Discover. Develop. Deploy.

Fast, accurate, and efficient. Illumina technology touches each step of the agrigenomics pipeline. Accelerating and enhancing agricultural research, advancing the development of high-value trait screening methods, and enabling the swift deployment of these applications in the real world.

Research Applications: Sequencing

De Novo Sequencing
Whether a research project is focused on a novel species or just one that has never been investigated before using genetic tools, de novo sequencing is a first step toward understanding the genetic underpinnings of a plant or animal’s functions and its interaction with the environment. With long-paired and mate-pair sequence data, some researchers use the assembled genome to assign map positions and stack diverse breed information for subsequent resequencing to discover SNPs and other genetic variations.
Articles
Argout X, Salse J, et al. (2011) The genome of Theobroma cacao. Nat Genet 43: 101-8.
Epigenetics
Adaptive responses to changes in the environment (food availability, drought conditions, etc.) can trigger phenotypic changes in plants and animals that affect their viability and reproductive fitness. By identifying changes in DNA methylation, chromatin structure, and small RNA expression, researchers can better understand how epigenetic factors contribute to controlling these and other traits in a species of interest.
Articles
Eaton CJ, Cox MP, Ambrose B, et al. (2010) Disruption of signaling in a fungal-grass symbiosis leads to pathogenesis. Plant Physiol 153: 1780-94.

Dunoyer P, Brosnan CA, et al. (2010) An endogenous, systemic RNAi pathway in plants. EMBO J 29: 1699-712.

Nowack EC, Vogel H, et al. (2011) Endosymbiotic gene transfer and transcriptional regulation of transferred genes in Paulinella chromatophora. Mol Biol Evol 28: 407-22.

Hirst M, Marra MA (2010) Next generation sequencing based approaches to epigenomics. Brief Funct Genomics 9: 455-465.

Smith ZD, Gu H, Bock C, et al. (2009) High-throughput bisulfite sequencing in mammalian genomes. Methods 48: 226-32.

Feng S, Cokus SJ, et al. (2010) Conservation and divergence of methylation patterning in plants and animals. Proc Natl Acad Sci U S A 107: 8689-94.

Fahlgren N, Jogdeo S, et al. (2010) MicroRNA gene evolution in Arabidopsis lyrata and Arabidopsis thaliana. Plant Cell 22: 1074-89.
Metagenomics
Sequencing has transformed metagenomics, enabling the study of large microbial communities directly in their natural environment without prior culturing. These studies can yield important information about the complex and diverse populations of microbes associated with animal and plant development, from rumen flora that enhance animal digestion to root-associated bacteria involved in nitrogen fixation.
Articles
Hess M, Sczyrba A, et al. (2011) Metagenomic discovery of biomass-degrading genes and genomes from cow rumen. Science 28: 463-467.

 

Targeted Resequencing
Targeted resequencing digs deeper into the exome or specific genomic regions of interest identified from large-scale association or linkage studies. This efficient and economical method sequences predetermined areas of genetic variation over a large number of samples, identifying common and rare variants (SNPs, CNVs, etc.). These variants may represent beneficial mutations that can help inform breeding decisions and may reveal causative mutations responsible for plant or animal disease, or parasite susceptibility.
Articles
Hyten DL, Cannon SB, et al. (2010) High-throughput SNP discovery through deep resequencing of a reduced representation library to anchor and orient scaffolds in the soybean whole genome sequence. BMC Genomics 11: 38.
Transcriptome Sequencing
RNA sequencing is revolutionizing the exploration of gene expression in plants and animals, providing novel insights into changing expression levels that occur in development, and during disease and stress conditions. It can be used to elucidate gene and protein function and interactions, identify tissue-specific list of RNA transcripts produced by an animal or plant genome (mRNAs, non-coding RNAs, and small RNAs), and for SNP discovery.
Articles
Wang XW, Luan JB, et al. (2010) De novo characterization of a whitefly transcriptome and analysis of its gene expression during development. BMC Genomics 11: 400.

Bonasio R, Zhang G, et al. (2010) Genomic comparison of the ants Camponotus floridanus and Harpegnathos saltator. Science 329: 1068-71.
Whole-Genome Resequencing
When a species’ reference genome is available, whole-genome resequencing is an efficient approach for discovering genes, SNPs, and structural variants, while simultaneously determining genotypes. Information from these studies will fill in the gaps that exist in the genetic maps of many plant and animal species, improving plant breeding and selection, and enabling definitive comparative genomic analyses within and across species.
Articles
Myles S, Chia JM, et al. (2010) Rapid genomic characterization of the genus vitis. PLoS One 5: e8219.

Research Applications: Genotyping

Fine Mapping and Candidate Gene Region Genotyping
Correlating the presence of certain genes with key phenotypic traits requires focused genotyping. Genotyping can be used to create fine map traits and/or test a genotype-phenotype hypothesis. Quantitative trait loci (QTL) analyses can be performed on the results to characterize how differential gene expression might contribute to phenotypic variation.
Articles
Pryce JE, Bolormaa S, et al. (2010) A validated genome-wide association study in 2 dairy cattle breeds for milk production and fertility traits using variable length haplotypes. J Dairy Sci 93: 3331-45.

