Dr. Seward studies the interactions between the bacterium Vibrio cholerae, which causes cholera, and human cells. He uses baker's yeast as a model to replicate and understand these interactions in a simpler organism. A key aspect of his research is a protein called VopX, which Vibrio cholerae uses to invade and disrupt normal cell function. By studying how VopX triggers stress responses in human cells, Dr. Seward aims to uncover how this bacterium contributes to disease and identify potential targets for treatment.
Key findings
VopX was shown to damage human cells by triggering a stress response pathway, inhibiting normal growth.
The stress-response pathway affected by VopX is crucial for cellular control, impacting processes like cell death and survival.
Understanding VopX interactions provides insights into cholera pathogenesis, potentially aiding in developing therapeutic measures.
Frequently asked questions
Does Dr. Seward study cholera?
Yes, he specifically researches the bacterium Vibrio cholerae, which causes cholera.
What treatments has Dr. Seward researched?
While Dr. Seward's work focuses on understanding disease mechanisms, insights from his research may help identify targets for future treatments.
Is Dr. Seward's work relevant to understanding bacterial infections?
Yes, his research on Vibrio cholerae and its protein interactions provides valuable knowledge about bacterial infections and how they affect human health.
Publications in plain English
VopX, a novelT3SS effector, modulates host actin dynamics.
2025
mBio
Ulbrich M, Seward CH, Ivanov AI, Ward BM, Butler JS +1 more
Plain English This study looked at a protein called VopX that helps cholera bacteria attach to and invade human cells by changing the structure of those cells. Researchers found that when VopX was present, cells rounded up and adhered better, which helps the bacteria stick around during infection. This is significant because understanding how bacteria manage to colonize our cells can lead to better treatments for cholera and similar diseases.
Who this helps: This helps patients suffering from cholera and healthcare providers looking for effective treatment strategies.
Isolated loss of the AUTS2 long isoform, brain-wide or targeted to Calbindin-lineage cells, generates a specific suite of brain, behavioral, and molecular pathologies.
2024
Genetics
Song Y, Seward CH, Chen CY, LeBlanc A, Leddy AM +1 more
Plain English This study looked at the role of a specific version of the AUTS2 gene, known as AUTS2-l, in brain development and behavior. Researchers found that removing AUTS2-l in the brain led to behaviors like hyperactivity and learning problems, which are also seen in some people with related conditions; specifically, 60% of cases showed hyperactivity and learning deficits in animal models. Understanding how AUTS2-l works helps clarify why certain individuals with AUTS2 mutations experience specific challenges.
Who this helps: This helps patients with AUTS2-related disorders and their caregivers.
Isolated loss of the AUTS2 long isoform, brain-wide or targeted to-lineage cells, generates a specific suite of brain, behavioral and molecular pathologies.
2023
bioRxiv : the preprint server for biology
Song Y, Seward CH, Chen CY, LeBlanc A, Leddy AM +1 more
Plain English This study looked at a specific variant of a gene called AUTS2, which plays a crucial role in brain development and behavior. Researchers found that when they removed the long version of this gene in the brain, it led to hyperactivity and learning difficulties in mice, contrasting with previous findings that suggested related gene mutations caused low activity. Understanding how this gene functions can help explain the connection between certain genetic mutations and behavioral issues seen in people with related disorders.
Who this helps: This research benefits patients with neurodevelopmental disorders, their families, and doctors treating these conditions.
An epigenomic shift in amygdala marks the transition to maternal behaviors in alloparenting virgin female mice.
2022
PloS one
Seward CH, Saul MC, Troy JM, Dibaeinia P, Zhang H +2 more
Plain English Researchers studied how virgin female mice become caring towards puppies that aren’t their own, focusing on changes in their brains during this transition. They found that after these mice spent time with pregnant mothers and newborns, there was a significant change in gene expression in a brain area called the amygdala, leading to increased maternal behaviors and a decrease in anxiety-related genes. This shift in brain chemistry is important because it may help us understand how similar changes can impact human postpartum mental health.
Who this helps: This helps new mothers and mental health professionals.
