Abstract
Background.
Sequencing of the SARS-CoV-2 viral genome from patient samples is an important epidemiological tool for monitoring and responding to the pandemic, including the emergence of new mutations in specific communities.
Methods.
SARS-CoV-2 genomic sequences were generated from positive samples collected, along with epidemiological metadata, at a walk-up, rapid testing site in the Mission District of San Francisco, California during November 22-December 2, 2020 and January 10-29, 2021. Secondary household attack rates and mean sample viral load were estimated and compared across observed variants.
Results.
A total of 12,124 tests were performed yielding 1,099 positives. From these, 811 high quality genomes were generated. Certain viral lineages bearing spike mutations, defined in part by L452R, S13I, and W152C, comprised 54.9% of the total sequences from January, compared to 15.7% in November. Household contacts exposed to “West Coast” variants were at higher risk of infection compared to household contacts exposed to lineages lacking these variants (0.357 vs 0.294, RR=1.29; 95% CI:1.01-1.64). The reproductive number was estimated to be modestly higher than other lineages spreading in California during the second half of 2020. Viral loads were similar among persons infected with West Coast versus non-West Coast strains, as was the proportion of individuals with symptoms (60.9% vs 64.1%).
Conclusions.
The increase in prevalence, relative household attack rates, and reproductive number are consistent with a modest transmissibility increase of the West Coast variants; however, additional laboratory and epidemiological studies are required to better understand differences between these variants.
Keywords: SARS-CoV-2, variant, spike mutation, secondary attack rates, household transmission
Summary:
We observed a growing prevalence and elevated attack rate for “West Coast” SARS-CoV-2 variants in a community testing setting in San Francisco during January 2021, suggesting its modestly higher transmissibility.
INTRODUCTION
Genomic surveillance during the SARS-CoV-2 pandemic is a critical source of situational intelligence for epidemiological control measures, including outbreak investigations and detection of emergent variants. Countries with robust, unified public health systems and systematic genomic surveillance have been able to rapidly detect SARS-CoV-2 variants with increased transmission characteristics, and mutations that potentially subvert both naturally acquired or vaccination-based immunity (e.g. COVID-19 Genomics UK Consortium). Examples include the rapidly spreading B.1.1.7 lineage documented in the UK and the B.1.351 lineage described from South Africa. The P.1/P.2 lineages originally discovered in Brazil harbor the E484K mutation within the spike protein which, along with other mutations, is associated with reduced neutralization in laboratory experiments[1-4].
In the US, genomic surveillance is sparse relative to the number of confirmed cases (27.8 million as of Feb 20, 2021), with 123,672 genomes deposited in the GISAID database, representing only 0.4% of the total reported cases. Despite the lower rates of overall US genomic surveillance, independent local programs and efforts have contributed to our understanding of variant emergence and spread[5]. The appearance of new nonsynonymous mutations highlight the utility of this approach in the US[6].
Genomic sequencing of SARS-CoV-2 in California has predominantly been conducted by academic researchers and non-profit biomedical research institutions (for example, the Chan Zuckerberg Biohub and Andersen Lab at the Scripps Research Institute) in conjunction with state and local public health partners. These efforts identified an apparent increase in the prevalence of lineages B.1.427 and B.1.429 (“West Coast” variant), which share S gene nonsynonymous mutations at sites 13, 152, 452, and 614, during December 2020 to February 2021 when California was experiencing the largest peak of cases observed during the pandemic. While the cluster of mutations was first observed in a sample from May 2020, these variants rose from representing <1% of the consensus genomes recovered from California samples collected in October 2020 (5/546; 0.91%) to over 50% of those collected during January, 2021 (2,309/4,305; 53.6%; GISAID accessed February 20, 2021).
The majority of efforts in the US utilize samples sent for clinical analysis from symptomatic individuals or outbreaks, introducing selection bias making interpretation of trends, such as the rise in lineage prevalence. Clinical remnant samples are most often delinked from case information, thus eliminating the possibility of evaluating genotypes with detailed geospatial information, household information, and other metadata useful for investigation of transmission dynamics.
Sequencing cases identified during intensive, longitudinal community-based testing may help address both limitations. Here, we describe an investigation of the prevalence of the West Coast variants as well as other variants among persons tested at a community testing site situated in the Mission District neighborhood, San Francisco with high COVID-19 incidence during two periods: November 22-December 2, 2020 and January 10-29, 2021. Using metadata collected at the testing site and Supplementary household testing, we estimated secondary household attack rate with respect to viral genotype to evaluate relative transmissibility of identified variants.
