MRDNA 16s DNA Sequencing Service

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Our Sequencing Platforms

MRDNA HiSeq 16s Sequencing
MRDNA MiSeq 16s Sequencing
MRDNA PGM 16s Sequencing

Illumina HiSeq

 

  The addition of the HiSeq 2500 to our portfolio of sequencers allows us to better serve you, our customers. The innate flexibility of this instrument provides us with the…

 

 

 

Illumina MiSeq

 

Illumina’s MiSeq is quickly becoming the sequencer of choice for researchers, such as yourself, to carryout their genomic and targeted resequencing studies. The highly experienced team at MR DNA is…

 

 

 

Pacbio Sequel

 

The PacBio Sequel is the newest sequencing platform released by Pacific Biosciences. The PacBio Sequel, aptly named, follows the release of the PacBio RS II System; one of the first to offer read lengths greater than 20Kb, and the PacBio Sequel is no different...

Ion Torrent PGM

 

The Ion PGM supplies an innovative approach to sequencing technology. Utilizing the semiconductor technology employed by the PGM, the scientists at MR DNA are able to provide you, our customer, with…

 

 

 

16s rRNA Sequencing

 

The 16s rRNA gene is the ideal target to complete metagenomic studies. Our in-house 16s sequencing primers are designed to target the nine hypervariable regions. MRDNA amplicon sequencing methods are not limited to bacteria, but include fungi, archaea, and eukaryotes.

Whole Genome Sequencing

 

We offer a wide range of NGS platforms, making whole genome sequencing all the more affordable. From small microbial genomes to larger eukaryote genomes, whole genome sequencing provides researchers the opportunity to identify disease causing variants without the labor of traditional microbiology techniques.

Microbiome Sequencing

 

MRDNA is passionate about microbiome research. In addition to our 16s sequencing service, we also offer Shotgun metagenome sequencing services. From targeted taxonomic analysis to a complete overview metabolic pathways, allow us to combine our experience in microbiome analysis to your research project.

Our Services

Today's Research

Transcriptome analysis of the epidermis of the purple quail-like (q-lp) mutant of silkworm, Bombyx mori

 

A new purple quail-like (q-lp) mutant found from the plain silkworm strain 932VR has pigment dots on the epidermis similar to the pigment mutant quail (q). In addition, q-lp mutant larvae are inactive, consume little and grow slowly, with a high death rate and other developmental abnormalities. Pigmentation of the silkworm epidermis consists of melanin, ommochrome and pteridine. Silkworm development is regulated by ecdysone and juvenile hormone. In this study, we performed RNA-Seq on the epidermis of the q-lp mutant in the 4th instar during molting, with 932VR serving as the control. The results showed 515 differentially expressed genes, of which 234 were upregulated and 281 downregulated in q-lp. BLASTGO analysis indicated that the downregulated genes mainly encode protein-binding proteins, membrane components, oxidation/reduction enzymes, and proteolytic enzymes, whereas the upregulated genes largely encode cuticle structural constituents, membrane components, transport related proteins, and protein-binding proteins. Quantitative reverse transcription PCR was used to verify the accuracy of the RNA-Seq data, focusing on key genes for biosynthesis of the three pigments and chitin as well as genes encoding cuticular proteins and several related nuclear receptors, which are thought to play key roles in the q-lp mutant. We drew three conclusions based on the results: 1) melanin, ommochrome and pteridine pigments are all increased in the q-lp mutant; 2) more cuticle proteins are expressed in q-lp than in 932VR, and the number of upregulated cuticular genes is significantly greater than downregulated genes; 3) the downstream pathway regulated by ecdysone is blocked in the q-lp mutant. Our research findings lay the foundation for further research on the developmental changes responsible for the q-lp mutant.