Miura K, Ashikari M, et al. (2011) The role of QTLs in the breeding of high-yielding rice. Trends Plant Sci, 2011 March 21.

Bolon YT, Joseph B, et al. (2010) Complementary genetic and genomic approaches help characterize the linkage group I seed protein QTL in soybean. BMC Plant Biol 10: 41.
Copy Number Variation (CNV)
A common form of natural diversity, copy number variation (CNV) is also heritable and appears to play an important role in agrigenomics. CNV differences can correlate to health and production traits, and contribute to phenotypic diversity. The distribution of high density probes can be used to identify CNV breakpoints and ultimately accelerate genetic improvements. Studies are on-going to quantify and characterize if the impact of CNVs is the result of differences in copy number for key genetic segments, structural modification of the genome, or a combination of both.
Articles
Mills RE, Walter K, et al. (2011) Mapping copy number variation by population-scale genome sequencing. Nature 470: 59-65.
Custom Genotyping
Not every non-human organism has been extensively genetically investigated, resulting in an absence of commercial genotyping arrays for certain plant and animal species. Illumina offers custom array panels that can be designed with all the discovered markers for species of interest, enabling genotyping studies to identify variants associated with desired phenotypic traits. Through its on-going work with major agrigenomics consortia, Illumina technology is being used to identify new, relevant markers in a wide range of species.
Articles
McMullen MD, Kresovich S, et al. (2009) Genetic properties of the maize nested association mapping population. Science 325: 737-40.
Whole-Genome Association
Association mapping across an entire genome provides insight into the genetic location and architecture of linking traits to species’ adaption (e.g. to a wide variety of environmental conditions). The results of these studies support whole-genome selection applications (fingerprinting, net merit, marker-assisted breeding) that enhance the value of commercial crops and herds.
Articles
Fortes MR, Reverter A, Zhang Y, et al. (2010) Association weight matrix for the genetic dissection of puberty in beef cattle. Proc Natl Acad Sci U S A 107:13642-13647.

Bolormaa S, Pryce JE, Hayes BJ, et al. (2010) Multivariate analysis of a genome-wide association study in dairy cattle. J Dairy Sci 93: 3818-33.

Cockram J, White J (2011) Genome-wide association mapping to candidate polymorphism resolution in the unsequenced barley genome. Proc Natl Acad Sci U S A 107:21611-21616.

Van Oeveren J, de Ruiter M, et al. (2011) Sequence-based physical mapping of complex genomes by whole genome profiling. Genome Res 21:618-625.

Commercial Applications

Genomic Selection/Trait Screening
Genetic markers linked to specific value traits can be used to screen large numbers of progeny to identify those with desired characteristics. Trait screening is ideal for multigenic traits that are difficult to manage using conventional breeding or propagation techniques, and even more difficult to identify phenotypically. Iterative screening of populations enables easier segregation of progeny possessing the desired traits for use as breeding stock.
Literature
Application Note: RAD-Seq Genotypes Less, But Offers More
Articles
Lunney JK, Chen H (2010) Genetic control of host resistance to porcine reproductive and respiratory syndrome virus (PRRSV) infection. Virus Res 154: 161-169.

Rolf MM, Taylor JF, Schnabel RD, et al. (2010) Impact of reduced marker set estimation of genomic relationship matrices on genomic selection for feed efficiency in Angus cattle. BMC Genet 11: 24.

Eberlein A, Takasuga A, Setoguchi K, et al. (2009) Dissection of genetic factors modulating fetal growth in cattle indicates a substantial role of the non-SMC condensin I complex, subunit G (NCAPG) gene. Genetics 183: 951-964.

Matukumalli LK, Lawley CT, Schnabel RD, et al. (2009) Development and characterization of a high density SNP genotyping assay for cattle. PLoS ONE 4: e5350.

Video: Genomics breeding
Marker-Assisted Backcrossing
The goal of backcrossing is to move a single trait of interest, such as drought-tolerance, high-productivity, or disease resistance, from a donor parent to progeny. Marker-assisted backcrossing enables researchers to monitor the transmission of the trait gene via a genetically-linked marker that can be easily screened, significantly accelerating backcrossing programs and reducing the time to release of commercially viable plant lines or breeding stock.
Articles
Kalendar R, Flavell AJ, Ellis TH, et al. (2011) Analysis of plant diversity with retrotransposon-based molecular markers. Heredity 106: 520-30.
Parentage
Genetic markers can be used to identify animals and understand the relationship of offspring to parents. Since a single marker may not yield definitive results, multiple markers are used to increase the probability of identifying the true parent. In linebreeding situations where multiple generations of males or females are present in the herd, the marker results are combined with the breeder’s knowledge of possible sires or dams to determine parentage.
Whole-Genome Enabled Selection/genetic selection
There are multiple plant and animal applications where whole-genome sequencing information can assist in identifying or selecting progeny with traits of interest.
  • Fingerprinting (plants) – genetic markers are used to track genes as they are isolated and transferred into crops, and to identify seeds with specific traits, patented seed types, and the presence or absence of GMO events
  • Genetic purity (plants) – genetic markers are used to assess the similarity of all seeds in a seed lot
  • Net merit (animals) – genetic markers are used to determine the genetic merit of an animal (possession of a combination of economically important traits) to simplify the selection of the correct sire or dam for breeding
  • Marker-assisted breeding (plants and animals) – genetic markers are used to identify and select favorable alleles and recombine them during repeated breeding cycles to generate herds or crops possessing high-value traits
  • Traceability – small number of markers used to uniquely identify animals and trace them from “farm to fork” to track outbreaks of food borne illness
Articles
Parker HG, VonHoldt BM, Quignon P, et al. (2009) An expressed fgf4 retrogene is associated with breed-defining chondrodysplasia in domestic dogs. Science 325: 995-8.

