Low Ca diet leads to increased Ca retention by changing the gut flora and ileal pH value in laying hens

IF 6.3
Sha Jiang , Xinyu Zou , Miao Mao , Mi Zhang , Wenjun Tu , Meilan Jin
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引用次数: 1

Abstract

Osteoporosis is a common degenerative metabolic bone disease in caged laying hens. Intensive egg production mobilizing large amounts of Ca from bone for eggshell formation, consequently leading to Ca deficiency, has been recognized as a critical factor causing osteoporosis in commercial laying hens. The aim of this study was to examine the effect of Ca deficiency on the function of the gut microbiota–bone axis and related egg production traits and bone health in laying hens. Twenty-four 48-week-old laying hens were fed a control diet (Control, 3.72%) or a low Ca diet (LC, 2.04%) for 60 d (n = 12). Compared to the Control hens, the LC hens had higher levels of alkaline phosphatase and tartrate resistant acid phosphatase (P < 0.05) with lower bone strength, eggshell thickness, and eggshell strength (P < 0.05). In addition, the LC hens had higher plasma estradiol concentrations, while having lower concentrations of interleukin-1 (IL-1) and IL-6. The LC hens also had a lower pH value in the ileum with an increased Ca retention. The principal co-ordinates analysis showed significantly separate cecal microbiota populations between the Control and LC hens. The Prevotellaceae_UCG-001, Subdoligranulum, Peptococcus, and Eubacterium_hallii_group (P < 0.05) were higher, while the CHKC1001 and Sutterella (P < 0.05) were lower at the genus level in the LC hens. In addition, Prevotellaceae_UCG-001, Subdoligranulum and Eubacterium_hallii_group had a negative correlation, while Sutterella was positively correlated with ileal pH values. The transcriptome analysis revealed that the low Ca diet caused 20 and 31 genes to be significantly up- and down-regulated, respectively. The gene expressions of cystic fibrosis transmembrane conductance regulator, solute carrier family 26 member 3 of the anion exchangers, and mitogen-activated protein kinase 12 of pro-inflammatory factors were lower in the LC birds, which was correlated with the lower ileal pH values. These results suggest that the hens with low Ca diet-induced osteoporosis have an increased intestinal Ca retention with a decreased ileal pH value, correlated with the changes in Prevotellaceae_UCG-001, Subdoligranulum, and Eubacterium_hallii_group of beneficial genera. The results provide insights for further understanding and preventing osteoporosis in laying hens.

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低钙饮食通过改变蛋鸡肠道菌群和回肠pH值来增加钙的保留
骨质疏松症是笼养蛋鸡常见的退行性代谢性骨病。密集的鸡蛋生产从骨骼中动员大量的钙来形成蛋壳,从而导致钙缺乏,已被认为是导致商品蛋鸡骨质疏松的关键因素。本研究的目的是研究钙缺乏对蛋鸡肠道微生物群-骨轴功能、相关产蛋性状和骨骼健康的影响。24只48周龄蛋鸡饲喂对照日粮(对照,3.72%)或低钙日粮(LC,2.04%)60天(n=12)。与对照母鸡相比,LC母鸡的碱性磷酸酶和抗酒石酸酸性磷酸酶水平较高(P<;0.05),骨强度、蛋壳厚度和蛋壳强度较低(P<!0.05)。此外,LC母鸡血浆雌二醇浓度较高,白细胞介素-1(IL-1)和IL-6浓度较低。LC母鸡回肠中的pH值也较低,Ca保留增加。主坐标分析显示对照和LC母鸡盲肠微生物群明显分离。在属水平上,LC母鸡的Prevotellaceae_UCG-001、Subdoligletum、Peptoccus和Eubacterum_halli_group(P<;0.05)较高,而CHKC101和Sutterella(P<)较低。此外,Prevotellaceae_UCG-001、Subdoligletum和Eubacterum_halli_group呈负相关,Sutterella与回肠pH值呈正相关。转录组分析显示,低钙饮食分别导致20个和31个基因显著上调和下调。LC鸟类中促炎因子的囊性纤维化跨膜电导调节剂、溶质载体家族26成员3和促分裂原活化蛋白激酶12的基因表达较低,这与较低的回肠pH值有关。这些结果表明,低钙饮食诱导的骨质疏松症母鸡的肠道钙滞留量增加,回肠pH值降低,这与有益属Prevotellaceae_UCG-001、Subdoligalleum和Eubacterum_halli_group的变化有关。研究结果为进一步了解和预防蛋鸡骨质疏松症提供了见解。
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来源期刊
Animal Nutrition
Animal Nutrition Animal Science and Zoology
CiteScore
9.70
自引率
0.00%
发文量
542
审稿时长
65 days
期刊介绍: Animal Nutrition encompasses the full gamut of animal nutritional sciences and reviews including, but not limited to, fundamental aspects of animal nutrition such as nutritional requirements, metabolic studies, body composition, energetics, immunology, neuroscience, microbiology, genetics and molecular and cell biology related to primarily to the nutrition of farm animals and aquatic species. More applied aspects of animal nutrition, such as the evaluation of novel ingredients, feed additives and feed safety will also be considered but it is expected that such studies will have a strong nutritional focus. Animal Nutrition is indexed in SCIE, PubMed Central, Scopus, DOAJ, etc.
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