Friday, 25 December 2020

COVID-19 time capsule captures pandemic moments for future researchers

 



The non-profit Social Science Research Council, based in Brooklyn, N.Y., has assembled a collection of images that aims to freeze in time the myriad ways the COVID-19 crisis is transforming societies worldwide. And unlike time capsules of yesteryear, this version will live entirely online. The capsule currently includes an eclectic mix of photographs, charts and even a drawing appearing to depict infectious diseases expert Anthony Fauci as a saint.

 

Further details, see Science Daily: https://www.sciencenews.org/article/covid-19-time-capsule-pandemic-moments-future-researchers


 

 Posted by Dr. Tim Sandle, Pharmaceutical Microbiology Resources (http://www.pharmamicroresources.com/)

Thursday, 24 December 2020

Season's greetings


 

Hello,

 I'd like to wish you all the best over the festive season and thank you for your continued support of Pharmaceutical Microbiology resources.

Best regards,

 Dr. Tim Sandle

 

 

Posted by Dr. Tim Sandle, Pharmaceutical Microbiology Resources (http://www.pharmamicroresources.com/)

Wednesday, 23 December 2020

Microbiota linked to dynamics of human immune system



 

In recent years, the microbiota -- the community of bacteria and other microorganisms that live on and in the human body -- has captured the attention of scientists and the public, in part because it's become easier to study. It has been linked to many aspects of human health.

 

A multidisciplinary team from Memorial Sloan Kettering has shown for the first time that the gut microbiota directly shapes the makeup of the human immune system. Specifically, their research demonstrated that the concentration of different types of immune cells in the blood changed in relation to the presence of different bacterial strains in the gut. The results of their study, which used more than ten years of data collected from more than 2,000 patients.

 

The data that were used in the study came from people receiving allogeneic stem cell and bone marrow transplants (BMTs). After strong chemotherapy or radiation therapy is used to destroy cancerous blood cells, the patient's blood-forming system is replaced with stem cells from a donor. For the first few weeks until the donor's blood cells -- including the white blood cells that make up the immune system -- have established themselves, the patients are extremely vulnerable to infections. To protect them during this time, patients are given antibiotics.

 

But many of these antibiotics have the unwanted side effect of destroying healthy microbiota that live in the gut, allowing dangerous strains to take over. When the patient's immune system has reconstituted, the antibiotics are discontinued, and the gut microbiota slowly starts to grow back.

 

For more than ten years, members of MSK's BMT service have regularly collected and analyzed blood and fecal samples from patients throughout the BMT process. The bacterial DNA were processed by the staff at MSK's Lucille Castori Center for Microbes, Inflammation, and Cancer, which played a key role in creating the massive microbiota dataset.

 

This wider effort has been led by Marcel van den Brink, Head of the Division of Hematologic Malignancies, and a team of infectious disease specialists, BMT doctors, and scientists.

 

Previous research using samples collected from this work has looked at how the gut microbiota affects patients' health during the BMT process. A study published in February 2020 reported that having a greater diversity of species in the intestinal microbiota is associated with a lower risk of death after a BMT. It also found that having a lower diversity of microbiota before transplant resulted in a higher incidence of graft-versus-host disease, a potentially fatal complication in which the donor immune cells attack healthy tissue.

 

See:

 

Jonas Schluter, Jonathan U. Peled, Bradford P. Taylor, Kate A. Markey, Melody Smith, Ying Taur, Rene Niehus, Anna Staffas, Anqi Dai, Emily Fontana, Luigi A. Amoretti, Roberta J. Wright, Sejal Morjaria, Maly Fenelus, Melissa S. Pessin, Nelson J. Chao, Meagan Lew, Lauren Bohannon, Amy Bush, Anthony D. Sung, Tobias M. Hohl, Miguel-Angel Perales, Marcel R. M. van den Brink, Joao B. Xavier. The gut microbiota is associated with immune cell dynamics in humans. Nature, 2020; DOI: 10.1038/s41586-020-2971-8

 

Posted by Dr. Tim Sandle, Pharmaceutical Microbiology Resources (http://www.pharmamicroresources.com/)

Tuesday, 22 December 2020

What makes certain groups more vulnerable to COVID-19?



 

What makes the elderly and people with underlying conditions more vulnerable to COVID-19? According to a new study led by McGill University researchers, clues can be found in the proteins involved in initiating infection, as the virus binds to host cells of different animals. Greater cellular oxidation with aging and sickness may explain why seniors and people with chronic illness get infected more often and more severely.

 

Over 60 million people have been infected and around 1.5 million have died from COVID-19. The virus is disrupting economies and food supply chains all over the world.

 

Understanding why some animals get infected and others do not could be the key to unlocking new treatments and therapies. In a study published in Computational and Structural Biotechnology Journal, researchers analyzed available protein sequences of the virus and host cell receptors across different spices to find out why.

 

Once inside a host cell, the virus hijacks the cell's metabolic machinery to replicate and spread. The virus's protein spikes attach to a protein receptor on the surface of the host cell called ACE2, fusing the membranes around the cell and the virus together. This process allows the virus to enter the cell and co-opt its protein-making machinery to make new copies of itself. The copies then go on to infect other healthy cells.

 

In analyzing the proteins and their amino acid building blocks, the researchers found that animals susceptible to the virus have a few things in common. Such animals like humans, cats, and dogs have two cysteine amino acids that form a special disulfide bond held together by an oxidizing cellular environment. This disulfide bond creates an anchor for the virus. "Our analysis suggests that greater cellular oxidation in the elderly or those with underlying health conditions could predispose them to more vigorous infection, replication and disease," says co-author Rajinder Dhindsa, an emeritus professor of biology at McGill University.

 

In the case of animals resistant to the virus, like pigs and cows, one of these two cysteine amino acids is missing, and the disulfide bond cannot be formed. As a result, the virus cannot anchor on to the cell.

 

According to the researchers, preventing the anchor from forming could be the key to unlocking new treatments for COVID-19. One strategy, they suggest, could be to disrupt the oxidizing environment that keeps the disulfide bonds intact.

 

See:

 

Jaswinder Singh, Rajinder S. Dhindsa, Vikram Misra, Baljit Singh. SARS-CoV2 infectivity is potentially modulated by host redox status. Computational and Structural Biotechnology Journal, 2020; 18: 3705 DOI: 10.1016/j.csbj.2020.11.016

 

Posted by Dr. Tim Sandle, Pharmaceutical Microbiology Resources (http://www.pharmamicroresources.com/)

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