12.12.12 on 12.12.12

Sorry – just had to have a post at 12.12.12 on 12.12.12.

Award: Ridiculous, absurd, offensive overselling of the microbiome from Chalmers & Gothenburg

Wow.  This is painful.  There is a press release that came out a few days ago: Changes in the gut bacteria protect against stroke.  In it they report on a new paper showing some interesting results comparing the metagenomes of gut microbiota in stroke patients vs healthy patients.  They found some interesting differences.  And they then made absurd, dangerous, self-serving claims that completely confuse the issue of correlation vs. causation.

Basically, they found carotenoid production genes to be more abundant in the people who were healthy.  And they then appear to have concluded that production of carotenoids by bacteria in the gut protects from strokes.  Completely ridiculous.  No evidence whatsoever is presented that such production of carotenoids by gut microbes does anything of the kind.   Compare the semi careful wording in the paper

Our finding of enriched levels of phytoene dehydrogenase in the metagenomes of healthy controls and its association with elevated levels of β-carotene in the serum may indicate that the possible production of this anti-oxidant by the gut microbiota may have a positive health benefit

To the drivel in the release

Our results indicate that long-term exposure to carotenoids, through production by the bacteria in the digestive system, has important health benefits. These results should make it possible to develop new probiotics. We think that the bacterial species in the probiotics would establish themselves as a permanent culture in the gut and have a long-term effect

As a bonus, they promote a new company of their Metabogen in the press release.   Here’s a suggestion.  Do not invest in this company and do not believe anything they do (unless they retract the claims in the PR).  The people involved in this press release, which also are associated with this company, are overselling their own work, do not seem to understand the difference between correlation and causation, and are making dangerous claims about health benefits.

And thus I am awarding them my coveted “Overselling the microbiome award.”  Past awards include:

UPDATE 1: 7:30 PM 12/11/12

Some of the other parts of the press release that are bad:

  • The title: “Changes in the gut bacteria protect against stroke.” Are you kidding me?  Ridiculous claim with no evidence.
  • Another line: “Jens Nielsen, Professor of Systems Biology at Chalmers, says that it may be preferable to take probiotics instead – for example dietary supplements containing types of bacteria that produce carotenoids.”  So now they have jumped from a correlation in what microbes are present to treating people with probiotics.  Just what priobiotics are they going to use? And is there any evidence that they help?

Guest post on "The phone microbiome" from Georgia Barguil in Jack Gilbert’s lab

From @Artologica on Etsy.  The Phonome. 

Today we have a very special guest post from Georgia Barguil in Jack Gilbert’s group at University of Chicago / Argonne National Lab.  Georgia has been coordinating analyses of microbial surveys that have been a collaboration between me and Jack (although really driven by Jack and his lab in most ways).  The study subject: cell phones and shoes.  The study locations: conferences and meetings in order to have participation in microbial surveys by “citizen” scientists of one kind or another.  We did this together at the AAAS meeting.  And then Gilbert’s lab did this at ThirstDC.  And then I did this at SciFoo at Google HQ.  We are working on a paper on this and wanted to get some results out to the community so Georgia wrote up this post.


Ever wanted to know what bacteria are on your shoes and phones? Of course you have! Here we explored the bacteria that call shoes and phones home; the shoes and phones belonged to employees at Google’s Headquarters, and to participants at the Thirst DC and AAAS annual meeting conferences over 2012 (Fig. 1). Altogether, 84 phones (34 from GoogleHQ, 23 from ThirstDC and 27 from AAAS) and 68 shoes (15 from SciFoo, 24 from ThirstDC and 29 from AAAS) were sampled. The DNA of these samples was extracted and the bacteria were identified by sequencing and subsequent computational analysis of a key gene (16SrRNA) found in all bacteria. Here we show some of the results.

Fig. 1: Map showing the 3 sampling locations: AAAS in Vancouver, SciFoo in California and ThirstDC in Washington

There are quite a lot of microorganisms found in these environments, as you can see in the graph below (Fig. 2), where each bar represents a sample and each color represents a group of bacteria. Also by looking at the chart you can see that the bacteria that live on phones and shoes are different, and found in different proportions. Actually, by comparing the bacterial profile from an unidentified sample with this collection, we could tell you whether that sample was from a phone or a shoe!

Fig. 2: Genus-level diversity and abundance of bacteria associated to phone and shoe samples.

