Research online! More from Advances in nutrigenomics

Read the entirety of Dr. Swanson's nutrigenomic research and a list of all references from his original June 2010 article

Recent Advances in Pet Genomics

The molecular age is upon us, creating exciting opportunities in the pet food industry. Genome sequence data, high-throughput functional genomics assays, and nanotools have several applications to pet health and the pet food industry. Such technology may be used to expand ingredient options (e.g., items enriched in functional nutrients), for pet food testing (e.g., contamination of microbes or toxins; identify ingredient origin; detection of GMOs), or for molecular-based animal research. Genomic biology may be used to gain a better understanding of dog and cat physiology and how nutrition contributes to health and disease. Because this last point will arguably have the greatest impact on pet health and the pet food industry, it will be the focus herein.

Genomic tools have greatly changed the landscape of all research fields pertaining to life sciences, including nutrition. In pets, such tools are being used to study microbial populations and gene expression changes in blood and various tissues. In the past, the field of microbiology was greatly limited by the methodology and inability to culture the majority of gastrointestinal microbiota. DNA-based techniques, which include quantitative polymerase chain reaction that is very sensitive and used to quantify specific microbial species, gel-based assays such as denaturing gradient gel electrophoresis that allows for a broad view of the population, and pyrosequencing that allows for widespread characterization of phylogeny (who is present?) and functional/metabolic capacity (what are they doing?), have many scientific and practical advantages. Intestinal microbes may be affected by host species, age, health status, and location in gastrointestinal tract. Our laboratory and others have begun using DNA-based sequencing techniques to characterize the canine and feline gastrointestinal tracts (Suchodolski et al ., 2008; Middelbos et al ., 2010; Swanson et al ., 2010; Barry, unpublished data). These initial experiments in healthy adult dogs and cats are providing a strong foundation for future initiatives that may be aimed at studying the microbial profile and metabolic pathways of animals with different health status (e.g., healthy vs. IBD), life stage (e.g., weanling vs. adult vs. geriatric), species (e.g., dog vs. cat), or dietary regimen.

Genomic biology is also being used to advance our understanding of nutrient-gene interactions within the dog and cat. The field of 'nutrigenetics' is focused on identifying how genetic background affects the response (e.g., absorption; metabolism; excretion; etc.) to a nutrient or diet. In contrast, 'nutrigenomics' is focused on measuring how a nutrient or diet affects gene expression. Most mammalian genomes contain ~20,000-25,000 genes, all interacting in complex ways. Identifying the genetic basis for disease may be difficult, even for monogenic diseases affected by a single mutation. One of the most popular examples of nutrigenetics in dogs is that of copper toxicosis in Bedlington Terriers (Klomp et al , 2003). In this example, dogs with a mutation in the MURR1 gene accumulate copper in hepatic tissue over time, eventually resulting in copper toxicosis. If undiagnosed and fed a diet containing standard copper concentrations, these dogs usually die between 3 and 7 years of age. A test is now available to detect this mutation at birth so that dietary management may be implemented long before clinical symptoms of the disease appear. If diagnosed and fed a low-copper diet, this population may live without complications. Other monogenic diseases have been identified in dogs and cats, but many are not directly related to diet. Moreover, while mutations of several monogenic diseases have been identified, the majority of diseases noted in pets are complex in nature. Diseases such as obesity or hip dysplasia, for example, are impacted by hundreds of genes and numerous environmental factors, including diet. While this field has enormous potential, we are many years away from devising a personalized food for any given dog or cat based solely on a blood (DNA) sample.

The field of nutrigenomics continues to enhance our understanding of canine and feline metabolism and has broad application to pet nutrition and health. Recently, researchers have applied canine- and feline-specific functional genomic assays to study adipose and skeletal muscle tissue biology, various disease states, the normal effects of aging, and diet-induced changes in gene expression. To lay the foundation for future studies in diseased or aged dogs, our lab initially focused on identifying gene expression differences in cerebral cortex (Swanson et al ., 2009b), skeletal muscle (Middelbos et al ., 2009), adipose (Swanson et al ., 2009a), colon (Kil et al ., 2010), and liver (Kil, unpublished data) tissues of healthy aged vs. young adult dogs. Biological systems highlighted in these datasets (e.g., immune function, stress response, etc) have provided targets of nutritional intervention in future projects focused on improving tissue function and/or longevity. Our lab and others have also used genomic biology to identify molecular changes in adipose and skeletal muscle tissues during weight gain/loss, after spay/neuter, or in obese cats and dogs (Leray et al ., 2008; Belsito et al . 2009; Vester et al ., 2009a; Vester et al ., 2009b). These studies have suggested the potential role of specific nutrients or phytochemicals, such as estrogenic-like compounds or green tea polyphenols, that may aid in healthy weight maintenance and deserve more attention in future research. Similarly, Brass et al . (2009) measured temporal gene expression patterns of skeletal muscle in Alaskan sled dogs to identify novel regulatory mechanisms and responses to exercise stimuli, which may lead to dietary strategies with the ability to prolong bouts of exercise or improve muscle recovery. Finally, other researchers have identified key genes or pathways differentially regulated in diseases such as atopic dermatitis (Merryman-Simpson et al ., 2008) and gastrointestinal diseases (Greger et al ., 2006).