Pooled resources. Reduced costs. Great results.

With a consortium, members work together privately or publicly to advance the collective understanding of agrigenomics and improve individual economics. Already there are consortia for a wide variety of plants and animals. Illumina coordinates. Members pool resources. Everyone benefits.

Genotyping panels based on Illumina BeadChips are the foundation of more than 25 different consortia products, with new groups being formed every year. In the sections below, you’ll learn about currently available consortia, publicly available BeadChips, and BeadChips that are in development. All Illumina BeadChips are designed to enable a broad range of agrigenomic applications to accelerate and enhance research, advance the development of high-value trait screening methods, and enable the swift deployment of these applications in the real world.

If you’d like to participate in consortia or are interested in starting a new one, fill out the Consortia interest form or contact your Illumina representative.

Crops and Other Plants

Apple, Peach, and Cherry (Consortia BeadChips available)

Three of the most flavorful members of the Rosaceae Family, apples, peaches, and cherries are also packed with nutrients and rich in antioxidant compounds, creating high-demand for these fruits worldwide. RosBREED is a multistate, multi-institutional, multi-national project dedicated to the improvement of rosaceous crops through targeted applications of genomics knowledge and tools to enhance the efficiency of breeding programs. Consortia-developed Infinium BeadChips are publically available, each possessing SNPs for use on worldwide breeding germplasm.

  • Apple (27 founder accessions) plus pear (2 accessions) totaling 8,788 SNPs
  • Peach (23 founder accessions) totaling 8,144 SNPs
  • Tart and Sweet Cherry (16 and 8 founder accessions, respectively) totaling 5,696 SNPs

To place an order, contact Illumina.

Maize (Commercial BeadChip available)

From its humble beginnings 10,000 years ago in Mesoamerica, maize is now grown in more than 50 countries worldwide with production exceeding 800 million metric tons in 2009. The MaizeSNP50 Consortium includes researchers from TraitGenetics, The French National Institute for Agricultural Research (INRA) and Syngenta, among others. Content contributor and decisionmakers worked with Illumina to develop an InfiniumHD BeadChip to perform genome-wide association studies in this important crop.

  • MaizeSNP50 BeadChip includes more than 50,000 markers derived from the B73 reference sequence that are evenly spaced across the entire maize genome.

Tomato (Consortium BeadChip available)

There are more than 7,000 different varieties of tomato, a plant that is native to South America and now enjoyed worldwide. The Solanaceae Coordinated Agricultural Project (SolCAP) has developed a tool primarily to address genetic diversity in cultivated varieties of tomato. SolCAP identified 28,380 potential SNPs, with 7,720 SNPs available on the SolCAP Tomato Consortium BeadChip.

To obtain additional information about the BeadChip or to place an order, contact Illumina.

Vitis/Grapevine (Consortium-designed BeadChip in development)

Once gracing the tables of the ancient Egyptians, Greeks, Phoenicians, and Romans, wine is now enjoyed by people around the world. More than 75,000 square kilometers are dedicated to grape cultivation worldwide, with over 70% focused on grape production for wine making. The GrapeReSeq Consortium consists of members from France, Spain, Italy, and Germany with the goal of developing a SNP genotyping tool to evaluate the diversity in the Vitaceae gene pool and support breeding programs that will reduce the use of chemical treatments in viticulture. Candidate Vitis SNPs identified from 17 different grapevine samples will be validated and optimized, with an estimated final BeadChip content of 10,000 SNPs.

To obtain additional information about the BeadChip or to place an order, contact Illumina.

Brassica (Consortium-designed BeadChip in development)

The over 30 plant species in the Brassica genus are members of the mustard family, ranging from radishes, cauliflower, and broccoli, to rapeseed and canola. The International Brassicas SNP Consortium consists of universities, agrigenomics, and seed companies, with the goal of developing a SNP genotyping tool to support trait/gene studies for enhanced cultivation and improved crop yields. Candidate Brassicas SNPs identified from 60 Brassica lines will be validated and optimized, with an estimated final BeadChip content between 50,000 and 54,000 SNPs.

To obtain additional information about the BeadChip or to place an order, contact Illumina.

Potato (Consortium BeadChip available)

This starchy nightshade vegetable is native to the Andes and now enjoyed worldwide, with over a thousand different varieties currently available. The Solanaceae Coordinated Agricultural Project (SolCAP) has developed a tool primarily to address genetic diversity in processing varieties of potato. SolCAP has ensured that 8,303 SNPs are available on the SolCAP Potato Consortium BeadChip.

