Susan Baker (virologist)

Last updated
Susan C. Baker
Alma mater Vanderbilt University (Ph.D.)
Scientific career
FieldsVirology, Immunology
InstitutionsLoyola University

Susan C. Baker is an American molecular virologist and professor at Loyola University Chicago, Illinois. She teaches microbiology and immunology within the Loyola Medicine Health System. She received her Ph.D. from Vanderbilt University. Currently, she has 80 publications, dating back to 1987, within each of the following disciplines: microbiology, infectious disease, and infectious disease control to name a few. [1] A list of her publications can be found here.

Contents

Research focus

Angiogram of Kawasaki Disease. KawasAngio.png
Angiogram of Kawasaki Disease.

Baker has done extensive research on many diseases, however her ongoing research revolves around Coronaviruses and Kawasaki disease and the pathogenesis of each.

Kawasaki Disease causes inflammation of arterial walls throughout the body. This disease also affects skin, mucous membranes, and the body's lymph nodes. [2] [3] [4] Baker's lab is investigating the possibility of a viral causative agent for the disease. This disease mostly affects children under the age of 5. Causes remain unknown, however it is treatable within days if the symptoms are recognized early enough. If left untreated, it can lead to serious problems for the heart. [5]

Coronavirus virion Coronavirus virion.jpg
Coronavirus virion

Baker has also worked closely with coronaviruses, the causative agent of severe acute respiratory syndrome. These are viruses that affect mostly the upper respiratory and GI tract of humans and are named because of their crown-like appearance under the electron microscope. Currently her lab is using a mouse model to test the function and inhibition of certain proteases involved in coronavirus infection. [6]

Publications

Baker has many published articles, mostly concerning Coronaviruses and Kawasaki Disease. The following are her most recent publications on these topics.

In this study, the function of ubiquitin-like domains (Ubl) is studied. To find the function, structures of papain-like proteases (PLP) and domains of coronaviruses (CoVs) were studied. It was found that an adjacent Ubl domain was present in different CoV domains.

This article shows the basis of the ubiquitin chain of PLpro and gene 15 specificity.

This article talks about miRNA and its function in Kawasaki Disease. They were not able to identify the cause for cardivascular miRNAs in Kawasaki Disease, though this study may guide future studies.

The article shows that differe coronaviruses work the same way, but are not the same efficiency. The two viruses studied included MERS-CoV and SARS-CoV. Though this was an important discovery, neither enzyme can be used as a model to explain the behavior of all CoV PLpros.

Coronaviruses and anteriviruses are positive strand RNA viruses. This article informs us on the nature of Nidoviruses and describes the PLP's role in viral pathogenesis.

Related Research Articles

Coronavirus Subfamily of viruses in the family Coronaviridae

Coronaviruses are a group of related RNA viruses that cause diseases in mammals and birds. In humans and birds, they cause respiratory tract infections that can range from mild to lethal. Mild illnesses in humans include some cases of the common cold, while more lethal varieties can cause SARS, MERS, and COVID-19. In cows and pigs they cause diarrhea, while in mice they cause hepatitis and encephalomyelitis.

<i>Severe acute respiratory syndrome–related coronavirus</i> Species of coronavirus causing SARS and COVID-19

Severe acute respiratory syndrome–related coronavirus is a species of coronavirus that infects humans, bats and certain other mammals. It is an enveloped positive-sense single-stranded RNA virus that enters its host cell by binding to the angiotensin-converting enzyme 2 (ACE2) receptor. It is a member of the genus Betacoronavirus and subgenus Sarbecovirus.

<i>Coronaviridae</i> Family of viruses in the order Nidovirales

Coronaviridae is a family of enveloped, positive-strand RNA viruses which infect amphibians, birds, and mammals. The group includes the subfamilies Letovirinae and Orthocoronavirinae; the members of the latter are known as coronaviruses.

<i>Nidovirales</i> Order of positive-sense, single-stranded RNA viruses

Nidovirales is an order of enveloped, positive-strand RNA viruses which infect vertebrates and invertebrates. Host organisms include mammals, birds, reptiles, amphibians, fish, arthropods, molluscs, and helminths. The order includes the families Coronaviridae, Arteriviridae, Roniviridae, and Mesoniviridae.

