Does scientific research back the claims made in this article?
Samiya

Amoebic Morality <http://www.damninteresting.com/amoebic-morality/ >

[image: Dictyostelium discoideum composite photo, Copyright © M.J. Grimson
& R.L. Blanton; Biological Sciences Electron Microscopy Laboratory, Texas
Tech University]
Dictyostelium discoideum composite photo, Copyright © M.J. Grimson & R.L.
Blanton; Biological Sciences Electron Microscopy Laboratory, Texas Tech
University
Once food had been plentiful, but no longer. In the early days of the
colony, the amoebas had feasted on a rich supply of bacteria. But as the
generations passed and the population swelled, they had hunted out their
food supply. Now starvation threatens. Their home-- a scrap of deer dung
which once provided all their needs-- has become a trap which they must
escape if they are to survive. At last, one amoeba sends out a cry for help.

The starving amoeba begins to emit a chemical signal in the form of *cyclic
adenosine monophosphate*, or cAMP. Nearby individuals sprout new pseudopods
and crawl toward the source. They also begin to give off cAMP themselves,
amplifying the call until the signal spreads to the far reaches of the
colony. Amoebas cannot concurrently detect and produce cAMP, so they
alternate, and the cells trace out intricate spiral patterns as they surge
forward in waves.

The amoebas pile on top of one another in growing numbers until so many of
them have joined the heap that this pile of microscopic single-celled
organisms becomes visible to the naked eye. At first their behavior might
seem odd; to gather together in the face of starvation surely ought to end
in cannibalism or death. Not so, for they are capable of an extraordinary
and rare transformation. The amoebas set aside their lives as individuals
and join ranks to form a new multicellular entity. Not all the amoebas will
survive this cooperative venture, however. Some will sacrifice themselves
to help the rest find a new life elsewhere.

These astonishing creatures are *Dictyostelium discoideum*, and they are a
member of the slime mold family. They are also known as social amoebas.
Aside from the novelty value of an organism that alternates between
unicellular and multicellular existence, D. discoideum is highly useful in
several areas of research. Among other things, this organism offers a
stellar opportunity to study cell communication, cell differentiation, and
the evolution of altruism.

In response to the cAMP distress call, up to one hundred thousand of the
amoebas assemble. They first form a tower, which eventually topples over
into an oblong blob about two millimeters long. The identical amoebas
within this *pseudoplasmodium*-- or slug-- begin to differentiate and take
on specialized roles.

The slug begins to seek out light, leaving a slimy trail behind. Some of
the amoebas take on the difficult role of sentinel, or immune-like
functions. They circulate through the slug, hunting for pathogens. If they
find any, they will engulf them in a process similar to the feeding
behavior they once displayed when in solitary form. The pseudoplasmodium
periodically sloughs off the sentinels-- and any pathogens they have
engulfed-- and abandons them in the trail of slime. More cells will then be
tapped to fill their place.

[image: Dictyostelium discoideum slug]
Dictyostelium discoideum slug
Once the slug finds a suitably sunny location, the unlucky cells at the
"head" of the slug form a stalk for the others to climb. These cells--which
make up roughly a fifth of the total population--will sacrifice themselves
in order to provide a path up for their comrades.

The remaining cells then climb the stalk and collect on its tip, eventually
resulting in a structure resembling a ping-pong ball balanced on top of a
floppy wire. This formation is known as a "fruiting body." They then form
spores, which are carried away by wind or passing animals or insects. Once
carried to a suitable location, the amoebas emerge from spore form and
begin the cycle again.

So long as all the amoebas which make up the slug are related, this
impressive display of self-sacrifice on the part of the stalk cells makes
sense. Though they will perish in the act of creating the stalk, they will
pass along their genetic legacy via their kin. In fact, when the amoebas
reproduce by division, they create an ever-increasing pool of genetically
identical clones. These clones suffer no genetic cost at all from
sacrificing their lives for each other.

More familiar multicellular organisms pool resources in a similar way. For
example, in a human being, a liver cell fills a very different role from a
lung or skin cell, but all of them harbor the same chromosomes. The result
is that the liver doesn't need to compete with the lungs concerning
reproduction. So long as the germ cells get lucky, all of the cells can be
(metaphorically) content knowing they will pass on their genetic legacy.

However, when the cAMP call goes out, it isn't only related amoebas that
answer it. Those of differing strains will come together to form a single
slug. If one strain could figure out a way to duck out of stalk and
sentinel duty, it would be expected to reproduce faster than its nobler
compatriots.

As is true with all organisms, some will evolve in such a way that they
can-- and will-- benefit from the colony's resources without contributing
anything back. In theory, such "leeches" could potentially have a survival
and reproductive advantage, thereby undermining the cooperative
Dictyostelid lifestyle. Such cheating does take place, but nonetheless D.
discoideum has been around for millions of years with no signs of imminent
extinction. Thus the mechanisms for keeping cheating under control must be
effective.

For one thing, the amoebas prefer to unite with kin. The amoebas are able
to recognize each other through molecular markers. They mingle with other
strains only when populations are low. At such times, the ability to form a
larger slug outweighs the risk of cooperating with strangers.