In the shoe samples you can see a lot more colors, which implies that the shoes are home to more bacterial groups than the phones. Out of 560 groups of bacteria found, there were 90 that favored either shoes or phones; 70 of these groups favored the shoe environment while the other 20 favored the phone. Some of the groups that preferred the phones were:

  • Streptococcus (dark green)- many streptococcal species are nonpathogenic, and form part of the commensal human microbiome of the mouth, skin, intestine, and upper respiratory tract.
  • Staphylococcus (brown)- most species of this genus are harmless and reside normally on the skin and mucous membranes of humans and other organisms.
  • Rothia (gray)- is a common inhabitant of the human oral cavity and respiratory tract. Some species were identified as gluten-degrading natural colonizers of the upper gastro-intestinal tract.
  • Actinomyces (army green)- normally present in the gingival area, they are part of the commensal flora, and are the cause of most common infection in dental procedures and oral abscesses. Many Actinomyces species are opportunistic pathogens of humans and other mammals, particularly in the oral cavity. In rare cases, these bacteria can cause actinomycosis, a disease characterized by the formation of abscesses in the mouth, lungs, or the gastrointestinal tract.
  • Prevotella (red)- has been a problem for dentists for years. As a human pathogen known for creating periodontal and tooth problems, Prevotella has long been studied in order to counteract its pathogenesis.
  • Gemella (bright yellow)- group of bacteria primarily found in the mucous membranes of humans and other animals, particularly in the oral cavity and upper digestive tract
  • Micrococcus (pale green)- have been isolated from human skin.
  • Corynebacterium (yellow)- occurs commonly in nature in the soil, water, plants, and food products. The non-pathogenic Corynebacterium species can even be found in the mucosa and normal skin flora of humans and animals.
  • Propionibacterium (pale blue)- members of this group are primarily facultative parasites and commensals of humans and other animals, living in and around the sweat glands, sebaceous glands, and other areas of the skin. They are virtually ubiquitous and do not cause problems for most people, but some propionobacteria have been implicated in acne and other skin conditions.

It is evident that all of these groups are commonly found in the skin and mucous membranes of humans, so it is expected that these groups occur in phones due to the close contact with the hands, face, mouth and breath.

In the plot below (Fig. 3), phones (blue squares) and shoes (orange triangles) from all sampling locations were analyzed together and you can see that phones harbor a very different community to shoes (in fact this is a statistically significant difference) – but shoes all look quite similar while phone microbiome are actually quite variable. It may be possible that the microbiome of your phone is reasonably unique to you, and that we could tell whose phones was who’s by the microbes that lived on the phone.

Fig. 3: Principal coordinate analysis (PCoA) plot using the UniFrac distance obtained for all phone (blue squares) and shoe (orange triangles) samples.

When dividing the samples according to geographical location instead of phones/shoes (Fig. 4), the three sampling locations do not form discrete clusters, and are not statistically significantly different (p>0.05), which suggests that no matter the geographical location you sample, you will find similar bacterial communities.

Fig. 4:PCoA plot using the UniFrac distance obtained for both phone and shoe samples from the 3 sampling locations. The red squares represent AAAS samples, while the blue circles and orange triangles represent SciFoo and ThirstDC, respectively.

However, if we only consider the bacteria found on shoes (Fig. 5), then GoogleHQ (green circle) is statistically different from both AAAS (red square) and ThirstDC (blue triangle). This difference is mostly due to a higher abundance of Corynebacterium and Kocuria groups found in the GoogleHQ shoe samples.

Fig. 5: PCoA plot using the UniFrac distance obtained for all shoe samples from SciFoo (green circles), AAAS (red squares) and ThirstDC (blue triangles).

The microbiota found in phones was highly similar among the three sampling locations (Fig. 6), indicating that phones tend to harbor the same groups of microorganisms even in different locations, regardless of the phone model and owner microbiota. As it can be observed in the plot below, phone samples from AAAS (red squares), ThirstDC (orange triangles) and SciFoo (blue circles) are interspersed.

Fig. 6: PCoA plot using the UniFrac distance obtained for all phone samples in the 3 sampling locations. GoogleHQ is represented by the blue circles, while Thirst DC and AAAS are represented by orange triangles and red squares, respectively.

In conclusion, there were more biological differences between shoes and phones than between the three geographical locations. Phones and shoes harbored microbiomes representing the environments they most often came into contact with. Phones were closely related to the skin and upper respiratory tract, and shoes reflected the bacteria found in soil and the environment.

Although many of the groups found both in shoes and phones have pathogenic representatives, you should not be scared, as it does not mean that you are going to get sick. Most of the isolated, characterized and sequenced bacterial groups available in the sequence databases are the pathogenic ones, exactly because of their importance to human health by aiding in the diagnosing and treatment of diseases. Some of the “relatives” of these pathogenic bacteria are actually good-guys that are usually present in your normal microbiota and do not represent any risks, in fact they may actually be preventing the ‘bad-guys’ from growing on your phone!  On the other hand, it is always a good idea to clean your cell phone screen once in a while, just to be safe.


