Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774705
Title: Barcoded Transposon Directed Insertion-site Sequencing (TraDIS) : a tool to improve our understanding of the functional genomics of Streptococcus equi subsp. equi
Author: Charbonneau, Amelia Rose Louise
ISNI:       0000 0004 7961 9083
Awarding Body: University of Cambridge
Current Institution: University of Cambridge
Date of Award: 2019
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Abstract:
Strangles, caused by Streptococcus equi (S. equi) remains the most frequently diagnosed infectious disease of horses and is a cause of significant welfare and economic cost. Vaccine research has been limited by the time taken to make mutations in individual genes to determine their role in the disease process. However, the development of transposon directed insertion-site sequencing (TraDIS) technologies provides an opportunity to simultaneously determine the importance of every gene in S. equi under disease relevant conditions, significantly enhancing the capacity to identify new vaccine targets. In this project, a novel barcoded TraDIS technique was designed, which identified that 19.5 percent of the S. equi genome is essential to basic survival in rich medium in vitro, 73.4 percent of genes being non-essential, with the remainder either not defined or of an ambiguous assignment. Comparative analysis revealed that more than 83 percent of the essential gene set of S. equi was concordant with the essential genomes of S. pyogenes and S. agalactiae, highlighting the close genetic relationships between these important pathogenic bacteria. Barcoded libraries were exposed to hydrogen peroxide (H2O2) and whole equine blood, to simulate the interaction with the equine immune system. Sequencing of surviving mutants enabled identification of genes important to S. equi under these conditions in vitro. Fifteen and 36 genes were implicated in the survival of S. equi in H2O2 and whole equine blood, respectively. Results were validated by generating deletion mutant strains in 4 of the genes (pyrP, mnmE, addA and recG). Mutant strains were exposed to H2O2 or whole equine blood and surviving bacteria measured over time. An additional 2 deletion strains in eqbE and hasA, generated prior to this project, were also utilised. Barcoded TraDIS is proposed to reduce the effects of stochastic loss commonly seen in similar datasets, enhancing the ability to resolve differences in the fitness of mutants. To determine the in vivo capabilities of barcoded TraDIS, 12 Welsh mountain ponies were each infected with 2 of 3 barcoded libraries. Viable mutants were recovered and sequenced from the abscess material of infected lymph nodes and data analysed both exploiting (barcoded analysis; BC) and disregarding (per animal analysis; PA) the input library barcodes. Exploiting the barcodes enables output data to be combined on a per input library basis, as opposed to a per animal basis as is traditionally completed in comparable in vivo transposon library studies. From the BC analysis, sequencing identified 368 genes required for fitness. Mutations in a further 85 genes conferred a fitness advantage in vivo. In the PA analysis, only 97 genes required for fitness were identified, which were all similarly identified in the barcoded analysis. No genes in which an insertion conferred a fitness advantage were identified in the PA analysis. To validate these results and confirm the benefit of applying a barcoded technique, 12 genes required for fitness were selected, plus 1 control gene where transposon insertions did not alter fitness, for tagged allelic replacement mutagenesis and repeat challenge in vivo. Seven genes required for fitness in both methods of analysis were selected, plus an additional 5 genes uniquely identified by the BC analysis. All deletion mutants appeared to be attenuated in vivo, however the control mutants and wild-type S. equi did not behave as expected, confounding statistical analysis. Thirty-nine percent (14/36) and 60 percent (9/15) of fitness genes identified in the whole equine blood and H2O2 TraDIS screens, respectively, were also identified as being required for in vivo fitness. Nine consensus genes were identified as required in all 3 experiments. Comparison of the genes implicated in in vivo survival of S. equi to those in S. pyogenes in a non-human primate model of necrotising myositis and in a mouse model of subcutaneous infection, uncovered a set of 23 pan-species fitness genes. Eighteen genes were also commonly identified between the S. equi in vivo data and S. pyogenes ex vivo in human saliva, alluding to the potential genes required by S. equi to survive in the nasopharynx before translocation to the local lymph nodes. The data presented in this thesis provide an unprecedented insight into the mechanisms employed by S. equi to cause disease in the natural host. The data also shed light on the pan-streptococcal pathways important for virulence that are likely to be important for future development of novel therapeutics and vaccines.
Supervisor: Waller, Andrew ; Sargan, David Sponsor: BBSRC ; Horse Trust HBLB Pet Plan
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.774705  DOI:
Keywords: Transposon ; strangles ; sequencing ; tradis ; tnseq ; essential
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