Book Review: Small and Packs a Punch

A Planet of Viruses
Carl Zimmer
The University of Chicago Press
109 pages

Interesting things happen when physicists decide to go into biological research. They ask questions that biologists generally won’t. For example, viruses have small genomes, but they also have very small storage space in their capsids. Bacteriophages inject their genetic material into the bacteria they infect like a combination of a lunar lander and a syringe. How much force does the coiled bacteriophage DNA have? As it turns out, bacteriophages pack quite a punch. The force required to insert the DNA into the capsid is fairly large, and requires quite a bit of ATP, stolen from the host cells by the infected virus before the cell is killed.

Carl Zimmer’s new book, A Planet of Viruses borrows its delivery technique from its subjects: in less than 100 pages, A Planet of Viruses packs quite a punch of information. The eradication of smallpox, the rise of HIV, the immigration of West Nile virus to the western hemisphere, the viruses in our genomes and the recent discovery mysteriously huge mimivirus are all treated here in delightfully short essays  describing the impact of viruses on mankind and on life in general.  To some of these topics Zimmer brings refreshing perspectives.  He proposes that the common cold virus, an unwelcome companion of man since ancient history, should be treated like a wise old tutor rather than an ancient enemy. Then he explains why we haven’t truly eradicated smallpox, and probably never will. Viruses, hovering between life and non-life have an impact on life so large it is hard to fathom. Viruses kill about half of marine microbes every day. Their sheer biomass (“…equal to [that of] 75 million blue whales”), huge host range, mind-boggling number of particles in the biosphere and, above all, the genetic diversity which is unmatched by all other life combined. They infect more than our cells: many are contained in our very genomes, transferred from generation to generation.

Having read the book in one sitting, I felt a bit lightheaded when I rose to drink my (now cold) coffee. Like compressed viral DNA injected into the host cell, the movement of this concentration of information from a small book into my brain had an almost palpable effect. As a microbiologist I knew quite a few of these stories about viruses, I just never had them put together in front of me in such a readable and concentrated fashion. Unlike larger books, which may be more elaborate on any single theme, Zimmer’s small book delivers its viral DNA in a short, sharp shock. I am happy to have been infected, and I recommend you do the same.

 

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You don’t get to 11 million papers without a few dodgy results

“The Science Network”: who stole PubMed?

Well, their accents don’t exactly fit the population in the NLM….

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Thursday Odds and Ends

 

A woman in Chesterfield, Ohio robbed a convenience store using her MRSA-infected arm as a weapon.  Warning: graphic picture of MRSA infected arm. Or a zombie limb. You can never know in northwestern Ohio.

Scanning Electron Microscope image of Methicillin-Resistant Staphylococcus aureus or MRSA. Credit: Janice Carr. Source: wikipedia

A US vector biologist got infected with Zika virus which is  a mosquito-borne pathogen causing joint pain and fatigue. He then passed in on to his wife during sexual intercourse. This would be the first documented case of sexual transmission of an insect-borne pathogen. Also, “Honey, Iswear, I got it from a mosquito bite” is the new excuse for two-timing spouses everywhere.

April’s fool came and went on the intertubes.  My favorite was the arsenic based sea-monkeys.

 

Great news for geeky kids of the 1980’s: the Commodore 64 is back!  Same nice bulky keyboard-in computer, with just a little bit more than 64K of RAM underneath:

 

 

“The upcoming Commodore 64 looks exactly like the ancient model which reshaped the home computer sector decades ago, though underneath the bonnet things have been brought well into the 21st century.

“Even though the computer refrains from relinquishing its old charm, it will come packed with modern computer hardware. The new Commodore 64 model will contain a mini-ITC motherboard, a dual core Intel 525 Atom processor, DDR3 RAM between 2GB and 4GB and Nvidia Ion2 graphics unit.

