Literature DB >> 32437764

Visualization of putative coronavirus in kidney.

Sara E Miller1, John K Brealey2.   

Abstract

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Year:  2020        PMID: 32437764      PMCID: PMC7206426          DOI: 10.1016/j.kint.2020.05.004

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


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To the editors: We read with concern the articles that report the presence of coronavirus in kidney based on electron microscopic evidence. , Neither article, in fact, demonstrates the presence of coronavirus in the kidney. Su et al. show purported virus particles in the cytoplasm of kidney tubular epithelium and podocytes. These structures are not viral particles, but rather clathrin-coated vesicles, normal cell organelles involved in intracellular transport. The objects in their Figure 2a and b (∼60 nm) are somewhat smaller than coronaviruses (∼80 to 140+ nm), but more importantly, their “spikes” (peplomers) are in contact with the cytosol, as are those on clathrin-coated vesicles; the larger particle in Figure 2d also has spikes that are touching the cytosol and does not have dense dots inside the particles corresponding to the coiled nucleocapsid, cut in cross section. Coronaviruses, on the other hand, have their projections either facing the extracellular space between cells or the space inside vacuoles within the cells.3, 4, 5 This phenomenon is due to the fact that coronaviruses receive their outer covering by budding into or on cellular membranes, thereby forming intracellular vacuoles with the viral projections in contact with the vacuolar content, not the cytosol. During assembly, viral structural proteins are incorporated into the endoplasmic reticulum–Golgi complex of the infected cell, and viral RNA, packaged with another protein, buds into these membranes, forming a membrane-bound sac containing mature virions; the spikes are on the outside of the virion, but inside the vacuole and not in direct contact with the cytosol (Figure 1 ). These virions get out of the cell by exocytosis when the vacuole membrane fuses with the plasma membrane and opens its contents to the outside; thus, complete virions with peplomers are seen within the cell inside the membrane container (sequestered from the cytosol) and outside of cells, frequently still attached to the opened vacuolar membrane that has fused with the plasma membrane. The particles shown in electron micrographs in the article by Su et al. have their spikes in contact with the cytoplasmic fluid, like endocytotic vesicles, that is, clathrin-coated vesicles (see Plate 523, Figures 3–5, pp. 1214–1215 in Ghadially; Figure 18c and d in Miller; and Miller).
Figure 1

Electron microscopic image of an isolate of severe acute respiratory syndrome coronavirus 2 seen here inside vacuoles (arrows). Note the dense membrane coat around the viral particles. This micrograph is of viral particles in a cell culture inoculated with infected patient nasopharyngeal and oropharyngeal fluids. Bar = 200 nm. Image provided by Cynthia S. Goldsmith, Centers for Disease Control and Prevention. To optimize viewing of this image, please see the online version of this article at www.kidney-international.org.

Electron microscopic image of an isolate of severe acute respiratory syndrome coronavirus 2 seen here inside vacuoles (arrows). Note the dense membrane coat around the viral particles. This micrograph is of viral particles in a cell culture inoculated with infected patient nasopharyngeal and oropharyngeal fluids. Bar = 200 nm. Image provided by Cynthia S. Goldsmith, Centers for Disease Control and Prevention. To optimize viewing of this image, please see the online version of this article at www.kidney-international.org. Likewise, the particles in Kissling et al. are not coronaviruses. While they are inside a vacuole, have spikes, and are approximately the correct size, they do not have the uniform appearance of virus particles with a membrane outer covering and dots inside indicating the nucleocapsid.3, 4, 5 These objects are inside a vesicle called a multivesicular body (see Plates 277–278, pp. 632–634 in Ghadially; Calomeni et al.; and Figure 3, p. 393 in Haguenau). The article by Kissling et al. is concerning, as electron microscopy is the only alleged evidence presented in support of the suggestion that coronaviruses are actually present in this kidney tissue; all other tests for coronavirus in kidney were negative. These micrographs do not support the statement that the particles are indeed viruses. Knowledge of virus morphology and morphogenesis, as well as of cellular architecture, is necessary to distinguish viral pathogens from normal subcellular organelles. This distinction is frequently difficult, because numerous cellular components can masquerade as viruses.7, 8, 9, 10, 11
  6 in total

1.  Renal histopathological analysis of 26 postmortem findings of patients with COVID-19 in China.

Authors:  Hua Su; Ming Yang; Cheng Wan; Li-Xia Yi; Fang Tang; Hong-Yan Zhu; Fan Yi; Hai-Chun Yang; Agnes B Fogo; Xiu Nie; Chun Zhang
Journal:  Kidney Int       Date:  2020-04-09       Impact factor: 10.612

2.  Collapsing glomerulopathy in a COVID-19 patient.

Authors:  Sébastien Kissling; Samuel Rotman; Christel Gerber; Matthieu Halfon; Frédéric Lamoth; Denis Comte; Loïc Lhopitallier; Salima Sadallah; Fadi Fakhouri
Journal:  Kidney Int       Date:  2020-04-15       Impact factor: 10.612

3.  Electron microscopy of SARS-CoV-2: a challenging task.

Authors:  Cynthia S Goldsmith; Sara E Miller; Roosecelis B Martines; Hannah A Bullock; Sherif R Zaki
Journal:  Lancet       Date:  2020-05-19       Impact factor: 79.321

4.  Multivesicular bodies mimicking SARS-CoV-2 in patients without COVID-19.

Authors:  Edward Calomeni; Anjali Satoskar; Isabelle Ayoub; Sergey Brodsky; Brad H Rovin; Tibor Nadasdy
Journal:  Kidney Int       Date:  2020-05-08       Impact factor: 10.612

