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Special Department of Microbiology and Immunology Seminar – Dr. Malika Grayson – November 9th at NOON

Friday, October 23, 2020

How do you make an impact when you are the only person in the room that looks like you? We hear the terms diversity and inclusion but forget that the term representation should be a reflection of diversity and inclusion combined. This isn't always the case. Dr. Grayson discusses her views on what it means to increase diversity and representation as an Individual Contributor. Learn more about her journey as the 2nd Black Woman to graduate with a PhD in  Mechanical Engineering from her graduate institution. Hear about her current work as both an engineer, a STEM Advocate, and her most recent success as author of 'HOODED: A Black Girl's Guide to the PhD' where she highlights her time and lessons learned during her PhD Program.

ChapinCavender

 

Can the Common Cold Help Protect You from COVID-19?

Thursday, October 1, 2020

Seasonal colds are by all accounts no fun, but new research suggests the colds you’ve had in the past may provide some protection from COVID-19. The study, authored by infectious disease experts at the University of Rochester Medical Center, also suggests that immunity to COVID-19 is likely to last a long time – maybe even a lifetime.

The study, published in mBio, is the first to show that the COVID-19-causing virus, SARS-CoV-2, induces memory B cells, long-lived immune cells that detect pathogens, create antibodies to destroy them and remember them for the future. The next time that pathogen tries to enter the body, those memory B cells can hop into action even faster to clear the infection before it starts.

Because memory B cells can survive for decades, they could protect COVID-19 survivors from subsequent infections for a long time, but further research will have to bear that out.

The study is also the first to report cross-reactivity of memory B cells – meaning B cells that once attacked cold-causing coronaviruses appeared to also recognize SARS-CoV-2. Study authors believe this could mean that anyone who has been infected by a common coronavirus – which is nearly everyone –  may have some degree of pre-existing immunity to COVID-19.

“When we looked at blood samples from people who were recovering from COVID-19, it looked like many of them had a pre-existing pool of memory B cells that could recognize SARS-CoV-2 and rapidly produce antibodies that could attack it,” said lead study author Mark Sangster, Ph.D., a research professor of Microbiology and Immunology at URMC.

Sangster’s findings are based on a comparison of blood samples from 26 people who were recovering from mild to moderate COVID-19 and 21 healthy donors whose samples were collected six to 10 years ago – long before they could have been exposed to COVID-19. From those samples, study authors measured levels of memory B cells and antibodies that target specific parts of the Spike protein, which exists in all coronaviruses and is crucial for helping the viruses infect cells.

Read More: Can the Common Cold Help Protect You from COVID-19?

Cells Sacrifice Themselves to Boost Immune Response to Viruses

Wednesday, September 30, 2020

Whether flu or coronavirus, it can take several days for the body to ramp up an effective response to a viral infection.  New research appearing in the journal Nature Immunology describes how different cells in the immune system work together, communicate, and – in the case of cells called neutrophils – bring about their own death to help fight off infections.  The findings could have important implications for the development of vaccines and anti-viral therapies.  

“The immune system consists of several different types of cells, all acting in coordination,” said Minsoo Kim, Ph.D., a professor of Microbiology and Immunology at the University of Rochester Medical Center (URMC) and senior author of the study.  “These findings show that cells called neutrophils play an important altruistic role that benefits other immune cells by providing key resources for their survival and, in the process, enhancing the body’s immune response against a virus.”

Neutrophils are a key component of the innate immune system, the part of the body’s defenses that is always switched on and alert for bacterial and viral invaders.  The vast majority of white cells circulating in blood are neutrophils and, as a result, these cells are the first on the scene to respond to an infection. 

However, neutrophils are not fully equipped to eliminate a viral threat by themselves.  Instead, when the respiratory tract is infected with a virus like influenza or COVID-19, a large number of neutrophils rush to the infection site and release chemical signals.  This triggers the production of specialized T cells, which are part of the body’s adaptive immune system, which is activated to produce a more direct response to specific infections.   Once mobilized in sufficient quantities, a process that typically takes several days, these T cells target and ultimately destroy the infected cells.     