“Commodore says that the device will run on the Ubuntu 10.04 LTS OS and will come with a DVD drive, with support for Blu-Ray, a multi-format memory card reader and five USB slots. The new Commodore 64 will also come with Wi-Fi support and will come pre-loaded with 3D games and other applications including a Microsoft Office compatible productivity suite.
Read more: http://www.itproportal.com/2011/04/06/iconic-commodore-64-all-set-comeback/#ixzz1IqxQ1LXX

 

Finally, remember the name: Zhuchengtyrannus magnus (zoo-CHENG TEER-ah-nus MAG-nus) or Z. magnus. A new dinosaur discovered in Zucheng, China. Related to Tyrannosaurus rex it is 4m tall, 11m long, 6 tons of carnivorous mass. The original paper.

 

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Reverse Translation Discovered?

 

We will never look at life at quite the same way again.

 

Until now, information flow in biology looked like this:

 

DNA gets transcribed to RNA, wheich in turn is translated to protein. While reverse transcription does take place with retroviruses using reverse transcriptase, the central dogma of molecular biology held that proteins is an end product, and there is no information flow back from protein to nucleic acids.

This has just changed.

Today, a press release and a paper by a joint group of scientists at Franklin National Lab and NASA reveals a new RNA-Protein complex that can read short protein sequences and reverse-translate them back to RNA.  The reverse-translation complex, which they call the  emosobir  (that’s “ribosme” in reverse) is larger even than the ribosome. This reverse translation activity has been initially observed in isolates of sludge-derived Amoeba lupicus from Lake Erie, but not published yet as the researchers wanted to duplicate the results in controlled lab conditions, which proved to be extremely challenging.  Apparently reverse translation is due to the activity of a new kind of intracellular parasite. The Emosobir Containing Particle (ECP) resembles a giant virus. However, it is devoid of chromosomal DNA or RNA. Rather, it contains the ebosomir itself. Once the amoeba is infected, the capsid dissolves, and the protein is reverse-translated to RNA. From that point on, the amoeba’s cellular machinery is hijacked just like in a virus to translate the ECP mRNA to new ebosomir and ECP capsids. The process of reverse-translation and RNA-dependent RNA replication and translation is considerably slower than a viral infection — it can take 14-30 days for enough ECPs  to accumulate to burst from an amoeba and infect another. The process is also quite inefficient, as it seems that in only 1% of the infected amoebas ongoing reverse translation is successful.

A Lattice of Ebosomirs in the infected Amoeba lupicus

The consequences of this finding are enormous. Although we are familiar with prions as replicating proteins without nucleic acids, and viroids as replicating nucleic acids without proteins, this is the first time that information flow from a protein to nucleic acids has been discovered.

The press conference will be held today at 4:00pm EDT.  More details here: http://www.nasa.gov/

UPDATE: (April 2)  too many people thought this was serious. Please check the date of this post. Then look up if there is even a Franklin National Lab or an A. lupicus. Then chill out.

 

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Ratting out landmines and tuberculosis

 
ResearchBlogging.org

Thanks to John Stevenson for drawing my attention to this one: Giant African Pouched Rats are trained as detectors; a good solution for low-income countries and communities. HeroRATS, as they are called, come in two “models”: landmine detectors and tuberculosis detectors. Rats born in captivity (captured rats are impossible to train) are trained to sniff out  landmines in historically war-ravaged zones where many landmines are laying unmapped, and using other detection or disposal techniques is too expensive. Their light weight is insufficient to trip the mines. Their veterinary requirements are less than those of dogs, and the rats are not dependent upon a single handler.

Tuberculosis is a serious public health problem affecting both developing and developed countries. But while developed countries may employ several molecular-based detection techniques (although see here for a new initiative supported by the Bill & Melinda Gates Foundation), the method of choice for developing countries is detection of the bacillus in the patient’s sputum using microscopy.  This can yield many false negatives (undetected infections), since the bacillus is slow growing, and may be present in an infected person’s sputum in undetectable amounts. The rats have been able to accurately detect infected sputum in concentrations that are normally missed by humans. Also, rats do it faster, and they work for bananas.