To obtain additional information about the BeadChip or to place an order, contact Illumina.

Companion Animals

Canine (Commercial BeadChip available)

Dogs are arguably man’s greatest invention, having been originally domesticated from grey wolves more than 100,000 years ago. Selective breeding over the last few centuries has led to an incredible amount of biological diversity among modern domestic dog breeds. In developing a canine BeadChip, Illumina collaborated with the LUPA Consortium, which includes 22 European universities such as Uppsala University, and other partners such as the Broad Institute.

  • The CanineHD BeadChip features more than 170,000 evenly spaced SNPs, with greater than 70 markers per megabase, providing ample SNP density for robust within-breed association and copy number variation studies.

Livestock

Bovine (Commercial BeadChips available)

Because of its economic importance, cattle was the first livestock animal to have its genome mapped. Illumina has worked with a variety of consortia to develop Infinium BeadChips that include novel SNP loci representing the genetic diversity of three populations of beef and dairy cattle, including Bos taurus taurus (Btt), Bos taurus indicus (Bti), and several Bti x Btt breeds, as well as temperate and tropically adapted breeds within these groupings. These BeadChips enable researchers to interrogate genetic variation across the genome for any breed of cattle.

  • Developed in collaboration with USDA-ARS, UNCEIA-INRA, Pfizer Animal Genetics, and the University of Missouri, the BovineHD BeadChip is the most comprehensive genome-wide genotyping array featuring 777,962 SNPs that uniformly span the entire bovine genome.
  • Developed in collaboration with USDA-ARS, USDA-MARC, University of Missouri, and the University of Alberta, the award-winning BovineSNP50 BeadChip features 54,609 informative SNP probes evenly spaced across the entire bovine genome.

Goat (Consortium BeadChip Available)

A good source of milk and meat, goats were domesticated by humans more than 10,000 years ago. The International Goat Genome Consortium was created in 2010, pooling efforts and resources to establish a goat reference genome. Several datasets generated by Consortium content contributors including INRA, Utrect Uni, Kunming Institute of Zoology, Chinese Academy of Sciences, Inner Mongolia Agricultural University, Beijing Genomics Institute (BGI), Università degli Studi della Tuscia, the Malaysian Agricultural Research and Development Institute, Universitat Autonoma De Barcelona (with funding from UNCEIA, Capgenes, Valogene, and Apis-gene) were used in SNP discovery. Candidate goat SNPs were validated and optimized for up to six breeds, with a final BeadChip content of 53,347 SNPs.

To obtain additional information about the BeadChip or to place an order, contact Illumina.

Ovine (Commercial and Consortium BeadChips available)

In the sheep industry, the most important animals are the “sires to breed sires”—the animals that produce the males that are used across the industry. By genotyping thousands of sires, researchers can evaluate a vast number of variants for economically important traits. To develop an ovine BeadChip, Illumina worked with the International Sheep Genomics Consortium (ISGC), comprising leading researchers from AgResearch, Baylor University, UCSC, and Australia’s Commonwealth Scientific and Industrial Research Organization (CSIRO). To develop the low density Ovine array, Illumina worked with AgResearch in New Zealand.

  • The OvineSNP50 BeadChip is a high-density array featuring more than 54,000 SNPs representing diverse Ovis aries breeds and outgroup species, providing a comprehensive solution for whole-genome ovine studies.
  • The AgResearch Ovine Imputation Low Density tool consists of approximately 5,000 SNPs intended for imputation to the OvineLD.

To obtain additional information about these BeadChips or to place an order, contact Illumina.

Porcine (Commercial BeadChip available)

With the average pig litter ranging from 8 to 14, pigs are one of the most prolific livestock animals. In developing a porcine BeadChip, Illumina collaborated with the International Porcine SNP Chip Consortium, comprising researchers from Wageningen University, Danish Institute of Agricultural Science, USDA-ARS, USMARC, Roslin Institute, University of Illinois, Iowa State University, INRA, University of Missouri, and Cambridge University.

  • Featuring more than 62,000 SNPs, the PorcineSNP60 BeadChip has been validated in seven economically important pig breeds, including Duroc, Landrace, Pietran, and Large White, enabling researchers to cost-effectively perform whole-genome studies in the porcine genome.

The Illumina Agricultural Greater Good Initiative Award

Agricultural Greater Good Initiative

We are pleased to announce the first recipient:

International Rice Research Institute (IRRI)

About the Illumina Agricultural Greater Good Initiative

Illumina is dedicated to making tangible contributions to the reduction of hunger, malnutrition and poverty. We are committed to enabling groundbreaking research that will result in increased sustainability, productivity and nutritional density of agricultural species. Nominees must be proficient in the use of ILMN technology and engaged in one or more projects aimed at breeding/identifying plants or animals.