For some other reading about the phone sampling efforts see

Some fun holiday reading about the UC Davis Medical Center neurosurgeon saga

Well, here are some new news stories to read:

For some background see my detailed post with much of the history in the story here.
I must say, it certainly seems time to replace the administration at the UC Davis Medical Center.  The Dean is stepping down, but not for some months (see Amid controversy, Claire Pomeroy to step down as UC Davis med).  The main administrator Ann Madden Rice is still there.  I wouldn’t expect her to stay for long.

Attention all metagenomicists: put your pinky in the corner of your mouth & say "1 million dollars"

Already posted this to Twitter and Facebook but had to post here too.  This is wild.  DTRA has announced a $1 million prize for metagenomic analysis: DTRA Algorithm Challenge | Landing Page.  From their page

The Prize:
As nth generation DNA sequencing technology moves out of the research lab and closer to the diagnostician’s desktop, the process bottleneck will quickly become information processing. The Defense Threat Reduction Agency (DTRA) and the Department of Defense are interested in averting this logjam by fostering the development of new diagnostic algorithms capable of processing sequence data rapidly in a realistic, moderate-to-low resource setting. With this goal in mind, DTRA is sponsoring an algorithm development challenge. 

The Challenge:
Given raw sequence read data from a complex diagnostic sample, what algorithm can most rapidly and accurately characterize the sample, with the least computational overhead?

My instinct is to keep this to myself because, well, I want to win.  But my sharing side of things won out and I am posting here.  Maybe we (i..e, the community) can develop an open, collaborative project to do this?  Just a thought …

Get the genomes of up to 12 type strains of bacteria and/or archaea sequenced, for free

Barny Whitman asked me to post this announcement and, well, I am.  I made one edit below (see strikethrough) in honor of Norm Pace.

Genomic Sequencing of Prokaryotic Bacterial and Archaeal Type Strains

The Community Sequencing Program (CSP) Quarterly Microbial call of the DOE Joint Genomes Institute provides a great opportunity to obtain draft genomic sequences of the type strains of bacterial and archaeal species. The type strains may also include proposed species prior to publication. Type strains must be relevant to DOE mission areas, such as bioenergy, biogeochemistry, bioremediation, carbon cycling, and phylogenetic diversity. However, strains of human pathogens and human associated species are not eligible. Proposals for genome sequencing of type strains can be submitted through the CSP Quarterly Microbial call, whose deadline is December 17, 2012, with approval usually being completed within one month. Up to 12 strains can be included in each proposal. Proposals for larger numbers of strains need to be submitted to the CSP annual call in the spring. If you cannot make the December call, Quarterly calls are also scheduled for March 25, June 17, and September 23, 2013.

Proposals may be completed on-line at: http://proposals.jgi-psf.org/proposals. You will need to register and sign in to this server. Once on the server, follow the links to the “CSP Quarterly Microbial/Metagenome”. All strains will have to have been deposited in a culture collection, including proposed type strains prior to publication. If a culture collection ID is not available, you can attach a copy of the Certification of Availability. Once approved, you will need to provide 5-10 µg of high molecular weight DNA.

For questions, contact Barny Whitman, University of Georgia (whitman@uga.edu).

Further signs that microbiome work is getting hot: more $$ from NIH

Just got an email about this NIH program: RFA-RM-12-021: Evaluation of Multi-omic Data in Understanding the Human Microbiomes Role in Health and Disease (U54)

Some key points

  • Up to 3$ million per year
  • 1 or 2 awards
  • U54 Specialized Center
The human microbiome is, well, hot, and there continues to be money available to work on it …

Guest post: uBiome puts microbiome science in the hands of the people

It is a fascinating time to be doing microbiology. One of the latest occurrences is the spread of work on the human microbiome and even more recently the launching of several crowdfunding / citizen science efforts in this area. (Full disclosure – I am a collaborator on one of these efforts – the American Gut Project).  Another one of these efforts is a startup called uBiome. After seeing the announcement of their launch I asked Zac Apte, one of the founders, if he would be interested in writing a guest post for my blog on what they are doing. And, well, he agreed. And it is below (the post title “uBiome puts microbiome science in the hands of the people is from him too – I added the pic).


uBiome puts microbiome science in the hands of the people

Most people think “germs” is a dirty word. That’s what we’re taught since preschool. But the truth is that microbes aren’t just good or bad — it’s a lot more complicated than that. We are surrounded by microbes (on and inside of us) that form a complex ecosystem that supports and nourishes our health.

uBiome (www.indiegogo.com/ubiome) is a citizen science startup focused on allowing people direct access to this cutting ed research. By amassing a large set of microbiome samples along with health and lifestyle data, we will perform a microbiome-wide association study, examining specific traits as well as diseases such as diabetes, heart disease, hypertension, and depression in the context of the human microbiome.

We hope participants will join our community and track themselves in the long term — as you change your diet or exercise regime, begin taking a new medication, such as an antibiotic, or simply as you age. Now is a great time for a first data point.

