Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
Function: GetPubMedArticleOutput_2016
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Our objective was to evaluate the inclusion of calcium-magnesium carbonate [CaMg(CO)] and calcium-magnesium hydroxide [CaMg(OH)] in corn silage-based diets and their impact on ruminal microbiome. Our previous work showed a lower pH and molar proportion of butyrate from diets supplemented with [CaMg(CO)] compared to [CaMg(OH)]; therefore, we hypothesized that ruminal microbiome would be affected by Mg source. Four continuous culture fermenters were arranged in a 4 × 4 Latin square with the following treatments defined by the supplemental source of Mg: 1) (100% MgO, plus sodium sesquicarbonate as a buffer); 2) [100% CaMg(CO)]; 3) [100% CaMg(OH)]; and 4) [50% Mg from CaMg(CO), 50% Mg from CaMg(OH)]. Diet nutrient concentration was held constant across treatments (16% CP, 30% NDF, 1.66 MCal NEl/kg, 0.67% Ca, and 0.25% Mg). We conducted four fermentation periods of 10 d, with the last 3 d for collection of samples of solid and liquid digesta effluents for DNA extraction. Overall, 16 solid and 16 liquid samples were analyzed by amplification of the V4 variable region of bacterial 16S rRNA. Data were analyzed with R and SAS to determine treatment effects on taxa relative abundance of liquid and solid fractions. Correlation of butyrate molar proportion with taxa relative abundance was also analyzed. Treatments did not affect alpha and beta diversities or relative abundance of phylum, class and order in either liquid or solid fractions. At the family level, relative abundance of in solid fraction was lower for CO and CO/OH compared to OH and Control ( < 0.01). For genera, abundance of ( = 0.01) and Lachnospiraceae ND3007 ( < 0.01) (both from Lachnospiraceae family) was lower and unclassified Ruminococcaceae ( = 0.03) was greater in CO than Control and OH in solid fraction; while abundance of ( = 0.10) and Lachnospiraceae FD2005 ( = 0.09) (both from Lachnospiraceae family) and ( = 0.09) tended to decrease in CO compared to Control in liquid fraction. Butyrate molar proportion was negatively correlated to Ruminococcaceae ( = -0.55) in solid fraction and positively correlated to ( = 0.61) and Lachnospiraceae FD2005 ( = 0.61) in liquid. Our results indicate that source of Mg has an impact on bacterial taxa associated with ruminal butyrate synthesis, which is important for epithelial health and fatty acid synthesis.
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Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9335223 | PMC |
http://dx.doi.org/10.1093/tas/txac092 | DOI Listing |
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