APOPO is the organization training people and rats to better detect tuberculosis and landmines.

Poling, A., Weetjens, B., Cox, C., Mgode, G., Jubitana, M., Kazwala, R., Mfinanga, G., & Huis in ‘t Veld, D. (2010). Using Giant African Pouched Rats to Detect Tuberculosis in Human Sputum Samples: 2009 Findings American Journal of Tropical Medicine and Hygiene, 83 (6), 1308-1310 DOI: 10.4269/ajtmh.2010.10-0180

Alan Poling, Bart J. Weetjens, Christophe Cox, Negussie W. Beyene, & Andrew Sully (2010). USING GIANT AFRICAN POUCHED RATS (CRICETOMYS GAMBIANUS) TO DETECT LANDMINES The Psychological Record, 60 (4), 715-728 Other: http://opensiuc.lib.siu.edu/tpr/vol60/iss4/11/

 

 

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Psychedelic Monday: Solitude is Bliss

 
From Tame Impala’s album Inner Speaker.

 

 

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Big Moon Rising

 

Unless you have been living on the, um, moon, then you have heard about the large moon expected tonight. The moon will be almost at perigee (closest point to earth in its orbit), and full. Luna is expected to be bigger & brighter. Best viewed when it is on the horizon, seems even bigger that way. You can find out the sunrise and sunset times of the moon for your neck of the woods here.

And contrary to John Fogerty’s advice, do go out tonight. Give the moon some Creedence.

 

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Why are there no (or almost no) disease-causing Archaea?

Some microbes are evil minions of Hell (but not all)

Quite a few people think that microbes are evil, disease causing minions of Hell that should be eradicated. Supermarkets are handing out sanitary wipes: wipe the handlebar if you want to live, never mind that 90% of the food in the supermarket is worse for you than anything you may catch off that cart handle.  Almost every public space looks like the secret basement level of the CDC, with alcoholic hand sanitizers and posters portraying the horrors of aerosol-borne infections. Microbes are the invisible enemy: you can’t see them, but they are deadly. You can sure kill them with copious amounts of ethanol.

 

Actually, only a minority of microbes are pathogens. Some eukaryotes are parasitic and disease causing.  There is Athlete’s foot (caused by a fungus) amoebal dysentery and other unpleasant experiences. But most are not. Also, most bacteria that live in us or on us are symbiotic and like us for our throwaway proteins, carbohydrates, nice 36.6C temperature, high humidity (armpit or mouth) and other goodies. Yes, some are pathogenic, and some do seem like evil little minions of the Devil.  Those have  ingenious mechanism which infect, wreak havoc, sometimes kill, and move on.  But for every plague bacillus or burger bug out there, there are millions of other kinds of bacteria that really don’t do much, good or bad.

 

About archaea

There is one group of microbes that have no known pathogens: Archaea.  Archaea are… different. An archaeon is as different from a bacterium as either is from a human. Superficially, bacteria and archaea look the same. Both are unicellular. Both do not have well-formed cellular organelles on the level that eukaryotes have. For those two reasons, archaea were thought, for a very long time, to be a type of bacteria. Today, virtually all microbiologists classify archaea in a domain of their own. Archaeal cell membranes are made up of their own unique type of building-blocks (lipids), the type which bacteria do not have, and neither do eukaryotes. Their cell wall is different than bacteria. Many live in extreme conditions: ocean smokers, geysers, hyper-saline lakes, the frozen Tundra, termite guts, cow stomachs and Charlie Sheen’s pants. Actually, the latter may be a bit too extreme even for archaea. Looking at phylogenetic marker genes, such as small subunit ribosomal RNA, (SSUrRNA) archaea indeed cluster as a domain unto themselves.

