Lysiphlebus fabarum: Aphid Rancher, Butcher

Dairy farmer meets Alien: The braconid wasp Lysiphlebus fabarum harvests honeydew from aphids before literally stabbing them in the back so their offspring can develop inside of the aphids’ bodies.

There are many unlikely relationships in the animal kingdom. Personally, I’m a fan of “Bonedigger” the lion and “Milo” the dachshund, but there are some pretty odd couples in the insect world as well. I recently stumbled across a research piece studying the behavior of a parasitoid wasp that attacks black bean aphids. Interestingly enough, the wasps mimic ant behavior to effectively “coax” the aphids into a false sense of security before stabbing them with their sharp ovipositor and inserting their eggs, which hatch to feed on the aphids from the inside out. Remarkably, these behaviors involve some degree of cooperation from the aphid, and when ants are present, there’s potential for some unlikely mutualism among all three species (although, admittedly, not so much between the aphids and wasps).

Lysiphlebus fabarum forages in ant-tended black bean aphid (Aphis fabae) colonies. Primarily, the aphid is the unfortunate host to developing L. fabarum larvae. In addition, adult wasps feed on aphid honeydew secretions, which is similar to host feeding in other parasitoid–host systems. But unlike host feeding, honeydew feeding does not harm the aphids, instead requiring host cooperation.

Female L. fabarum wasps promote honeydew secretion by mimicking the anntenal drumming of ants, and employ similar antennal movements while probing potential hosts prior to oviposition. Switching between the roles of ant mimic and parasitoid overall reduce the defensive responses of aphids: kicking, thrashing, dispersing, and secreting a waxy, glue-like substance from their cornicles (these cornicle secretions can fuse mandibles, antennae, legs, etc., leading to the death of the wasp).

F5.large
L. fabarum mimicking ant antennal behavior.
Image credit: Rasekh et al., J Ins Sci, 10(1)

Lysiphlebus spp. also possess cuticular hydrocarbons and lipids that identify them as aphids to help mask their presence from ants. Apparently their chemical camouflage is so good that it can be difficult for wasps to identify their conspecifics. This camouflage is an evolutionary response to ant aggression, since ants ferociously protect the aphids they tend to. And for L. fabarum, mimicry of ant behavior provides additional protection—not because the ants themselves are fooled, but because it makes aphids more inclined to secrete honeydew in the future.

So a few aphids are lost to parasitism, but the others are more productive—a benefit for hungry wasps as well as ants. In turn, ants offer protection for wasp offspring, albeit unintentionally. Ultimately there is potential for mutualism between ants and L. fabarum, as long as the wasps continue to parasitize only a small fraction of the aphid population. Of course, none of this could have happened if the parasitoid wasps didn’t take advantage of the already-existing mutualism between ants and aphids.


Further Reading:
Rasekh A, Michaud JP, Kharazi-Pakdel A, & Allahyari H. (2010). Ant mimicry by an aphid parasitoid, Lysiphlebus fabarum. Journal of Insect Science, 10(1). doi:10.1673/031.010.12601

When the Stingless Bee F. schrottkyi Made Headlines, We Made Generalizations

Sure, honey bees are important. They’re worth about $1.6 billion annually to U.S. agriculture. But take the blueberry plant, for example: southeastern blueberry bees, bumble bees, carpenter bees, orchard bees, Bradley’s andrena bee, and many others lend a “tarsus” in pollinating flowers. Together, all these “other” pollinators are more important than honey bees economically (by about $5 billion) and ecologically (enhancing productivity and stability).

While honey bees are the center of public attention—partly because they’re dying from Varroa destructor mites, the Nosema apis fungus, and insecticides—native bees modestly continue to pollinate in the face of similar environmental challenges.

operaria_inteiro_friesella_schrottkyiHowever, the stingless bee Friesella schrottkyi (Hymenoptera: Apinae) made headlines this week because of new research by Rodrigues et al. identifying copper sulfate-containing leaf fertilizers as mind-altering and lethal when consumed by F. schrottkyi. (Image credit: Sylvia Maria Matsuda, Laboratório de Abelhas)

Science Today

Ento Today

Wait a second. The research article only investigated the effects of certain leaf fertilizers on one species of stingless bee. Our friend F. schrottkyi’s only been famous for a week, and already we’re speculating and generalizing.

A key point to this research is in understanding the differences in pollination behavior and agrochemical toxicity among bee species. And stingless bees are not a single species, but rather a very diverse group in and of themselves. The effects of biopesticides, fungicides, and other agrochemicals on all kinds of bees (as well as other pollinators, and the surrounding ecosystem as a whole) is incredibly important.

So let’s take a quick look at what the Rodrigues et al. paper actually says:

  • The authors are implicitly concerned about the effects of all agrochemicals (especially non-insecticides) on a wide diversity of native pollinators.
  • Their research focused on Friesella schrottkyi and two commonly used fertilizers.
  • A series of bioassays (experiments run in the laboratory, not in the field) assessed the toxicity of a micronutrient mix and a fertilizer containing 24% copper sulfate.
  • The copper sulfate-containing fertilizer was surprising deadly when consumed, while contact exposure affected flight and foraging behavior.
  • Consuming the micronutrient mix did not affect F. schrottkyi survival, but did reduce respiration rate.
  • Copper, manganese, molybdenum, zinc, sulfur, and boron may all be involved in the toxic effects of leaf fertilizers on bees.

It’s important to take a step back and think about what this research really means. We should not be making broad conclusions, but we do need to ask questions about how other leaf fertilizers and other agrochemicals are affecting a wider spectrum of animals. While in a general sense it’s true that at high enough concentrations, all leaf fertilizers are probably toxic to all stingless bees, this conclusion is beyond the scope of the Rodrigues et al. article.

