microBEnet
Website    Blog    Resources    Sloan Program     Events    About
Resource
Welcome to microBEnet News
February 2013 

Resource of the Month 

Focusing on resources found on microBE.net

 

 

This month we would like to draw attention to our microBEnet YouTube channel. This contains videos ranging from Mendeley tutorials, to talks from conferences, to our "People Behind the Science" series of interviews.

microBEnetBlogs
MicroBEnet Blogs

A brief summary of the recent topics posted on microBE.net  

 

This month we've seen a couple of changes in the blog, most notably activation of a feature whereby discussion of a blog post on Twitter is automatically posted as comments to a blog post.

 

There have also been a few guest posts this month:

 

There were a couple of posts ranting about misleading press releases and media campaigns:

 

Hal Levin wrote up a couple posts on his troubles finding building science blogs and a review of building science journals.

 

Legionella is the ever-recurring topic

 

Other topics included:   

MicroBEnet is always seeking new blogs relevant to microbiology and the built environment. Your suggestions are always welcome.  

PeopleBehind
People Behind the Science
People Behind the Science

 

An interview with  Greg Caporaso from Northern Arizona University.   During this interview, he discusses his new Sloan-funded project, "Office Surface Microbiomes Across Climates."

 

Complete video interview can be seen here. 

 

Question: How did you become interested in microbiology of the built environment?

 

Greg: I first became interested in studying the built environment because, relative to some of the other environments I have worked in, it is relatively stable and it is very easily accessible. We can work on studies in our offices and homes and we don't necessarily need to be going out in the field to be collecting things like longtime series data. It is easier to get started and there are also a lot of really important questions. Specifically the types of things I am interested in are how are communities that establish in the built environment affecting human health, and ultimately can we make predictions about whether a community is going to establish that effects human health or accelerates the rate of building degradation.

 

Question: Can you tell us about the project that you just received funding through the Sloan Foundation?

 

Greg: This is a study to look at microbial succession in the built environment. At this point, we know that communities that establish indoors can affect things like human health and building rates of degradation. But we don't have a good idea about what different factors are contributing to what communities are establishing indoors. In this study we will be looking at the affect of surface material, climate and then various other environmental metadata and parameters that are affecting the succession of microbial communities. So the idea is that we will start in three different cities: Flagstaff, Arizona, which is where I am, San Diego, and Toronto. What we will do is identify three different offices in three different buildings in each of these cities, and we will install in each of these offices, three different surface materials. We will install carpet tile, ceiling tile and fiberboard. It will be your classic IKEA desk surface material. We will make some attempts to clean these materials in the beginning the same way to make an attempt at sterilizing them so we get to the point where they are all coming from the same starting condition. We install these and then monitor them over the course of about a year. In four 6-week blocks over the period of a year we will do regular sampling. So somewhere in the order of two days to eight days we will collect the sample from each of these surfaces. At the same time we will be collecting environmental metadata; outdoor environmental metadata such as temperature, relative humidity; indoor environmental metadata such as room temperature, light intensity, and activity in the room using motion sensors. We will also be looking at some micro environmental parameters such as water activity and proximity of objects or people to these materials. We will do this by installing motion sensors with each of these materials that have a very small range so they are only detecting things very close. Over the period of a year, we will have four of these six-week sampling periods. At the end we will be able to look at which of these factors were affecting what communities that are establishing over time and additionally, whether climate seems to play a role. Are materials that were installed in the same city more similar to each other in their succession patterns than materials that were installed in different cities?

 

Question: And you are doing some cool bioinformatics comparison as well with subsampling the communities after?