Severe acute respiratory syndrome coronavirus Virus strain causing severe acute respiratory syndrome

Severe acute respiratory syndrome coronavirus is a strain of virus that causes severe acute respiratory syndrome (SARS). It is an enveloped, positive-sense, single-stranded RNA virus which infects the epithelial cells within the lungs. The virus enters the host cell by binding to angiotensin-converting enzyme 2. It infects humans, bats, and palm civets.

Deubiquitinating enzyme

Deubiquitinating enzymes (DUBs), also known as deubiquitinating peptidases, deubiquitinating isopeptidases, deubiquitinases, ubiquitin proteases, ubiquitin hydrolases, ubiquitin isopeptidases, are a large group of proteases that cleave ubiquitin from proteins. Ubiquitin is attached to proteins in order to regulate the degradation of proteins via the proteasome and lysosome; coordinate the cellular localisation of proteins; activate and inactivate proteins; and modulate protein-protein interactions. DUBs can reverse these effects by cleaving the peptide or isopeptide bond between ubiquitin and its substrate protein. In humans there are nearly 100 DUB genes, which can be classified into two main classes: cysteine proteases and metalloproteases. The cysteine proteases comprise ubiquitin-specific proteases (USPs), ubiquitin C-terminal hydrolases (UCHs), Machado-Josephin domain proteases (MJDs) and ovarian tumour proteases (OTU). The metalloprotease group contains only the Jab1/Mov34/Mpr1 Pad1 N-terminal+ (MPN+) (JAMM) domain proteases.

<i>Human coronavirus NL63</i> Species of virus

Human coronavirus NL63 (HCoV-NL63) is a species of coronavirus, specifically a Setracovirus from among the Alphacoronavirus genus. It was identified in late 2004 in a seven-month-old child with bronchiolitis in the Netherlands. The virus is an enveloped, positive-sense, single-stranded RNA virus which enters its host cell by binding to ACE2. Infection with the virus has been confirmed worldwide, and has an association with many common symptoms and diseases. Associated diseases include mild to moderate upper respiratory tract infections, severe lower respiratory tract infection, croup and bronchiolitis.

<i>Murine coronavirus</i>

Murine coronavirus (M-CoV) is a species of coronavirus which infects mice. It is an enveloped, positive-sense, single-stranded RNA virus which enters its host cell by binding to the CEACAM1 receptor. It has, like other coronaviruses from genus Betacoronavirus, subgenus Embecovirus, an additional hemagglutinin esterase (HE) gene.

Coronavirus packaging signal Regulartory element in coronaviruses

The Coronavirus packaging signal is a conserved cis-regulatory element found in Betacoronavirus. It has an important role in regulating the packaging of the viral genome into the capsid. As part of the viral life cycle, within the infected cell, the viral genome becomes associated with viral proteins and assembles into new infective progeny viruses. This process is called packaging and is vital for viral replication.

Transmissible gastroenteritis virus

Transmissible gastroenteritis virus or Transmissible gastroenteritis coronavirus (TGEV) is a coronavirus which infects pigs. It is an enveloped, positive-sense, single-stranded RNA virus which enters its host cell by binding to the APN receptor. The virus is a member of the genus Alphacoronavirus, subgenus Tegacovirus, species Alphacoronavirus 1.

3C-like protease

The 3C-like protease (3CLpro), formally known as C30 Endopeptidase, is the main protease found in coronaviruses. It cleaves the coronavirus polyprotein at eleven conserved sites. It is a cysteine protease and a member of the PA clan of proteases. It has a cysteine-histidine catalytic dyad at its active site and cleaves a Gln–(Ser/Ala/Gly) peptide bond.

Middle East respiratory syndrome Viral respiratory infection

Middle East respiratory syndrome (MERS), also known as camel flu, is a viral respiratory infection caused by the MERS-coronavirus (MERS-CoV). Symptoms may range from none, to mild, to severe. Typical symptoms include fever, cough, diarrhea, and shortness of breath. The disease is typically more severe in those with other health problems.

<i>Human coronavirus HKU1</i>

Human coronavirus HKU1 (HCoV-HKU1) is a species of coronavirus in humans. It causes an upper respiratory disease with symptoms of the common cold, but can advance to pneumonia and bronchiolitis. It was first discovered in January 2004 from one man in Hong Kong. Subsequent research revealed it has global distribution and earlier genesis.

