Neil A. R. Gow

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Neil Gow

Professor Neil Gow FMedSci FRS.jpg
Neil Gow at the Royal Society admissions day in London in 2016
Born (1957-11-30) 30 November 1957 (age 65)
Education Madras College
Perth Academy [1]
Alma mater University of Edinburgh (BSc)
University of Aberdeen (PhD)
Scientific career
Fields Microbiology
Mycology
Immunology
Cell biology [2]
Institutions University of Exeter
University of Aberdeen
Thesis Growth, physiology and ultrastructure of the pathogenic fungus Candida albicans  (1982)
Doctoral advisor Graham W. Gooday
Website www.abdn.ac.uk/ims/profiles/n.gow

Neil Andrew Robert Gow (born 30 November 1957) [3] FRS FRSE FMedSci FRSB [4] [5] is a professor of Microbiology and deputy Vice Chancellor at the University of Exeter. [6] Previously he served at the University of Aberdeen for 38 years [1] [2] and retains an honorary Chair there. [7]

Contents

Education

Gow was educated Madras College and Perth Academy. [1] He studied at the University of Edinburgh and the University of Aberdeen where he was awarded a PhD in 1982 for research on the pathogenic fungus Candida albicans supervised by Graham Gooday. [8] [9]

Research and career

Gow's research career has been in the field of fungal biology and medical mycology. He is known for his discoveries in fungal biology and genetics, morphogenesis and pathogenesis. His studies of how the cell walls of fungal pathogenic species is assembled, responds to antifungal antibiotics and is recognised by the human immune system directly impacts on the design and use of antifungal drugs, diagnostics and immunotherapies for fungal diseases. [10] [11] [12] [13]

After his PhD, Gow worked in Denver before returning to Aberdeen, where he has developed a team that has recently[ when? ] become a Medical Research Council (MRC) Centre for Medical Mycology and is one of the largest centres in this field worldwide. He has helped co-ordinate UK training and research in medical mycology and has acted as President of the British Mycological Society, the International Society for Human and Animal Mycology (ISHAM) and the Microbiology Society. [4]

Awards and honours

Gow has received several awards for his research, he was elected a Fellow of the Academy of Medical Sciences (FMedSci),[ when? ] the Royal Society of Edinburgh (FRSE) [5] [ when? ] and the American Academy of Microbiology. He was elected a Fellow of the Royal Society (FRS) in 2016 [4] and a Fellow of the Royal Society of Biology (FRSB). [1] [ when? ]

Related Research Articles

<span class="mw-page-title-main">Candidiasis</span> Fungal infection due to any type of Candida

Candidiasis is a fungal infection due to any type of Candida. When it affects the mouth, in some countries it is commonly called thrush. Signs and symptoms include white patches on the tongue or other areas of the mouth and throat. Other symptoms may include soreness and problems swallowing. When it affects the vagina, it may be referred to as a yeast infection or thrush. Signs and symptoms include genital itching, burning, and sometimes a white "cottage cheese-like" discharge from the vagina. Yeast infections of the penis are less common and typically present with an itchy rash. Very rarely, yeast infections may become invasive, spreading to other parts of the body. This may result in fevers along with other symptoms depending on the parts involved.

<span class="mw-page-title-main">Hypha</span> Long, filamentous structure in fungi and Actinobacteria

A hypha is a long, branching, filamentous structure of a fungus, oomycete, or actinobacterium. In most fungi, hyphae are the main mode of vegetative growth, and are collectively called a mycelium.

<i>Candida dubliniensis</i> Species of fungus

Candida dubliniensis is a fungal opportunistic pathogen originally isolated from AIDS patients. It is also occasionally isolated from immunocompetent individuals. It is of the genus Candida, very closely related to Candida albicans but forming a distinct phylogenetic cluster in DNA fingerprinting. It is most commonly isolated from oral cavities, and is also occasionally found in other anatomical sites.