About IRRI

Established in 1960, the International Rice Research Institute (IRRI) is among the largest non-profit agricultural research centers in Asia, with headquarters in the Philippines and offices in 14 nations. Supported by donors and partners around the globe, IRRI is known as the home of the Green Revolution in Asia. IRRI helps feed almost half the world’s population. IRRI’s mission is to reduce poverty and hunger, improve the health of rice farmers and consumers, and ensure that rice production is environmentally sustainable.

IRRI is a customer and strong ILMN supporter. IRRI breeders utilize our BeadExpress platform installed at IRRI’s headquarters in Los Banos. They have a global reach and influence through their offices in 14 different nations and an extensive network of rice breeders globally.

Our award will facilitate:

  • IRRI testing service for rice breeding programs in countries in need and aimed at developing varieties with increased sustainability
  • A hands on testing component of a rice breeding course given at IRRI and aimed at developing the next generation of rice breeders. This will result in these breeders being trained specifically in Illumina technology.

Innovating together.

From facilitating species-specific consortia to collaborating with agriculture leaders, Illumina is a part of the community. Making technology accessible. Bringing groups together. Enabling research.

Learn more about how the Illumina Community is advancing agrigenomics.

René Hogers, Ing., uses Illumina technology to save time and money while developing highly desirable plants. More »

René Hogers, Ing.
KeyGene, Netherlands

Ing. René Hogers works at KeyGene, a private research company that develops innovative applications and provides genetic analysis services for plant breeding groups in an effort to speed up the process of selecting plants with desirable traits. Currently, breeders are required to grow several generations to confirm the presence or absence of a particular phenotype. This can take years and waste precious resources on plants that will end up holding no value to the grower. To minimize this generational breeding process, Ing. Hogers is using Illumina's technology to enable breeders to realize significant savings while producing highly desirable agricultural products.

Illumina solutions for marker-assisted selection

Using VeraCode technology with the BeadXpress Reader, Ing. Hogers works with his customers to screen for genetically fit plants, a practice known as marker-assisted selection. Plants carrying the SNPs of interest are identified, allowing researchers to "decide which of the plants they should take and go on with and which ones they can throw away when the plants are still very small and with a just a few leaves. Picking out the right plants to go with the breeding processes saves a lot of time and also space in the greenhouses." For now, Ing. René Hogers has applied this technique to fruit and vegetable crops such as tomato, melon, pepper, lettuce, and cucumber, as well as field crops such as maize, barley, and potato.

Faster more, effective way to evaluate crops

Ing. René Hogers chose the BeadXpress Reader for several reasons, including the throughput. "We can screen for over 200 selected markers that will be informative, even for closely related species or parental lines, in one assay," he states. "This saves us time and costs." When asked about the BeadXpress workflow, Ing. Hogers replies, "It's more or less plug and play. With the availability of the [VeraCode] GoldenGate Assay, it will be easier to perform the assays. If we have a 384-plex [SNP assay], it takes about two to two-and-a-half hours to scan a whole plate of 96 samples." In addition, Ing. Hogers is pleased with the results. "The quality is quite good, it's very reproducible."


Excerpted from the September 2008, iCommunity article "Is Genetic Testing the Next Revolution in Agriculture?"

Richard Crooijmans, Ph.D., uses Illumina technology to select the most advantageous chickens and pigs for breeding. More »

Richard Crooijmans, Ph.D.
Wageningen University

Dr. Richard Crooijmans is working to overcome new farming challenges. As a molecular geneticist at Wageningen University, he applies VeraCode technology and the BeadXpress Reader to genetic studies involving over 20,000 chickens and pigs. Many of these chicken and pig screenings are performed in an effort to remove a particular allele from the population, or as a way to study inheritance patterns. After analysis, only the desired animals are selected for breeding. To do this, Dr. Crooijmans needed a straightforward, accessible system.

Improving animal husbandry using Illumina technology

"We chose the VeraCode technology because it's pretty easy to use and everything is digital. You don't have to go through PCR where you have to load gels, with the potential to make mistakes. You don't have to check all the genotypes and enter them into a computer, where you can make mistakes again. With the VeraCode system, it's there and it's ready." A second reason for choosing VeraCode technology was the flexibility. "We have several regions we want to fine map, and [with VeraCode technology] we can just take specific SNPs and type them. This makes it very flexible. With other systems you have to do rather complicated assays and it also costs you more," he states. He sums up his experience by saying that VeraCode technology was "the easiest of the systems" he evaluated. When screening a large number of animals, the savings in time, cost, and effort add up significantly.

Faster more, cost-effective screening

With Dr. Crooijmans' efforts, SNPs associated with specific traits can be quickly and easily identified, eliminating the need for generational breeding. For example, a broiler chicken (one meant for consumption) has different desirable genetic traits than one destined for egg laying duties (a layer chicken). "Current commercial testing looks for a phenotype. It costs a large amount of money every time. You have to phenotype quite a lot of individuals and then screen them, and follow in time. We want to replace these very expensive phenotyping systems," states Dr. Crooijmans. If these can be replaced with faster, cost-effective molecular screening tests, the quality of the livestock population can be improved at a relatively rapid pace with minimal time and expense. When asked what the BeadXpress system has given him, Dr. Crooijmans answers, "knowledge and proven reliability as a partner in the animal sciences community. We showed that we can create and handle large data sets. With the help of commercial breeding partners, we have access to a wide range of animal material. Now we can get things done much more easily. Many of the grant proposals we submitted have been approved."