But  of the hundreds of disease-causing microbes or pathogens that we know of, none are archaea. Which is odd. Plenty of disease causing eukaryotes and bacteria, but no archaea? Why is that? In a new paper published in Bioessays, Erin Gill and Fiona Brinkman try to answer this question.

First, Gill and Brinkman examined the most trivial hypothesis: we may just not have discovered archaeal pathogens yet. Their statistical analysis shows that this is possible, but unlikely. Here is the way the authors explain this: about 0.36% of known bacterial species cause disease (585 out of about 151,000 known cultured and uncultured species, a very low-bound estimate). Assuming that the diversity in archaea is about the same, we should have identified a few (the authors estimate .0036 x 4,508 species of archaea = 16) archaeal species which cause disease. This somewhat back-of-the-envelope calculation is a bit rough and laden with assumptions: one, that the diversity among known archaea is the same as among known bacteria. It was recently discovered that there is a huge marine diversity of mesophilic archaea for which we only have metagenomic (fragmented DNA sequence) data.  Also, there may be many diseases we know nothing about, simply because our census of life on earth is far less than complete. Some of these archaea (and more of these bacteria) may be pathogens, only many have not been identified as such. Finally, historically, with bacteria, we were biased towards looking for pathogens. Bacteriology started as a medical discipline, and to this day many microbiology departments reside in universities’ medical schools. On the other hand, archaea were studied mostly by environmental microbiologists, who are not looking for pathogens necessarily, but are more interested in biogeochemical cycles and the diversity of life. But its claim does cause us to raise an eyebrow: not even one known archaeal pathogen? OK that’s odd. Quite worth looking into. Although the number of archaea we can examine may be too small.

So what exactly is going on?

Bacteria don’t kill people. Bacteriophages kill people?

A clue may lie in how virulence genes are arranged in the bacterial genome. Virulence genes are genes that code for proteins that let bacteria invade our body, cause disease and evading the immune system and drugs. Many of these genes are recognized as mobile: they can easily jump together from a disease causing strain to a benign strain, causing the latter to now become virulent. In many cases they can jump between different species. The vector that carries those genes is typically a bacterial virus, or bacteriophage. When a virus invades bacteria, it can uptake some of its DNA and incorporate it into its own genome. This DNA may later be deposited in another bacterium, turning a benign strain into a virulent one. The process of moving DNA between bacteria with a virus is called transduction, and viruses may also leave very specific “fingerprints” in transduced DNA.

Generalized transduction. Source: Indian River State College

 

One might say that pathogenic bacteria are actually a vehicle to help bacteriophages proliferate. Better yet, bacteriophages and bacteria both can be viewed as vehicles to help virulence genes proliferate.

ResearchBlogging.org

However, as far as we know, bacteriophages do not invade archaea. Archaea do have their own viruses, but those are different from bacteriophages. Archaea are a separate domain of life, and whatever parasitises one domain would be ill fit to parasitise another. After all, viruses that invade eukaryotes are also quite different from bacteriophages. (As an aside, this is what makes bacteriophages such an attractive idea as an anti-bacterial treatment method: after all, if we can inundate the human body with viruses that only infect bacteria, moreover only specific disease-causing bacteria leaving those that we need unharmed, that would make for a great silver bullet. But bacteriophage treatment is a matter for another post.) The differences are in shape, biochemistry  and in genomes. There is little to no similarity in the genomic sequences of archaeal viruses and bacteriophages. No bacteriophages are known to infect archaea and vice-versa. That said, we know precious little about the diversity of bacteriophages, and close to nothing about archaeal viruses.

We do know that archaea have a very different cell-wall biochemistry than bacteria, and lack the receptor proteins which bacteriophages use to infect bacteria. So bacteriophages cannot infect archaea, cannot transmit virulence genes, and cannot transmit virulence. Gill and Brinkman present virulence from the bacteriophage’s (or rather the bacteriophage’s genes) point of view: both bacteria and their hosts are vehicles for propagating bacteriophage genes. A rather complex evolutionary mechanism.