<i>Candida albicans</i> Species of fungus

Candida albicans is an opportunistic pathogenic yeast that is a common member of the human gut flora. It can also survive outside the human body. It is detected in the gastrointestinal tract and mouth in 40–60% of healthy adults. It is usually a commensal organism, but it can become pathogenic in immunocompromised individuals under a variety of conditions. It is one of the few species of the genus Candida that causes the human infection candidiasis, which results from an overgrowth of the fungus. Candidiasis is, for example, often observed in HIV-infected patients. C. albicans is the most common fungal species isolated from biofilms either formed on (permanent) implanted medical devices or on human tissue. C. albicans, C. tropicalis, C. parapsilosis, and C. glabrata are together responsible for 50–90% of all cases of candidiasis in humans. A mortality rate of 40% has been reported for patients with systemic candidiasis due to C. albicans. By one estimate, invasive candidiasis contracted in a hospital causes 2,800 to 11,200 deaths yearly in the US. Nevertheless, these numbers may not truly reflect the true extent of damage this organism causes, given new studies indicating that C. albicans can cross the blood–brain barrier in mice.

<i>Candida</i> (fungus) Genus of ascomycete fungi

Candida is a genus of yeasts and is the most common cause of fungal infections worldwide. Many species are harmless commensals or endosymbionts of hosts including humans; however, when mucosal barriers are disrupted or the immune system is compromised they can invade and cause disease, known as an opportunistic infection. Candida is located on most mucosal surfaces and mainly the gastrointestinal tract, along with the skin. Candida albicans is the most commonly isolated species and can cause infections in humans and other animals. In winemaking, some species of Candida can potentially spoil wines.

<span class="mw-page-title-main">Oral candidiasis</span> Fungal infection

Oral candidiasis, also known as oral thrush among other names, is candidiasis that occurs in the mouth. That is, oral candidiasis is a mycosis of Candida species on the mucous membranes of the mouth.

<i>Candida glabrata</i> Species of fungus

Candida glabrata is a species of haploid yeast of the genus Candida, previously known as Torulopsis glabrata. Despite the fact that no sexual life cycle has been documented for this species, C. glabrata strains of both mating types are commonly found. C. glabrata is generally a commensal of human mucosal tissues, but in today's era of wider human immunodeficiency from various causes, C. glabrata is often the second or third most common cause of candidiasis as an opportunistic pathogen. Infections caused by C. glabrata can affect the urogenital tract or even cause systemic infections by entrance of the fungal cells in the bloodstream (Candidemia), especially prevalent in immunocompromised patients.

<span class="mw-page-title-main">Sertaconazole</span>

Sertaconazole, sold under the brand name Ertaczo among others, is an antifungal medication of the Benzothiophene class. It is available as a cream to treat skin infections such as athlete's foot.

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

Gliotoxin is a sulfur-containing mycotoxin that belongs to a class of naturally occurring 2,5-diketopiperazines produced by several species of fungi, especially those of marine origin. It is the most prominent member of the epipolythiopiperazines, a large class of natural products featuring a diketopiperazine with di- or polysulfide linkage. These highly bioactive compounds have been the subject of numerous studies aimed at new therapeutics. Gliotoxin was originally isolated from Gliocladium fimbriatum, and was named accordingly. It is an epipolythiodioxopiperazine metabolite.

<i>Candida lusitaniae</i> Species of fungus

Candida lusitaniae is a species of yeast in the genus Candida.

<span class="mw-page-title-main">Dimorphic fungus</span>

Dimorphic fungi are fungi that can exist in the form of both mold and yeast. This is usually brought about by change in temperature and the fungi are also described as thermally dimorphic fungi. An example is Talaromyces marneffei, a human pathogen that grows as a mold at room temperature, and as a yeast at human body temperature.

