Elizabeth S Greene, Brooklee Roach, Maria Fernandez Cuadrado, Sara Orlowski, Sami Dridi
{"title":"热应激对高、低水效率肉鸡回肠上皮屏障完整性的影响。","authors":"Elizabeth S Greene, Brooklee Roach, Maria Fernandez Cuadrado, Sara Orlowski, Sami Dridi","doi":"10.3389/fphys.2025.1558201","DOIUrl":null,"url":null,"abstract":"<p><p>Water scarcity and rising global temperatures are two of the greatest current and future threats to poultry sustainability. Therefore, selection for water efficiency (WE) and heat resilience are of vital importance. Additionally, intestinal integrity is of critical importance under challenging conditions to maintain nutrient absorption and therefore, growth and performance of broilers. Here, we examined the effect of chronic cyclic heat stress (HS) on the ileal expression profile of tight-junction, gap-junction, adherens, and desmosome genes in the fourth generation of divergently selected low (LWE)- and high water efficient (HWE)-chicken lines. LWE birds exhibited higher levels of gut permeability, regardless of temperature, as measured by fluorescein isothiocyanate-dextran (FITC-D). Among the claudins (CLDN), <i>Cldn1</i> showed greater expression in the HWE as compared to LWE, regardless of temperature. <i>Cldn5</i>, -<i>16</i>, -<i>20</i>, and -<i>34</i> genes were all greater in LWE and lower in HWE during HS. Conversely, <i>Cldn25</i> was decreased in LWE but increased HWE under HS. <i>Cldn4</i> was increased in the HWE line and decreased by HS. Cingulin (<i>Cgn</i>) gene expression was lower in HWE as compared to LWE and lower in HS as compared to thermoneutral (TN) condition. Gap junction protein α1 (<i>Gja1</i>) and desmoglein 4 (<i>Dsg4</i>) were greater in the HWE as compared to the LWE. Cadherin 1 (<i>Cdh1</i>) gene expression was greatest in the HWE in TN conditions and lowest in HWE under HS, whereas catenin α2 (<i>Ctnna2</i>) and desmocollin 1 (<i>Dsc1</i>) were highest in HWE during HS compared to all other groups. This differential expression of key genes associated with intestinal barrier integrity likely contributes to the water efficiency phenotype and the response of these birds to HS.</p>","PeriodicalId":12477,"journal":{"name":"Frontiers in Physiology","volume":"16 ","pages":"1558201"},"PeriodicalIF":3.2000,"publicationDate":"2025-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12009728/pdf/","citationCount":"0","resultStr":"{\"title\":\"Effect of heat stress on ileal epithelial barrier integrity in broilers divergently selected for high- and low-water efficiency.\",\"authors\":\"Elizabeth S Greene, Brooklee Roach, Maria Fernandez Cuadrado, Sara Orlowski, Sami Dridi\",\"doi\":\"10.3389/fphys.2025.1558201\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Water scarcity and rising global temperatures are two of the greatest current and future threats to poultry sustainability. Therefore, selection for water efficiency (WE) and heat resilience are of vital importance. Additionally, intestinal integrity is of critical importance under challenging conditions to maintain nutrient absorption and therefore, growth and performance of broilers. Here, we examined the effect of chronic cyclic heat stress (HS) on the ileal expression profile of tight-junction, gap-junction, adherens, and desmosome genes in the fourth generation of divergently selected low (LWE)- and high water efficient (HWE)-chicken lines. LWE birds exhibited higher levels of gut permeability, regardless of temperature, as measured by fluorescein isothiocyanate-dextran (FITC-D). Among the claudins (CLDN), <i>Cldn1</i> showed greater expression in the HWE as compared to LWE, regardless of temperature. <i>Cldn5</i>, -<i>16</i>, -<i>20</i>, and -<i>34</i> genes were all greater in LWE and lower in HWE during HS. Conversely, <i>Cldn25</i> was decreased in LWE but increased HWE under HS. <i>Cldn4</i> was increased in the HWE line and decreased by HS. Cingulin (<i>Cgn</i>) gene expression was lower in HWE as compared to LWE and lower in HS as compared to thermoneutral (TN) condition. Gap junction protein α1 (<i>Gja1</i>) and desmoglein 4 (<i>Dsg4</i>) were greater in the HWE as compared to the LWE. Cadherin 1 (<i>Cdh1</i>) gene expression was greatest in the HWE in TN conditions and lowest in HWE under HS, whereas catenin α2 (<i>Ctnna2</i>) and desmocollin 1 (<i>Dsc1</i>) were highest in HWE during HS compared to all other groups. This differential expression of key genes associated with intestinal barrier integrity likely contributes to the water efficiency phenotype and the response of these birds to HS.</p>\",\"PeriodicalId\":12477,\"journal\":{\"name\":\"Frontiers in Physiology\",\"volume\":\"16 \",\"pages\":\"1558201\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2025-04-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12009728/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Frontiers in Physiology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3389/fphys.2025.1558201\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"PHYSIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Physiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3389/fphys.2025.1558201","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"PHYSIOLOGY","Score":null,"Total":0}
Effect of heat stress on ileal epithelial barrier integrity in broilers divergently selected for high- and low-water efficiency.
Water scarcity and rising global temperatures are two of the greatest current and future threats to poultry sustainability. Therefore, selection for water efficiency (WE) and heat resilience are of vital importance. Additionally, intestinal integrity is of critical importance under challenging conditions to maintain nutrient absorption and therefore, growth and performance of broilers. Here, we examined the effect of chronic cyclic heat stress (HS) on the ileal expression profile of tight-junction, gap-junction, adherens, and desmosome genes in the fourth generation of divergently selected low (LWE)- and high water efficient (HWE)-chicken lines. LWE birds exhibited higher levels of gut permeability, regardless of temperature, as measured by fluorescein isothiocyanate-dextran (FITC-D). Among the claudins (CLDN), Cldn1 showed greater expression in the HWE as compared to LWE, regardless of temperature. Cldn5, -16, -20, and -34 genes were all greater in LWE and lower in HWE during HS. Conversely, Cldn25 was decreased in LWE but increased HWE under HS. Cldn4 was increased in the HWE line and decreased by HS. Cingulin (Cgn) gene expression was lower in HWE as compared to LWE and lower in HS as compared to thermoneutral (TN) condition. Gap junction protein α1 (Gja1) and desmoglein 4 (Dsg4) were greater in the HWE as compared to the LWE. Cadherin 1 (Cdh1) gene expression was greatest in the HWE in TN conditions and lowest in HWE under HS, whereas catenin α2 (Ctnna2) and desmocollin 1 (Dsc1) were highest in HWE during HS compared to all other groups. This differential expression of key genes associated with intestinal barrier integrity likely contributes to the water efficiency phenotype and the response of these birds to HS.
期刊介绍:
Frontiers in Physiology is a leading journal in its field, publishing rigorously peer-reviewed research on the physiology of living systems, from the subcellular and molecular domains to the intact organism, and its interaction with the environment. Field Chief Editor George E. Billman at the Ohio State University Columbus is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.