5.  Ultrastructural characterization of SARS coronavirus.

Authors:  Cynthia S Goldsmith; Kathleen M Tatti; Thomas G Ksiazek; Pierre E Rollin; James A Comer; William W Lee; Paul A Rota; Bettina Bankamp; William J Bellini; Sherif R Zaki
Journal:  Emerg Infect Dis       Date:  2004-02       Impact factor: 6.883

6.  Detection and identification of viruses by electron microscopy.

Authors:  Sara E Miller
Journal:  J Electron Microsc Tech       Date:  2005-02-04
  6 in total
  52 in total

1.  COVID-19-Associated Kidney Injury: A Case Series of Kidney Biopsy Findings.

Authors:  Purva Sharma; Nupur N Uppal; Rimda Wanchoo; Hitesh H Shah; Yihe Yang; Rushang Parikh; Yuriy Khanin; Varun Madireddy; Christopher P Larsen; Kenar D Jhaveri; Vanesa Bijol
Journal:  J Am Soc Nephrol       Date:  2020-07-13       Impact factor: 10.121

2.  Histopathologic and Ultrastructural Findings in Postmortem Kidney Biopsy Material in 12 Patients with AKI and COVID-19.

Authors:  Pouneh Golmai; Christopher P Larsen; Maria V DeVita; Samuel J Wahl; Astrid Weins; Helmut G Rennke; Vanesa Bijol; Jordan L Rosenstock
Journal:  J Am Soc Nephrol       Date:  2020-07-16       Impact factor: 10.121

3.  Caution in Identifying Coronaviruses by Electron Microscopy.

Authors:  Sarah E Miller; Cynthia S Goldsmith
Journal:  J Am Soc Nephrol       Date:  2020-07-10       Impact factor: 10.121

4.  Authors' Reply.

Authors:  Evan A Farkash; Allecia M Wilson; Jeffrey M Jentzen
Journal:  J Am Soc Nephrol       Date:  2020-08-12       Impact factor: 10.121

5.  Clinicopathological Features and Outcomes of Acute Kidney Injury in Critically Ill COVID-19 with Prolonged Disease Course: A Retrospective Cohort.

Authors:  Peng Xia; Yubing Wen; Yaqi Duan; Hua Su; Wei Cao; Meng Xiao; Jie Ma; Yangzhong Zhou; Gang Chen; Wei Jiang; Huanwen Wu; Yan Hu; Sanpeng Xu; Hanghang Cai; Zhengyin Liu; Xiang Zhou; Bin Du; Jinglan Wang; Taisheng Li; Xiaowei Yan; Limeng Chen; Zhiyong Liang; Shuyang Zhang; Chun Zhang; Yan Qin; Guoping Wang; Xuemei Li
Journal:  J Am Soc Nephrol       Date:  2020-08-21       Impact factor: 10.121

6.  Kidney Biopsy Findings in Patients with COVID-19.

Authors:  Satoru Kudose; Ibrahim Batal; Dominick Santoriello; Katherine Xu; Jonathan Barasch; Yonatan Peleg; Pietro Canetta; Lloyd E Ratner; Maddalena Marasa; Ali G Gharavi; M Barry Stokes; Glen S Markowitz; Vivette D D'Agati
Journal:  J Am Soc Nephrol       Date:  2020-07-17       Impact factor: 10.121

7.  COVID-19-associated Nephropathy Includes Tubular Necrosis and Capillary Congestion, with Evidence of SARS-CoV-2 in the Nephron.

Authors:  Antoine Bouquegneau; Pauline Erpicum; Stéphanie Grosch; Lionel Habran; Olivier Hougrand; Justine Huart; Jean-Marie Krzesinski; Benoît Misset; Marie-Pierre Hayette; Philippe Delvenne; Christophe Bovy; Dominik Kylies; Tobias B Huber; Victor G Puelles; Pierre Delanaye; Francois Jouret
Journal:  Kidney360       Date:  2021-02-12

8.  Association between Postmortem Kidney Biopsy Findings and Acute Kidney Injury from Patients with SARS-CoV-2 (COVID-19).

Authors:  Jesús Rivero; Maribel Merino-López; Rossana Olmedo; Rubén Garrido-Roldan; Bernardo Moguel; Gustavo Rojas; Alfonso Chavez-Morales; Pablo Alvarez-Maldonado; Pablo Duarte-Molina; Rodolfo Castaño-Guerra; Ivon Karina Ruiz-Lopez; Elizabeth Soria-Castro; Cesar Luna; Alejandro Bonilla-Méndez; Francisco Baranda; Carlos Zabal; Magdalena Madero; Rafael Valdez-Ortiz; Ma Virgilia Soto-Abraham; Armando Vazquez-Rangel
Journal:  Clin J Am Soc Nephrol       Date:  2021-03-29       Impact factor: 8.237

Review 9.  Evidence For and Against Direct Kidney Infection by SARS-CoV-2 in Patients with COVID-19.

Authors:  Luise Hassler; Fabiola Reyes; Matthew A Sparks; Paul Welling; Daniel Batlle
Journal:  Clin J Am Soc Nephrol       Date:  2021-06-14       Impact factor: 8.237

Review 10.  Pathophysiology of COVID-19-associated acute kidney injury.

Authors:  Matthieu Legrand; Samira Bell; Lui Forni; Michael Joannidis; Jay L Koyner; Kathleen Liu; Vincenzo Cantaluppi
Journal:  Nat Rev Nephrol       Date:  2021-07-05       Impact factor: 42.439

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