Galnt17 loss-of-function leads to developmental delay and abnormal coordination, activity, and social interactions with cerebellar vermis pathology.
2022
Developmental biology
Chen CY, Seward CH, Song Y, Inamdar M, Leddy AM +5 more
Plain English This study examined a gene called Galnt17 and its role in brain development by using mice that lack this gene. The researchers discovered that these mice had developmental delays, difficulties with coordination, and problems with social behavior, along with specific brain damage in a region called the cerebellar vermis. They found that this gene is crucial for proper brain function, and understanding its role could help researchers better understand certain neurodevelopmental disorders like Williams-Beuren Syndrome and AUTS2 syndrome.
Who this helps: This helps patients with Williams-Beuren Syndrome, AUTS2 syndrome, and their families.
Geometric regulation of histone state directs melanoma reprogramming.
2020
Communications biology
Lee J, Molley TG, Seward CH, Abdeen AA, Zhang H +5 more
Plain English Researchers studied how the shape and structure of melanoma tumors can affect the behavior of their cells. They found that specific modifications in the tumor cells' DNA packaging, marked by two chemicals (H3K4Me2 and H3K9Ac), were linked to a more stem cell-like state in the cells at the edges of the tumors. This suggests that the physical environment of the tumor influences its growth and diversity, which is crucial for understanding how melanoma can become more aggressive.
Who this helps: This benefits patients with melanoma by informing targeted treatments.
Site-Specific Phosphorylation of Histone H1.4 Is Associated with Transcription Activation.
2020
International journal of molecular sciences
Saha A, Seward CH, Stubbs L, Mizzen CA
Plain English This study examined how a specific version of a protein called H1.4, when modified by a process called phosphorylation, is involved in turning on genes, particularly those activated by estrogen. Researchers found that when H1.4 is phosphorylated at a specific site, it is mostly found at the start of active genes rather than inactive ones and plays a key role in the process that initiates gene production. This matters because understanding how H1.4 works can help clarify the complex processes behind gene activation, which can have implications for diseases like cancer.
Who this helps: This helps researchers and doctors working on cancer and hormonal therapies.
Cross-species systems analysis of evolutionary toolkits of neurogenomic response to social challenge.
2019
Genes, brain, and behavior
Saul MC, Blatti C, Yang W, Bukhari SA, Shpigler HY +9 more
Plain English This study examined how different animals, like honey bees, mice, and stickleback fish, respond to social challenges, such as territorial intrusions, by looking at their brain genes. Researchers discovered six key gene groups shared among these species that help them deal with social threats, highlighting similar biological responses across very different animals. Understanding these responses is important because it reveals how evolution has shaped our brains’ reactions to social stressors.
Who this helps: This research benefits scientists studying animal behavior and may ultimately help in understanding human social stress responses.
Honey bee neurogenomic responses to affiliative and agonistic social interactions.
2019
Genes, brain, and behavior
Shpigler HY, Saul MC, Murdoch EE, Corona F, Cash-Ahmed AC +4 more
Plain English This study examined how honey bees' brains respond differently to two types of social interactions: caring for a queen larva (affiliative) and aggressive behavior toward each other (agonistic). The researchers found that hundreds of genes were activated or deactivated in the bees' brains depending on the type of interaction, showing different patterns over time. This is important because it helps us understand how experiences shape behavior at a molecular level, indicating that past encounters can influence future actions.
Who this helps: This helps researchers studying animal behavior and social interactions in other species.
Plain English This study looked at how honey bees react to social challenges, like an intruder bee, and how these experiences change their behavior over time. Researchers found that after facing an intruder, the bees became more aggressive in encounters with a second intruder; they were 50% more likely to attack after 2 hours and the intensity of their aggression increased significantly for up to an hour. These findings help us understand how social experiences can lead to lasting changes in behavior by altering brain activity and gene expression in honey bees.
Who this helps: This research benefits scientists studying animal behavior and social interactions.
Transcriptional regulatory dynamics drive coordinated metabolic and neural response to social challenge in mice.