Pathogenic fungi are fungi that cause disease in humans or other organisms. Approximately 300 fungi are known to be pathogenic to humans. Markedly more fungi are known to be pathogenic to plant life than those of the animal kingdom. The study of fungi pathogenic to humans is called "medical mycology". Although fungi are eukaryotic, many pathogenic fungi are microorganisms. The study of fungi and other organisms pathogenic to plants is called plant pathology.

<span class="mw-page-title-main">Blastoconidium</span>

A blastoconidium is an asexual holoblastic conidia formed through the blowing out or budding process of a yeast cell, which is a type of asexual reproduction that results in a bud arising from a parent cell. The production of a blastoconidium can occur along a true hyphae, pseudohyphae, or a singular yeast cell. The word "conidia" comes from the Greek word konis and eidos, konis meaning dust and eidos meaning like. The term "bud" comes from the Greek word blastos, which means bud. Yeasts such as Candida albicans and Cryptococcus neoformans produce these budded cells known as blastoconidia.

<span class="mw-page-title-main">Hwp1</span>

Hwp1 is a protein (glycoprotein) located on the surface of an opportunistic diploid fungus called Candida albicans.

<span class="mw-page-title-main">James Naismith (chemist)</span> British structural biologist

James Henderson Naismith is Professor of Structural Biology at the University of Oxford, former Director of the Research Complex at Harwell and Director of the Rosalind Franklin Institute. He previously served as Bishop Wardlaw Professor of Chemical Biology at the University of St Andrews. He was a member of Council of the Royal Society (2021-2022). He is currently the Vice-Chair of Council of the European X-ray Free Electron Laser and Vice-President (non-clinical) of The Academy of Medical Sciences.

Pneumocandin B<sub>0</sub> Chemical compound

Pneumocandin B0, also known as pneumocandin B0, pneumocandin B(0), and hydroxy echinocandin, is an organic chemical compound with the formula C50H80N8O17, produced by the fungus Glarea lozoyensis.

Graham William Gooday (1942–2001) was a British molecular biologist. He was Professor of Microbiology at Aberdeen University. He was presented with the inaugural Fleming Prize Lecture for the Microbiological Society in 1976. He served as Director of the Institute of Marine Biology.

Beatrice B. "Bebe" Magee is an American biochemist and geneticist with expertise in molecular mycology and fungal genetics. She earned her B. A. in chemistry from Brandeis University in 1962 and her M. A. in biochemistry from the University of California, Berkeley, in 1964. She has been co-author on over 40 publications in peer-reviewed journals and an invited speaker at scientific meetings including Woods Hole and Cold Spring Harbor courses as well as at professional mycology societies.

Carol Kumamoto is an American microbiologist who is Professor of Molecular Biology & Microbiology at Tufts University. She investigates the filamentous growth of Candida albicans, a fungal pathogen that causes several diseases. She is also interested in how C. albicans interacts with its host during colonisation and invasive diseases. She is a Fellow of the American Association for the Advancement of Science and the American Academy of Microbiology.

<span class="mw-page-title-main">Frank Odds</span> English mycologist (1945–2020)

Frank C. Odds was an English mycologist. He studied Candida albicans, establishing how modern researchers study fungal pathogens and the diseases they cause.

