing (timepoint 1) and at the onset of clinical PDS (timepoint 2). Piglets from PDS sows had lower average daily gain and higher mortality than piglets from CON (P < 0.01). Aspartate aminotransferase was increased (20%; P ≤ 0.06) in PDS sows compared to CON at both timepoints. Additionally, blood urea nitrogen was increased in PDS sows at timepoint 1 and timepoint 2 (13%; P = 0.08 and 16%; P = 0.01, respectively). At timepoint 2, total protein, globulin, magnesium, and cholesterol were increased (P ≤ 0.03) while γ-glutamyl transferase and albumin were decreased (P ≤ 0.02) in PDS sows. Lipopolysaccharide-binding protein, an inflammatory biomarker, was increased (48%; P = 0.07) at timepoint 2 in PDS compared to CON sows. Collectively, these data indicate PDS sows have altered metabolism and appear immune activated compared to healthy herd-mates, and further investigation is needed to determine if PDS can be predicted at farrowing.</description><identifier>ISSN: 0021-8812</identifier><identifier>ISSN: 1525-3163</identifier><identifier>EISSN: 1525-3163</identifier><identifier>DOI: 10.1093/jas/skae270</identifier><identifier>PMID: 39298285</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Animals ; Biomarkers - blood ; Colostrum - immunology ; Female ; Inflammation - blood ; Inflammation - veterinary ; Lactation ; Lactation and Mammary Gland Biology ; Lactation Disorders - blood ; Lactation Disorders - veterinary ; Milk - chemistry ; Postpartum Period ; Pregnancy ; Swine ; Swine Diseases - blood ; Swine Diseases - immunology</subject><ispartof>Journal of animal science, 2024-01, Vol.102</ispartof><rights>The Author(s) 2024. Published by Oxford University Press on behalf of the American Society of Animal Science.</rights><rights>The Author(s) 2024. Published by Oxford University Press on behalf of the American Society of Animal Science. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c233t-9d214ebc012879e5308f208bebceecfbe55a7f24447ad52a3c691451ace27563</cites><orcidid>0000-0002-3064-2384 ; 0000-0002-1907-0709 ; 0000-0003-1913-3383 ; 0000-0001-6597-009X ; 0000-0003-4950-2258</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11452653/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11452653/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39298285$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Studer, Jamie M</creatorcontrib><creatorcontrib>Kiefer, Zoë E</creatorcontrib><creatorcontrib>Koester, Lucas R</creatorcontrib><creatorcontrib>Johnson, Erika M</creatorcontrib><creatorcontrib>Schmitz-Esser, Stephan</creatorcontrib><creatorcontrib>Farkas, Attila</creatorcontrib><creatorcontrib>Galina Pantoja, Lucina</creatorcontrib><creatorcontrib>Vonnahme, Kimberly A</creatorcontrib><creatorcontrib>Greiner, Laura L</creatorcontrib><creatorcontrib>Keating, Aileen F</creatorcontrib><creatorcontrib>Baumgard, Lance H</creatorcontrib><creatorcontrib>Ross, Jason W</creatorcontrib><title>Evaluation of circulating immune cells, analytes, and inflammatory markers in sows affected with postpartum dysgalactia syndrome</title><title>Journal of animal science</title><addtitle>J Anim Sci</addtitle><description>Postpartum dysgalactia syndrome (PDS) is a condition affecting periparturient sows, characterized by a reduction in milk and colostrum synthesis shortly after farrowing. Insufficient milk production results in substantial economic losses due to increased piglet morbidity/mortality and premature sow culling. Since PDS develops within a few days following farrowing, the study objectives were to determine if periparturient immune cell profiles and circulating biomarkers differ in sows affected by PDS. We hypothesized differences in immune cells, circulating analytes, and inflammatory markers would exist at farrowing in sows that subsequently developed PDS compared to healthy herd-mates. Thirty-six sows with PDS symptoms were matched by parity and day of lactation with 36 healthy control (CON) sows. Diagnosis of PDS (timepoint 2) occurred on average 9.25 ± 2.67 d after farrowing. Blood samples and litter weights were collected at farrowing (timepoint 1) and at