War of the worms

A battlefield

Some of the most successful animals on earth live in societies characterised by a division of labour between reproducing and non-reproducing castes.  One role non-reproducing members may undertake is defence. Spectacular examples include the heavily armoured termites and ants. Recently a soldier caste was discovered in an entirely new and unexpected battleground, inside the bodies of snails. The soldiers? Tiny parasitic flatworms.

Flatworms, or trematodes, have complicated life cycles, involving several different stages infecting a variety of host species. In one host, often a snail, a single trematode undergoes repeated clonal reproduction. Clones produce more clones or go on to produce the next infective stage, which leaves the snail to infect the final host. While working with trematode colonies of Himasthla sp. infecting the Californian horn snail Cerithidea californica, researchers at the University California Santa Barbara observed that the trematode occurred in two distinct morphological forms. There was a large reproducing primary morph, which appeared to be the form typically described in the literature, and a secondary smaller, thinner morph.

These secondary morphs had a number of other features which set them apart. They rarely showed any signs of reproduction and were far more active. They also had huge muscular pharynxes and guts relative to their larger sisters. When researchers preformed behavioural tests, they discovered just what those large mouth parts were for. The secondary morphs attacked and killed other trematode species and unrelated conspecifics. This behaviour is not unknown in trematodes; a number of species attack and kill other trematodes. What was novel was that the smaller morphs appeared to be doing all attacking. The behaviour was rarely observed in the primary morphs. There was also a spatial segregation of morphs. Primary morphs were located in the visceral mass, mainly in the region of the gonads. The secondary morphs were more widely distributed though mainly found within the mantle. The snail mantle is the main entry point for trematodes, a strategic area to defend against invading armies. Finally, the researcher found very few intermediate morphs, suggesting that the smaller morphs were not simply juvenile stages of the primary morphs. They were a distinct, permanent caste whose function appeared to be defence – soldiers. The researchers had discovered eusociality in a completely new taxonomic group.  Previously, eusocial systems consisting of morphologically distinct, specialised reproductive and non-reproductive castes had only been recognised in insects, snapping shrimp, a sea anemone and mole rats. The researchers have already suggested a further five species of trematodes that may have soldier castes.

Work from New Zealand, published this year, on another species (Philophthalmus sp.) has expanded the list of trematodes with soldier castes. The authors also showed that interspecific competition has a heavy impact on colony numbers. This is just the sort of pressure that favours adaptive strategies to reduce competition, such as a permanent soldier caste. However, competition may not be the only selective pressure driving or maintaining caste differentiation in trematodes. In the absence of competition, the presence non-reproducing morphs were found to provide a benefit to the colony, as measured by the number of infective stages produced. Precisely how this benefit comes about is not yet known. The authors suggest some form of communication or nutrient exchange may be taking place between the two morphs. This gives tantalising hints that these colonies are even more complex and interactive than previously thought.

Not only has the discovery of the eusociality in trematodes widened the taxonomic range of this phenomenon, it has also provided researchers with an exciting new tool to study its evolution. The Trematoda class contains at least 20, 000 species with a wide variety of life-histories and ecologies. The discovery is also a great example of how new and unexpected results can still come from well-studied animals. The Himasthla sp. /Californian horn snail system had been studied for over 65 years.

Author

Karen Loxton: loxtonk[at]tcd.ie

Photo credits

wikimedia commons

The not so black and white story of why the zebra got its stripes

Why are zebra black and white? I would hazard a guess your answer is camouflage, and you would be right… well, mostly. I would then bet you got the beast from which the zebra is hiding wrong. While the black and white stripes might disrupt outline of a zebra in the eyes of an ambushing lion or sprinting cheetah, the scientific evidence points to a much smaller blood thirsty devourer of zebra.

Since the 1970s, experiments have shown that Tsetse flies are less attracted to black and white striped patterns than plain black, white or grey colours. Most recently, a series of experiments conclusively showed that another group of flies, the horseflies, are far less attracted to zebra-stripe patterns than plain, black, white, brown or grey surfaces. Furthermore, narrow bands of stripes are even more effective at keeping hidden from the horseflies, and it’s perhaps no surprise that the legs and heads of zebra contain the closest spaced stripes where blood vessels lie perilously close to the skin surface of these key anatomical locations. The legs being needed to flee from the lions and the head for thinking.

Of course, there may be other factors that simultaneously favour such a striking colour pattern. Regardless though, some interesting evolutionary points follow the “camouflage from flies” idea. Chief among them being: if stripes are so good at hiding from horseflies, then why do Eurasian horses not possess the same pattern where horseflies are also common and a nuisance?

So while the “why” of the zebras stripes seems to have some scientific evidence at last, the “how” they got their stripes is another blog topic for another day and involves leopards, cells, computers and a bit of maths.

Author

Andrew Jackson: a.jackson@tcd.ie

Photo credit

Andrew Jackson

The plight of the bumble bee; diapause, immunity and parasitic attack

Sphaerularia bombi with an everted uterus.

Bee populations are in severe decline, an alarming and worrying trend when you consider their vital importance as commercial and ecological pollinators. Research and media attention often focuses on afflictions of honeybees such as the Varroa mite and colony collapse disorder. However, parasites are also major contributors to the plight of the bumble bee.

Bumble bee queens spend 6-9 months in diapause, a hibernation-like state which allows them to survive harsh winter weather. My research demonstrated that queens have reduced immune function during this time, leaving them vulnerable to infections and parasitic attack.

Sphaerularia bombi is a common yet poorly studied nematode which is found primarily in the Northern hemisphere, infecting up to 50% of queen bumble bees in some areas. Adult female Sphaerularia present in the soil infect diapausing queens. My project showed that, with their immunological guards down, the queens cannot mount an effective response to invading parasites.

Sphaerularia exerts significant influence on its host after the queens emerge from diapause. The nematodes evert their uterus to a structure 300 times the volume of the rest of their body (see picture above). This enormous uterus releases numerous eggs into the host and also extracts nutrients from the bees.

Sphaerularia castrate the queens so they don’t form new colonies. The parasite also changes queens’ behaviour so they go to sites suitable for diapause even though it’s the wrong time of year. Having released larval stage nematodes into the soil, parasitised queens die while the nematodes are then poised to infect new queens entering diapause.

Sphaerularia clearly has a significant impact on a host species with high ecological and commercial value yet it remains very poorly studied.  In collaboration with research currently being performed by PhD student Joe Colgan (Trinity College Dublin: Supervisor Dr. Mark Brown) and Dr. Jim Carolan (National University of Ireland, Maynooth), my project filled some of the gaps in our understanding of the molecular interactions between host and parasite. One particularly interesting finding was that S.bombi infection seems to change the protein expression in bees, indicating a complex interaction between host and parasite at the molecular level in parallel to the dramatic physiological and behavioural changes in the bees.

Continuation of this research on a fascinating host-parasite system will bring us closer to understanding and hopefully eventually combatting the plight of the bumble bee.

References

1. Society of Biology News Page http://www.societyofbiology.org/newsandevents/news/view/469

Author

Sive Finlay: sfinlay[at]tcd.ie

Sive is a PhD student from Trinity College Dublin, who recently won Best Biology student at the 2012 SET awards for her undergraduate project detailed here

Photo credit

Mike Kelly