But why haven’t archaea developed virulence of their own, independently of bacteria? Wouldn’t archaeal viruses develop a similar mechanisms? The authors claim the reason is that virulence evolution is a rare event. They argue that the evolution of virulence, at least the virus-transmitted secondary type is a multi-step process, and is therefore rare. My take on this argument: yes, it might be true for phage-transmitted virulence, but both bacteria and eukarya have evolved virulence mechanisms independent of viruses, encompassing many diverse mechanism that appear to have evolved independently. Hence, virulence itself is not so rare, even if the gene-island type may be.

All-in-all a thought provoking paper, which was very exciting to read.  The authors qualify their hypothesis heavily, knowing that with bacterial, archaeal and their viruses, there are unknown unknowns, as the following bit of poetry illustrates:

 

The Unknown
As we know,
There are known knowns.
There are things we know we know.
We also know
There are known unknowns.
That is to say
We know there are some things
We do not know.
But there are also unknown unknowns,
The ones we don’t know
We don’t know.

—Donald Rumsfeld, Feb. 12, 2002, Department of Defense news briefing


 

 

Gill, E., & Brinkman, F. (2011). The proportional lack of archaeal pathogens: Do viruses/phages hold the key? BioEssays, 33 (4), 248-254 DOI: 10.1002/bies.201000091

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Function predictor? Submit your work to the CAFA meeting

 

Last July I introduced CAFA: Critical Assessment of (Gene and Protein) Function Annotations. Recap: the number of genomic and metagenomic sequences is growing at a horrendous rate. We are inundated with sequence data, yet the fraction of useful information we can glean from these sequences is steadily decreasing. There are simply too many sequences, and they are getting extremely diverse. Even when we have the sequences of the genes and their RNA or protein products, we are clueless as to what many (by some estimates most) of them do. There are many algorithms to predict the function of proteins, but they have not been compared on a large scale yet. We, the CAFA challenge organizers decided to have some fun: we released the sequences of some 50,000 proteins whose functions are unknown. Some 35 research groups predicted the functions of these proteins using their own software, and uploaded their predictions to our server.

Credit: Brazma et al, European Bioinformatics Insititute

 

The first phase of CAFA is over: the predictions are now in, and we will be assessing them soon. But if you  want to participate in the AFP (Automated Function Prediction) / CAFA meeting you still can. Even if you  were not a predictor this round, but you are a bioinformatician developing gene function prediction algorithms, please consider submitting an abstract to the AFP/CAFA meeting. The best abstracts will be selected for oral or poster presentations. And at the authors’ discretion, they may be extended to a full publication in a peer-review journal.

Important dates:

  • April 18, 2011: Deadline for submitting abstracts.
  • May 9, 2011: Notifications for accepted abstracts e-mailed to corresponding authors.
  • May 16, 2011: Deadline for presenters to confirm acceptance of invitation to speak.
  • July 15-16, 2011: The AFP/CAFA meeting, Vienna, Austria (an ISMB/ECCB 2011 Special Interest Group meeting).

Looking forward to seeing you in Vienna!

 

 

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Giggity

The authors and editor knew exactly what they were doing with this one:

Thanks to Ed Yong for tweeting this.

Chau, R., Hamel, S., & Nellis, W. (2011). Chemical processes in the deep interior of Uranus Nature Communications, 2 DOI: 10.1038/ncomms1198

ResearchBlogging.org

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You know your graduate student is frustrated when…

…you find this on the top of the paper pile on his desk:

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February: a Good Month for Music

Some good things happened in music this month.

The Black Keys won Grammy awards for Best Alternative Album, (Brothers) Best Rock Performance By A Duo Or Group With Vocals, Best Recording Package and Producer of the Year, Non Classical. Arcade Fire won a Grammy for Album of the Year, The Suburbs.

