Gerry Wright

Last updated
Gerry Wright
Gerard D. Wright
Nationality Canadian
Education University of Waterloo (BSc 1986, PhD 1990)
Known forAntibiotic research [1]
Scientific career
Fields Biochemistry
Institutions McMaster University
Thesis Investigation of the lanosterol 14[alpha]-demethylase (P-45014DM) from Saccharomyces cerevisiae  (1990)

Gerard D. Wright, PhD, FRSC, is a professor in the Department of Biochemistry and Biomedical Sciences, and Canada Research Chair in Antibiotic Biochemistry at McMaster University [2] who studies chemical compounds that can combat antibiotic resistance in bacteria. [3] [4] [5] He is also an Associate member of the Departments of Chemistry and Chemical Biology and Pathology and Molecular Medicine. Wright was Chair of the Department of Biochemistry and Biomedical Sciences from 2001 to 2007. He was the Director of McMaster's Michael G. DeGroote Institute for Infectious Disease Research from 2007 to 2022. He is currently the executive director of Canada's Global Nexus for Pandemics and Biological Threats. [6] He is also founding director of the McMaster Antimicrobial Research Centre, and co-founder of the McMaster High Throughput Screening Facility.

Wright obtained his BSc in Biochemistry and his PhD in chemistry from the University of Waterloo. He did his post-doctoral training at Harvard Medical School before joining McMaster University in 1993.

Wright is a Fellow of the Royal Society of Canada and the American Academy of Microbiology. He currently serves as an associate editor of ACS Infectious Diseases , and he is a member of the editorial boards of Chemistry and Biology, The Journal of Antibiotics, Annals of the New York Academy of Sciences, and Antimicrobial Therapeutics Reviews.

Wright coined the term antibiotic resistome, which is used to describe the collection of all the antibiotic resistant genes and their precursors in both pathogenic and non-pathogenic bacteria. [7]

In 2014, Wright was the senior author on a study in Nature which described the discovery that the previously known Aspergillomarasmine A was a new antibiotic. [1] [8] [9]

Related Research Articles

<span class="mw-page-title-main">Antibiotic</span> Antimicrobial substance active against bacteria

An antibiotic is a type of antimicrobial substance active against bacteria. It is the most important type of antibacterial agent for fighting bacterial infections, and antibiotic medications are widely used in the treatment and prevention of such infections. They may either kill or inhibit the growth of bacteria. A limited number of antibiotics also possess antiprotozoal activity. Antibiotics are not effective against viruses such as the ones which cause the common cold or influenza; drugs which inhibit growth of viruses are termed antiviral drugs or antivirals rather than antibiotics. They are also not effective against fungi; drugs which inhibit growth of fungi are called antifungal drugs.

<span class="mw-page-title-main">Antimicrobial resistance</span> Resistance of microbes to drugs directed against them

Antimicrobial resistance (AMR) occurs when microbes evolve mechanisms that protect them from the effects of antimicrobials. All classes of microbes can evolve resistance where the drugs are no longer effective. Fungi evolve antifungal resistance, viruses evolve antiviral resistance, protozoa evolve antiprotozoal resistance, and bacteria evolve antibiotic resistance. Together all of these come under the umbrella of antimicrobial resistance. Microbes resistant to multiple antimicrobials are called multidrug resistant (MDR) and are sometimes referred to as superbugs. Although antimicrobial resistance is a naturally occurring process, it is often the result of improper usage of the drugs and management of the infections.

<i>Klebsiella pneumoniae</i> Species of bacterium

Klebsiella pneumoniae is a Gram-negative, non-motile, encapsulated, lactose-fermenting, facultative anaerobic, rod-shaped bacterium. It appears as a mucoid lactose fermenter on MacConkey agar.

<span class="mw-page-title-main">Phage therapy</span> Therapeutic use of bacteriophages to treat bacterial infections

Phage therapy, viral phage therapy, or phagotherapy is the therapeutic use of bacteriophages for the treatment of pathogenic bacterial infections. This therapeutic approach emerged at the beginning of the 20th century but was progressively replaced by the use of antibiotics in most parts of the world after the Second World War. Bacteriophages, known as phages, are a form of virus that attach to bacterial cells and inject their genome into the cell. The bacteria's production of the viral genome interferes with its ability to function, halting the bacterial infection. The bacterial cell causing the infection is unable to reproduce and instead produces additional phages. Phages are very selective in the strains of bacteria they are effective against.