METHODS
Study setting and population
From January 10-29, 2021, BinaxNOW™ rapid antigen tests were performed at the 24th & Mission BART (public transit) station in the Mission District of San Francisco, a setting of ongoing community transmission, predominantly among Latinx persons[7]. Tests for SARS-CoV-2 were performed free of charge on a walk-up, no-appointment basis, including persons ≥ 1 year of age, regardless of symptoms through Unidos en Salud, an academic, community (Latino Task Force) and city partnership. Certified lab assistants collected 2 bilateral anterior nasal swabs. The first was tested with BinaxNOW™, immediately followed by a separate bilateral swab for SARS-CoV-2 genomic sequencing[8,9]. Results were reported to participants within 2 hours, and all persons in a household corresponding to a positive BinaxNOW case were offered same-day BinaxNOW testing. All persons testing BinaxNOW positive were offered participation in longitudinal Community Wellness Team support program[10,11].
SARS-CoV-2 genomic sequence recovery and consensus genome generation
SARS-CoV-2 genomes were recovered using ARTIC Network V3 primers[12] and sequenced on an Illumina NovaSeq platform. Consensus genomes generated from the resulting raw .fastq files using IDseq [13] were used for subsequent analysis. Full details are included in Supplementary Methods.
Household attack rate analyses
Households (n=327) meeting the following inclusion criteria were eligible for secondary attack rate analyses: 1) ≥1 adult (aged ≥18 years) with a positive BinaxNOW result; 2) ≥1 case in household sequenced; and, 3) ≥2 persons tested with BinaxNOW during the study period. Households in which sequences represented both West Coast and non-West Coast variants were excluded (n=9). The index was defined as the first adult to test positive. Crude household attack rates, stratified by variant classification, were calculated as i) the proportion of positive BinaxNOW results among tested household contacts; and, ii) as the mean of household-specific secondary attack rate, with 95% CI based on cluster-level bootstrap. Generalized estimating equations were used to fit Poisson regressions, with cluster-robust standard errors and an exchangeable working covariance matrix. Because symptoms and disease severity may be affected by strain, these factors were not included in the a priori adjustment set. We evaluated for overdispersion[14], and conducted sensitivity analyses using targeted maximum likelihood estimation (TMLE) combined with Super Learning to relax parametric model assumptions; influence curve-based standard error estimates used household as the unit of independence[15].
Bayesian Phylogenetic Analysis
We compared the growth rates of B.1.427 and B.1.429 PANGO lineages against two other lineages, B.1.232 and B.1.243 that had been circulating in California during the latter half of 2020. To do this, we built a Bayesian phylogeny for each lineage in BEAST v.1.10.4 and estimated the effective population size over time using the Bayesian SkyGrid model. We fit an exponential model to the median SkyGrid curve and inferred the reproductive numbers based on the exponential growth rates and generation time estimates from literature. Full analysis details are included in Supplementary Methods.
Ethics statement
The UCSF Committee on Human Research determined that the study met criteria for public health surveillance. All participants provided informed consent for dual testing.
RESULTS
Low-Barrier SARS-CoV-2 Testing and Sequencing
From January 10-29, 8,822 rapid direct antigen tests were performed on 7,696 unique individuals, representing 5,239 households (Supplementary Table 1). Test subjects originated from addresses in 8 Bay Area counties, indicating a wide catchment area (Figure 1). During this time period, there were 885 (10.0%) samples from 863 unique persons that were BinaxNOW positive for SARS-CoV-2 infection. From this set, a total of 165 samples were sequenced for the S gene only, of which 96 had S gene coverage over 92%. In addition, full SARS-CoV-2 genome sequencing was attempted on a total of 674 samples, of which 620 samples resulted in a genome coverage over 92% (Supplementary Table 2, sequences deposited in GISAID). These 716 samples, together with an additional 191 SARS-CoV-2 genome sequences generated from the same testing site during the period of November 22-December 2, 2020[16], had adequate coverage of the full genome or spike protein for further analysis based on S gene sequence (Supplementary Table 3). Classification as either a West Coast variant or a non-West Coast variant was determined for 830 of all samples sequenced.
Figure 1. Testing catchment area.
The location of the 24th & Mission testing site is denoted by the yellow symbol. Negative tests are in grey, and positive tests are shown in red. Household locations shown have a random offset of up to 750 meters. The testing catchment area is concentrated within San Francisco County (A), but substantial numbers of individuals reside in the surrounding 8 Bay Area Counties (B). Map tiles by Stamen Design and data by OpenStreetMap.
Similar to our previous observations in San Francisco[17], full length sequences were distributed among the major clades (Supplementary Figure 1). Notably, mutations at spike position 501 were not observed, and thus no instances of the B.1.1.7 strain or any other strain bearing the N501Y mutation were detected in any sample during this period. A single individual was found to have been infected with the P.2 strain, which carries the spike E484K mutation and was described in Brazil from a re-infection case[4]. This mutation has been associated with decreased neutralization in numerous laboratory experiments[1,3].
