Biology subjects

Jones-Burrage, S. E.

Publications and source records attributed to Jones-Burrage, S. E..

3 recordsLinked to original sources

bioRxiv2019

Identification of Chikungunya virus nucleocapsid core assembly modulators

AbstractThe alphavirus Chikungunya virus is transmitted to humans via infected mosquitos. Most infected humans experience symptoms which can range from short-term fatigue and fever to debilitating arthritis that can last for months or years. Some patients relapse and experience symptoms months or years after the initial bout of disease. The capsid protein of Chikungunya virus forms a shell around the viral RNA genome; this structure is called the nucleocapsid core. The core protects the genome during virus transmission and with the correct environmental trigger, this proteinaceous shell dissociates and releases the viral genome to initiate infection. We hypothesized that targeting compounds to interfere with the nucleocapsid cores function would constrain virus spread either by inhibiting the release of viral genomes during entry or by reducing the number of infectious virus particles assembled. We implemented a high throughput, in vitro, FRET-based assay to monitor nucleic acid packaging by purified Chikungunya capsid protein as a proxy for nucleocapsid core assembly and disassembly. We screened 10,000 compounds and found 45 that substantially modulated the assembly of core-like particles. A subset of compounds was selected to study their effects in virus-infected vertebrate cells. Our results show that four compounds inhibit infectious virus production by at least 90% in a dose-dependent manner. The most promising inhibitor was tested and found to reduce the amount of nucleocapsid cores inside the cell during Chikungunya virus infection. These compounds could be the foundation for anti-viral therapeutics.\n\nHighlightsO_LIA FRET-based assay to detect nucleic acid packaging by Chikungunya virus capsid protein\nC_LIO_LIIdentification of small molecules that modulate core-like particle assembly\nC_LIO_LIA subset of compounds that interfere with in vitro assembly also inhibit Chikungunya virus production in cell culture\nC_LIO_LIIdentification of antiviral molecules that may not be identified by assays using reporter viruses\nC_LIO_LIPotential starting compounds for developing direct-acting antivirals\nC_LI

microbiology↗

bioRxiv2019

Cell aggregation and aerobic respiration facilitate survival of Zymomonas mobilis ZM4 in an aerobic minimal medium

Zymomonas mobilis produces ethanol from glucose near the theoretical maximum yield, making it a potential alternative to yeast for industrial ethanol production. A potentially useful industrial feature is the ability to form multicellular aggregates called flocs, which can settle quickly and exhibit higher resistance to harmful chemicals. While spontaneous floc-forming Z. mobilis mutants have been described, little is known about the natural conditions that induce Z. mobilis floc formation and the genetic factors involved. Here we found that wild-type Z. mobilis forms flocs in response to aerobic growth conditions but only in a minimal medium. We identified a cellulose synthase gene cluster and a single diguanylate cyclase that are essential for both floc formation and survival in an aerobic minimal medium. We also found that NADH dehydrogenase 2, a key component of the aerobic respiratory chain, is important for survival in an aerobic minimal medium, providing a physiological role for this enzyme which has previously been found to be disadvantageous in aerobic rich media. Supplementation of the minimal medium with vitamins also promoted survival but did not inhibit floc formation.

microbiology↗

bioRxiv2017

Pantothenate auxotrophy in Zymomonas mobilis ZM4 is due toa lack of aspartate decarboxylase activity

The bacterium Zymomonas mobilis naturally produces ethanol at near theoretical maximum yields, making it of interest for industrial ethanol production. Z. mobilis requires the vitamin pantothenate for growth. Here we characterized the genetic basis for the Z. mobilis pantothenate auxotrophy. We found that this auxotrophy is due to the absence of a single gene, panD, encoding aspartate-decarboxylase. Heterologous expression of Escherichia coli PanD in Z. mobilis or supplementation of the growth medium with the product of PanD activity, {beta}-alanine, eliminated the need for exogenous pantothenate. We also determined that IlvC, an enzyme better known for branched-chain amino acid synthesis, is required for pantothenate synthesis in Z. mobilis, as it compensates for the absence of PanE, another pantothenate synthesis pathway enzyme. In addition to contributing to an understanding of the nutritional requirements of Z. mobilis, our results have led to the design of a more cost-effective growth medium.

microbiology↗