Multiple drug resistance (MDR), multidrug resistance or multiresistance is antimicrobial resistance shown by a species of microorganism to at least one antimicrobial drug in three or more antimicrobial categories. Antimicrobial categories are classifications of antimicrobial agents based on their mode of action and specific to target organisms. The MDR types most threatening to public health are MDR bacteria that resist multiple antibiotics; other types include MDR viruses, parasites.

<span class="mw-page-title-main">Medical microbiology</span> Branch of medical science

Medical microbiology, the large subset of microbiology that is applied to medicine, is a branch of medical science concerned with the prevention, diagnosis and treatment of infectious diseases. In addition, this field of science studies various clinical applications of microbes for the improvement of health. There are four kinds of microorganisms that cause infectious disease: bacteria, fungi, parasites and viruses, and one type of infectious protein called prion.

The resistome has been used to describe to two similar yet separate concepts:

<span class="mw-page-title-main">New Delhi metallo-beta-lactamase 1</span> Enzyme

NDM-1 is an enzyme that makes bacteria resistant to a broad range of beta-lactam antibiotics. These include the antibiotics of the carbapenem family, which are a mainstay for the treatment of antibiotic-resistant bacterial infections. The gene for NDM-1 is one member of a large gene family that encodes beta-lactamase enzymes called carbapenemases. Bacteria that produce carbapenemases are often referred to in the news media as "superbugs" because infections caused by them are difficult to treat. Such bacteria are usually sensitive only to polymyxins and tigecycline.

<span class="mw-page-title-main">Plasmid-mediated resistance</span> Antibiotic resistance caused by a plasmid

Plasmid-mediated resistance is the transfer of antibiotic resistance genes which are carried on plasmids. Plasmids possess mechanisms that ensure their independent replication as well as those that regulate their replication number and guarantee stable inheritance during cell division. By the conjugation process, they can stimulate lateral transfer between bacteria from various genera and kingdoms. Numerous plasmids contain addiction-inducing systems that are typically based on toxin-antitoxin factors and capable of killing daughter cells that don't inherit the plasmid during cell division. Plasmids often carry multiple antibiotic resistance genes, contributing to the spread of multidrug-resistance (MDR). Antibiotic resistance mediated by MDR plasmids severely limits the treatment options for the infections caused by Gram-negative bacteria, especially family Enterobacteriaceae. The global spread of MDR plasmids has been enhanced by selective pressure from antimicrobial medications used in medical facilities and when raising animals for food.

Julian Edmund Davies is a British-born microbiologist and Professor Emeritus in the Department of Microbiology and Immunology at the University of British Columbia.

<span class="mw-page-title-main">Aspergillomarasmine A</span> Chemical compound

Aspergillomarasmine A is an polyamino acid naturally produced by the mold Aspergillus versicolor. The substance has been reported to inhibit two antibiotic resistance carbapenemase proteins in bacteria, New Delhi metallo-beta-lactamase 1 (NDM-1) and Verona integron-encoded metallo-beta-lactamase (VIM-2), and make those antibiotic-resistant bacteria susceptible to antibiotics. Aspergillomarasmine A is toxic to leaves of barley and other plants, being termed as "Toxin C" when produced by Pyrenophora teres.

<span class="mw-page-title-main">One Health Model</span> Concept of interaction between all components of the global ecosystem determining its health

The concept of One Health is the unity of multiple practices that work together locally, nationally, and globally to help achieve optimal health for people, animals, and the environment. When the people, animals, and environment are put together they make up the One Health Triad .The One Health Triad shows how the health of people, animals, and the environment is linked to one another. With One Health being a worldwide concept, it makes it easier to advance health care in the 21st century. When this concept is used, and applied properly, it can help protect people, animals, and the environment in the present and future generations.

