Identifying biosynthetic gene clusters whose products inhibit cystic fibrosis derived pathogens

Bibliographic Details
Main Author: Basalla, Joseph
Language:English
Published: Bowling Green State University / OhioLINK 2018
Subjects:
Online Access:http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1530795688583696
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spelling ndltd-OhioLink-oai-etd.ohiolink.edu-bgsu15307956885836962021-08-03T07:07:21Z Identifying biosynthetic gene clusters whose products inhibit cystic fibrosis derived pathogens Basalla, Joseph Biology Microbiology Molecular Biology Antibiotic resistance cystic fibrosis environmental microbiology Pseudomonas The emergence of pathogens resistant to all known antibiotics has become a serious threatto our healthcare systems. In 2050, infections from antibiotic resistant bacteria are predicted tobecome the leading cause of death worldwide, reaching over 300,000 per year in the U.S. alone.Unfortunately, pharmaceutical companies have stopped research and development of new drugsdue to low profitability, so university research labs have begun leading efforts to discover newcompounds. In concordance with this, the Wildschutte lab uses environmental Pseudomonas spp.as a source for novel antibiotics. We hypothesize that pathogenic bacteria have evolvedadaptations to their host, and that these adaptations may result in a decreased fitness whencompeted against bacteria from non-host, natural environments. To support this, we have shownthat environmental Pseudomonas from different habitats produce diverse compounds that inhibitpathogens isolated from human hosts. Specifically, 495 environmental Pseudomonas strains wereisolated from U.S. derived soil, freshwater lakes in Hungary, and estuaries in Germany. Theseenvironmental strains were then competed against a panel of 70 pathogens isolated from thelungs of cystic fibrosis patients. In total, over 2,000 of these interactions were seen as inhibitory,suggesting that the environmental strains represent an underutilized source of antibiotics.Additionally, environmental strains that were shown to inhibit a number of pathogens werestudied using transposon-mutagenesis to uncover the underlying genetic elements responsible forinhibition. Through this process, we have identified a number of putative metabolites capable ofinhibiting the growth of human pathogens. 2018-07-23 English text Bowling Green State University / OhioLINK http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1530795688583696 http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1530795688583696 unrestricted This thesis or dissertation is protected by copyright: all rights reserved. It may not be copied or redistributed beyond the terms of applicable copyright laws.
collection NDLTD
language English
sources NDLTD
topic Biology
Microbiology
Molecular Biology
Antibiotic resistance
cystic fibrosis
environmental microbiology
Pseudomonas
spellingShingle Biology
Microbiology
Molecular Biology
Antibiotic resistance
cystic fibrosis
environmental microbiology
Pseudomonas
Basalla, Joseph
Identifying biosynthetic gene clusters whose products inhibit cystic fibrosis derived pathogens
author Basalla, Joseph
author_facet Basalla, Joseph
author_sort Basalla, Joseph
title Identifying biosynthetic gene clusters whose products inhibit cystic fibrosis derived pathogens
title_short Identifying biosynthetic gene clusters whose products inhibit cystic fibrosis derived pathogens
title_full Identifying biosynthetic gene clusters whose products inhibit cystic fibrosis derived pathogens
title_fullStr Identifying biosynthetic gene clusters whose products inhibit cystic fibrosis derived pathogens
title_full_unstemmed Identifying biosynthetic gene clusters whose products inhibit cystic fibrosis derived pathogens
title_sort identifying biosynthetic gene clusters whose products inhibit cystic fibrosis derived pathogens
publisher Bowling Green State University / OhioLINK
publishDate 2018
url http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1530795688583696
work_keys_str_mv AT basallajoseph identifyingbiosyntheticgeneclusterswhoseproductsinhibitcysticfibrosisderivedpathogens
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