Towards this goal, I work with a specific family of reading comprehension tasks, normally referred to as the Non-Extractive Reading Comprehension (NRC), where the given passage does not contain enough information and to correctly answer sophisticated reasoning and ``additional knowledge" is required. I have organized the NRC tasks into three categories. Here I present my solutions to the first two categories and some preliminary results on the third category.
Category 1 NRC tasks refer to the scenarios where the required ``additional knowledge" is missing but there exists a decent natural language parser. For these tasks, I learn the missing ``additional knowledge" with the help of the parser and a novel inductive logic programming. The learned knowledge is then used to answer new questions. Experiments on three NRC tasks show that this approach along with providing an interpretable solution achieves better or comparable accuracy to that of the state-of-the-art DL based approaches.
The category 2 NRC tasks refer to the alternate scenario where the ``additional knowledge" is available but no natural language parser works well for the sentences of the target domain. To deal with these tasks, I present a novel hybrid reasoning approach which combines symbolic and natural language inference (neural reasoning) and ultimately allows symbolic modules to reason over raw text without requiring any translation. Experiments on two NRC tasks shows its effectiveness.
The category 3 neither provide the ``missing knowledge" and nor a good parser. This thesis does not provide an interpretable solution for this category but some preliminary results and analysis of a pure DL based approach. Nonetheless, the thesis shows beyond the world of pure DL based approaches, there are tools that can offer interpretable solutions for challenging tasks without using much resource and possibly with better accuracy.
Salmonella enterica serovar Typhimurium, a gram-negative facultative rod-shaped bacterium causing salmonellosis and foodborne disease, is one of the most common isolated Salmonella serovars in both developed and developing nations. Several S. Typhimurium genomes have been completed and many more genome-sequencing projects are underway. Comparative genome analysis of the multiple strains leads to a better understanding of the evolution of S. Typhimurium and its pathogenesis. S. Typhimurium strain UK-1 (belongs to phage type 1) is highly virulent when orally administered to mice and chickens and efficiently colonizes lymphoid tissues of these species. These characteristics make this strain a good choice for use in vaccine development. In fact, UK-1 has been used as the parent strain for a number of nonrecombinant and recombinant vaccine strains, including several commercial vaccines for poultry. In this study, we conducted a thorough comparative genome analysis of the UK-1 strain with other S. Typhimurium strains and examined the phenotypic impact of several genomic differences. Whole genomic comparison highlights an extremely close relationship between the UK-1 strain and other S. Typhimurium strains; however, many interesting genetic and genomic variations specific to UK-1 were explored. In particular, the deletion of a UK-1-specific gene that is highly similar to the gene encoding the T3SS effector protein NleC exhibited a significant decrease in oral virulence in BALB/c mice. The complete genetic complements in UK-1, especially those elements that contribute to virulence or aid in determining the diversity within bacterial species, provide key information in evaluating the functional characterization of important genetic determinants and for development of vaccines.
Uropathogenic Escherichia coli (UPEC), a member of extraintestinal pathogenic E. coli, cause ∼80% of community-acquired urinary tract infections (UTI) in humans. UPEC initiates its colonization in epithelial cells lining the urinary tract with a complicated life cycle, replicating and persisting in intracellular and extracellular niches. Consequently, UPEC causes cystitis and more severe form of pyelonephritis. To further understand the virulence characteristics of UPEC, we investigated the roles of BarA-UvrY two-component system (TCS) in regulating UPEC virulence. Our results showed that mutation of BarA-UvrY TCS significantly decreased the virulence of UPEC CFT073, as assessed by mouse urinary tract infection, chicken embryo killing assay, and cytotoxicity assay on human kidney and uroepithelial cell lines. Furthermore, mutation of either barA or uvrY gene reduced the production of hemolysin, lipopolysaccharide (LPS), proinflammatory cytokines (TNF-α and IL-6) and chemokine (IL-8). The virulence phenotype was restored similar to that of wild-type by complementation of either barA or uvrY gene in trans. In addition, we discussed a possible link between the BarA-UvrY TCS and CsrA in positively and negatively controlling virulence in UPEC. Overall, this study provides the evidences for BarA-UvrY TCS regulates the virulence of UPEC CFT073 and may point to mechanisms by which virulence regulations are observed in different ways may control the long-term survival of UPEC in the urinary tract.