The new study, which was conducted in mice infected with the flu virus, shows that in addition to jump-starting the adaptive immune response, neutrophils have one more important mission that requires that they sacrifice themselves.  As T cells arrive at the infection site, the neutrophils initiate a process called apoptosis, or controlled death, which releases large quantities of a molecule called epidermal growth factor (EGF).  EGF provides T cells with the extra boost in energy necessary to finish the job. 

“This study represents an important paradigm shift and shows that the adaptive immune system doesn’t generate a successful response without instruction and help from the innate immune system,” said Kim.  “The findings reveal, for the first time, how different immune cells work together, and even sacrifice themselves, to accomplish the same goal of protecting the host from the viral infection.”

Read More: Cells Sacrifice Themselves to Boost Immune Response to Viruses

RNA Essay Contest Results and Congratulations

Wednesday, August 26, 2020

The UR Center for RNA Biology offered an exercise during the time when COVID-19 became a sufficient threat to largely shut-down our research enterprise. We’re pleased to announce the winners of the UR’s Center for RNA Biology Essay Contest on “The role of RNA research in community health”. These awards are sponsored by a grant from the RNA Society & Lexogen to the UR Center for RNA Biology, and funds from UR RNA Structure & Function Cluster.

Our Gold prize (~$1,000 value) award goes to Sydney Simpson, an Immunology, Microbiology & Virology graduate student in Steve Dewhurst’s lab in the Department of Microbiology & Immunology, for her essay: “Nucleoside Analog Inhibitors: Timeless & Timely Beacons of Hope”.

The Silver Prize (~$250 value) award goes to Omar Hedaya, a Biochemistry & Molecular Biology graduate student in Peng Yao’s lab in the Department of Medicine/Department of Biochemistry & Biophysics, for his essay: “Know the Fundamentals when Seeking the Future”.

Omar Hedaya

Sydney Simpson

Both awardees have become members of the RNA Society and will use their winnings toward technology needs for the upcoming semester.

The RNA Society now features our contest results, including the winning essays, in its latest RNA Salon update: https://www.rnasociety.org/featured-salons, see bullet #3.

We would like to acknowledge Honorable Mentions for the following applicants:

  • Sai Shashank Chavali – Graduate student; Biophysics, Structural & Computational Biology; Wedekind Lab
  • Lily Cisco – Graduate student; Cellular and Molecular Pharmacology & Physiology; Lueck Lab
  • Gabrielle Kosoy – Graduate student; Biophysics, Structural & Computational Biology; Miller Lab
  • Ashwin Kumar – Graduate student; Biophysics, Structural & Computational Biology; Topham Lab
  • Li Xie – Graduate student; Genetics, Development & Stem Cells; Pröschel Lab

We thank all who participated – and our judges, too!

Thakar Lab publishes article on the Impact of vaccine type on HIV-1 vaccine elicited antibody durability and B cell gene signature

Monday, August 10, 2020

Abstract

Efficacious HIV-1 vaccination requires elicitation of long-lived antibody responses. However, our understanding of how different vaccine types elicit durable antibody responses is lacking. To assess the impact of vaccine type on antibody responses, we measured IgG isotypes against four consensus HIV antigens from 2 weeks to 10 years post HIV-1 vaccination and used mixed effects models to estimate half-life of responses in four human clinical trials. Compared to protein-boosted regimens, half-lives of gp120-specific antibodies were longer but peak magnitudes were lower in Modified Vaccinia Ankara (MVA)-boosted regimens. Furthermore, gp120-specific B cell transcriptomics from MVA-boosted and protein-boosted vaccines revealed a distinct signature at a peak (2 weeks after last vaccination) including CD19, CD40, and FCRL2-5 activation along with increased B cell receptor signaling. Additional analysis revealed contributions of RIG-I-like receptor pathway and genes such as SMAD5 and IL-32 to antibody durability. Thus, this study provides novel insights into vaccine induced antibody durability and B-cell receptor signaling.

