Sunday, December 6, 2015

Getting the Hologenome Concept Right

Related publication: Getting the hologenome concept right: an eco-evolutionary framework for hosts and their microbiomes (2016)

What is the target of natural selection in animals and plants? From a phenotypic perspective, selection sees trait variation that influences who passes on offspring and who does not. Given this rather obvious tenet, selection at the individual level is effectively selection on the holobiont - the community of microrganisms and its host. Consequently, variation in the collective genomes of the holobiont - i.e, the hologenome - yields variation in phenotypes upon which evolution can act. This hologenome concept of evolution distinguishes itself by placing emphasis on the vast symbiotic complexity and transmission routes inherent in holobiont animals and plants. As we emphasized in a recent perspective, it is also true that just as  large parts of the nuclear genome can evolve neutrally or be in conflict, so too can large parts the hologenome.

Yesterday, I read a skeptical essay on the hologenome concept by Nancy Moran and Daniel Sloan.  I have several thoughts on it. In short, it was great to see the attention on the topic, as all opinions and analyses are welcome at this nascent stage of the framework. Raising the profile of this area was precisely the intent of a recent publication with Kevin Theis, in which we clarified the history and use of the terms, revised the hologenome concept to include new perspectives such as neutrality, and laid a foundation for hypothesis-driven research and theoretical analyses for the field. This article subsequently calls for some of the same, which is great, but it is unnecessarily narrow and divisive at times. I briefly lay out the misconceptions about the article.

From the start in paragraph 2, it wasn't clear if M&S read our publication in detail. They attribute the origin of the word "holobiont" to Mindell (1992) but we showed that it was first used by Lynn Margulis in 1991. I had the pleasure of corresponding with Mindell prior to our publication, and he humbly tipped us off to the false credit. As we state...
The term "holobiont" traces back to Lynn Margulis and refers to symbiotic associations throughout a significant portion of an organism's lifetime, with the prefix holo- derived from the Greek word holos, meaning whole or entire. Amid the flourishing of host microbiome studies, holobiont is now generally used to mean every macrobe and its numerous microbial associates [19,22]
Second, M&S read our article well enough to extract some quotes, which I fully stand by. But they seem to be skeptical while at the same time they do not elaborate on the justifications spelled out in the paper. Take the example of thinking about host-microbe interactions as interspecific epistasis, similar to gene-gene interactions in the same genome. This is just scaling well accepted population genetic epistasis to community genetic epistasis and it has been done by many eco-evolutionary biologists. As we discuss in our essay, theory shows that there is an intellectual continuum between epistasis in the same genome and interspecific epistasis between different genomes, even for symbionts that are horizontally transmitted. This is not controversial or problematic. What is up for experimentation is the degree to which the epistasis comes and goes versus persist for selection to operate on it. The challenges are interestingly the same for both genetic epistasis in the same genome and intergenomic epistasis. There is nothing out of the ordinary here.

Third, I heartily agree with M&S that coevolution has run amok in the microbiome field (without any evidence) and has been applied incorrectly in most cases. Glad to see this getting more attention. It is precisely why I came up with the word "phylosymbiosis" in 2012-2013 because it does not confer coevolution or codiversification apriori to the observed pattern of microbial community relationships recapitulating host phylogenetics.  It does, however, provide evidence for community selection in controlled studies of the microbiota where microbes are assembled in a deterministic manner that parallels host genetic relationships. Controlled studies of Nasonia wasps and Hydra best show this pattern. I also like their Figure 1 on phylosymbiosis and think that it could be improved as both models could be operating at the same time. Some microbes could be strictly evolving in synchrony with hosts by vertical transmission while other microbes may be horizontally transmitted.

Fourth, the essay ignores that hologenomic models fully accommodate mutualism and parasitism. It is a misconception that it does not. Just as selfish genes are part of the nuclear genome, pathogens are part of the hologenome. See Principle 8 of our essay.

  1. VIII. The hologenome is shaped by selection and neutrality
    • Natural selection can work to remove deleterious nuclear mutations or microbes while spreading advantageous nuclear mutations or microbes; in the absence of selection, the neutral spread of hologenomic variation through populations is an inherently stochastic process.
    • Mixed ecological models of stochastic and deterministic community assembly likely reflect natural systems, and partitioning the microbiota into stochastic versus deterministic subunits will be an important future goal of the field.
Fifth, the hologenome concept fits squarely into multi-level selection theory. Most would agree that it is not correct to say that it is the only unit of selection, but it is equally not correct to say that the concept fails as a whole if there are others level of selection operating. Many levels are operating simultaneously. Moreover, for phenotypic selection, the key point is that nearly all individual selection is holobiont-level selection given the pervasive affects of the microbiota on host biology. The genetic response to selection is what's clearly more challenging to unravel and whether this occurs at a holobiont-level or not is indeed an experimental question worthy of future attention that people are working on.

  1. VII. The hologenome concept fits squarely into genetics and accommodates multilevel selection theory
    • Multilevel selection theory asserts that selection operates across multiple levels of genetic variation with phenotypic effects, from genes to hologenomes and beyond.
    • Holobionts are exclusive to hosts and their associated microbiota; different holobionts, such as a pollinator and a flower, interact with each other under standard ecological principles.
Sixth, the paper frequently plays both sides of the debate. Obligate endosymbionts and organelles are presented as hologenomic entities, but then the paper at times claims hologenomic evolution could be relatively insignificant or rare. These statements are contradictory.

The paper's abstract concludes that "Although selection at the level of the symbiotic community, or hologenome, occurs in some cases, it should not be accepted as the null hypothesis for explaining features of host-symbiont associations". This opinion is largely based on the inaccurate pretense that scientists are claiming holobiont-level selection without evidence or that holobionts are a kumbaya conglomerate. Neither is true. It is easy to oversimplify any concept to death if one wants to. Yet as Einstein once noted "Everything should be made as simple as possible but not simpler".


1 comment:

  1. "While biologists would agree that microorganisms have important roles in host evolution, this statement is a far cry from the claim that they are fused with hosts to form the primary units of selection, or that hosts and microorganisms provide different portions of a unified genome."

    It seems this statement reflects the fact that science has not said the last word yet and there are still many surprises ahead.

    See for instance this paper:

    Novel Symbiotic Protoplasts Formed by Endophytic Fungi Explain Their Hidden Existence, Lifestyle Switching, and Diversity within the Plant Kingdom (2014)

    http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0095266

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