the onset of clinical PDS (timepoint 2). Piglets from PDS sows had lower average daily gain and higher mortality than piglets from CON (P < 0.01). Aspartate aminotransferase was increased (20%; P ≤ 0.06) in PDS sows compared to CON at both timepoints. Additionally, blood urea nitrogen was increased in PDS sows at timepoint 1 and timepoint 2 (13%; P = 0.08 and 16%; P = 0.01, respectively). At timepoint 2, total protein, globulin, magnesium, and cholesterol were increased (P ≤ 0.03) while γ-glutamyl transferase and albumin were decreased (P ≤ 0.02) in PDS sows. Lipopolysaccharide-binding protein, an inflammatory biomarker, was increased (48%; P = 0.07) at timepoint 2 in PDS compared to CON sows. Collectively, these data indicate PDS sows have altered metabolism and appear immune activated compared to healthy herd-mates, and further investigation is needed to determine if PDS can be predicted at farrowing.</description><subject>Animals</subject><subject>Biomarkers - blood</subject><subject>Colostrum - immunology</subject><subject>Female</subject><subject>Inflammation - blood</subject><subject>Inflammation - veterinary</subject><subject>Lactation</subject><subject>Lactation and Mammary Gland Biology</subject><subject>Lactation Disorders - blood</subject><subject>Lactation Disorders - veterinary</subject><subject>Milk - chemistry</subject><subject>Postpartum Period</subject><subject>Pregnancy</subject><subject>Swine</subject><subject>Swine Diseases - blood</subject><subject>Swine Diseases - immunology</subject><issn>0021-8812</issn><issn>1525-3163</issn><issn>1525-3163</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpVUU1P3DAQtaqisqU99V75WKkN-CPeJKcKIUqRkHrhbs06k8Xgj63tgHLrT6-BBbWnmXnz9ObjEfKJs2POBnlyC_kk3wGKjr0hK66EaiRfy7dkxZjgTd9zcUje53zLGBdqUO_IoRzE0Itercif83twMxQbA40TNTaZ2dUybKn1fg5IDTqXv1EI4JaCT9lIbZgceA8lpoV6SHeYcgVpjg-ZwjShKTjSB1tu6C7msoNUZk_HJW_BgSkWaF7CmKLHD-RgApfx4z4ekesf59dnP5urXxeXZ6dXjRFSlmYYBW9xY-oJfTegkqyfBOs3FUI00waVgm4Sbdt2MCoB0qwH3ioOpv5FreUR-f4su5s3HkeDoSRwepds3X7REaz-vxPsjd7Ge82rilgrWRW-7BVS_D1jLtrb_PgcCBjnrCVnHVeKMVapX5-pJsWcE06vczjTj57p6pnee1bZn_9d7ZX7YpL8CxMPmGk</recordid><startdate>20240103</startdate><enddate>20240103</enddate><creator>Studer, Jamie M</creator><creator>Kiefer, Zoë E</creator><creator>Koester, Lucas R</creator><creator>Johnson, Erika M</creator><creator>Schmitz-Esser, Stephan</creator><creator>Farkas, Attila</creator><creator>Galina Pantoja, Lucina</creator><creator>Vonnahme, Kimberly A</creator><creator>Greiner, Laura L</creator><creator>Keating, Aileen F</creator><creator>Baumgard, Lance H</creator><creator>Ross, Jason W</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-3064-2384</orcidid><orcidid>https://orcid.org/0000-0002-1907-0709</orcidid><orcidid>https://orcid.org/0000-0003-1913-3383</orcidid><orcidid>https://orcid.org/0000-0001-6597-009X</orcidid><orcidid>https://orcid.org/0000-0003-4950-2258</orcidid></search><sort><creationdate>20240103</creationdate><title>Evaluation of circulating immune cells, analytes, and inflammatory markers in sows affected with postpartum dysgalactia syndrome</title><author>Studer, Jamie M ; Kiefer, Zoë E ; Koester, Lucas R ; Johnson, Erika M ; Schmitz-Esser, Stephan ; Farkas, Attila ; Galina Pantoja, Lucina ; Vonnahme, Kimberly A ; Greiner, Laura L ; Keating, Aileen F ; Baumgard, Lance H ; Ross, Jason W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c233t-9d214ebc012879e5308f208bebceecfbe55a7f24447ad52a3c691451ace27563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>Biomarkers - blood</topic><topic>Colostrum - immunology</topic><topic>Female</topic><topic>Inflammation - blood</topic><topic>Inflammation - veterinary</topic><topic>Lactation</topic><topic>Lactation and Mammary Gland Biology</topic><topic>Lactation Disorders - blood</topic><topic>Lactation Disorders - veterinary</topic><topic>Milk - chemistry</topic><topic>Postpartum Period</topic><topic>Pregnancy</topic><topic>Swine</topic><topic>Swine Diseases - blood</topic><topic>Swine Diseases - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Studer, Jamie M</creatorcontrib><creatorcontrib>Kiefer, Zoë