Distinct whole-blood transcriptome profile of children with metabolic healthy overweight/obesity compared to metabolic unhealthy overweight/obesity

Author(s):  
Abel Plaza-Florido ◽  
Signe Altmäe ◽  
Francisco J. Esteban ◽  
Cristina Cadenas-Sanchez ◽  
Concepción M. Aguilera ◽  
...  
2021 ◽  
Vol 12 ◽  
Author(s):  
Janelle Jiminez ◽  
Edouard Timsit ◽  
Karin Orsel ◽  
Frank van der Meer ◽  
Le Luo Guan ◽  
...  

Bovine respiratory disease (BRD) is one of the main factors leading to morbidity and mortality in feedlot operations in North America. A complex of viral and bacterial pathogens can individually or collectively establish BRD in cattle, and to date, most disease characterization studies using transcriptomic techniques examine bronchoalveolar and transtracheal fluids, lymph node, and lung tissue as well as nasopharyngeal swabs, with limited studies investigating the whole-blood transcriptome. Here, we aimed to identify differentially expressed (DE) genes involved in the host immune response to BRD using whole blood and RNA sequencing. Samples were collected from heifers (average arrival weight = 215.0 ± 5.3 kg) with (n = 25) and without (n = 18) BRD at a commercial feedlot in Western Canada. RNAseq analysis showed a distinct whole-blood transcriptome profile between BRD and non-BRD heifers. Further examination of the DE genes revealed that those involved in the host inflammatory response and infectious disease pathways were enriched in the BRD animals, while gene networks associated with metabolism and cell growth and maintenance were downregulated. Overall, the transcriptome profile derived from whole blood provided evidence that a distinct antimicrobial peptide-driven host immune response was occurring in the animals with BRD. The blood transcriptome of the BRD animals shows similarities to the transcriptome profiles obtained from lung and bronchial lymph nodes in other studies. This suggests that the blood transcriptome is a potential diagnostic tool for the identification of biomarkers of BRD infection and can be measured in live animals and used to further understand infection and disease in cattle. It may also provide a useful tool to increase the understanding of the genes involved in establishing BRD in beef cattle and be used to investigate potential therapeutic applications.


2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Marianthi Kalafati ◽  
Martina Kutmon ◽  
Chris T. Evelo ◽  
Carla J. H. van der Kallen ◽  
Casper G. Schalkwijk ◽  
...  

Abstract Background Worldwide, the prevalence of obesity and insulin resistance has grown dramatically. Gene expression profiling in blood represents a powerful means to explore disease pathogenesis, but the potential impact of inter-individual differences in a cell-type profile is not always taken into account. The objective of this project was to investigate the whole blood transcriptome profile of insulin-resistant as compared to insulin-sensitive individuals independent of inter-individual differences in white blood cell profile. Results We report a 3% higher relative amount of monocytes in the insulin-resistant individuals. Furthermore, independent of their white blood cell profile, insulin-resistant participants had (i) higher expression of interferon-stimulated genes and (ii) lower expression of genes involved in cellular differentiation and remodeling of the actin cytoskeleton. Conclusions We present an approach to investigate the whole blood transcriptome of insulin-resistant individuals, independent of their DNA methylation-derived white blood cell profile. An interferon-related signature characterizes the whole blood transcriptome profile of the insulin-resistant individuals, independent of their white blood cell profile. The observed signature indicates increased systemic inflammation possibly due to an innate immune response and whole-body insulin resistance, which can be a cause or a consequence of insulin resistance. Altered gene expression in specific organs may be reflected in whole blood; hence, our results may reflect obesity and/or insulin resistance-related organ dysfunction in the insulin-resistant individuals.


2012 ◽  
Vol 31 (1) ◽  
pp. 76 ◽  
Author(s):  
Adel M Zaatar ◽  
Chun Lim ◽  
Chin Bong ◽  
Michelle Mei Lee ◽  
Jian Ooi ◽  
...  

2019 ◽  
Vol 143 (2) ◽  
pp. AB423
Author(s):  
Paul J. Turner ◽  
Nandinee Patel ◽  
Monica Ruiz-Garcia ◽  
Isabel J. Skypala ◽  
Stephen R. Durham ◽  
...  

Vaccine ◽  
2019 ◽  
Vol 37 (13) ◽  
pp. 1743-1755 ◽  
Author(s):  
Peris M. Munyaka ◽  
Arun Kommadath ◽  
Janelle Fouhse ◽  
Jamie Wilkinson ◽  
Natalie Diether ◽  
...  

BMC Genomics ◽  
2017 ◽  
Vol 18 (S8) ◽  
Author(s):  
Guan Wang ◽  
Jérôme Durussel ◽  
Jonathan Shurlock ◽  
Martin Mooses ◽  
Noriyuki Fuku ◽  
...  

PLoS ONE ◽  
2015 ◽  
Vol 10 (10) ◽  
pp. e0139678 ◽  
Author(s):  
Valérie Rodrigues ◽  
Philippe Holzmuller ◽  
Carinne Puech ◽  
Hezron Wesonga ◽  
François Thiaucourt ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document