Read More: Thakar Lab publishes article on the Impact of vaccine type on HIV-1 vaccine elicited antibody durability and B cell gene signature

Sangster Weighs in on COVID-19 Vaccine, Antibodies

Wednesday, August 5, 2020

With millions of lives on the line, researchers have been working at an unprecedented pace to develop a COVID-19 vaccine.

But that speed—and some widely touted breakthroughs—belie the enormous complexity and potential risks involved. Researchers have an incomplete understanding of the coronavirus and are using technology that’s largely unproven.

Among many worries: A handful of studies on COVID-19 survivors suggest that antibodies—key immune system proteins that fight infection—begin to disappear within months. That’s led scientists to worry that the protection provided by vaccines could fade quickly as well. Some even question whether vaccines will really end the pandemic. If vaccines produce limited protection against infection, experts note, people will need to continue wearing masks and social distancing even after vaccines roll out.

People with severe symptoms from COVID-19 tend to have higher antibody levels than those with milder cases.

Some people fail to generate antibodies because they have compromised immune systems, said Mark Sangster, a research professor at the University of Rochester Medical Center.

Even when people do generate antibodies against the novel coronavirus, studies suggest the antibodies may not last long.

Read More: Sangster Weighs in on COVID-19 Vaccine, Antibodies

IMV Grad Student Megan Ulbrich Wins the Melville A. Hare Award for Excellence in Teaching

Friday, June 5, 2020

Please join the department in congratulating Megan Ulbrich, this year’s winner of the Melville A. Hare Award for Excellence in Teaching.  This award is given annually by the Department of Microbiology and Immunology to a graduate student who has displayed outstanding qualities of mentoring and teaching in one or more MBI courses.  The award will be officially conferred at URMC Convocation in the late summer.

Megan is currently an IMV graduate student in Michelle Dziejman's lab working on multidisciplinary approaches to uncover novel effector protein functions. Megan grew up in Buffalo, NY and received her B.S. in Microbiology from the University of Pittsburgh. 

Dr. Deborah Fowell appointed next Chair of the Department of Microbiology and Immunology

Tuesday, May 12, 2020

Photo of Dr. FowellWe congratulate Dr. Deborah Fowell on her new position as Chair of the Department of Microbiology and Immunology at Cornell University College of Veterinary Medicine, where she will start this fall. As a valued faculty member and Dean’s Professor in the Department of Microbiology and Immunology, Center for Vaccine Biology and Immunology, this is a bittersweet goodbye – but a wonderful new opportunity for Deb!

Since joining UR in April 2000, Dr. Fowell has achieved great success in her research program. One example is her organization and leadership of an accomplished, interdisciplinary team of investigators in an NIH funded program project to visualize the immune system in action, which was recently renewed. Her efforts have led to tremendous advancements in the field and will continue to enhance our understanding of tissue inflammation and immune responses, while also providing new therapeutic targets for mitigation of a wide variety of inflammatory diseases.

Not only is Dr. Fowell an outstanding researcher, she is also deeply committed to excellence in graduate education. She recently took over as Program Director and successfully renewed the University’s Predoctoral Training Grant in Immunology. In addition, she has received multiple mentoring awards at the UR, including the 2015 Graduate Alumni Award, which is the most prestigious student teaching and mentoring award here at the School of Medicine and Dentistry.

Dr. Fowell has a strong reputation among her peers as a highly innovative researcher with rigorous intellectual standards, and as a consistent advocate of the highest quality science and long-term success for academic research. Her collaborative approach to research, commitment to enriching learning and intellectual discourse, coupled with her drive and energy, will ensure her success at Cornell.

It’s with pride, warm wishes and anticipation of exciting future collaborations that we wish Deb every success in her new role!

Read More: Dr. Deborah Fowell appointed next Chair of the Department of Microbiology and Immunology