Notes from the Field: SARS-CoV-2 Omicron Variant Infection in 10 Persons Within 90 Days of Previous SARS-CoV-2 Delta Variant Infection — Four States, October 2021–January 2022
Weekly / April 8, 2022 / 71(14);524–526
Mellisa Roskosky, PhD*,1,2; Brian F. Borah, MD*,1,3; Peter M. DeJonge, PhD1,4; Catherine V. Donovan, PhD5; Lynn Zanardi Blevins, MD3; Allison G. Lafferty, MD3; Julia C. Pringle, PhD6; Patsy Kelso, PhD3; Jonathan L. Temte, MD7; Emily Temte7; Shari Barlow7; Maureen Goss, MPH7; Amra Uzicanin, MD8; Allen Bateman, PhD9; Kelsey Florek, PhD9; Vance Kawakami, DVM2; James Lewis, MD2; Julie Loughran2; Sargis Pogosjans, MPH2; Meagan Kay, DVM2; Jeff Duchin, MD2; Stephanie Lunn, MPH, MS10; Hannah Schnitzler, DVM10; Shivani Arora5; Jacqueline Tate, PhD11; Jessica Ricaldi, MD11; Hannah Kirking, MD11 (View author affiliations)View suggested citation
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Vaccination protects against infection with SARS-CoV-2 (the virus that causes COVID-19) and related hospitalizations (1,2), and surviving a previous infection protects against B.1.1.7 (Alpha) and B.1.617.2 (Delta) variant reinfections† (2). Since the SARS-CoV-2 B.1.1.529 (Omicron) variant became predominant in the United States in late December 2021, reported reinfections have increased§ (3). Early reinfections (those occurring within 90 days of previous infection) are not well understood (4). Because some persons have prolonged detection of viral RNA after infection,¶ repeat positive nucleic acid amplification test (NAAT) results within 90 days could reflect prolonged shedding from earlier infection, presenting technical challenges to documenting and characterizing early reinfections. This report describes 10 patients from four states, with whole genome sequencing (WGS)–confirmed Omicron variant infections within 90 days of a previous Delta infection. This activity was reviewed by CDC, approved by respective institutional review boards, and was conducted consistent with applicable federal law and CDC policy.**
An early reinfection was defined as a SARS-CoV-2 WGS test result (performed at a state, university, or contracted commercial laboratory††) from a new NAAT-positive specimen, collected during October 2021–January 2022 and <90 days after a first positive specimen from a previous WGS-confirmed SARS-CoV-2 infection, that demonstrated a different lineage from the first infection. Vermont Department of Health case investigators noted an increase in suspected early reinfections; five of these cases were confirmed through Vermont’s passive WGS surveillance system, which sequences the highest percentage (15.8%) of total state cases nationwide.§§ Wisconsin Department of Health Services was notified by university researchers of suspected early reinfections in members of a household enrolled in a longitudinal respiratory disease surveillance study.¶¶ Public Health – Seattle & King County was notified after Washington testing guidance for K–12 schools led to identification of a suspected early reinfection in a student at a school sporting event. Rhode Island screening protocols for hospitals and long-term care facilities led to collection of two NAAT-positive specimens within 90 days from a long-term care facility resident.
Ten patients with early reinfections were identified (Table). WGS identified Delta variant in all specimens from first infections and Omicron in all reinfection specimens.*** Median age at first infection was 11 years. Eight patients were aged <18 years, one was a long-term care facility resident, and one was a health care worker†††; five were male. Intervals between initial and subsequent specimen collections ranged from 23 to 87 days (median = 54.5 days). Patient E had completed a 2-dose mRNA COVID-19 vaccination series 6–10 weeks before the first infection; patients A and B each had received a single dose of mRNA COVID-19 vaccine between infections. The seven remaining patients were unvaccinated. In Wisconsin, household transmission during patient G’s reinfection likely resulted in reinfections of patients F and H.§§§,¶¶¶ Nine patients were symptomatic during first infection (median duration = 9 days; range = 0–20 days).**** Among eight patients with available clinical data during reinfection, six were symptomatic during reinfection (median duration = 5 days; range = 0–10 days).