In addition to highlighting genes or pathways associated with disease that may aid in developing preventative or treatment strategies, such studies have suggested that genomic tests may also be an effective diagnostic tool to distinguish closely-related diseases from one another (Greger et al ., 2006).

In summary, genomic biology is rapidly changing the research environment, providing for new and exciting avenues of research geared toward improving the health or longevity of pets. Even though this field is in its infancy, initial publications have shown great promise, highlighting dietary strategies for further testing or inclusion in pet foods.

Literature cited:

  1. Belsito, K. R., B. M. Vester, T. Keel, T. K. Graves, and K. S. Swanson. 2009. Impact of ovariohysterectomy and food intake on body composition, physical activity, and adipose gene expression in cats. J. Anim. Sci. 87:594-602.
  2. Brass, E. P., M. A. Peters, K. W. Hinchcliff, Y. D. He, and R. G. Ulrich. 2009. Temporal pattern of skeletal muscle gene expression following endurance exercise in Alaskan sled dogs. J. Appl. Physiol . 107:605-612.
  3. Greger, D. L., F. Gropp, C. Morel, S. Sauter, and J. W. Blum. 2006. Nuclear receptor and target gene mRNA abundance in duodenum and colon of dogs with chronic enteropathies. Domest. Anim. Endocrinol. 31:327-339.
  4. Kil, D. Y., B. M. Vester, C. J. Apanavicius, L. B. Schook, and K. S. Swanson. 2010. Age and diet influence gene expression profiles of canine colonic tissue. Arch. Anim. Nutr. (submitted).
  5. Klomp, A. E., B. van de Sluis, L. W. Klomp, and C. Wijmenga. 2003. The ubiquitously expressed MURR1 protein is absent in canine copper toxicosis. J. Hepatol. 39:703-709.
  6. Leray, V., S. Serisier, S. Khosniat, L. Martin, H. Dumon, and P. Nguyen. 2008. Adipose tissue gene expression in obese dogs after weight loss. J. Anim. Physiol. Anim. Nutr. 92:390-398.
  7. Merryman-Simpson, A. E., S. H. Wood, N. Fretwell, P. G. Jones, W. M. McLaren, N. A. McEwan, D. N. Clements, S. D. Carter, W. E. Ollier, and T. Nuttall. 2008. Gene (mRNA) expression in canine atopic dermatitis: microarray analysis. Vet. Dermatol. 19:59-66.
  8. Middelbos, I. S., B. M. Vester, L. K. Karr-Lilienthal, L. B. Schook, and K. S. Swanson. 2009. Age and diet affect gene expression profile in canine skeletal muscle. PLoS ONE 4 :e4481. doi:10.1371/journal.pone.0004481.
  9. Middelbos, I. S., B. M. Vester Boler, A. Qu, B. A. White, K. S. Swanson, and G. C. Fahey, Jr. 2010. Phylogenetic characterization of fecal microbial communities of dogs fed diets with or without supplemental dietary fiber using 454 pyrosequencing. PLoS ONE 5 :e9768. Doi:10.1371/journal.pone.0009768.
  10. Suchodolski, J. S., J. Camacho, and J. M. Steiner. 2008. Analysis of bacterial diversity in the canine duodenum, jejunum, ileum, and colon by comparative 16S rRNA gene analysis. FEMS Microbiol. Ecol. 66:567-578.
  11. Swanson, K. S., K. R. Belsito, B. M. Vester, and L. B. Schook. 2009a. Adipose tissue gene expression profiles of healthy young adult and geriatric dogs. Arch. Anim. Nutr. 63:160-171.
  12. Swanson, K. S., B. M. Vester, C. J. Apanavicius, N. A. Kirby, and L. B. Schook. 2009b. Implications of age and diet on canine cerebral cortex gene transcription. Neurobiol. Aging 30:1314-1326.
  13. Swanson, K. S., S. E. Dowd, J. S. Suchodolski, I. S. Middelbos, B. M. Vester, K. A. Barry, K. E. Nelson, M. Torralba, B. Henrissat, P. M. Coutinho, I. K. O. Cann, B. A. White, and G. C. Fahey, Jr. 2010. Phylogenetic and gene-centric metagenomics of the canine gastrointestinal microbiome reveals similarities with human and mouse gut metagenomes. ISME J. (submitted).
  14. Vester, B. M., S. M. Sutter, T. L. Keel, T. K. Graves, and K. S. Swanson. 2009a. Ovariohysterectomy alters body composition and adipose and skeletal muscle gene expression in cats fed a high-protein or moderate-protein diet. Animal 3 :1287-1298.
  15. Vester, B. M., K. J. Liu, T. L. Keel, T. K. Graves, and K. S. Swanson. 2009b. In utero and postnatal exposure to a high-protein or high-carbohydrate diet leads to differences in adipose tissue mRNA expression and blood metabolites in kittens. Brit. J. Nutr. 102:1136-1144.
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