Listen to an introduction to our synthetic biology research:
Studying Evolution and Engineering Bee Guts (EBRC in Translation Podcast)
Watch a public seminar on our microbial evolution research at UT Tyler 2024 Darwin Day:
The Long-Term Evolution Experiment: Watching Bacteria Evolve for More Than Three Decades
See also: Previous Research Projects
Current Funding: ARO MURI, NSF EDGE, USDA NIFA
Past Funding: DARPA BRICS, DARPA Insect Allies, ERDC
Overview Publication
Current Researchers: Zuberi Ashraf, Kadena Cope, Korin Jones, Kathleen Sotelo, PJ Lariviere, Lucio Navarro, Dennis Mishler
News: Bacteria Engineered to Protect Bees from Pests and Pathogens
Representative Publications
Aphids are plant pests and model systems for studying bacteria-insect symbioses. We have developed tools for engineering strains of Serratia symbiotica that colonize the aphid gut. We are now using these tools to unravel how these strains, which can be pathogenic to their hosts, are related to strains of S. symbiotica that live within insect cells, are inherited across aphid generations, and can benefit their aphid hosts. We have showed that cultured S. symbiotica strains are capable of maternal transmission within aphids, suggesting that they possess a latent capacity to evolve a long-term symbiotic relationship with their hosts. We are also exploring applications of these engineered bacteria related to pest control, especially through symbiont-mediated RNAi.
Current Researchers: Anthony VanDieren, Lucio Navarro
News: Turning Plant Pests into Helpers
Representative Publications
Synthetic biology applies engineering principles to create living systems with predictable and useful behaviors from collections of standardized genetic parts. However, living systems – unlike mechanical devices – inevitably evolve when their DNA sequences accumulate copying errors, often resulting in "broken" cells that no longer function as they were programmed. We are addressing this challenge by better characterizing how engineered cells evolve and using this information to design DNA sequences and host cells that are more robust against unwanted evolution. Also, precisely defining the function, extent, and provenance of genetic parts can be complicated because variation in these parts can arise from engineering or intentional evolution. This work includes: (1) developing "negative design" software to alert researchers to genetically unstable and unintentionally burdensome DNA designs; (2) using experimental evolution and engineering to create "antimutator" variants of host organisms that have lower-than-natural mutation rates; and (3) developing databases and software tools for improved annotation of engineered DNA sequences and common variants of those sequences.
Current Researchers: Dennis Mishler, Cameron Roots
Representative Publications
Current Funding: NIH R01; Past Funding: NSF CAREER, DARPA BRICS, DARPA Insect Allies
Current Researchers: Alexa Morton, Pranesh Rao, Ira Zibbu
News: Legendary bacterial evolution experiment enters new era
Representative Publications
Funding: NSF LTREB, UT-CNS SPARK, NSF EEID, NASA Past Funding: NSF K99/R00
Naturally competent bacteria have expanded evolutionary potential because they can readily acquire new DNA from their environment. We are using experimental evolution of the model organism Acinetobacter baylyi ADP1 to understand how horizontally acquired genes and mobile genetic elements become domesticated after their incorporation into a new genome and the broader effects of gene acquisition on the rest of the genome. We are also studying the role of chemical specificity in determining the fate of acquired DNA as either nutrition or genetic information. These bacteria also provide an improved platform for studying microbial genome engineering due to the ease of reconstructing mutations and introducing new genes. We are investigating sources of genetic instability in ADP1 and engineering a clean genome version of this strain by deleting transposable elements and prophages. This will promote the use of ADP1 in synthetic biology by reducing rates of mutations that lead to inactivation of introduced genes. Further, we are using ADP1 as a platform to understand the limits to streamlining bacterial genomes and identifying adaptations to overcome the fitness costs of reduced genomes.
Current Researchers: Isaac Gifford, Meghna Vergis
Representative Publications
Funding: NSF, UT-CNS SPARK Past Funding: Welch Foundation, NSF CAREER
Bartonella are diverse blood-borne parasites that can cause zoonotic infections of humans. The Hawlena Lab studies Bartonella species that circulate in gerbil populations in the Negev Desert in southwestern Israel. In these natural wildlife communities, multiple species of Bartonella infect and co-infect multiple host species, making it a dynamic system for studying host-parasite interactions. Our laboratory collaborates on projects characterizing how the genomes of these Bartonella evolve within and over multiple infection cycles in wild and lab-reared rodents. Our lab is particularly interested in mechanisms for genome evolvability utilized by these bacteria to escape host immune responses, including simple-sequence repeat contingency loci, gene accordions, and recombination during co-infections.
Current Researchers: Isaac Gifford
Representative Publications
Funding: BSF Past Funding: NSF EEID