Below is a summary of the abstract you submitted. Presenting author(s) is shown in bold.
If any changes need to be made, you can modify the abstract or change the authors.
You can also download a .docx version of this abstract.
If there are any problems, please email Dan at dar78@pitt.edu and he'll take care of them!
This abstract was last modified on March 16, 2022 at 12:22 a.m..

We isolated phages on Microbacterium paraoxydans as well as the more commonly used host, Microbacterium foliorum. Two M. paraoxydans phage genomes were sequenced and analyzed. One of these phages, Cassita, is in cluster GB, which consists of four phages that were all isolated on M. paraoxydans. The cluster GB phages have Siphoviral morphology and genomes that are 59,253-62,439 kb with large direct terminal repeats (1350-1807 bp). These genomes have very little nucleotide similarity with other phages in the database. However, they share overall genome structure and several phams, including structural proteins and DNA modification enzymes, with cluster ED phages. The second phage sequenced, Fransoyer, is in cluster EG. There are two other M. paraoxydans phages in this cluster, SadLad and RubyRalph, and these three phages form a group that is more similar to each other (>85% gene content similarity) than to the other cluster EG phages isolated on M. foliorum (<60% gene content similarity). These phages have Siphoviral morphology and 61,880-62,801 bp genomes with 209-211 bp direct terminal repeats. We are conducting host range experiments to determine whether these M. paraoxydans phages can infect M. foliorum or other Microbacterium species.