Giardia

Not so special, after all?

Article metrics

The parasite Giardia was thought to represent a throwback to the earliest days of advanced cellular life. But biologists are now arguing over its true status. Jonathan Knight reports.

Body of evidence: it was thought that Giardia had never evolved mitochondria, but electron micrographs (above) have now revealed it contains sacs that resemble diminished versions of this cellular equipment. Credit: J. LUCOCQ

Intestinal cramps rarely inspire deep thoughts about evolution. But anyone who has suffered an infection of the gut parasite Giardia intestinalis can boast of having an intimate, if painful, familiarity with an icon of evolutionary theory. Textbooks have for years held up this single-celled parasite as a living relic of the very early days in the evolution of plants, animals and other higher life forms.

But this may have to change. A new discovery about Giardia's own innards, which makes the parasite look rather more run-of-the-mill, has caused a rift among evolutionary biologists. Some argue that its role in the history of life will have to be reconsidered. But others are fighting to retain Giardia's iconic status.

At the heart of this debate lie mitochondria, sacs of enzymes that use oxygen to generate energy for cells. Organisms from people, through house flies and elm trees, to single-celled yeast and algae, all have them. These are the eukaryotes, whose cells contain many types of other useful sacs, or ‘organelles’, as well as a nucleus, all packaged in the same sort of fatty membrane that surrounds the cell.

The rest of life lacks this equipment. Prokaryotes, which include bacteria and archaea — ancient, single-celled creatures found in extreme environments such as volcanic springs — are devoid of mitochondria and other specialized organelles.

Biologists now believe that eukaryotes gained their mitochondria sometime between 1.5 billion and 2.2 billion years ago1. At the time, rising oxygen levels in Earth's atmosphere were causing problems for organisms adapted to life without the gas. The theory goes that the ancestor of mitochondria was a prokaryotic cellular parasite that could process oxygen. It took up residence inside an ancestral eukaryote and helped it by soaking up toxic dissolved oxygen. Over time, this parasite became an indispensable source of chemical energy for the host, using oxygen to ‘burn’ sugars. Most of its genes relocated to the host's nucleus, sealing the partnership.

Primitive appearance

Until a few months ago, Giardia was thought to represent a throwback to the time before this union. Mitochondria are relatively easy to see under the microscope because they are large and have a characteristic appearance. But none were ever seen in Giardia, so it was thought to be a direct descendent of pre-mitochondrial eukaryotes. Partly as a result, resources have been ploughed into Giardia research, including a project to sequence its genome. “A lot of people's efforts were invested in the idea that Giardia was the most primitive eukaryote,” says Andrew Roger, who studies molecular evolution at Dalhousie University in Nova Scotia, Canada.

Doubts about Giardia's evolutionary position first began to emerge in 1998, when Roger and his colleagues found a strong similarity between a Giardia gene, called cpn60, and a gene from the α-proteobacteria2. These bacteria, which include the pathogen that causes typhus, are thought to be the closest living relatives to the prokaryotes that gave rise to mitochondria. Given the genetic similarity, Roger and his colleagues concluded that Giardia once had mitochondria but had lost them.

But the gene might also have been acquired from another invader that took up residence in eukaryotic cells and did not evolve into mitochondria. This is not as improbable as it might sound — hundreds of examples of such ‘endosymbiosis’ are known3. So far as we know, in billions of years, endosymbiosis has led to the formation of only two cellular organelles: mitochondria and chloroplasts, the site of photosynthesis in plants and algae, which are believed to be related to modern cyanobacteria.

But the real bombshell came last November, thanks to an international team led by molecular parasitologist Jorge Tovar of Royal Holloway, a college of the University of London in Egham, Surrey. His team found in Giardia a number of proteins related to those associated with mitochondria in other eukaryotes. More significantly, these proteins were clustered together at discrete locations in the organism's cells. Using electron microscopy, the researchers saw tiny sacs at those spots, which they identified as mitochondrial relics called mitosomes4.

Gut feeling

A question of timing: did advanced cellular life gain mitochondria after Giardia branched off from the evolutionary tree or before? Credit: SOURCE: N. R. PACE PROC. NATL ACAD. SCI. USA 98, 805–808 (2001)

Tovar first identified mitosomes in 1999 in an unrelated organism called Entamoeba histolytica, a deadly intestinal parasite5. Like Giardia, Entamoeba was once considered to have branched off the trunk of the eukaryotic evolutionary tree before mitochondria came on the scene, and the two were lumped together in a class called Archezoa6. But in the 1980s, DNA sequence evidence showed that Entamoeba branched much later than other organisms with fully fledged mitochondria7. To many researchers, this suggested that it had lost its mitochondria at some point. Tovar's discovery of mitosomes indicated that they were not entirely gone, only much reduced.