References

  1. 1 2 3 4 Anon (2017). "Gow, Prof. Neil Andrew Robert" . Who's Who . ukwhoswho.com (online Oxford University Press  ed.). A & C Black, an imprint of Bloomsbury Publishing plc. doi:10.1093/ww/9780199540884.013.U286513.(Subscription or UK public library membership required.)(subscription required)
  2. 1 2 Neil A. R. Gow publications indexed by Google Scholar OOjs UI icon edit-ltr-progressive.svg
  3. Neil A. R. Gow at Library of Congress Authorities
  4. 1 2 3 Anon (2016). "Professor Neil Gow FMedSci FRS". London: Royal Society. Archived from the original on 29 April 2016. One or more of the preceding sentences incorporates text from the royalsociety.org website where:
    "All text published under the heading 'Biography' on Fellow profile pages is available under Creative Commons Attribution 4.0 International License." -- "Royal Society Terms, conditions and policies". Archived from the original on 25 September 2015. Retrieved 9 March 2016.{{cite web}}: CS1 maint: bot: original URL status unknown (link)
  5. 1 2 "Royal Society of Edinburgh Fellows as of 2016-05-13" (PDF). Edinburgh: Royal Society of Edinburgh. Archived from the original (PDF) on 30 March 2016.
  6. "University of Exeter". Exeter.ac.uk. Retrieved 28 November 2018.
  7. "Professor Neil Gow: Chair in Microbiology, University of Aberdeen". Aberdeen: abdn.ac.uk. Archived from the original on 17 May 2016.
  8. Gow, Neil Andrew Robert (1982). Growth, physiology and ultrastructure of the pathogenic fungus Candida albicans. jisc.ac.uk (PhD thesis). University of Aberdeen. OCLC   646445444. EThOS   uk.bl.ethos.354942.
  9. Gow, Neil A. R.; Gooday, Graham W. (1982). "Growth kinetics and morphology of colonies of the filamentous form of Candida albicans". Journal of General Microbiology. 128 (9): 2187–2194. doi: 10.1099/00221287-128-9-2187 . PMID   6757383.
  10. Odds, Frank C.; Brown, Alistair J.P.; Gow, Neil A.R. (2003). "Antifungal agents: mechanisms of action". Trends in Microbiology. 11 (6): 272–279. doi:10.1016/S0966-842X(03)00117-3. PMID   12823944.
  11. Netea, Mihai G.; Brown, Gordon D.; Kullberg, Bart Jan; Gow, Neil A. R. (2008). "An integrated model of the recognition of Candida albicans by the innate immune system". Nature Reviews Microbiology. 6 (1): 67–78. doi:10.1038/nrmicro1815. PMID   18079743. S2CID   1477651.
  12. Cormack, B. P.; Bertram, G.; Egerton, M.; Gow, N. A. R.; Falkow, S.; Brown, A. J. P. (1997). "Yeast-enhanced green fluorescent protein (yEGFP): a reporter of gene expression in Candida albicans". Microbiology. 143 (2): 303–311. doi: 10.1099/00221287-143-2-303 . PMID   9043107.
  13. Butler, Geraldine; Rasmussen, Matthew D.; Lin, Michael F.; Santos, Manuel A. S.; Sakthikumar, Sharadha; Munro, Carol A.; Rheinbay, Esther; Grabherr, Manfred; Forche, Anja; Reedy, Jennifer L.; Agrafioti, Ino; Arnaud, Martha B.; Bates, Steven; Brown, Alistair J. P.; Brunke, Sascha; Costanzo, Maria C.; Fitzpatrick, David A.; de Groot, Piet W. J.; Harris, David; Hoyer, Lois L.; Hube, Bernhard; Klis, Frans M.; Kodira, Chinnappa; Lennard, Nicola; Logue, Mary E.; Martin, Ronny; Neiman, Aaron M.; Nikolaou, Elissavet; Quail, Michael A.; Quinn, Janet; Santos, Maria C.; Schmitzberger, Florian F.; Sherlock, Gavin; Shah, Prachi; Silverstein, Kevin A. T.; Skrzypek, Marek S.; Soll, David; Staggs, Rodney; Stansfield, Ian; Stumpf, Michael P. H.; Sudbery, Peter E.; Srikantha, Thyagarajan; Zeng, Qiandong; Berman, Judith; Berriman, Matthew; Heitman, Joseph; Gow, Neil A. R.; Lorenz, Michael C.; Birren, Bruce W.; Kellis, Manolis; Cuomo, Christina A. (2009). "Evolution of pathogenicity and sexual reproduction in eight Candida genomes". Nature. 459 (7247): 657–662. Bibcode:2009Natur.459..657B. doi:10.1038/nature08064. PMC   2834264 . PMID   19465905.