» Articles » PMID: 33720333

Comparison of In Situ Hybridization, Immunohistochemistry, and Reverse Transcription-Droplet Digital Polymerase Chain Reaction for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Testing in Tissue

Abstract

Context.—: Small case series have evaluated severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) detection in formalin-fixed, paraffin-embedded tissue using reverse transcription-polymerase chain reaction, immunohistochemistry (IHC), and/or RNA in situ hybridization (RNAish).

Objective.—: To compare droplet digital polymerase chain reaction, IHC, and RNAish to detect SARS-CoV-2 in formalin-fixed, paraffin-embedded tissue in a large series of lung specimens from coronavirus disease 2019 (COVID-19) patients.

Design.—: Droplet digital polymerase chain reaction and RNAish used commercially available probes; IHC used clone 1A9. Twenty-six autopsies of COVID-19 patients with formalin-fixed, paraffin-embedded tissue blocks of 62 lung specimens, 22 heart specimens, 2 brain specimens, and 1 liver, and 1 umbilical cord were included. Control cases included 9 autopsy lungs from patients with other infections/inflammation and virus-infected tissue or cell lines.

Results.—: Droplet digital polymerase chain reaction had the highest sensitivity for SARS-CoV-2 (96%) when compared with IHC (31%) and RNAish (36%). All 3 tests had a specificity of 100%. Agreement between droplet digital polymerase chain reaction and IHC or RNAish was fair (κ = 0.23 and κ = 0.35, respectively). Agreement between IHC and in situ hybridization was substantial (κ = 0.75). Interobserver reliability was almost perfect for IHC (κ = 0.91) and fair to moderate for RNAish (κ = 0.38-0.59). Lung tissues from patients who died earlier after onset of symptoms revealed higher copy numbers by droplet digital polymerase chain reaction (P = .03, Pearson correlation = -0.65) and were more likely to be positive by RNAish (P = .02) than lungs from patients who died later. We identified SARS-CoV-2 in hyaline membranes, in pneumocytes, and rarely in respiratory epithelium. Droplet digital polymerase chain reaction showed low copy numbers in 7 autopsy hearts from ProteoGenex Inc. All other extrapulmonary tissues were negative.

Conclusions.—: Droplet digital polymerase chain reaction was the most sensitive and highly specific test to identify SARS-CoV-2 in lung specimens from COVID-19 patients.

Citing Articles

SARS-CoV-2 (COVID-19) Experience at an Academic Medical Examiner's Office.

Prahlow J, Jones P, Bailey K, Grande A, Obead A, Pink C Acad Forensic Pathol. 2024; 14(3):87-107.

PMID: 39246388 PMC: 11380442. DOI: 10.1177/19253621231224532.


The Role of TLR-2 in Lethal COVID-19 Disease Involving Medullary and Resident Lung Megakaryocyte Up-Regulation in the Microthrombosis Mechanism.

Pannone G, Pedicillo M, De Stefano I, Angelillis F, Barile R, Pannone C Cells. 2024; 13(10.

PMID: 38786077 PMC: 11120208. DOI: 10.3390/cells13100854.


Immunohistochemical and Morphometric Analysis of Lung Tissue in Fatal COVID-19.

Gheban-Rosca I, Gheban B, Pop B, Mironescu D, Siserman V, Jianu E Diagnostics (Basel). 2024; 14(9).

PMID: 38732328 PMC: 11082993. DOI: 10.3390/diagnostics14090914.


COVID-19: detection methods in post-mortem samples.

Tedesco I, Marino F, Ronchi A, Duarte Neto A, Dolhnikoff M, Municino M Pathologica. 2023; 115(5):263-274.

PMID: 38054901 PMC: 10699333. DOI: 10.32074/1591-951X-933.


Identification of SARS-CoV-2 from Human Lung Formalin-Fixed Paraffin-Embedded Tissue Sections Using Mass Spectrometry.

Mangalaparthi K, Singh S, Garapati K, Garcia J, Kipp B, Roden A OMICS. 2023; 27(10):494-496.

PMID: 37815798 PMC: 10615085. DOI: 10.1089/omi.2023.0157.