<i>Betacoronavirus</i> Genus of viruses in the subfamily Orthocoronavirinae

Betacoronavirus is one of four genera of coronaviruses. Member viruses are enveloped, positive-strand RNA viruses that infect mammals. The natural reservoir for betacoronaviruses are bats and rodents. Rodents are the reservoir for the subgenus Embecovirus, while bats are the reservoir for the other subgenera.

Human coronavirus OC43 Species of virus

Human coronavirus OC43 (HCoV-OC43) is a member of the species Betacoronavirus 1, which infects humans and cattle. The infecting coronavirus is an enveloped, positive-sense, single-stranded RNA virus which enters its host cell by binding to the N-acetyl-9-O-acetylneuraminic acid receptor. OC43 is one of seven known coronaviruses to infect humans. It is one of the viruses responsible for the common cold. It has, like other coronaviruses from genus Betacoronavirus, subgenus Embecovirus, an additional shorter spike protein called hemagglutinin esterase (HE).

Human coronavirus 229E (HCoV-229E) is a species of coronavirus which infects humans and bats. It is an enveloped, positive-sense, single-stranded RNA virus which enters its host cell by binding to the APN receptor. Along with Human coronavirus OC43, it is one of the viruses responsible for the common cold. HCoV-229E is a member of the genus Alphacoronavirus and subgenus Duvinacovirus.

Severe acute respiratory syndrome coronavirus 2 Virus strain that causes coronavirus disease 2019 (COVID-19)

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the strain of coronavirus that causes coronavirus disease 2019 (COVID-19), the respiratory illness responsible for the COVID-19 pandemic. Colloquially known as simply the coronavirus, it was previously referred to by its provisional name, 2019 novel coronavirus (2019-nCoV), and has also been called human coronavirus 2019. The World Health Organization declared the outbreak a Public Health Emergency of International Concern on 30 January 2020, and a pandemic on 11 March 2020.

Susan R. Weiss is an American microbiologist who is a Professor of Microbiology at the Perelman School of Medicine at the University of Pennsylvania. Her research considers the biology of coronaviruses, including SARS, MERS and SARS-CoV-2. As of March 2020, Weiss serves as Co-Director of the University of Pennsylvania Coronavirus Research Center.

Karen Louise Mossman is a Canadian virologist who is a professor of Pathology and Molecular Medicine at McMaster University. Mossman looks to understand how viruses get around the defence mechanisms of cells. She was part of a team of Canadian researchers who first isolated SARS-CoV-2.

History of coronavirus

The history of coronaviruses is a reflection of the discovery of the diseases caused by coronaviruses and identification of the viruses. It starts with the first report of a new type of upper-respiratory tract disease among chickens in North Dakota, US, in 1931. The causative agent was identified as a virus in 1933. By 1936, the disease and the virus were recognised as unique from other viral disease. The became known as infectious bronchitis virus (IBV), but later officially renamed as Avian coronavirus.

References

  1. "Susan Baker". ResearchGate. Retrieved 15 April 2015.
  2. Baker, Susan. "The Baker Lab Home Page". Microbiology & Immunology: Dr. Susan Baker. Loyola University. Retrieved 15 April 2015. Old Page
  3. Rowley AH, Baker SC, Orenstein JM, Shulman ST (2008). "Searching for the cause of Kawasaki disease--cytoplasmic inclusion bodies provide new insight". Nat. Rev. Microbiol. 6 (5): 394–401. doi:10.1038/nrmicro1853. PMC   7097362 . PMID   18364728.
  4. "Kawasaki Disease". Mayo Clinic. Retrieved 15 May 2015.
  5. Ravin, Karen. "Kawasaki Disease". KidsHealth. Retrieved 2 August 2020. Old Page
  6. Mielech AM, Deng X, Chen Y, Kindler E, Wheeler DL, Mesecar AD, Thiel V, Perlman S, Baker SC (2015). "Murine coronavirus ubiquitin-like domain is important for papain-like protease stability and viral pathogenesis". J. Virol. 89 (9): 4907–17. doi:10.1128/JVI.00338-15. PMC   4403493 . PMID   25694594.