![\"v_butoday_15-8765-FEARNS-023\"](\"\/federal\/files\/2015\/06\/v_butoday_15-8765-FEARNS-023.jpg\")
<\/a>Rachel Fearns, a MED associate professor of microbiology and winner of a 2014 Hartwell Individual Biomedical Research Award, studies the molecular mechanisms within RSV, a common virus that is a major cause of pneumonia in infants and young children. Photo (to the left) by Cydney Scott.<\/em><\/p>\nRespiratory syncytial virus<\/a>, or RSV, is a highly contagious virus that attacks people\u2019s lungs and airways. For healthy adults, infection often leads to mild symptoms that feel like a cold. But for children and babies, the effects can be severe. RSV is a major cause of pneumonia in infants and young children in the United States, and the leading cause of viral death in infants.<\/p>\n Rachel Fearns<\/a>, a\u00a0School of Medicine associate professor of microbiology, hopes that a deeper understanding of RSV may lead to better treatments. She has won a 2014 Hartwell Individual Biomedical Research Award <\/a>from the Hartwell Foundation, which gives her $300,000 over three years to study the molecular mechanisms that allow RSV to replicate and multiply. Fearns hopes that her research might eventually lead to antiviral drugs and vaccines to treat and prevent RSV disease and give insight into how related viruses could also be controlled.<\/p>\n Fearns studies a protein within the virus called a polymerase, a complicated enzyme with two different jobs: first, it copies the RSV genome into messenger RNAs to make viral proteins, a process called transcription; it also makes more copies of the genome, a process called replication. She was the first scientist to isolate and purify RSV polymerase, a \u201ctechnically challenging\u201d process, she says, that took her six years, from 2004 to 2010. One of the challenges was that RSV polymerase is so large\u2014more than five times larger than the average cellular protein\u2014and therefore is difficult to make efficiently and correctly. \u201cMost normal people would have given up,\u201d she says, with a smile.<\/p>\n Fearns wanted a pure copy of the protein so she could study its function in detail. \u201cWe wanted something we could work with in a test tube,\u201d she says. \u201cHow does this one protein do both transcription and replication, and how does it choose which one to do? It\u2019s a big scientific question.\u201d<\/p>\n So far, scientists studying RSV polymerase have learned that it has at least three distinct parts with three different functions, as well as other parts that are not well understood. \u201cWe want to understand those unexplained parts,\u201d says Fearns, \u201cbecause any essential protein activity is potentially a good target for antiviral drugs.\u201d She also notes that RSV is closely related to measles, mumps, and some emerging viruses such as Marburg and Ebola. \u201cIn the long term, anything we learn with RSV would likely be applicable to those other viruses,\u201d she says.<\/p>\n Each year, the Hartwell Foundation awards grants to faculty who are involved in innovative, cutting-edge biomedical research that will potentially benefit children. For each researcher funded, the sponsoring participating institution will also receive a Hartwell Fellowship to fund one postdoctoral candidate. For Fearns, it means a chance to pursue science that is high risk, with a potentially large payoff. \u201cIt\u2019s exciting science,\u201d she says, \u201cand I\u2019m glad to have the opportunity to work on it.\u201d<\/p>\n A version of this article originally appeared on<\/em> BU Research<\/a>.<\/p>\n