I also feel it shouldn’t come as a surprise to anyone that the heavy metals in fertilizers, administered orally or in high concentrations, have a negative affect on, well, any insect, plant, or animal. Heavy metals play an important role as cofactors for proteins and enzymes (think hemoglobin, in blood). But at higher levels, heavy metals start to interfere with enzymes, cellular structures, and even DNA.

The point is to take these broad ideas—like the stuff we think can be toxic, the pollinators we think are useful—and learn as much as we can about it, which is exactly what Rodrigues et al. did: figuring how and why a commonly used fertilizer affects one of their native bees. The best way we can preserve our ecosystems and protect our agriculture is to have detailed knowledge of how it works—and then we can ask even more questions and create new hypotheses about how stuff works.

Tweet: Native pollinators are important, too! #savethebees is not just for honeybees anymore. #saveALLthebees via @rudimik

 

DNA Thief: How a Braconid Wasp Used a Stolen Virus to Hack Its Prey

In a long con lasting nearly 100 million years, a crafty braconid wasp stole a virus’s DNA to control the immune system of its prey.

1323021-PPT
Braconid wasp (Aleiodes indiscretus) parasitizing a gypsy moth larva (Lymantria dispar)
Image credit: Scott Bauer, USDA Agricultural Research Service

Braconid wasps are unique parasites that lay their eggs inside unsuspecting butterfly or moth larvae, in which newly hatched wasps feed on relatively nonessential organs. Normally the immune system of the host defends against these attacks, but the wasps have a secret weapon in their arsenal: a domesticated virus from the Cretaceous period used to ensure the prey stays incapacitated but alive…until the young wasps are old enough to search out alternative food sources, that is.

The viruses coopted by braconid wasps are a type of polydnavirus (PDV), an infectious agent barely recognizable as a virus at all. Typical “everyday” viruses—like influenza or the common cold—contain all of the genetic information needed to replicate, but the genes involved in PDV reproduction are stored within the wasp’s DNA, which is an odd habit for a virus. As a result, the wasps more or less control the manufacture of the viruses and produce them at will.

Nearly 100 million years ago when the DNA coding for PDV replication was integrated into the wasp’s genome, virulence genes encoding wasp venom were transferred into the virus. Like Cold War-era microfilm, these DNA sequences contain sensitive information capable of great destruction. With these genes packaged into the shell of the stolen virus, braconid wasps literally invented nanotechnology for use in predator–prey warfare.

Think not what your virus can do for you, but what your virus can do for your baby wasps. After the mother wasp transmits the modified virus while laying its eggs, the prey’s blood cells read the DNA message inside the virus. Traditionally, this is how viruses hijack cellular machinery in order to reproduce, but after the braconid wasp’s slight-of-hand millions of years ago, the host’s cells are tricked into producing wasp venom instead of new viruses—effectively silencing the host’s own immune system so the young wasps can develop in secret.

By tricking larvae into poisoning themselves, braconid wasps save a lot of time and energy they would have otherwise used to produce their own venoms. They also gained more control over venom delivery—if the PDV integrates into a host larva’s genome, infected cells can be reprogrammed to deliver small doses of venom days or even weeks after the initial attack.

Using viruses for genetic hacking is unique among braconid wasps and several species of ichneumons, but many other wasps transmit viruses as well. Ascoviruses and baculoviruses, for example, are two types of contagion that infect butterfly and moth larvae. The parasitic wasp is only a disease vector in this case, just as mosquitoes transmit West Nile Virus to humans without infecting themselves. Ascovirus and baculovirus infections lower the immune defenses of the prey, making it easier for immature wasps to feed and grow without interference.

The relationship between wasps and viruses is symbiotic. The wasp’s young are able to develop without fear of an immune system attack and the viruses have better access to hosts. But for braconid wasps and their PDVs, the virus completely relies on the wasp for reproduction. PDVs can be selfish, though. If a caterpillar survives being parasitized by young wasps, small pieces of the virus may join with the host’s DNA to be inherited by future offspring. This is not an ideal situation for the virus, but it does remove some the virus’s reliance on the wasp for reproduction and transmission. However, these fragments of virus DNA would need to hijack DNA from another virus in order to become infectious again…but that’s just science fiction.

Or is it science fiction? In the laboratory, scientists have successfully made super-viruses from pieces of Langet and mosquito-borne dengue viruses. These and other “Frankenviruses” are typically inactive and used to create vaccines against dangerous diseases, but as for our friendly neighborhood PDVs…perhaps over the next 100 million years another insect will reengineer them in newer, even more unimaginable ways.


Further Reading:

Herniou, Huguet, Thézé, Bézier, Periquet, & Drezen. (2013). When parasitic wasps hijacked viruses: genomic and functional evolution of polydnaviuses. Phil Trans R Soc B, 368, 20130051. doi: 10.1098/rstb.2013.0051

Gunderson–Rindal & Pedroni. (2005). Characterization and transcriptional analysis of protein tyrosine phosphatase genes and an ankyrin repeat gene of the parasitoid Glyptapanteles indiensis polydnavirus in the parasitized host. J Gen Virol, 87(2), 311–322. doi: 10.1099/vir.0.81326-0

Pletnev, Bray, Hanley, Speicher, & Elkins. (2001). Tick-borne Langat/mosquito-borne dengue flavivirus chimera, a candidate live attenuated vaccine for protection against disease caused by members of the tick-borne encephalitis virus complex: evaluation in rhesus monkeys and in mosquitoes. J Virol, 75(17), 8259–8267. doi: 10.1128/JVI.75.17.8259-8267.2001