We observed SARS-CoV-2 genome sequences that belonged to PANGO lineages B.1.427 and B.1.429, both of which share a trio of recent mutations in the spike protein (S13I, W152C, and L452R) (Figure 2). These lineages are separated by differing mutations ORF1a and ORF1b, including ORF1b:P976L and ORF1a:I4205V, respectively. Sequencing of 191 viral genomes from November 22 – December 2, 2020 revealed that sequences carrying this trio of mutations represented only 15.7% of the total. A trend of increasing frequency was observed on a daily basis during the January testing period (Figure 2A), and the frequency of these lineages were observed to have increased to 54.9% of the total, representing an increase of more than 3-fold in approximately 1.5 months (Figure 2B,C). As noted, this increase in frequency is consistent with an expansion of viruses more broadly in California carrying these same mutations[18].
Figure 2. Variants observed at 24th & Mission.
(A) The proportion of daily cases belonging to West Coast and non-West Coast variants, and (B) the total number of samples per day. (C,D) Area maps [25] showing the relative proportion of PANGO lineages acquired from full length genomes from the November (N=191) and January (N=671) time periods respectively. (E) Genome maps for variants detected in this study. Dominant mutations (filled black circles), and non-synonymous mutations detected at lower frequency in combination with existing lineages (filled grey circles) are shown in grey.
Additional non-synonymous mutations were observed throughout the genome, including 100 unique non-synonymous mutations in the spike gene, of which several are within functionally-significant regions of the protein (Figure 2C, Supplementary Table 3). Eleven unique mutations were observed in the receptor binding domain, most of which have yet to be investigated for possible effects on ACE2 binding, transmissibility, or antibody neutralization. Additionally, seven unique mutations were found adjacent to the polybasic furin cleavage site at the S1/S2 junction, which is reported to have a potential role in determination of virulence and host cell tropism[19-22]. Moderately prevalent mutations were observed at spike position 681 (P681H, n=29 and P681R, n=1), which is within the furin recognition site, and at spike position 677, where two different amino acid substitutions were observed in this cohort (Q677H, n=21 and Q677P, n=10). Multiple mutations at both of these sites have been observed across a wide geographical range with previous reports noting the likelihood of positive selection accounting for convergent evolution[6].
Disease Severity
The SARS-CoV-2 RT-PCR cycle thresholds (Ct) for nasal swab samples from which whole genomes corresponding to the West Coast variant were recovered were compared to parallel non-West Coast variant samples. Mean Ct values did not differ significantly between persons infected with West Coast (mean Ct 23.62; IQR 6.6) versus non-West Coast (mean Ct 23.67; IQR 8.0) strains (95% CI: −0.63-0.83, p-value = 0.79) (Supplementary Figure 2, Supplementary Table 2). The proportion of individuals with symptoms was similar among persons infected with West Coast (272/447, 60.9%) versus non-West Coast (248/387, 64.1%) strains. Among 347 sequenced cases with longitudinal follow up by the Community Wellness Team, 4 (1.2%) were hospitalized (3/184, and 1/175, for West Coast and non-West Coast, respectively).
Household Secondary Attack Rate
A total of 327 households met inclusion criteria for evaluation of secondary attack rate; of these, 9 households had individuals with mixed strains, and thus were excluded from analyses. Among the remaining 318 households, characteristics including race/ethnicity, ages of other household members, household size, density, and location were similar, regardless of whether the members were positive for West Coast or non-West Coast variants. (Table 1, Supplementary Table 4).
Table 1:
Characteristics of households included in the household attack rate analysis, stratified by strain.