 

 

 

 

Wang P, Qiu Z, Xia D, Tang S, Shen X, Zhao Q (2017) Transcriptome analysis of the epidermis of the purple quail-like (q-lp) mutant of silkworm, Bombyx mori. PLoS ONE 12(4): e0175994. https://doi.org/10.1371/journal.pone.0175994

February 17, 2017

According to the Crohn's and Colitits Foundation of America, 1.6 million Americans have been diagnosed with some form of inflammatory bowel disease.  Due to the prevalence  and the nature of IBD, Chrohn's disease and Ulcerative Colitis are popular targets to complete microbiome studies. Studying the human microbiome via 16s rRNA sequencing may be one of the more popular research topics in the literature today. Dr. Dirk Haller from the Technical Univerisity of Munich recently investigated the implications of iron deficiency treatments in patients with IBD. Due to the inflammation present in the tissue of IBD patients cause these patients to also be anemic. In order to account for this nutrient deficiency, patients with IBD typically undergo sometype of Iron replacement therapy. Dr. Haller and his team found that while patients with Chrohn's disease and Ulcerative Colitis can experience noticeable shifts in their microbiome, these shift cannot always be attributed to their primary pathology. Over short periods of time, Iron replacement therapy also caused shifts in the microbial characterization of the GI tract of these patients. These shifts were detected by targeted sequencing of the V4 region of the 16s rRNA gene on the Illumina MiSeq system.

 

Lee T, Clavel T, Smirnov K, et al. Oral versus intravenous iron replacement therapy distinctly alters the gut microbiota and metabolome in patients with IBD. Gut. 2016;

February 13, 2017

In The News

In The News

We all know that physical exercise is important to our health. Exercise can influence the health of our heart, the health of our brain, and...you guessed it, the health of our gut. A research team from the European University conducted a study evaluating the gut microbiome of women who led active or sedentary lifestyles. Using a combination of 16s rRNA sequencing and quantitative PCR, Bressa, C. et al., discovered that not only does the activity level in women alter the characterization of the gut microbiome, but women who led a more active lifestyle had an increased abundance of probiotics in their microbiota. The research team began their study by sampling the stool of women aged 18-40 with a similar body mass index. Subsequent to DNA extraction, Bressa, C. et al., targeted the V3-V4 region of the 16s rRNA gene and completed sequencing using the Illumina MiSeq. Interestingly, the research team from Spain did not find a significant increase in bacterial diversity in those women who led a more active lifestyle. However, there was a negative correlation between a sedentary life and the diversity of the bacteria found in the gut microbiome.

 

Bressa C, Bailén-Andrino M, Pérez-Santiago J, González-Soltero R, Pérez M, Montalvo-Lominchar MG, et al. (2017) Differences in gut microbiota profile between women with active lifestyle and sedentary women. PLoS ONE 12(2): e0171352. doi:10.1371/journal.pone.0171352

16s Sequencing

16s sequencing is one of the go to sequencing methods to complete microbiome studies. 16s sequencing involves sequencing of the 16s rRNA gene found in all bacteria and archaea. The fact that the 16s rRNA gene can be found in all prokaryotes make the 16s gene the ideal candidate to characterize the microbiome of numerous environments. Another key factor that makes the 16s gene an ideal candidate for microbiome characterization is the fact that there are both highly conserved regions and highly variable regions within the gene. The highly conserved regions within the 16s rRNA gene make great targets for PCR primers bind to and replicate thereby producing millions of copies of the targeted hypervariable region that is flanked by the highly conserved regions. The 16s rRNA gene contains 9 hypervariable regions that can be targeted in order to gain insight into the diversity amongst prokaryotes.

 

16s rRNA sequencing has grown in popularity over the last decade due in large part to next-generation sequencing. NGS, also known as high-throughput sequencing, has drastically reduced the cost of DNA sequencing due to its capability to sequence hundreds of samples at a time. In the past, capillary electrophoresis was able to produce ~1Mb per run, and today, with instruments such as the Illumina HiSeq, we are able to produce ~500 Gb per run. Until recently, one metric that Sanger sequencing had as an advantage over NGS instruments such as the Illumina MiSeq and Ion Torrent was read length. On average, capillary electrophoresis was able to achieve read lengths up to 1,000bp in comparison to the 400-600bp read lengths provided by Illumina and Ion Torrent. However, the PacBio Sequel now allows researchers the ability to achieve read lengths ranging from 10-30Kb. What does this mean for 16s rRNA sequencing? We can now sequence the entire 16s rRNA gene, which is approximately 1.5Kb in length. Whether your goal is to target one specific hypervarible region or the entire 16s rRNA gene, there is a NGS platform for you.