[image: A typical amoeba]
A typical amoeba
In addition, evidence suggests that some social amoebas have evolved to
link reproductive genes with altruistic ones. In the case of D. discoideum,
researchers created a mutant strain of cells which are "deaf" to the
chemical signal to become a self-sacrificing stalk cell. They then watched
to see if these cells would gain a reproductive advantage. Just the
opposite took place. The "cheater" mutant cells did not join in stalk
formation, yet they rarely made it up the stalk to become spores, and
therefore they died out. The traits of self-sacrifice and reproduction had
become genetically entangled, it seems, allowing only the altruistic
amoebas to produce offspring.

Finally, opportunities for cheating simply aren't very common. In the wild,
these creatures spend much of their lives reproducing via division, and
surrounding themselves with identical copies. Outside of laboratory
experiments, cases where social amoebas run across strangers to exploit are
rare. Cheater genes peter out once the cheaters run out of nobler amoebas
to sponge off of. When exploiting one's clone mates, greed doesn't pay.

In addition to studies of altruism, study of D. discoideum is shedding
light on how cells communicate. D. discoideum uses many of the same
signaling processes found in all multicellular creatures. But unlike fish
or frogs, D. discoideum can be frozen, thawed, grown by the millions in a
matter of days, and stored away for years if need be. A website called
DictyBase offers an impressive list of breakthroughs which can be credited
to the social amoeba.

The consistency with which these amoebas act in the common good might
inspire admiration in many. Yet a more cynical observer might point out
that the amoebas are moved not by love of family and friends, nor by moral
scruples, but by the cold mechanics of natural selection. Amoebas behave
altruistically only because natural selection has led to a stable state in
which self-sacrifice is the best way for them to pass on their genes. But
the end result is the same, regardless of the natural forces that have
shaped it. Altruism triumphs, and through their mutual selflessness the
amoebas arrive at a new patch of bacteria-laden dung to call home.
Written by Carol Otte <http://www.damninteresting.com/?page_id=886>, posted
on 09 October 2007. Carol is a contributing editor for DamnInteresting.com.



On Thu, Apr 24, 2014 at 6:54 PM, Bruno Marchal <[email protected]> wrote:

>
> On 24 Apr 2014, at 12:26, Richard Ruquist wrote:
>
> Microbes provide insights into evolution of human language
> April 23rd, 2014 in Biology / Cell & Microbiology
>
> Gram-stained Pseudomonas aeruginosa bacteria (pink-red rods). Credit:
> GFDL, CC-by-sa
>
> Big brains do not explain why only humans use sophisticated language,
> according to researchers who have discovered that even a species of pond
> life communicates by similar methods.
>
> Dr Thom Scott-Phillips of Durham University led research into Pseudomonas
> aeruginosa, a type of bacteria common in water and soil, which showed that
> they communicated in a way that was previously thought to be unique to
> humans and perhaps some other primates.
>
> The bacteria used combinatorial communication, in which two signals are
> used together to achieve an effect that is different to the sum of the
> effects of the component parts. This is common in human language. For
> example, when we hear 'boathouse', we do not think of boats and houses
> independently, but of something different - a boathouse.
>
> This type of communication had never been observed in species other than
> humans and some other primates, until colonies of Pseudomonas aeruginosa
> were shown to be using the same technique - not, of course, with spoken
> words but with chemical messengers sent to each other that signalled when
> to produce certain proteins necessary for the bacteria's survival.
>
> By blocking one signal, then the other, the researchers showed if both
> signals were sent separately, the effect on protein production was
> different from both signals being sent together.
>
> Dr Scott-Phillips, a research fellow in evolutionary anthropology at
> Durham University, conducted the research in collaboration with a team of
> experts in bacteriology from the universities of Nottingham and Edinburgh.
>
> He commented: "We conducted an experiment on bacterial communication, and
> found that they communicate in a way that was previously thought to be
> unique to humans and perhaps some other primates.
>
> "This has serious implications for our understanding of the origins of
> human communication and language. In particular, it shows that we can
> assume that combining signals together is unique to the primate lineage."
>
> More information: 'Combinatorial communication in bacteria: Implications
> for the origins of linguistic generativity', Scott-Phillips et al,
> published in PLOS One, 23 April 2014.
> www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0095929
>
> Provided by Durham University
>
> "Microbes provide insights into evolution of human language." April 23rd,
> 2014.
> http://phys.org/news/2014-04-microbes-insights-evolution-human-language.html
>
>
>
> The contrary would have astonished me a lot, but it is nice this is
> confirmed and studied (I was sure it was). Comparison with language might
> be slightly stretched as there is no symbolic role in the messages, but may
> be it can make sense (I am not sure, I will read the paper ... but that
> does not seem really in his topics). I have few doubts that our own cells
> communicate in very sophisticate chemical ways, and there are evidences
> that plants does communicate through their roots, may be even through
> bacteria. (But no proof of such explicit double "words" nuancing, although
> again, its non existence would be astonishing). I would have bet this was
> already discovered on Escherichia Coli, but not in that apparently explicit
> way.
> Hmm... I'm not sure that they verified enough that the two compounds don't
> react to get a third molecule, which would trivialize the discovery.
> So interesting, but has to be continued and confirmed, ...
>
> Bruno
>
>
>
>
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> http://iridia.ulb.ac.be/~marchal/
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>
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