Here are The Black Keys in Howlin’ for You from Brothers:

Lady Gaga should have won the WTF award for this:

In other news, North Mississippi Allstars have a new album out, Keys to the Kingdom, February 1. Less blues, more gospel and folk. Probably their most main-streamish album to date. Here’s The Meeting:

Drive By Truckers have been extremely prolific lately. Less than a year after their latest album, they came out with Go-Go Boots two days ago. The tradition of stories of hardhsip  in small southern towns continues. Go Go Boots is quite dark, even for DBT who are not known for a cheerful demeanor. Used to be a Cop:

Finally, a new video from The New Pornographers. Nice take on the “Rise and Fall of a Rock Band”  genre, posted last week on YouTube:

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Humans draw the LINE at Gonorrhea. Not that it helps.

א וַיְדַבֵּר יְהוָה, אֶל-מֹשֶׁה וְאֶל-אַהֲרֹן לֵאמֹר.  ב דַּבְּרוּ אֶל-בְּנֵי יִשְׂרָאֵל, וַאֲמַרְתֶּם אֲלֵהֶם:  אִישׁ אִישׁ, כִּי יִהְיֶה זָב מִבְּשָׂרוֹ–זוֹבוֹ, טָמֵא הוּא.  ג וְזֹאת תִּהְיֶה טֻמְאָתוֹ, בְּזוֹבוֹ:  רָר בְּשָׂרוֹ אֶת-זוֹבוֹ, אוֹ-הֶחְתִּים בְּשָׂרוֹ מִזּוֹבוֹ–טֻמְאָתוֹ, הִוא.  ד כָּל-הַמִּשְׁכָּב, אֲשֶׁר יִשְׁכַּב עָלָיו הַזָּב–יִטְמָא; וְכָל-הַכְּלִי אֲשֶׁר-יֵשֵׁב עָלָיו, יִטְמָא. ,

The Ebers Papyrus Credit: the US National Library of Medicine

The day after Valentine’s Day. Ah! What better day in the year can we find to discuss gonorrhea? In the US alone 700,000 people are infected each year, and 5 million are infected worldwide.  In most infected men gonorrhea causes urethral discharge and pain while urinating. The reason is that  Neisseria gonhorrea have little hair-like structures called fimbriae. This makes them very sticky and they stick to the urethra’s walls.  Then you get inflammation, urethritis and urination becomes difficult and painful. In women, if left untreated, gonorrhea can lead to pelvic inflammatory disease, a painful condition that can cause sterility or ectopic pregnancy.

This doesn't help! Source: Wikipedia

For those of you who are wondering, gonorrhea actually predates college dormitories by a few millenia.  The opening paragraph of this post is taken from Leviticus 15, 1-4. The first 15 verses of this chapter deal with male discharge, presumably gonorrhea. Strict quarantine and washing procedures were required from infected men. That’s a lot of verses and instructions. Gonorrhea must have been considered to serious problem back then, as now. The Ebers papyrus, dating back to ~1500 BCE also mentions cures for burning urination.

I certainly hope you used condoms last night.

Recently, researchers at Northwestern Medical School have found evidence of a human DNA fragment in Neisseria gonorrhoeae. The gene transfer appears to be quite recent, in evolutionary terms. So “they” have a bit of “us” in them. Given that N. gonorrhoeae have been sticking to mankind for thousands of years, human DNA in the bacterial genome is more than plausible: it is almost expected. The human DNA was found in three of fourteen bacterial isolates that were sequenced. The question is: does the human DNA provide fitness to the bacteria? Probably not. But it may just provide fitness to itself, as selfish DNA: DNA which spreads by forming additional copies of itself, and has no positive contribution to the reproductive success of the organism. The human DNA found in N. gonorrhoeae fits the description of selfish DNA. This bit of DNA, nicknamed LINE is found in 500,000 copies in the human genome. Long Interspersed Nuclear Elements or LINEs are transcribed from DNA to RNA by an RNA polymerase II enzyme which they encode. LINEs  code for a reverse transcriptase: the enzyme that can get the RNA encoded as DNA in another place in the genome. Since LINEs code for their own genome integration, they are actually a semi-autonomous replicating element within the human genome. A small  “genome” within a genome, constantly replicating  and embedding itself. Indeed, over the years we have amassed some 500,000 LINEs in our genome, making up 17% of our total genomic content. Think of LINEs as the Tribbles of evolution, replicating themselves constantly. It seems that now LINEs have jumped species, and are infecting our infectors. (UPDATE: Thanks to Joe H for the correction. LINEs do not encode for RNA Polymerase II, they use the human one.)