 

 

Metagenome Sequencing

Metagenome sequencing is a term that can cause a lot of confusion, as well as bring so much joy to microbiologists around the world.  Metagenome sequencing is a sequencing method that investigates the DNA extracted from an environmental sample as a whole. Whereas certain DNA sequencing techniques will target a specific organism from a specific environment, metagenome sequencing targets all microbial organisms found in a certain environment. There are predominantly two methods used to completely metagenomics studies, 16s rRNA sequencing and Shotgun metagenome sequencing. The difference between the two sequencing methods can be found in their names. 16s rRNA sequencing, as you would expect, targets only the 16s rRNA gene, while Shotgun metagenome sequencing targets all genes present in your sample. How is this accomplished?

 

Shotgun metagenome sequencing involves the random shearing of all DNA present in a particular sample. These smaller fragments are sequenced on NGS platforms such the Illumina MiSeq and then reassembled. Because shotgun metagenomics is non-discriminatory, not only are you able to gain taxonomic information, similar to 16s sequencing, but you are also able to gain insight to the presence of functional genes as well. Overall, shotgun metagenome sequencing provides a more complete picture of your environmental sample. NGS platforms such as the Illumina HiSeq allow researchers to ability to sequence their metagenome samples to a much greater depth. Why is sequencing depth important? Naturally, the most abundant organisms in your sample will receive the most amounts of data, and because you are not specifically targeting certain organisms, without sufficient sequencing coverage, you run the risk of not identifying those organisms that may be underrepresented. From the human microbiome, to pond water, and to the rumen of cattle, shotgun metagenome sequencing paired with NGS platforms has the ability to take your ecological study to the next level.

 

 

February 10, 2017

The  human microbiome continues to be a field of major focus, not just for the scientific community, but for scientists and average joe alike. Whether you're a teenager searching for the next self-help tip to clear up your acne, or your a leading researcher investigating the link between the bacteria in our GI tract and disease such as Alzheimer's or Diabetes, the secrets the human microbiome can provide are becoming all encompassing. Not only is the human microbiome a point of interest for everyone across the world, but is now a point of interest for everyone out of this world. Astronaut Scott Kelly was the first man to spend a full year in space. As if being the first person to spend a year in space didn't make him unique enough, Scott is also a twin. Scott and his brother, Mark, a fellow astronaut, have undergone numerous studies upon Scott's return to Earth. A research group from Northwestern University has undertaken the task of investigating the effects of gravity on the human microbiome. The scientific community is well aware that certain changes to your diet can alter the Bacteroidetes and Firmicutes ratio, but we now know that this ratio is not only altered by our diet but by the force of gravity placed on our bodies. While still early in the study, Fred W. Turek and the rest of the team have found something of significant interest when comparing the microbiomes of the Kelly twins. The bacterial diversity found in Scott remained more constant in comparison to his earth-bound brother. So if you're one of the few who has booked the next rocket ship to space, along side Richard Branson, remember to take a few samples while in space and become a part of not just citizen science, but galactic science.

 

Source: Fellman, M., (2017). Change in astronaut’s gut bacteria attributed to spaceflight. Northwestern Now. https://news.northwestern.edu/stories/2017/february/change-in-astronauts-gut-bacteria-attributed-to-spaceflight/

January 19, 2017

Type 1 diabetes, also known as juvenile diabetes, only comprises ~5% of those diagnosed with diabetes. Unlike type 2 diabetes, individuals diagnosed with Type 1 diabetes cannot resort to change in lifestyle or diet with the hopes of no longer being diabetic. Type 1 diabetes is a result of an autoimmune process where cells that should produce insulin are destroyed thereby eliminating that individual from processing sugar into energy. While the onset of Type 1 diabetes cannot be prevented or cured with a change in diet per se, researchers have discovered that the gut microbiota may play a key role in reducing the likelihood of disease occurrence. Stewart et al., have used previous research, documenting the relationship between Type 1 diabetes and the gut microbiota, as a launching point towards investigating the microbiome of individuals diagnosed with Type 1 diabetes with good glycaemic control and a high level of physical fitness in comparison with healthy individuals. The research team successfully characterized the gut microbiota by sampling 20 stool samples and performing 16s rRNA sequencing using the Illumina MiSeq platform. The results of this study indicate that the microbiome of Type 1 diabetics who have optimal glycemic control and good physical fitness closely resembles that found in non-diabetic individuals. Future research may find that, because it is possible to exhibit a diverse and well balanced microbiota under well-maintained Type 1 diabetes, alterations to the gut microbiota may be able to influence the onset of such a disease.

