VS 17-25: A Soil Isolate with Activity Against Multidrug-Resistant Pathogens
Presenter: Vinuji Senalya Siriwardena
Faculty Sponsor: Verena Carvalho
School: UMass Amherst
Research Area: Biology
Session: Poster Session 5, 3:15 PM - 4:00 PM, 163, C18
ABSTRACT
Antibiotic resistance is a rapidly escalating global health crisis, mainly in hospital-acquired
(nosocomial) infections, where treatment options are increasingly limited. ESKAPE pathogens
(Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas
aeruginosa, Enterococcus, and Enterobacter spp.) account for the majority of multidrug-resistant
infections worldwide and are responsible for increased healthcare costs and mortalities.
Soil is one of the most diverse microbial habitats on Earth, with complex microbial communities
engaging in constant competition for nutrients and space. Microorganisms naturally produce
antibiotics as part of their competitive strategies, and many antibiotics used in modern clinical
practice were originally derived from soil microbes, posing soil as a promising source for the
discovery of novel antimicrobial compounds.
The Tiny Earth Project approach aims to address the dire need for finding new, effective
antimicrobial compounds by engaging students in individual research projects in which they
isolate and characterize antibiotic-producing soil bacteria. In this project, we performed soil
sampling, serial dilution, bacterial isolation, screening activity against ESKAPE pathogens,
physiological characterization, Kirby-Bauer susceptibility testing, and a chemical extraction
assay.
Here, we present the data about the discovery of soil isolate VS-17-25, which can produce
inhibition zones against Acinetobacter baumannii and Enterobacter cloacae. The isolate is a
Gram-negative, rod-shaped, motile, obligate aerobic bacterium that is susceptible to ampicillin,
ciprofloxacin, and cefepime. Our study demonstrates that soil microbes are a promising source for
antibiotic discovery and the future development of new, effective therapeutics.
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