 

Greg: Yes. We are at the point right now where these studies are getting a lot more accessible. The cost of sequencing is going down and the bioinformatics techniques are becoming a lot more advanced and becoming a lot more accessible. With the introduction of things like easily accessible cloud computing, and even computing resources are getting pretty accessible. So, we are moving to a really exciting period where we will be able to do things like routine monitoring of buildings to develop things like early warning systems of communities that might have a negative impact on human health or on building health. So, one of the key questions is, how often do we need to be sampling to detect what might be shifts in the community towards an unhealthy community? So what we will do in our first 6-week sampling period, we are going to collect very dense time series data. We are going to sample every two days from nine different sites in each office included in this study. What we will be able to do with that information is sequence right away on the Illumina MiSeq, which is the bench top sequencer for Illumina. We will sequence all these samples right away and what we will do, which one of the main goals of this study, is determine if we can develop predictive models. Can we make predictions about the abundance of, just for simplicity, one specific taxa based on environmental data, or other taxa that are present in the environment?  We can develop our model using all of the data, dense time series data and then we can subsample from that. So rather than using data from every two days, we can use data for every four days or every six days and see what effect that has on our ability to develop predictive models. Using that we can then figure out the right balance of accuracy of our methodology and our models versus the cost of sequencing. So, obviously the every two day time series is more expensive than to do it every four days. So if doing it every two days doesn't buy us a lot in terms of accuracy, then we know that maybe it is ok to go with sampling every four days.

 

Questions: What is one big scientific question now in the built environment research community?

 

Greg: The big one I am thinking about is the one that is driving this project. What factors are contributing to the establishment of communities in the built environment? Is it things like outdoor temperature, indoor light availability and so on? Or do none of those things matter and the only thing that matters is the cleaning schedule in the building and so on? I think that's one of the big questions in my mind is what factors are affecting what communities are establishing?

Mendeley
Latest in Mendeley Collection
To see the complete collection, visit the microBEnet Mendely Group. 

 
 Quick Links

Social Media
View our profile on LinkedIn

Like us on Facebook

View our videos on YouTube

Join Our Mailing List



Blogosphere
Around the Blogosphere

Microbiology Blogroll
Built Environment Blogroll

 

 


Featured Articles


 

The Spread Of Hospital-Acquired Bacteria Revealed By Computational Methods 

 

By David Coil  


Another short post here, this time on modeling the spread of hospital-acquired bacteria.  Horizontal gene transfer between bacteria is a huge problem in hospitals and these researchers have developed some models for how this process actually occurs in hospitals.    They've applied their techniques in a couple of real-life situations with interesting results.   They found for example that over half of the genetic variation in MRSA is caused by horizontal gene transfer.  From these results they can start to get a handle on the epidemiology of problematic strains with potential implications for management of outbreaks.



 by   Rachel Adams

One of our broad goals at BIMERC, the UC Berkeley group funded by Sloan, is to look at what microbes are found indoors and why. We first tackled this in homes and decided to survey in a university family housing complex - in essence, getting replication in the built environment while eliminating potential sources of variation in buildings, such as design, building material, age, etc.

 

Sampling one-month collections of airborne dust at two different seasons, we  found some things we expected, and others we didn't.

 

First, the unsurprising. When you don't limit sampling to what will grow in culture, you can a shocking number of taxa. In our case, over 1000 fungal "species" were detected indoors, the far majority of which were clearly coming in from the outdoors. For example, types like a puffball known as the "dog-turd" and Glomeromycota that (for what we can tell) are obligate symbiotic associates with plants.

 

What we didn't expect to see was that the features of the dust sample and the unit - for example, what kind of room the sample came from or how often the residents clean - had no effect on what kinds of fungi were found indoors. Instead, the airborne fungi indoors were singularly dominated by what was coming in from the outdoors.

 

And what is coming in from outdoors in this housing complex that spans hundreds of meters is not a uniform source pool. Instead, the fungi appear to dispersal limited on even this small geographic scale, so that two air samples separated by 100 meters have more species in common that two air samples separated by 400 meters.  While this "distance-decay" effect would not be surprising across regions, its occurrence for airborne propagules of microbes on this small scale is practically undocumented.

 

Turns out, those fungi that make our homes sick or unsightly are just a tiny fraction of what can end up inside. It would be interesting to do this in a different region than the Bay Area, where the climate is not so conducive for "natural" ventilation year around. Davis, CA?


 



Like us on Facebook  View our profile on LinkedIn  View our videos on YouTube       Join Our Mailing List