LINEs, LINEs, LINEs

The similarity between the LINEs in the bacteria and the human LINEs is very high. The authors hypothesize that 1) the gene transfer may have happened recently or 2) LINEs are extremely conserved in the bacteria due to some selective pressure. A third hypothesis is that this gene transfer happens multiple times, with a high frequency. In any infected host, there is a certian probability that LINE (or another human genomic element) shall be transferred from human to Nisseria, then replicate with the bacteria for a while (maybe thousands of generations), but eventually drop out of the bacterial genome. Bacteria don’t tolerate too much dead weight in their genome, unlike eukaryotes. But just as humans get reinfected with gonorrhea all the time, we keep transferring our genomic elements to them.

So, Nisseria. For thousands of years, you have been giving us the clap. But now, we give you LINEs. Take that!
ResearchBlogging.org


(OK, not much of a revenge. Safe sex is probably a better option.)

I think it is high time we looked for LINEs in other human pathogens, and for more genomic evidence of host-pathogen DNA transmission.  Finally,  at this point, I would like to let Frank Zappa continue our discussion (slightly NSFW.)

Mark T. Anderson, & H. Steven Seifert (2011). Opportunity and Means: Horizontal Gene Transfer from the Human Host to a Bacterial Pathogen mBio, 1-4 : 10.1128/​mBio.00005-11

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Playboy Pleasure Palace Provides Pneumophila?

It seems like an outbreak of Legionnaire’s disease (in a mild form, Pontiac Fever)  has occurred at the DOMAINFest this year at Santa Monica, California. Legionnaire’s disease  is caused by gram-negative bacterium, Legionlla pneumophila. Legionella typically inhabits the water tanks of central air conditioning systems, but any aerosolized  fresh water such as from fog machines or desert coolers, jacuzzis and breathing apparatuses may be a source. First identified in an American Legion conference in 1976,  it is now estimated that there are between 10,000 and 50,000 cases each year in the US alone.

Legionella pneumophila source: Wikipedia. Credit: US Center for Disease Control and Prevention.

So what’s special about this outbreak? The delegates who got sick all attended a fundraiser held by Jenny McCarthy at the Playboy Mansion. Yup, the same lady who is so prominent and vocal in the anti-vaccination movement. The fundraiser was for her anti-vaccination foundation, Generation Rescue. The Playboy Mansion is now being investigated by Los-Angeles County health officials as the source of the outbreak. Although there is no vaccine for legionelliosis, the air is still quite thick with irony. As thick as it was with the aerosol from the fog machine that may have started it all.

(Or the outbreak may have started at the Fairmont Hotel in Santa Monica where most of the conference sessions were held.)

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Open Positions in Structural Bioinformatics

Posting for a colleague, who leads a great structural bioinformatics group in Valencia.

Structural Genomics Unit

Bioinformatics & Genomics Department – Príncipe Felipe Research Center

Seeking a Bioniformatician and a Postdoc

The Structural Genomics Unit at the CIPF (Valencia, Spain) seeks candidates for two open positions:

If you were interested, please read the linked PDF and follow the instructions.

Deadline 18th of February 2011

Research Positions

Postdocs and PhD candidates interested in molecular structure and function are always encouraged to apply by sending an email to Marc A. Marti-Renom.

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