For Tovar and many others, the evidence that Giardia once had mitochondria is solid. For example, the electron micrographs of its mitosomes revealed a double membrane surrounding the sacs. This is a property of only three known cellular structures: chloroplasts, the nucleus and mitochondria. Furthermore, contained within those membranes are two proteins that process iron–sulphur clusters, complex structures that are essential to the mitochondrial job of energy production. “We now know that Giardia diverged after the evolution of mitochondria,” Tovar asserts.

But Patricia Johnson, an evolutionary biologist at the University of California, Los Angeles, is among those who are not convinced. Johnson studies the evolution of hydrogenosomes, another cellular sac that may similarly be the product of mitochondrial reduction. One problem, she says, is that the protein produced by cpn60 does not migrate to Tovar's mitosomes. Yet in fully fledged mitochondria and in other microorganisms with mitosomes or hydrogenosomes, it does. “The data make it a toss-up, but it's not being treated with that kind of caution,” she says. To strengthen his case, Tovar is trying to identify all the proteins in Giardia mitosomes, to see if more of those normally associated with mitochondria are present.

Mitchell Sogin of the Marine Biological Laboratory in Woods Hole, Massachusetts, who heads the Giardia genome project, also wants to see more evidence before changing his mind about the parasite's evolutionary status. He points out that sequence analysis shows Giardia's iron–sulphur cluster genes to be only weakly related to mitochondrial genes8. “Evolutionary trees must be strong if you are making strong statements about evolutionary history,” he says.

This attitude frustrates people such as William Martin, who studies molecular evolution at Heinrich Heine University in Düsseldorf, Germany. He is convinced that the best and simplest explanation for the data is that Giardia once had mitochondria9. Some people, he argues, refuse to accept this because they have spent too many years working on the opposite assumption. “They don't want it to have mitochondria because it spoils their soup,” he says. “This thinking is deeply ingrained.”

The thinking has its roots in the concept of the Archezoa, Martin argues, the group that was conceived to bring together a range of single-celled eukaryotes thought to lack mitochondria. Giardia was the grandaddy, having branched off on its own before any other eukaryote, according to evolutionary trees built using sequences of RNA from ribosomes, the organelles in which proteins are made (see Figure, below left).

Family ties

But one by one, the Archezoa all proved to have either a set of mitochondrial genes in their nuclei, or relics of mitochondria such as mitosomes or hydrogenosomes. This isn't entirely surprising, because many of these organisms are parasites, which tend over evolutionary time to become stripped-down versions of their former selves as they become increasingly dependent on their hosts.

Giardia's status as the earliest branching eukaryote has also been questioned. Some recent evolutionary trees that take into account the variable rates at which different DNA bases mutate paint a much muddier picture of the early branches10.

If Tovar, Roger and Martin are correct, how bad is the news for Giardia research? Sogin contends that even if Giardia is shown definitively to have once had mitochondria, it would have no adverse impact on his genome project. Apart from the organism's importance to human health, its sequence should still reveal much about evolution because it branched off the eukaryotic tree very early, he says.

But Giardia's status as a uniquely important throwback to the earliest days of the eukrayotes surely would be usurped if someone discovers a new member of the Archezoa, sans mitochondria or mitosomes, lurking in the oxygen-starved muck at the bottom of a lake. This possibility hasn't escaped the notice of Roger and others, who are still collecting samples in the hope of finding something new. “There is a lot more out there, and it's possible that such organisms still exist,” Roger says.

References

  1. 1

    Dyall, S. D., Brown, M. T. & Johnson, P. J. Science 304, 253–257 (2004).

  2. 2

    Roger, A. J. et al. Proc. Natl Acad. Sci. USA 95, 229–234 (1998).

  3. 3

    Buchner, P. Endosymbiosis of Animals with Plant Microorganisms (Interscience, New York, 1965).

  4. 4

    Tovar, J. et al. Nature 426, 172–176 (2003).

  5. 5

    Tovar, J., Fischer, A. & Clark, C. G. Mol. Microbiol. 32, 1013–1021 (1999).

  6. 6

    Cavalier-Smith, T. in Endocytobiology II (eds Schwemmler, W. & Schenk, H. E. A.) 265–279 (de Gruyter, Berlin, 1983).

  7. 7

    Sogin, M. L., Edman, U. & Elwood, H. in The Hierarchy of Life (eds Fernholm, B., Bremer, K. & Jörnvall, H.) 133–143 (Elsevier Science, Amsterdam, 1989).

  8. 8

    Tachezy, J., Sánchez, L. B. & Müller, M. Mol. Biol. Evol. 18, 1919–1928 (2001).

  9. 9

    Henze, K. & Martin, W. Nature 426, 127–128 (2003).

  10. 10

    Simpson, A. G. B. & Roger, A. J. Curr. Biol. 12, R691–R693 (2002).

Download references

Author information

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Knight, J. Not so special, after all?. Nature 429, 236–237 (2004) doi:10.1038/429236a

Download citation

Further reading

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.