Expansion of SARS-CoV-2 WGS, through public health surveillance and longitudinal research,†††† might enable rapid identification of reinfections with distinct lineages and detection of novel variants. Current CDC guidance for identifying early reinfections requires demonstration of different lineages by genetic sequencing.§§§§ Limited capacity for strain testing, including WGS, diminishes opportunities for first and reinfection NAAT specimens from the same person to undergo additional testing.¶¶¶¶ Moreover, antigen tests are increasingly performed at home, resulting in specimens being unavailable for strain testing. Thus, most early reinfections are likely not identified.
The findings from this case series might not be generalizable to the U.S. population and are specific to the transition period between Delta and Omicron variant predominance. Nonetheless, this study highlights potential limits of infection-induced immunity against novel variants.
One patient in this case series had received a full primary COVID-19 vaccine series but was not yet eligible for a booster. No other eligible patient was up to date on recommended COVID-19 vaccinations,***** which provides additional protection, even among those with previous infection (2,5). These patients might have had increased risk for SARS-CoV-2 infection because of low vaccination rates††††† and high rates of close contact§§§§§ in school-aged cohorts, and higher frequency and intensity of exposures in health care and congregate settings. Although the epidemiology of COVID-19 might change as new variants emerge, vaccination remains the safest strategy for preventing future SARS-CoV-2 infections (2,5).
Vermont case investigation and contact tracing team; Broad Institute of MIT and Harvard; Public Health – Seattle & King County COVID-19 contact tracing and case investigation team; students and families in the ORCHARDS study; Kristin Carpenter-Azevedo.
Corresponding author: Brian Borah, email@example.com.
1Epidemic Intelligence Service, CDC; 2Public Health – Seattle & King County, Seattle, Washington; 3Vermont Department of Health; 4Wisconsin Department of Health Services; 5Rhode Island Department of Health; 6Career Epidemiology Field Officer Training Program, CDC; 7University of Wisconsin, Madison, Wisconsin; 8National Center for Emerging and Zoonotic Infectious Diseases, CDC; 9Wisconsin State Laboratory of Hygiene, Madison, Wisconsin; 10Washington State Department of Health; 11CDC COVID-19 Emergency Response Team.
All authors have completed and submitted the International Committee of Medical Journal Editors form for disclosure of potential conflicts of interest. Lynn Zanardi Blevins reports ownership of Pfizer stock. Allison G. Lafferty reports ownership of Arena Pharmaceuticals stock. Jonathan L. Temte reports institutional support from Quidel Corporation receipt of payment or honoraria from Elsevier Publishing as member of the Advisory Board of Primary Care PracticeUpdate. No other potential conflicts of interest were disclosed.
* These authors contributed equally to this report.
** Inclusion of Wisconsin case data was approved by University of Wisconsin-Madison, Minimal Risk Research Institutional Review Board; 45 C.F.R. part 46; 21 C.F.R. part 56. Remaining activity was determined not to be research; 45 C.F.R. part 46, 21 C.F.R. part 56; 42 U.S.C. Sect. 241(d); 5 U.S.C. Sect. 552a; 44 U.S.C. Sect. 3501 et seq.
†† Despite potential differences in established WGS protocols among laboratories, all lineage and sublineage determinations, which are based upon universally accepted genetic sequence markers, are comparable among laboratories.
§§ In the 90 days preceding April 4, 2022, the percentage of state cases sequenced and shared with GISAID ranged from 0.45% (Oklahoma) to 15.83% (Vermont). https://www.gisaid.org/submission-tracker-usaexternal icon
*** Multiple Delta variant sublineages (AY.3, AY.4, AY.25, AY.33, AY.44, AY.47, and AY.100) and two Omicron variant sublineages (BA.1 and BA1.1) were identified.