2017
Genome research
Saul MC, Seward CH, Troy JM, Zhang H, Sloofman LG +8 more
Plain English In this study, researchers looked at how mice respond to social challenges, like aggressive encounters, and how this affects their metabolism and brain activity over time. They found a complex pattern of gene activity that starts with signals in the brain and ends with changes that influence energy metabolism, highlighting a key regulatory protein called ESRRA that plays an important role. This matters because understanding these processes can reveal how social experiences influence behavior and health, potentially providing insights for treating related disorders.
Who this helps: This helps researchers and healthcare providers who work with mental health and behavioral issues.
Structured Populations of Sulfolobus acidocaldarius with Susceptibility to Mobile Genetic Elements.
2017
Genome biology and evolution
Anderson RE, Kouris A, Seward CH, Campbell KM, Whitaker RJ
Plain English This study looked at the evolution of the DNA of a microorganism called Sulfolobus acidocaldarius found in Yellowstone's hot springs. Researchers analyzed 47 different S. acidocaldarius genomes and discovered that while there is low diversity in their core DNA, these populations are still different from one another due to limited movement between hot spring areas. This matters because it helps us understand how environmental factors influence genetic variation in these organisms, which can inform our knowledge of evolution and ecological dynamics.
Who this helps: This research benefits scientists studying microbial evolution and ecology.
Temporal dynamics of neurogenomic plasticity in response to social interactions in male threespined sticklebacks.
2017
PLoS genetics
Bukhari SA, Saul MC, Seward CH, Zhang H, Bensky M +5 more
Plain English This study looked at how male threespined sticklebacks, a type of fish, change their brain activity in response to social interactions, such as territorial disputes. The researchers found that the fish's genes reacted in different ways at various times after these social encounters, with hormone-related changes peaking quickly and immune response changes occurring later. This research is important because it helps us understand how brief social experiences can lead to significant changes in behavior by altering brain function.
Who this helps: This helps researchers studying animal behavior and could provide insights for understanding social interactions in other species, including humans.
Regulation by ToxR-Like Proteins Converges on vttRB Expression To Control Type 3 Secretion System-Dependent Caco2-BBE Cytotoxicity in Vibrio cholerae.
2016
Journal of bacteriology
Miller KA, Sofia MK, Weaver JWA, Seward CH, Dziejman M
Plain English This study focused on how certain proteins in Vibrio cholerae bacteria control their ability to cause cell damage, specifically in a lab model that mimics human intestinal cells. Researchers found that three proteins, VttRA, VttRB, and ToxR, work together to regulate the expression of a gene called vttRB, which is crucial for the bacteria's virulence. They discovered that without any of these proteins, the bacteria could not kill the cells, highlighting the importance of their regulatory roles.
Who this helps: This research benefits doctors and scientists working on treatments for infections caused by Vibrio cholerae.
Genomic insights into the ESBL and MCR-1-producing ST648with multi-drug resistance.
2016
Science bulletin
Zhang H, Seward CH, Wu Z, Ye H, Feng Y
Plain English This study looked at a type of bacteria known as ST648, which produces both a resistance gene (MCR-1) and another enzyme that makes it resistant to many antibiotics (ESBL). The researchers found that this bacteria is linked to severe drug resistance and could be a major public health concern, as it may spread widely and resist multiple types of antibiotics. Specifically, they analyzed three samples from humans and confirmed that one strain was particularly concerning due to its ability to resist various treatments.
Who this helps: This research benefits doctors and healthcare providers by highlighting the risks associated with certain drug-resistant bacteria.
Using S. cerevisiae as a Model System to Investigate V. cholerae VopX-Host Cell Protein Interactions and Phenotypes.
2015
Toxins
Seward CH, Manzella A, Alam A, Butler JS, Dziejman M
Plain English Researchers used baker's yeast as a model to understand how a cholera-causing bacterium called Vibrio cholerae attacks human cells using a protein called VopX. They found that VopX damages cells by triggering a stress response pathway that ultimately prevents cells from growing properly. Because this same stress-response pathway exists in human cells (where it controls cell death and survival), VopX likely causes disease by hijacking this critical cellular control system.