Finally, we’re not just polling people for their poop. We’re also polling them for their creativity in scientific research. When our first dataset goes live, we’re going to ask our citizen scientists to form their own cohorts and we’ll empower them (statistically speaking) to test their own hypotheses. That’s our vision.

Our team has expertise in metagenomics as well as roots in population genetics, computer science, and network mathematics. We also have a team of scientific advisors which includes inventor and MacArthur Genius award winner Dr. Joseph DeRisi, biotechnology pioneer and inventor of the recombinant Hepatitis B vaccine Pablo Valenzuela, as well as doctors, bioinformaticians, and researchers.

We really appreciate Jonathan Eisen reaching out to give us this opportunity to say hello on the Tree of Life blog — and we look forward to engaging with you!

By Zac, Will and Jessica – the uBiome team

Genomics Standards Consortium meeting – GSC15, Bethesda, April 22-24, 2013

The 15th Workshop of the Genomic Standards Consortium (GSC15)

April
22-24, 2013, Bethesda, Maryland, USA.

Registration and EasyChair abstract submission website now open.

Theme: Standards-enabled Research in Genomics
URL: http://gensc.org/gc_wiki/index.php/GSC_15

The 15th Genomic Standards Consortium (GSC15) meeting will be held at
NIH (Bethesda, Maryland) from April 22-24th. This meeting will
highlight the utilization of genome metadata standards for the
enhancement of our biological understanding of microbes, the interaction
between microbial genomes, human health and disease. GSC15 will provide
a forum for standards developers, genome and metagenome researchers and
biological database developers to discuss their research, initiate
collaborations, join GSC working groups and engage in panel
discussions. The conference will include two days of plenary talks
featuring GSC projects and community standards efforts along with a
keynote speaker, discussion of standards among a government panel and
groups discussion panel. Day 3 of GSC15 will include concurrent GSC
working groups open to GSC15 participants.

Key Dates:
October 15, 2012: Registration opens, EasyChair abstract submission opens
December 20, 2012: Deadline for submission of abstracts
January 7, 2013: Decisions released on abstract
February 15, 2013: Registration closes

Abstract Submission:
Abstract for Outreach I and II session talks and GSC15 posters may be
submitted through EasyChair
(https://www.easychair.org/conferences/?conf=gsc15).

Outreach I and II and poster topics: Standards in Genomic and
Metagenomic projects. Development, integration and research findings
related to human, model organism or environmental projects, resources,
tools or databases.

Location: Natcher Conference Center, Building 45, NIH Campus, Bethesda,
Maryland, USA

For more detailed information, please visit the GSC 15 website at
gensc.org/gc_wiki/index.php/GSC_15

Daphne Koller (Coursera, MOOCs): Dec 6 3:30 pm Kemper 1003

Forwarding this:

Daphne Koller to Visit Davis

We are pleased to announce that Daphne Koller, co-founder of Coursera, a major provider of Massive Open Online Courses (MOOCs), will be visiting the UC Davis campus on Thursday, December 6 to deliver a lecture on this exciting new development in online learning. Please join us to learn more about the MOOC movement.

The Online Revolution: Education for Everyone
Thursday, December 6
3:30 – 4:30 pm
Kemper Hall 1003

Abstract: We are at the cusp of a major transformation in higher education. In the past year, we have seen the advent of MOOCs – massively open online classes (MOOCs) – top-quality courses from the best universities offered for free. These courses exploit technology to provide a real course experience to students, including video content, interactive exercises with meaningful feedback, using both auto-grading and peer-grading, and rich peer-to-peer interaction around the course materials. At Coursera, as of November 2012, we offer 207 courses from our 33 university partners, and over 1.9 million students from 196 countries. The courses start from bridge/gateway courses all the way through graduate courses, and span a range of topics including computer science, business, medicine, science, humanities, social sciences, and more. In this talk, I’ll report on this far-reaching experiment in education, and why we believe this model can provide both an improved classroom experience for our on-campus students, via a flipped classroom model, as well as a meaningful learning experience for the millions of students around the world who would otherwise never have access to education of this quality.

Daphne Koller
Professor of Computer Science, Stanford University; Co-Founder and co-CEO, Coursera

Daphne Koller is a Professor of Computer Science at Stanford University and the co-founder of Coursera, a social entrepreneurship company that works with top universities to make the best education freely accessible to everyone. In her research life, Koller works in the area of machine learning. She has received the Presidential Early Career Award for Scientists and Engineers, the MacArthur Foundation Fellowship, the ACM/ Infosys award, and membership in the National Academy of Engineering. She is an award-winning teacher who pioneered many of the ideas that underlie the Coursera user experience. She received her BSc and MSc from the Hebrew University of Jerusalem, and her PhD from Stanford in 1994.