Kaci Resau, MA, MLIS (She/her/hers), E-Resources Manager
I am a plant lover, and luckily, I was born with my great-grandmother’s green thumb. Anytime I visit a new city, I always explore whatever gardens or forests I can find. So, when I heard that the Royal Botanic Gardens, Kew was releasing a podcast series, I knew I had to listen.
Royal Botanic Gardens, Kew aims to protect biodiversity while supporting sustainability. Currently, the gardens preserve 8.25 plant and fungal specimens and 200,000 botanical illustrations. In 2020, Kew released a new podcast, “Unearthed: Mysteries from an unseen world,” hosted by ethnobotanist & broadcaster/writer, James Wong. The 8-episode podcast (to date) series looks at how fungi and plants play a role in everything from crime-solving, to body healing, to new laws. Most of the podcasts are about 30 minutes, with a few around 1 hour. It’s a great listen for a commute or while you’re taking a walk.
Listeners can learn about how a zombie fungus can make ants explode, how the Kew was able to help solve a murder by identifying a plant that the murderer used to kill their spouse, food safety, plant/fungi based medical cures, and the seedy underbelly of plant culture via plant trafficking. The podcast brings in horticulturists, toxicologists, climate change experts, and more. My favourite episode focuses on ecocide (the destruction of natural environment by humans deliberately or negligently) and whether or not it is a crime.
Give this podcast a chance and you’ll surely look at plants a lot differently – plus, that James Wong is a fun-gi!
“Unearthed: Mysteries from an unseen world” can be downloaded directly at https://www.kew.org/about-us/virtual-kew-wakehurst/unearthed-kew-podcast or wherever you find your favourite podcasts. You can learn more about Royal Botanic Gardens, Kew, here.
Each month Levy Library showcases the achievements of Mount Sinai faculty and researchers by highlighting an article and its altmetrics. Altmetrics are alternative measures of impact that capture non-traditional data like abstract views, article downloads, and social media activity. Our altmetrics data is provided by the PlumX platform.
This month we highlight Evolution of antibody immunity to SARS-CoV-2. This article was written in part by Saurabh Mehandru, MD.
Citation Data
Nature, ISSN: 1476-4687, Vol: 591, Issue: 7851, Page: 639-644
Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has infected 78 million individuals and is responsible for over 1.7 million deaths to date. Infection is associated with the development of variable levels of antibodies with neutralizing activity, which can protect against infection in animal models1,2. Antibody levels decrease with time, but, to our knowledge, the nature and quality of the memory B cells that would be required to produce antibodies upon reinfection has not been examined. Here we report on the humoral memory response in a cohort of 87 individuals assessed at 1.3 and 6.2 months after infection with SARS-CoV-2. We find that titres of IgM and IgG antibodies against the receptor-binding domain (RBD) of the spike protein of SARS-CoV-2 decrease significantly over this time period, with IgA being less affected. Concurrently, neutralizing activity in plasma decreases by fivefold in pseudotype virus assays. By contrast, the number of RBD-specific memory B cells remains unchanged at 6.2 months after infection. Memory B cells display clonal turnover after 6.2 months, and the antibodies that they express have greater somatic hypermutation, resistance to RBD mutations and increased potency, indicative of continued evolution of the humoral response. Immunofluorescence and PCR analyses of intestinal biopsies obtained from asymptomatic individuals at 4 months after the onset of coronavirus disease 2019 (COVID-19) revealed the persistence of SARS-CoV-2 nucleic acids and immunoreactivity in the small bowel of 7 out of 14 individuals. We conclude that the memory B cell response to SARS-CoV-2 evolves between 1.3 and 6.2 months after infection in a manner that is consistent with antigen persistence.
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