Electron microscopy of SARS-CoV-2: a challenging task – Authors' reply
Published:May 19, 2020DOI:https://doi.org/10.1016/S0140-6736(20)31185-5
We thank Cynthia Goldsmith and colleagues for their interest in our recent Correspondence.
We described autopsy findings from patients who had died from COVID-19
and showed a systemic endotheliitis with evidence of loss of integrity
of the endothelial monolayer.
The
framework of endotheliitis provides an explanation for the unique
predilection of severe acute respiratory syndrome coronavirus 2
(SARS-CoV-2) in those individuals with hypertension, diabetes, or
established cardiovascular disease, a group known to have pre-existing
endothelial dysfunction. COVID-19-endotheliitis could also explain
impaired microcirculatory function across different organs and the
frequently observed prothrombotic state with in-situ clot formation.
Endothelial infection and injury by SARS-CoV-1 has been shown.
Our demonstration of viral particles using electron microscopy (EM) is
supported by several reports independently describing ultrastructural
round virus-like particles in the setting of a SARS-CoV-2 infection.
,
We demonstrated tubulo-reticular structures in the immediate vicinity
of the spherical particles that are strikingly identical to
SARS-CoV-1-associated membrane changes described by Goldsmith and
colleagues in 2004.
In our EM thin-section images, the virus-like particles were relatively
large (mean diameter 180 nm [SD 10]). However, subsequent analysis of
more EM images has revealed a mean particle size of 67 nm (SD 15 nm,
median 65 nm, 95% CI 41–102; n=33). Zhu and colleagues
noted that SARS-CoV-2 virions ranged from “about 60 to 140 nm”. In another recent study,
virus-like particles in patients with confirmed SARS-CoV-2 infection
were 70–110 nm in diameter. By comparison, SARS-CoV-1 viral particles
analysed with the same technique (ultrathin EM imaging) were 50–80 nm in
diameter.
Goldsmith
and colleagues have studied coronavirus isolates grown in cell culture,
whereas our EM data of virus-like particles were obtained from a
post-mortem kidney allograft obtained during autopsy. Since most other
recent reports of patients with COVID-19 also describe postmortem
findings, it remains unclear to what extent tissue type (cell culture,
fresh biopsy material, or autopsy material), time to fixation, and
postmortal autolysis alter subcellular structures in preparation for EM.
This notwithstanding, these observed particles in patients with
COVID-19 should be best designated as virus-like particles because
definitive assignment of these structures as SARS-CoV-2 virions requires
immuno-EM.
Investigations with vascular organoids that preceded our observations
showed that SARS-CoV-2 can infect human blood vessels via the ACE2
pathways, providing the first and direct evidence that the virus can
indeed invade human vasculature.
Our findings have also been confirmed in descriptions of renal tropism
of SARS-CoV-2, with detection of SARS-CoV-2 protein in human glomerular
endothelial and epithelial cells.
Importantly, our demonstration of virus cell infection in the kidney and endotheliitis
points to a general host inflammatory response causing
hyperinflammation as a principal participant in the vascular pathology
of COVID-19. Endothelial cell dysfunction, which might subsequently
induce a prothrombotic state, could thus explain the vascular
microcirculatory complications seen in different organs in patients with
COVID-19.
.. Sitaatti artikkelista : ..cell infection and endotheliitis in COVID-19. Lancet. 2020; 395: 1417-1418
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