 

 

Source: Stewart CJ, Nelson A, Campbell MD, et al. Gut microbiota of Type 1 diabetes patients with good glycaemic control and high physical fitness is similar to people without diabetes: an observational study. Diabet Med. 2017;34(1):127-134.

January 17, 2017

One of the key areas of metagenomic and microbiome research has been on the transmission of bacteria from mother to infant . Asnicar et al., recently published a study where they sampled 5 mother-infant pairs collecting both fecal and breast milk samples. In order to characterize the microbiome of each pair, DNA was extracted and prepared for metagenomic sequencing on the Illumina HiSeq 2500. Both breast feeding and delivery method have both been seen to play an important role in the diversity of the microbiome of infants relative to their mothers. A vaginal delivery has been documented as providing the infant with a much more diverse microbiome thereby decreasing the likelihood of the infant from succumbing to certain health risks a newborn would experience following a C-section. The research team from Italy postulates that the seemingly apparent transmission of bacteria from mother to infant based on species commonality may not be the most thorough investigative method. "It is therefore imperative to assess whether shared microbes belong to the same genetic variant (i.e., strain) to support the hypothesis of vertical transmission.", states Asnicar et al. Through shotgun metagenomics, the research team was able to assess that based on strain similarity, there does appear to be evidence in support of vertical transmission of the mother's microbiome to their infant. Even as early as 3 months does the microbiome of the infant begin to shift to to what the research team describes as "mother-like".

 

Source: Studying Vertical Microbiome Transmission from Mothers to Infants by Strain-Level Metagenomic Profiling. mSystems. 2017;2(1):e00164-16.

January 16, 2017

Have we entered a new era DNA sequencing? An era where DNA sequencing has become so commonplace that the curiosity of the general public is able to inspire new scientific studies. An era of "cultural genomics". The latest study of the Canadian beaver seems to be one of the first endeavors in "cultural genomics." The research team, based in Toronto, states , "We release the beaver genome to mark Canada’s sesquicentennial, and hope the initiative will catalyze other exploratory investigations in “cultural genomics,” of which this project was motivated by a nation’s curiosity and the pride in the animal that has most shaped its history." The world of DNA sequencing and genomics has come a long way since the human genome project. Popularized by "CSI" TV shows and citizen science projects, the general public has become very familiar with the overall concept of DNA sequencing and the capabilities available to the scientific community. As DNA sequencing methods, such as whole genome sequencing, continue to drop in price, the more the scientific community can take an interest in the concerns and ideas of their surrounding communities and investigate topical issues like the history of the Canadian beaver. Lok et al., utilized both the PacBio RSII and Illumina HiSeq X systems to preform de novo genome and de novo transcriptome sequencing. Both of these technologies have allowed the cost of genome and transcriptome sequencing to decrease dramatically and the sequencing power to increase. The results of the genome assembly generated by the Illumina HiSeq X indicate that the research team was able to achieve 160x coverage of the 4 billion bp beaver genome. As sequencing power and popularity continue to progress, it is not difficult to imagine whole genome sequencing becoming a routine test ordered by your family physician.