<span class="mw-page-title-main">Squire Booker</span> American biochemist

Squire Booker is an American biochemist at Penn State University. Booker directs an interdisciplinary chemistry research program related to fields of biochemistry, enzymology, protein chemistry, natural product biosynthesis, and mechanisms of radical dependent enzymes. He is an associate editor for the American Chemical Society Biochemistry Journal, is a Hughes Medical Institute Investigator, and an Eberly Distinguished Chair in Science at Penn State University.

Asad Ullah Khan is an Indian microbiologist, biochemist and a professor at the Interdisciplinary Biotechnology Unit of the Aligarh Muslim University. He is known for his studies on multidrug resistant clinical strains as well as for the first sighting in India of Aligarh super bug (NDM-4), a variant of New Delhi metallo-beta-lactamase 1 (NDM-1). He is an elected fellow of the Royal Society of Chemistry, the Biotech Research Society, India and the Indian Academy of Microbiological Sciences. The Department of Biotechnology of the Government of India awarded him the National Bioscience Award for Career Development, one of the highest Indian science awards, for his contributions to biosciences, in 2012.

Houra Merrikh is an Iranian-American microbiologist. She is a full professor at Vanderbilt University in the Department of Biochemistry. Her field of work is antibiotic resistance and bacterial evolvability.

Helen Boucher is Dean of Tufts University School of Medicine and Chief Academic Officer of Tufts Medicine, the parent health system for Tufts Medical Center in Boston. Prior to this, she served as Chief of the Division of Geographic Medicine and Infectious Diseases at Tufts Medical Center, a Professor of Medicine at Tufts University School of Medicine, and Director of the Stuart B. Levy Center for Integrated Management of Antimicrobial Resistance at Tufts.

<span class="mw-page-title-main">Georg Peters</span> German physician

Georg Peters was a German physician, microbiologist and university professor. From 1992 until his fatal mountain accident he headed the Institute of Medical Microbiology at the University of Münster. He was an internationally recognised expert in the field of staphylococci and the infectious diseases caused by them, to which he had devoted himself since the beginning of his scientific career.

Laura Piddock is a microbiologist, specialising in antibiotics and antibiotic resistance in bacteria. She is Professor Emerita at the University of Birmingham, UK and also Scientific Director within the Global Antibiotic Research and Development Partnership.

Lori Lee Burrows is a Canadian microbiologist. She is a Tier 1 Canada Research Chair in Microbe-Surface Interactions at McMaster University.

References

  1. 1 2 Crowe, Kelly (25 June 2014). "Antibiotic-resistant bacteria disarmed with fungus compound". CBC News. Retrieved 19 August 2015.
  2. "Gerry's Bio". Thewrightlab.com. Retrieved 19 August 2015.
  3. Waters, Hannah (25 April 2011). "Drugs boost antibiotic function". The Scientist. Retrieved 19 August 2015.
  4. "Unravelling the secrets of the superbugs". Hamilton Spectator. 24 October 2013. Retrieved 19 August 2015.
  5. "Canada Research Chair in Molecular Studies of Antibiotics". McMaster University. Retrieved 19 August 2015.
  6. "Contact Us". McMaster University. Retrieved 6 March 2023.
  7. Sello, Jason K. (October 2012). "Mining the Antibiotic Resistome". Chemistry & Biology. 19 (10): 1220–1221. doi: 10.1016/j.chembiol.2012.10.005 . PMID   23102216.
  8. King, Andrew M.; Reid-Yu, Sarah A.; Wang, Wenliang; King, Dustin T.; De Pascale, Gianfranco; Strynadka, Natalie C.; Walsh, Timothy R.; Coombes, Brian K.; Wright, Gerard D. (25 June 2014). "Aspergillomarasmine A overcomes metallo-β-lactamase antibiotic resistance". Nature. 510 (7506): 503–506. Bibcode:2014Natur.510..503K. doi:10.1038/nature13445. PMC   4981499 . PMID   24965651.
  9. Yang, Jennifer (25 June 2014). "Superbug NDM-1's antibiotic foe may lie in a handful of soil". Toronto Star. Retrieved 19 August 2015.