Called Wolbachia, the bacterium acts as a “pathogen blocker” in mosquitoes, which means insects infected with it are unable to pass along certain viruses to new hosts, including people.
“Amazingly, Wolbachia-infected mosquitos have been quite effective at reducing transmission of RNA viruses, including human pathogens,” said Newton, an associate professor in the IU Bloomington College of Arts and Sciences’ Department of Biology. “The phenomenon was first discovered in fruit flies and later moved into mosquitos by scientists through a difficult process in order to stop virus transmission to humans.
“What we still don’t know is how Wolbachia actually does any of these things, and that’s what my lab is poised to find out.”
Under the grant, Newton’s research will identify the biological building blocks involved in pathogen blocking. It’s important to understand these mechanisms because Wolbachia-infected mosquitoes are already used in some parts of the world, including the Asia Pacific islands, northern Australia, South America and Mexico. More information about how the bacteria colonizes new hosts, and the processes that stop it from spreading disease, could increase its effectiveness – as well as prevent unintended consequences from releasing modified organisms into the wild.
The class of viruses that Wolbachia stops from spreading are arboviruses, or viruses spread by arthropods, which include mosquitoes and ticks. Other lesser-known arboviruses include Japanese encephalitis virus, Rift Valley fever virus and tick-borne encephalitis virus.
Last year, Newton and colleagues at IU discovered that a gene called Mt2, which encodes a type of enzyme known as a methyltransferase, plays a role in pathogen blocking. This work – as well as new research under the grant – uses fruit flies, or Drosophila, as a model species for mosquitoes, and leverages IU’s world-class facilities in fruit fly genetics, including the Bloomington Drosophila Stock Center, the Drosophila Genomics Resource Center and FlyBase.
“Access to all the genetic constructs and cell lines in the DGRC – as well as the genetic stocks in the BDSC – will allow our research to progress rapidly,” Newton said. “In this project, we will use resources from the DGRC to see how different proteins impact Wolbachia infection in flies as well as genetic mutants from the BDSC to reveal other variables related to infection.”
Specifically, Newton’s work will focus on proteins known as effectors. Wolbachia inject these proteins into host organisms through a needle-like apparatus called a type IV secretion system, which modifies the insects’ biology to make a “cozy niche” for the bacteria.
Newton’s lab has already found that an effector called WalE1 interacts with a cellular protein called actin in hosts to facilitate transmission of Wolbachia from female insects to their offspring. She and colleagues are working to identify additional effector proteins.
The need to know more about effectors is great since the process of infecting mosquitoes with Wolbachia – to create insects unable to transmit disease – does not occur naturally or easily, Newton said.
“The identification of effectors is important since they can help make the process of infection easier,” she added. “The more we know about the role of effectors, the more control we can gain over the process of infection, and the greater our ability to safely and effectively to stop disease.”