What is the ‘Wuhan coronavirus (2019-nCoV)’ and what do we know about
it so far?
Dr John Tregoning from Imperial’s Department
of Infectious Disease spoke to the School of Public Health’s Prof Steven Riley
about the ‘Wuhan
coronavirus’ outbreak that recently began in China.
·
Who has been working on the outbreak
epidemiology at Imperial College London?
SR: I work as part of the MRC
Centre for Global Infectious Disease Analysis
and the Abdul Latif
Jameel Institute for Disease and Emergency Analytics centre with Professor
Neil Ferguson, Dr Natsuko Imai, Dr Ilaria Dorigatti and Dr Anne Cori.
·
So what is the ‘Wuhan coronavirus'?
It is a viral infection that was
first discovered in the Chinese city of Wuhan in 2019 that has been associated
with a number of cases of pneumonia – an infection of the tissue in the lungs. You
might see it being called ‘2019-nCoV’, which stand for novel (or new)
coronavirus. More information has been provided by the World
Health Organisation.
·
What
is a coronavirus?
JT: Viruses are infectious organisms that rely upon the
cells in our bodies to replicate. A virus needs to enter our cells and hijack
them to make copies of itself. They enter our cells by sticking to the outside
of the cell, using viral proteins to recognise proteins made by the human
cells.
Coronavirus are respiratory viruses, which means they are viruses that infect the nose and the lungs. They are a large family of different viruses causing a range of different illnesses from colds to more severe diseases. The coronavirus family is known to be potentially zoonotic, so able to jump between different species. They are from a broader group of viruses called RNA viruses, which means their genetic material is carried on RNA molecules, not DNA molecules, which is important when it comes to thinking about how they can mutate.
Coronavirus are respiratory viruses, which means they are viruses that infect the nose and the lungs. They are a large family of different viruses causing a range of different illnesses from colds to more severe diseases. The coronavirus family is known to be potentially zoonotic, so able to jump between different species. They are from a broader group of viruses called RNA viruses, which means their genetic material is carried on RNA molecules, not DNA molecules, which is important when it comes to thinking about how they can mutate.
·
What are the symptoms?
SR: Since nCoV is a respiratory virus, it will cause
symptoms ranging from a cold (blocked nose) and a cough, to chest infection and
pneumonia. Fever (a temperature over 38°C or 100.4°F) has been commonly observed with nCoV infections. As the
virus was first identified in a cluster of pneumonia patients, we can probably assume
that it can cause pneumonia in the more severe cases.
·
Is it anything like SARS, MERS or Ebola?
SR: The novel coronavirus (nCoV) associated with this
outbreak, is somewhat similar to SARS (Severe acute respiratory syndrome) which emerged in 2003 and
MERS (Middle east respiratory
syndrome)
which emerged in 2012. Both of these infections, SARS and MERS, are caused by
coronaviruses and are respiratory infections.
It is nothing like Ebola, which is caused by a different
virus type altogether (Filoviridae). Ebola spreads from person to person by
contact with bodily fluids from infected individuals.
·
How does nCoV spread?
SR: We don’t fully know. However, we can compare it to other
respiratory viruses. Most of which are spread by respiratory droplets, for
example from a sneeze to a hand to a surface, which is then picked up by a new
person who then touches their face. Sometimes the virus can be airborne and
then inhaled, but it’s more difficult to measure how much transmission happens this
way.
·
How was it discovered?
SR: There was a cluster of pneumonia cases in Wuhan, China. Genetic
material was isolated from these patients and this coronavirus was found.
The team that found it have rapidly shared this information with the global
research community, which has enabled research towards new vaccines and
diagnostics.
·
How do you test patients for a new virus like this?
SR: Following the identification of the virus causing the
infection, we can use pre-existing technology called PCR to test patients. PCR (polymerase
chain reaction) is a highly specific test that recognises a genetic sequence
and amplifies it so that its presence can be detected.
·
Where did it come from – did it ‘jump’ from
reptiles or bats?
SR:
The first cases have been closely tied to a specific market in Wuhan. These no reliable evidence for it
coming from snakes. The closest known virus is found in bats, but we don’t know
for sure if this is where it came from.
·
And how did it jump to humans?
JT: Viruses, and in particular RNA viruses, mutate over time.
This is because when they use your cells to make copies of themselves they have
poor proofreading, so each copy is not quite the same as the original. Most of
these changes will make the virus less infectious, but some might enable them
to infect a slightly different type of cell or species.
SR: For other zoonotic viruses (viruses which spread between
animals and humans), the viruses normally move from a species with which we are
closely physically associated, so for example influenza can move from pigs and
chickens to people. The huge number of animals raised for meat and their close
physical proximity to people can make these jumps more likely.
·
How
is it spreading now?
SR: One of the tools we use as epidemiologists is the R0
value. This is the number of new individuals infected by the first infected
person. So for example an R0 of 2 means that each infected person infects 2
more people: in an unbroken transmission chain these 2 people would then infect
2 more each – so 2 becomes 4, which becomes 8 and so on. We then want to apply
behavioural and treatment approaches to reduce the R0 to less than 1 so the
infection contracts. We do not know the R0 value for nCoV yet and it is too
early to be confident about what it is.
·
Is the virus mutating?
SR: It is very hard to tell. Viruses mutate all the time as
part of their replication process. It’s very difficult to detect significant
mutations that really change the behaviour of a virus.
·
Is
this virus any more or less dangerous than seasonal flu?
SR: We don’t know. We are concerned that it is more
dangerous than the 2009 strain of influenza, which was milder than other
influenza pandemics. One way to think about this is the difference between case
fatality rate and infection fatality rate. Very roughly speaking case fatality
rate (CFR) is the number of deaths per confirmed cases of the virus (so in this
example people who have gone to a doctor or a hospital and had a confirmed
diagnosis of the virus). Infection fatality rate (IFR) is the number of deaths
of all the people who have been infected.
·
Why
is the difference between IFR and CFR important?
JT: If the majority of people who get infected with the
virus do not have severe enough illness to need to go to hospital or the Doctor,
then the case fatality rate will be higher than the infection fatality rate and
the disease will be less serious than it appears. Essentially clinical cases,
those that require medical assistance is the tip of an iceberg and the question
is how big is the underlying iceberg? If most people infected don’t develop any
symptoms, then it is a mild disease, if most people infected need
hospitalisation, it is a cause for concern.
·
Why don’t our existing vaccines or antiviral drugs
work?
JT: Vaccines work by training your immune system to
recognise specific features (called antigens) of the virus it is protecting you
against. Since this is a new virus, which looks different to other viruses and
has different antigens, current vaccines cannot provide protection.
JT speaking to Professor
Robin Shattock (Imperial College London). Vaccines take time to manufacture,
even with our best new platforms, any new vaccine takes at least 3 months to
manufacture enough material to test in people for safety. It is then a big step
from there to manufacture enough doses of vaccine to cover the world
population.
Likewise, antiviral drugs target key components of the viral
replication. They have been developed for other families of viruses and so are
not necessarily specific enough to inhibit the coronaviruses.
·
Is
there anything people can do to reduce their risk: for example wearing facemasks
or washing hands?
JT: Masks are important in clinical settings when properly
used, however they have little value for the general public. Handwashing and
reducing contact from hands to face can be helpful, as this helps stop the spread
of the virus through respiratory droplets from coughs and sneezes.
·
Will
the quarantine in Wuhan work?
SR: It is an unprecedented step, so we have no evidence
either way. But it is a strong statement from the government and this will
increase the awareness of the infection and therefore reduce spread.
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