Excerpted from the September 2008, iCommunity article "Is Genetic Testing the Next Revolution in Agriculture?"

Martien Groenen, Ph.D., relied on Illumina technology to help develop the first whole-genome genotyping array for pigs. More »

Martien Groenen, Ph.D.
Professor, Animal Genomes
Wageningen University, Netherlands
Co-developer of the PorcineSNP60 BeadChip

A molecular biologist by training, Dr. Martien Groenen has been studying complex traits in animals for more than 20 years at Wageningen University. He started out scanning the genome for microsatellites, looking for genetic markers associated with traits of interest. When Illumina's GoldenGate Genotyping panels hit the market, he quickly adopted these high-multiplex, high-throughput arrays for his research. Pleased with Illumina's technology, Groenen and collaborators decided to stay with Illumina to develop the first whole-genome genotyping array for the pig through the iSelect program.

i: What was your experience designing iSelect BeadChips?

For the PorcineSNP60 BeadChip, my group took a leading role in identifying a large number of SNPs through sequencing. In four months, using the Genome Analyzer, we identified 350,000 SNPs in the porcine genome. Within that same time frame we selected 70,000 and submitted them to be synthesized by Illumina. The results were great, 59,000 SNPs worked. I presented the design of the chip at the 2009 Plant and Animal Genome conference, and for the first time several groups heard the results. Everybody was really enthusiastic, which was very nice to hear.

And more or less we have done the same in chicken, but faster. We were involved in designing a 60K iSelect BeadChip in chicken. In this case, there were already three million known SNPs in the chicken genome. But we still used the Genome Analyzer to specifically identify new SNPs and to calculate the minor allele frequencies in the breeds that we wanted to use later on. This allowed us to have the maximum information content of the SNPs that were put on the chip. Once we had our sequence data, the whole process took six to seven weeks: analyzing the data, selecting the SNPs, and then submitting our SNP list to Illumina.

i: Why did you decide to go with Illumina for custom arrays?

Well, we began using Illumina's GoldenGate Assay a couple of years ago. We have continued using Illumina's technologies for two very important reasons. One is the reliability of the data and the quality of the data. The other thing is also the contact with Illumina itself, working with people at Illumina who have helped us get the results that we want. It's not just that you buy a product and that's it. You feel that for Illumina [the final product] is something that they want to bring to a good end.

i: Where do you see your research heading in the next few years?

The Genome Analyzer and iSelect, these different tools, are allowing much more rapid progress in agricultural research. Talking to my colleagues, we are very excited about these technologies, that's for sure. Looking ahead it's clear that at some point we will be completely resequencing individuals and I think we can expect a lot of information coming out of that.

If you would have asked me this question two or three years ago, what do you think you will be doing two or three years from now, I wouldn't have expected to do 60,000 SNPs on thousands of individuals or producing hundreds of millions of sequences in these species. Looking ahead for a couple of years and seeing developments in the field it's almost beyond imagining what is possible. I'm extremely excited working in this field and really in this period of time.


Excerpted from the September 2008, iCommunity article "Is Genetic Testing the Next Revolution in Agriculture?"

John McEwan uses Illumina technology to improve the genetic quality of the world's sheep and deer population. More »

John McEwan
Principal Scientist
AgResearch, New Zealand
Co-developer of the OvineSNP50 BeadChip

John McEwan is trying to improve the pastoral industry—specifically grazing animals and the products that come from them. As a member of the International Sheep Genomics Consortium, McEwan played a leading role in the development of the iSelect OvineSNP50 BeadChip, the first whole-genome genotyping array for sheep. His work primarily focuses on increasing the rate of genetic gain of sheep. To that end, he is currently attempting to identify a broad set of informative DNA markers for the sheep industry.

i: What was your strategy for designing a whole-genome array without a draft genome?

We just didn't have the money and we didn't have the time to sequence the sheep de novo, so we jumped onto next-generation sequencing technologies. We had a strategy where we used a long-read next-gen technology to get lumps of ovine sequence. We assembled those reads against the bovine genome to order and orientate the ovine contigs. Then we used the Illumina Genome Analyzer with the shorter reads and reduced representational library sequencing to provide the depth to find SNPs.

Doing this, we discovered more than 600,000 SNPs. We had about 300,000 good ones that passed the Illumina Infinium Assay design process. From these, we selected 60,000, and most of those made it onto the final OvineSNP50 BeadChip. A key point was that the assembly process allowed us to identify the SNP order and spacing, which greatly helped the quality of the final product.

Our goal in the sheep industry, is to move from the current situation of a having just a few DNA markers that can predict only a small proportion of the variation in performance to where we've got hundreds or thousands of markers and a much better prediction of the animal performance. With the Ovine BeadChip, people can now go directly from BeadChip results to markers that are immediately useful in the industry.

i: Will this strategy work for others in the agriculture community?

