2026-09-19T00:43:06Zhttps://dspace.mit.edu/server/oai/requestoai:dspace.mit.edu:1721.1/1644742026-01-13T03:35:32Zcom_1721.1_7582com_1721.1_7581col_1721.1_131022
Blainey, Paul C.
Hacohen, Nir
Carlson, Rebecca J.
Harvard-MIT Program in Health Sciences and Technology
2026-01-12T19:39:10Z
2026-01-12T19:39:10Z
2023-06
2023-06-13T20:48:46.636Z
https://hdl.handle.net/1721.1/164474
https://orcid.org/0000-0002-5423-9717
Host-pathogen interactions represent a complex interplay between hosts and pathogens that can evolve over millions of years. Interactions between bacteria or viruses and human cells, and the resulting evolved antipathogenic signaling pathways, are processes responsible for pathologies ranging from infectious diseases to autoimmune conditions and cancer. In addition, engineered designs inspired by pathogen interactions with hosts are increasingly being used to both treat and diagnose many pathologies that need not originate from infection with a pathogen. Therefore, it is critical to build and deploy scalable tools to better understand host-pathogen dynamics in order to both better treat conditions where pathogens or antipathogenic signaling contribute directly to disease pathology as well as to engineer new treatments to address a broader range of disease states.
In this thesis, I describe approaches to leverage functional genomics and image-based screening to perturb and profile host-pathogen interactions, including responses to two RNA viruses, Sendai virus and Ebola virus. These provide case studies highlighting the utility of high-content image-based screening for revealing new genes regulating predefined phenotypes of interest as well as for generating single-cell imaging profiles that can be used to infer new genetic functions and phenotypic states directly from screening data without a priori specification. I also highlight an example of a genetic screen that revealed a robust negative result, leading to hypothesis and validation of a novel function of the STING protein as a proton channel.
Ph.D.
Massachusetts Institute of Technology
Attribution-ShareAlike 4.0 International (CC BY-SA 4.0)
Copyright retained by author(s)
https://creativecommons.org/licenses/by-sa/4.0/
Functional Genomic and Image-Based Screening Approaches for Probing Host-Pathogen Interactions
Thesis
application/pdf
Doctoral
Doctor of Philosophy
Publication
unknown
unknown
<Publication xmlns="https://www.openaire.eu/cerif-profile/1.1/" id="cab59c1c-b105-4e1e-8e5d-75ec911b21ee">
<Type xmlns="https://www.openaire.eu/cerif-profile/vocab/COAR_Publication_Types">http://purl.org/coar/resource_type/c_1843</Type>
<Title>Functional Genomic and Image-Based Screening Approaches for Probing Host-Pathogen Interactions</Title>
<PublishedIn>
<Publication>
</Publication>
</PublishedIn>
<PublicationDate>2023-06</PublicationDate>
<Authors>
<Author>
<DisplayName>Carlson, Rebecca J.</DisplayName>
<Affiliation>
<OrgUnit>
</OrgUnit>
</Affiliation>
</Author>
</Authors>
<Editors>
</Editors>
<Publishers>
<Publisher>
<DisplayName>Massachusetts Institute of Technology</DisplayName>
<OrgUnit />
</Publisher>
</Publishers>
<License>https://creativecommons.org/licenses/by-sa/4.0/</License>
<Abstract>Host-pathogen interactions represent a complex interplay between hosts and pathogens that can evolve over millions of years. Interactions between bacteria or viruses and human cells, and the resulting evolved antipathogenic signaling pathways, are processes responsible for pathologies ranging from infectious diseases to autoimmune conditions and cancer. In addition, engineered designs inspired by pathogen interactions with hosts are increasingly being used to both treat and diagnose many pathologies that need not originate from infection with a pathogen. Therefore, it is critical to build and deploy scalable tools to better understand host-pathogen dynamics in order to both better treat conditions where pathogens or antipathogenic signaling contribute directly to disease pathology as well as to engineer new treatments to address a broader range of disease states.
In this thesis, I describe approaches to leverage functional genomics and image-based screening to perturb and profile host-pathogen interactions, including responses to two RNA viruses, Sendai virus and Ebola virus. These provide case studies highlighting the utility of high-content image-based screening for revealing new genes regulating predefined phenotypes of interest as well as for generating single-cell imaging profiles that can be used to infer new genetic functions and phenotypic states directly from screening data without a priori specification. I also highlight an example of a genetic screen that revealed a robust negative result, leading to hypothesis and validation of a novel function of the STING protein as a proton channel.</Abstract>
<Access xmlns="http://purl.org/coar/access_right"
>
</Access>
</Publication>