E</creatorcontrib><creatorcontrib>Koester, Lucas R</creatorcontrib><creatorcontrib>Johnson, Erika M</creatorcontrib><creatorcontrib>Schmitz-Esser, Stephan</creatorcontrib><creatorcontrib>Farkas, Attila</creatorcontrib><creatorcontrib>Galina Pantoja, Lucina</creatorcontrib><creatorcontrib>Vonnahme, Kimberly A</creatorcontrib><creatorcontrib>Greiner, Laura L</creatorcontrib><creatorcontrib>Keating, Aileen F</creatorcontrib><creatorcontrib>Baumgard, Lance H</creatorcontrib><creatorcontrib>Ross, Jason W</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of animal science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Studer, Jamie M</au><au>Kiefer, Zoë E</au><au>Koester, Lucas R</au><au>Johnson, Erika M</au><au>Schmitz-Esser, Stephan</au><au>Farkas, Attila</au><au>Galina Pantoja, Lucina</au><au>Vonnahme, Kimberly A</au><au>Greiner, Laura L</au><au>Keating, Aileen F</au><au>Baumgard, Lance H</au><au>Ross, Jason W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of circulating immune cells, analytes, and inflammatory markers in sows affected with postpartum dysgalactia syndrome</atitle><jtitle>Journal of animal science</jtitle><addtitle>J Anim Sci</addtitle><date>2024-01-03</date><risdate>2024</risdate><volume>102</volume><issn>0021-8812</issn><issn>1525-3163</issn><eissn>1525-3163</eissn><abstract>Postpartum dysgalactia syndrome (PDS) is a condition affecting periparturient sows, characterized by a reduction in milk and colostrum synthesis shortly after farrowing. Insufficient milk production results in substantial economic losses due to increased piglet morbidity/mortality and premature sow culling. Since PDS develops within a few days following farrowing, the study objectives were to determine if periparturient immune cell profiles and circulating biomarkers differ in sows affected by PDS. We hypothesized differences in immune cells, circulating analytes, and inflammatory markers would exist at farrowing in sows that subsequently developed PDS compared to healthy herd-mates. Thirty-six sows with PDS symptoms were matched by parity and day of lactation with 36 healthy control (CON) sows. Diagnosis of PDS (timepoint 2) occurred on average 9.25 ± 2.67 d after farrowing. Blood samples and litter weights were collected at farrowing (timepoint 1) and at the onset of clinical PDS (timepoint 2). Piglets from PDS sows had lower average daily gain and higher mortality than piglets from CON (P < 0.01). Aspartate aminotransferase was increased (20%; P ≤ 0.06) in PDS sows compared to CON at both timepoints. Additionally, blood urea nitrogen was increased in PDS sows at timepoint 1 and timepoint 2 (13%; P = 0.08 and 16%; P = 0.01, respectively). At timepoint 2, total protein, globulin, magnesium, and cholesterol were increased (P ≤ 0.03) while γ-glutamyl transferase and albumin were decreased (P ≤ 0.02) in PDS sows. Lipopolysaccharide-binding protein, an inflammatory biomarker, was increased (48%; P = 0.07) at timepoint 2 in PDS compared to CON sows. Collectively, these data indicate PDS sows have altered metabolism and appear immune activated compared to healthy herd-mates, and further investigation is needed to determine if PDS can be predicted at farrowing.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>39298285</pmid><doi>10.1093/jas/skae270</doi><orcidid>https://orcid.org/0000-0002-3064-2384</orcidid><orcidid>https://orcid.org/0000-0002-1907-0709</orcidid><orcidid>https://orcid.org/0000-0003-1913-3383</orcidid><orcidid>https://orcid.org/0000-0001-6597-009X</orcidid><orcidid>https://orcid.org/0000-0003-4950-2258</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biomarkers - blood Colostrum - immunology Female Inflammation - blood Inflammation - veterinary Lactation Lactation and Mammary Gland Biology Lactation Disorders - blood Lactation Disorders - veterinary Milk - chemistry Postpartum Period Pregnancy Swine Swine Diseases - blood Swine Diseases - immunology |
title | Evaluation of circulating immune cells, analytes, and inflammatory markers in sows affected with postpartum dysgalactia syndrome |
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