I think that vertebrate genomes are not the most complicated. Probably some of these large multi-ploid plant genomes will be more difficult. Within our institution there are a number of people who work with different plant species that are quite keen on the approach we took. I think with the current next-generation sequencing technology you should be able to quite rapidly and cost-effectively go from no sequence at all to an Illumina BeadChip. If you wanted to really push it, you could probably do it in a year and you could probably find all the SNPs required for less than several hundred thousand dollars.

i: How has the OvineSNP50 BeadChip performed?

I'm primarily interested in breeding sheep that can better resist diseases and, in particular, parasites. So we've genotyped 3,000 sheep, mainly sires, with the chip. Most of these sires have been evaluated for between approximately 40 to 200 progeny each for parasite resistance, growth, and various other traits. We got over 97% of the animals that passed the genotyping quality threshold on the first pass through and finally achieved 98.6% after rerunning a few samples. And we've got well over 99% genotype calls on the samples that passed the quality threshold. The performance of the BeadChip is really good. We're really happy about that.

i: What was you're experience working with Illumina to develop the OvineSNP50 BeadChip?

You obviously look over the fence at what other groups are doing and the experiences they are having and I think it would be fair to say that the experience in the bovine community was very good with Illumina, and the bovine community evaluated a number of platforms. Internally, our research group has also used a number of SNP genotyping technologies. I think Illumina has got a good, robust product and it's at a very good price.

We developed this BeadChip through a consortium. The great benefit of consortia is that people can do things that they couldn't do by themselves. Another hidden benefit is that there are many more people involved, each with different points of view. Often what finally comes out of the mix is actually a better solution. But, of course, that means all these people have to work together and communication becomes a very big issue.

This is where the Illumina staff comes in, particularly for the mechanical arrangements and the financial arrangements. They gave a lot of support to the community in getting the product out. The final product is much better because it involves animals from around the world, but it's also good for Illumina because they can sell a product that can be used anywhere in the world. The other benefit is technical advice. Obviously, Illumina works with a lot of other species. They've been down this path before and they can give you a lot of help and support in what they think is right, as well as what has worked well previously.

5 Most Recent Companion Animal Publications

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Hospital and community ampicillin-resistant Enterococcus faecium are evolutionarily closely linked but have diversified through niche adaptation.
de Regt MJ, van Schaik W, van Luit-Asbroek M, Dekker HA, van Duijkeren E, Koning CJ, Bonten MJ, Willems RJ

Abstract

Ampicillin-resistant Enterococcus faecium (ARE) has emerged as a nosocomial pathogen. Here, we quantified ARE carriage in different community sources and determined genetic relatedness with hospital ARE.

PLoS One 7 e30319 2012
Dissemination of pHK01-like incompatibility group IncFII plasmids encoding CTX-M-14 in Escherichia coli from human and animal sources.
Ho PL, Lo WU, Yeung MK, Li Z, Chan J, Chow KH, Yam WC, Tong AH, Bao JY, Lin CH, Lok S, Chiu SS

Abstract

Few studies have compared CTX-M encoding plasmids identified in different ecological sources. This study aimed to analyze and compare the molecular epidemiology of plasmids encoding CTX-M-14 among strains from humans and animals. The CTX-M-14 encoding plasmids in 160 Escherichia coli isolates from animal faecal (14 pigs, 16 chickens, 12 cats, 8 cattle, 5 dogs and 3 rodents), human faecal (45 adults and 20 children) and human urine (37 adults) sources in 2002-2010 were characterized by molecular methods. The replicon types of the CTX-M-14 encoding plasmids were IncFII (n=61), I1-I? (n=24), other F types (n=23), B/O (n=10), K (n=6), N (n=3), A/C (n=1), HI1 (n=1), HI2 (n=1) and nontypeable (n=30). The genetic environment, ISEcp1 -bla(CTX-M-14) - IS903 was found in 89.7% (52/58), 87.7% (57/65) and 86.5% (32/37) of the animal faecal, human faecal and human urine isolates, respectively. Subtyping of the 61 IncFII incompatibility group plasmids by replicon sequence typing, plasmid PCR-restriction fragment length polymorphism and marker genes (yac, malB, eitA/eitC and parB/A) profiles showed that 31% (18/58), 30.6% (20/65) and 37.8% (14/37) of the plasmids originating from animal faecal, human faecal and human urine isolates, respectively, were pHK01-like. These 52 pHK01-like plasmids originated from diverse human (20 faecal isolates from 2002, 2007 to 2008, 14 urinary isolates from 2004) and animal (all faecal, 1 cattle, 1 chicken, 5 pigs, 9 cats, 1 dog, 1 rodent from 2008 to 2010) sources. In conclusion, this study highlights the importance of the IncFII group, pHK01-like plasmids in the dissemination of CTX-M-14 among isolates from diverse sources.

