Serologic Testing of US Blood Donations to Identify Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2)–Reactive Antibodies: December 2019–January 2020

Author:

Basavaraju Sridhar V1,Patton Monica E1,Grimm Kacie2,Rasheed Mohammed Ata Ur2,Lester Sandra2,Mills Lisa3,Stumpf Megan3,Freeman Brandi1,Tamin Azaibi1,Harcourt Jennifer1,Schiffer Jarad1,Semenova Vera1,Li Han1,Alston Bailey4,Ategbole Muyiwa5,Bolcen Shanna1,Boulay Darbi1,Browning Peter1,Cronin Li1,David Ebenezer6,Desai Rita1,Epperson Monica1,Gorantla Yamini5,Jia Tao1,Maniatis Panagiotis1,Moss Kimberly4,Ortiz Kristina4,Park So Hee4,Patel Palak6,Qin Yunlong4,Steward-Clark Evelene1,Tatum Heather5,Vogan Andrew4,Zellner Briana7,Drobeniuc Jan1,Sapiano Matthew R P1,Havers Fiona1,Reed Carrie1,Gerber Susan1,Thornburg Natalie J1,Stramer Susan L2

Affiliation:

1. Centers for Disease Control and Prevention, Atlanta, Georgia, USA

2. American Red Cross, Scientific Affairs, Gaithersburg, Maryland, USA

3. Synergy America, Inc, Atlanta, Georgia, USA

4. Eagle Global Scientific, Atlanta, Georgia, USA

5. IHRC, Atlanta, Georgia, USA

6. CFD Research Corporation, Huntsville, Alabama, USA

7. Oak Ridge Institute for Science and Education, Oak Ridge, Tennessee, USA

Abstract

Abstract Background Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus that causes coronavirus disease 2019 (COVID-19), was first identified in Wuhan, China, in December 2019, with subsequent worldwide spread. The first US cases were identified in January 2020. Methods To determine if SARS-CoV-2–reactive antibodies were present in sera prior to the first identified case in the United States on 19 January 2020, residual archived samples from 7389 routine blood donations collected by the American Red Cross from 13 December 2019 to 17 January 2020 from donors resident in 9 states (California, Connecticut, Iowa, Massachusetts, Michigan, Oregon, Rhode Island, Washington, and Wisconsin) were tested at the Centers for Disease Control and Prevention for anti–SARS-CoV-2 antibodies. Specimens reactive by pan-immunoglobulin (pan-Ig) enzyme-linked immunosorbent assay (ELISA) against the full spike protein were tested by IgG and IgM ELISAs, microneutralization test, Ortho total Ig S1 ELISA, and receptor-binding domain/ACE2 blocking activity assay. Results Of the 7389 samples, 106 were reactive by pan-Ig. Of these 106 specimens, 90 were available for further testing. Eighty-four of 90 had neutralizing activity, 1 had S1 binding activity, and 1 had receptor-binding domain/ACE2 blocking activity >50%, suggesting the presence of anti–SARS-CoV-2–reactive antibodies. Donations with reactivity occurred in all 9 states. Conclusions These findings suggest that SARS-CoV-2 may have been introduced into the United States prior to 19 January 2020.

Funder

US government work

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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