Can environmental stress reshape the genomes of marine bacteria?

Temple University
Seattle, Washington
BiologyEcology
DOI: 10.18258/97486
Grant: What Ifs? 2026
$7,340
Raised of $7,340 Goal
100%
Funded on 10/27/26
Successfully Funded
  • $7,340
    pledged
  • 100%
    funded
  • Funded
    on 10/27/26

About This Project

Urban development is changing coastal waterways, altering salinity and pollution in ways that affect marine life. I study bioluminescent bacteria living inside cardinalfish in Australia and found that bacteria from polluted areas carry far more mobile DNA elements, which copy themselves across the genome and disrupt normal bacterial functions. I hypothesize that environmental stress drives this, and I will test it by sequencing bacterial communities across a pollution/salinity gradient.

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What is the context of this research?

Urban development is altering coastal waterways, exposing marine bacteria to novel salinity fluctuations and environmental pollutants. One response that bacteria have to combat this stress is the proliferation of mobile genetic elements (MGEs), which can lead to rapid adaptation to changing environments but can also disrupt normal gene function. I became interested in mobile genetic elements in early 2025 when I sequenced bioluminescent bacterial DNA from siphonfish I collected from Sydney Harbor. Though I originally wanted to identify bacterial species, I instead found a dramatic proliferation of mobile elements in bacteria isolated from highly polluted areas. Prior work shows that stress can activate mobile elements, but it is unknown whether this occurs in coastal marine ecosystems. I hypothesize that environmental stressors in coastal water can trigger mobile element proliferation in marine bacteria.

What is the significance of this project?

Mobile genetic elements (MGEs) are a major engine of rapid bacterial evolution, as they can spread useful traits but also disrupt important functions. This project will reveal whether salinity and pollution levels in coastal waters can directly trigger MGE activity, giving biologists, conservationists, and lawmakers a new lens for understanding how urbanization affects bacterial communities. This matters because if what we put into coastal waters triggers large-scale genomic changes in bacteria, we may need to rethink how we assess the biological impact of urban runoff and pollution. By connecting genomics, microbial ecology, and environmental change across a pollution and salinity gradient, this project generates data directly relevant to bacterial adaptation in an era of increasing coastal urbanization and climate-driven salinity shifts.

What are the goals of the project?

To test whether mobile genetic element (MGE) density increases with environmental stress, I will travel to Sydney, Australia in March 2027 and collect triplicate water samples from four Harbour sites spanning a gradient from urban runoff to open marine. I’ll measure pollution levels (e.g., heavy metals), salinity, and temperature, filter the water, extract DNA, and sequence it with Nanopore long-read metagenomics, which is needed to resolve repetitive MGEs that short-read sequencing cannot. I’ll quantify MGEs per megabase and test whether density correlates with each water parameter, with sequencing and analysis finished by July 2027. Funds cover flights, lodging, meals, sampling supplies, extraction kits, and Nanopore flow cells and library prep. If a signal emerges, it will motivate future lab experiments to test which stressors drive MGE expansion. I’ll publish the results and share the data openly.

Budget

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The proposed budget will allow me to travel to Sydney, Australia, and collect samples at four sites in the Sydney Harbour area. The field supplies will cover all filters, preservation buffer, water-parameter testing, and shipping materials needed to collect water samples and isolate bacteria. I am requesting funds to extract high-molecular-weight DNA from the filtered water and sequence the bacterial DNA through Oxford Nanopore long-read sequencing. Long-read sequencing is necessary for this project because mobile genetic elements are not reliably picked up by other types of genomic sequencing. These funds will allow me to turn bacterial samples into genomic data that I can compare across a pollution and salinity gradient.

Project Timeline

By February 1st, 2027, I will have travel, permits, and supplies organized. In March 2027, I will spend ten days sampling four Sydney Harbour sites along a pollution and salinity gradient, then filter and preserve samples on site. I will ship the samples to Temple University and spend April and May extracting DNA and completing the Nanopore sequencing. By July 1st, 2027, I will analyze the data to see whether insertion sequence density tracks environmental factors.

Feb 01, 2027

Travel, permits, and sampling supplies arranged.

Apr 01, 2027

Water samples collected, filtered, and preserved at four Sydney Harbour sites.

May 01, 2027

Samples received at Temple and DNA extracted.

Jun 01, 2027

Nanopore long-read sequencing complete.

Jul 01, 2027

MGE density quantified and tested against water parameters.

Meet the Team

Hannah Osland
Hannah Osland
PhD Candidate

Affiliates

Temple University
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Hannah Osland

I'm Hannah Osland, a PhD student in biology at Temple University in Philadelphia, where I study fish and the glowing bacteria that live inside them.

I have always loved the water, which is what led me to want to study marine life and how big and small beings interact with each other. I received my bachelor's degree in Biology from Pomona College, and my master's in environmental science degree from Alaska Pacific University. Like many scientists, I have been affected by recent reductions in funding, but still want to be able to try and answer some of the questions I have.

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