 

Source: Lok S, Paton TA, Wang Z, et al. De novo genome and transcriptome assembly of the Canadian beaver (Castor canadensis). G3 (Bethesda). 2017;

January 13, 2017

In the past few years the world of DNA sequencing has seen a rapid appearance of new next-generation sequencing instruments. Some the new comers include the Illumina NextSeq and the recently announced Illumina NovaSeq. Other companies that are making a niche for themselves in this market are PacBio, with their Sequel system, and Oxford Nanopore, with their MinIon. Ma, Stachler, and Bibbly, recently published a study evaluating the abilities of the Oxford Nanopore MinIon to successfully complete 16s rRNA microbiome studies. With run costs similar to that of the more popular Illumina MiSeq, and a footprint the size of your thumbdrive, it is easy to see what scientists from all over the world are eager to see this "mini" sequencer in action. One of the immediate benefits of the MinIon over some of the more popular NGS platforms is its ability to perform real-time data analysis. But can we have speed without sacrificing accuracy? The team from the University of Pittsburgh found that the data generated by the MinIon did not successfully characherize 6 of the 11 phyla detected by the Illumina Platfrom. Overall, Oxford Nanopore's MinIon is not able to produce the necessary results to successfully capture the microbial diversity in 16s rRNA microbiome studies. The high error rates that are known to plague the MinIon contribute greatly the lack of taxonomic identification. The entire research world is waiting to see if Oxford Nanopore can increase their run quality, because with their run cost and speed, paired with their read length, the MinIon is on the verge of being a vital part of the world of microbiome research.

 

Source: Ma, X., Stachler, E., & Bibby, K. (2017). Evaluation of Oxford Nanopore MinION Sequencing for 16S rRNA Microbiome Characterization. doi:10.1101/099960

January 12, 2017

On January 10, 2017, The National Institutes of Health opened an initiative to encourage applicants for funding of genomic research with a special interest in identifying variants in the human genome that may be linked to substance abuse. Previous studies have provided evidence for the existence of a link between the our DNA and the likelihood of an individual developing an addition to habit forming substances. There are ~ 3.5 billion Americans addicted to alcohol, tobacco, and/or illicit drugs, and it is safe to say this initiative set forth by the NIH is a necessary step in improving the public health of this country. With the hopes of identifying genetic risk factors via whole-genome sequencing, this type of federal funding may be just what scientists need to reduce the millions of deaths that result each year stemming from addiction. Researchers such as Wang et al., have focused their efforts on investigating the rare variants related to addiction. In order to identify these rare variants, investigators are utilizing the sequencing power of next-generation sequencing instruments to complete whole-genome and whole-exome sequencing studies. The sequencing depth that NGS instruments such as the Illumina HiSeq provide has uncovered thousands of variants, but unfortunately, the majority of these variants have only been identified from a select group of candidate genes linked to substance abuse. Clearly, based on this funding initiative, this is an area of research the NIH is looking to expand and not limit to only identifying certain variants, but to gain a greater comprehension on gene expression, the effects of small RNAs, and disease progression.

 

Source: Wang S, Yang Z, Ma JZ, Payne TJ, Li MD. Introduction to deep sequencing and its application to drug addiction research with a focus on rare variants. Mol Neurobiol. 2014;49(1):601-14.

January 11, 2017

Next-generation sequencing is not only opening doors into the future, but also provides a window into the past. Once limited to only mitochondrial sequencing, DNA sequencing of ancient organisms has excelled leaps and bounds since the early 1980s. This amount of growth in such a short amount of time is due to technological advancements in high-throughput sequencers developed by Illumina, PacBio, and Ion Torrent (Thermo Fisher). From mtDNA sequencing to whole genome sequencing, NGS platforms offer researchers the opportunity to sequencing ancient DNA with much greater specificity and depth than ever before. Devault et al., recently published a study in eLIFE documenting the sequencing of bacteria extracted from 30 year old woman buried 800 years ago near the ancient city of Troy. The research team was able to take advantage of modern DNA extraction kits, such as the MoBio PowerSoil kit, as well as the Illumina MiSeq  and HiSeq sequencing platform to not only perform mtDNA sequencing, but whole genome sequencing with up to ~300x coverage. This type of sequencing depth even a few years ago would have been unheard of, but today is common place for both modern day and ancient DNA samples. The two bacterial species sequenced were Staphylococcus saprophyticus and Gardnerella vaginalis. Devault et al. discovered that while G. vaginalis closely resembled that which we would find today, S. saprophyticus more closely resembles that which would be found in the from the time period this woman was buried.

 

Source: Devault AM, Mortimer TD, Kitchen A, et al. A molecular portrait of maternal sepsis from Byzantine Troy. Elife. 2017;6

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