Vet Microbiol 2012
Parallel mapping and simultaneous sequencing reveals deletions in BCAN and FAM83H associated with discrete inherited disorders in a domestic dog breed.
Forman OP, Penderis J, Hartley C, Hayward LJ, Ricketts SL, Mellersh CS

Abstract

The domestic dog (Canis familiaris) segregates more naturally-occurring diseases and phenotypic variation than any other species and has become established as an unparalled model with which to study the genetics of inherited traits. We used a genome-wide association study (GWAS) and targeted resequencing of DNA from just five dogs to simultaneously map and identify mutations for two distinct inherited disorders that both affect a single breed, the Cavalier King Charles Spaniel. We investigated episodic falling (EF), a paroxysmal exertion-induced dyskinesia, alongside the phenotypically distinct condition congenital keratoconjunctivitis sicca and ichthyosiform dermatosis (CKCSID), commonly known as dry eye curly coat syndrome. EF is characterised by episodes of exercise-induced muscular hypertonicity and abnormal posturing, usually occurring after exercise or periods of excitement. CKCSID is a congenital disorder that manifests as a rough coat present at birth, with keratoconjunctivitis sicca apparent on eyelid opening at 10-14 days, followed by hyperkeratinisation of footpads and distortion of nails that develops over the next few months. We undertook a GWAS with 31 EF cases, 23 CKCSID cases, and a common set of 38 controls and identified statistically associated signals for EF and CKCSID on chromosome 7 (P(raw) 1.9×10(-14); P(genome)?=?1.0×10(-5)) and chromosome 13 (P(raw) 1.2×10(-17); P(genome)?=?1.0×10(-5)), respectively. We resequenced both the EF and CKCSID disease-associated regions in just five dogs and identified a 15,724 bp deletion spanning three exons of BCAN associated with EF and a single base-pair exonic deletion in FAM83H associated with CKCSID. Neither BCAN or FAM83H have been associated with equivalent disease phenotypes in any other species, thus demonstrating the ability to use the domestic dog to study the genetic basis of more than one disease simultaneously in a single breed and to identify multiple novel candidate genes in parallel.

PLoS Genet 8 e1002462 2012
Rates of mutation and host transmission for an Escherichia coli clone over 3 years.
Reeves PR, Liu B, Zhou Z, Li D, Guo D, Ren Y, Clabots C, Lan R, Johnson JR, Wang L

Abstract

Although over 50 complete Escherichia coli/Shigella genome sequences are available, it is only for closely related strains, for example the O55:H7 and O157:H7 clones of E. coli, that we can assign differences to individual evolutionary events along specific lineages. Here we sequence the genomes of 14 isolates of a uropathogenic E. coli clone that persisted for 3 years within a household, including a dog, causing a urinary tract infection (UTI) in the dog after 2 years. The 20 mutations observed fit a single tree that allows us to estimate the mutation rate to be about 1.1 per genome per year, with minimal evidence for adaptive change, including in relation to the UTI episode. The host data also imply at least 6 host transfer events over the 3 years, with 2 lineages present over much of that period. To our knowledge, these are the first direct measurements for a clone in a well-defined host community that includes rates of mutation and host transmission. There is a concentration of non-synonymous mutations associated with 2 transfers to the dog, suggesting some selection pressure from the change of host. However, there are no changes to which we can attribute the UTI event in the dog, which suggests that this occurrence after 2 years of the clone being in the household may have been due to chance, or some unknown change in the host or environment. The ability of a UTI strain to persist for 2 years and also to transfer readily within a household has implications for epidemiology, diagnosis, and clinical intervention.

PLoS One 6 e26907 2011
Viral transcriptome analysis of feline immunodeficiency virus infected cells using second generation sequencing technology.
Ertl R, Birzele F, Hildebrandt T, Klein D

Abstract

Feline immunodeficiency virus (FIV) is a widespread pathogen causing immunodeficiency in domestic cats and related wild cat species. The virus genome includes the main structural genes common to all retroviruses as well as accessory genes displaying essential functions during the viral life cycle. Expression of viral genes involves transcription of provirus genomes into full-length transcripts, which are partially processed into several spliced mRNA variants for the translation of particular proteins. Among several FIV isolates derived from domestic cats, notable differences in pathogenicity could be observed leading to identification of low and high pathogenic virus isolates. This study investigates the viral transcriptome of two differentially virulent FIV strains using second generation sequencing (SGS) technology. The expression levels of viral genes as detected by SGS were additionally determined by reverse transcription quantitative PCR analysis in order to compare two methods of mRNA quantification. The different properties of both methods, especially regarding normalization between samples, had to be considered when comparing the resulting data. SGS turned out to be a suitable technique for comparing mRNA transcription between both FIV infected cell lines and the identification of spliced viral transcripts. In contrast to this, the quantification of these spliced isoforms using SGS data was impeded by the short length of sequencing reads. In summary, SGS analysis revealed very consistent mRNA levels for the majority of viral genes between the low pathogenic Petaluma and the more highly pathogenic Glasgow 8 isolate. Notable differences among the two FIV strains could be observed in the viral mRNA splicing where Glasgow 8 displays similarities to the transcription pattern seen in the early stages of natural lentivirus infections. Thus, divergences in the regulation of post-transcriptional RNA processing might represent an additional contributor to the diverse pathogenic effects of individual FIV isolates. Taken together, this study aims to investigate the viral transcriptome as one part of the complex network of virus-host interactions, which will contribute to gaining deeper insights into FIV pathogenesis.

Vet Immunol Immunopathol 143 314-24 2011

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