††† Patient E was a non-Vermont resident who was living and working as a health care worker (caring for COVID-19 patients) in Vermont during both infections.
§§§ The index member in this household cluster of persons with early reinfections with SARS-CoV-2 was patient G, who began to experience respiratory illness symptoms on January 3, 2022, and was the only person to receive a positive SARS-CoV-2 test result the next day when specimens were collected from all household members. On January 8, patient F began to experience respiratory illness symptoms and was the only person to receive a positive SARS-CoV-2 test result when specimens from remaining household members (including patient G) were tested on January 11. On January 15, patient H began to experience symptoms of respiratory illness and was the only person to receive a positive SARS-CoV-2 test result when specimens from remaining household members (including patients F and G) were tested on January 18.
¶¶¶ Household secondary transmission during patient B’s early reinfection likely also resulted in an early reinfection in a parent, but WGS data from this parent’s reinfection were not available for confirmation. This parent is not included in this case series.
**** Calculation of median duration of symptoms during first infection does not include patient D because information on the full duration of this patient’s symptoms was unavailable.
†††† The Seattle Flu Study, like the Oregon Child Absentee due to Respiratory Disease Study (ORCHARDS), is a community-based, longitudinal surveillance study of influenza and viral respiratory diseases. Seattle Flu Study researchers were instrumental in the first identification of COVID-19 in the Seattle area. http://www.seattleflu.org/external icon
¶¶¶¶ Although S-gene target failure, which detects a deletion in the gene that encodes for the SARS-CoV-2 spike protein, is a commonly used screening method for the Omicron variant, this deletion is not unique to this variant and is not present in all Omicron variant sublineages. Other strain testing methods only target a portion of a strain’s genome. In contrast, WGS analyzes a strain’s entire genome and is therefore the preferred method for lineage confirmation.
- Danza P, Koo TH, Haddix M, et al. SARS-CoV-2 infection and hospitalization among adults aged ≥18 years, by vaccination status, before and during SARS-CoV-2 B.1.1.529 (Omicron) variant predominance—Los Angeles County, California, November 7, 2021–January 9, 2022. MMWR Morb Mortal Wkly Rep 2022;71:177–81. https://doi.org/10.15585/mmwr.mm7105e1external icon PMID:35113851external icon
- León TM, Dorabawila V, Nelson L, et al. COVID-19 cases and hospitalizations by COVID-19 vaccination status and previous COVID-19 diagnosis—California and New York, May–November 2021. MMWR Morb Mortal Wkly Rep 2022;71:125–31. https://doi.org/10.15585/mmwr.mm7104e1external icon PMID:35085222external icon
- Altarawneh HN, Chemaitelly H, Hasan MR, et al. Protection against the Omicron variant from previous SARS-CoV-2 infection. N Engl J Med 2022;386:1288–90. https://doi.org/10.1056/NEJMc2200133external icon PMID:35139269external icon
- Wang J, Kaperak C, Sato T, Sakuraba A. COVID-19 reinfection: a rapid systematic review of case reports and case series. J Investig Med 2021;69:1253–5. https://doi.org/10.1136/jim-2021-001853external icon PMID:34006572external icon
- Cavanaugh AM, Spicer KB, Thoroughman D, Glick C, Winter K. Reduced risk of reinfection with SARS-CoV-2 after COVID-19 vaccination—Kentucky, May–June 2021. MMWR Morb Mortal Wkly Rep 2021;70:1081–3. https://doi.org/10.15585/mmwr.mm7032e1external icon PMID:34383732external icon
Suggested citation for this article: Roskosky M, Borah BF, DeJonge PM, et al. Notes from the Field: SARS-CoV-2 Omicron Variant Infection in 10 Persons Within 90 Days of Previous SARS-CoV-2 Delta Variant Infection — Four States, October 2021–January 2022. MMWR Morb Mortal Wkly Rep 2022;71:524–526. DOI: http://dx.doi.org/10.15585/mmwr.mm7114a2external icon.
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