| Non-West Coast (N=156) |
West coast | Total (N=318) |
|||
|---|---|---|---|---|---|
| B.1.427 (N=78) |
B.1.429 (N=60) |
All West coast (N=162)+ |
|||
| Race/Ethnicity (most common in household) | |||||
| Hispanic/Latinx | 143 (91.7%) | 68 (87.2%) | 58 (96.7%) | 145 (89.5%) | 288 (90.6%) |
| Asian | 5 (3.2%) | 4 (5.1%) | 1 (1.7%) | 8 (4.9%) | 13 (4.1%) |
| White/Caucasian | 4 (2.6%) | 2 (2.6%) | 0 (0%) | 3 (1.9%) | 7 (2.2%) |
| Black or African American | 2 (1.3%) | 2 (2.6%) | 1 (1.7%) | 4 (2.5%) | 6 (1.9%) |
| Other | 2 (1.3%) | 2 (2.6%) | 0 (0%) | 2 (1.2%) | 4 (1.3%) |
| Has Children | |||||
| Does not have children | 105 (67.3%) | 62 (79.5%) | 32 (53.3%) | 109 (67.3%) | 214 (67.3%) |
| Has children | 51 (32.7%) | 16 (20.5%) | 28 (46.7%) | 53 (32.7%) | 104 (32.7%) |
| Location | |||||
| San Francisco | 118 (75.6%) | 64 (82.1%) | 36 (60.0%) | 114 (70.4%) | 232 (73.0%) |
| Outside San Francisco | 38 (24.4%) | 14 (17.9%) | 24 (40.0%) | 48 (29.6%) | 86 (27.0%) |
| Household Size | |||||
| 2 persons | 13 (8.3%) | 9 (11.5%) | 4 (6.7%) | 20 (12.3%) | 33 (10.4%) |
| 3-4 persons | 64 (41.0%) | 28 (35.9%) | 20 (33.3%) | 56 (34.6%) | 120 (37.7%) |
| 5+ persons | 79 (50.6%) | 41 (52.6%) | 36 (60.0%) | 86 (53.1%) | 165 (51.9%) |
| Household Density* | |||||
| Mean (SD) | 1.86 (0.858) | 1.92 (0.911) | 2.28 (1.21) | 2.04 (1.04) | 1.95 (0.956) |
| Median [Min, Max] | 1.88 [0.250, 7.00] | 1.63 [0.444, 5.00] | 2.00 [0.857, 6.00] | 1.71 [0.444, 6.00] | 1.75 [0.250, 7.00] |
22 households with S gene only sequence available.
Household density missing for 17 households.
The 318 index cases had a total of 1,241 non-index household members; of these, 866 (69.8%) had a BinaxNOW test result available (451/655 [68.9%] for West Coast variant households; 415/586 [70.8%] of non-West Coast variant households). A total of 35.7% (161/451) of household contacts exposed to the West Coast variant tested BinaxNOW positive (33.0%, 68/206 for B1.427; 41.4%, 77/186 for B.1.429), while 29.4% (122/415) of contacts exposed to non-West Coast variant tested positive (Table 2). Secondary cases were identified a median of 1 day after index cases (IQR 0-4).
Table 2:
Secondary household attack rates for West Coast variants, combined and disaggregated by B.1.427 and B.1.429. Relative risks estimated based on Poisson regression using generalized estimating equations and cluster-robust standard errors. Adjustment variables included age group, latinx/hispanic race, household size, and household density.
| Unadjusted | Adjusted | |||||
|---|---|---|---|---|---|---|
| Positives Among Tested Contacts (%) |
Mean Household Attack Rate (95% CI) |
RR (95%CI) | p-value | aRR | p-value | |
| Class | ||||||
| Non-West Coast | 122/415 (29.4%) | 25.6% (20.3-31) | - | - | - | - |
| West Coast | 161/451 (35.7%) | 36.1% (30.3-42.2) | 1.29 (1.01-1.64) | 0.044 | 1.25 (0.98-1.60) | 0.068 |
| Lineage | ||||||
| B.1.427 | 68/206 (33%) | 31.7% (23.6-40.1) | 1.18 (0.87-1.59) | 0.3 | 1.22 (0.90-1.64) | 0.2 |
| B.1.429 | 77/186 (41.4%) | 42.2% (32.7-52.1) | 1.48 (1.11-1.98) | 0.008 | 1.39 (1.03-1.87) | 0.030 |
Based on unadjusted Poisson regression with cluster-robust standard errors, household contacts exposed to the West Coast variant had an estimated 29% higher risk of secondary infection, compared to household contacts exposed to a non-West Coast variant (RR: 1.29, 95% CI: 1.01-1.64, p-value = 0.044). When exposure to West Coast variants was disaggregated by B.1.427 and B.1.429, corresponding risks of secondary infections relative to exposure to non-West Coast variants were 1.18 (95% CI: 0.87-1.59, p-value = 0.3) and 1.48 (95% CI: 1.11-1.98, p-value = 0.008), respectively. Dispersion ratios were greater than 0.9 in all regression analyses. Estimated relative risks of infection after household exposure to West Coast versus non-West Coast variants were similar after adjustment for household and individual-level characteristics of secondary contacts (aRR: 1.25, 95% CI: 0.98-1.60, p-value: 0.068 for West Coast vs non-West Coast variants; aRR: 1.22, 95%CI: 0.90-1.64, p-value = 0.2 and aRR: 1.39, 95%CI: 1.03-1.87, p-value = 0.030 for B.1.427 and B.1.429, respectively.) Relative attack rates were generally similar when stratified by household characteristics and by the characteristics of secondary contacts (Table 3); secondary attack rates among children aged <12 years were 51.9% (41/79) and 39.7% (31/78) when exposed to West Coast and non-West Coast strains, respectively. Sensitivity analyses in which parametric assumptions were relaxed using TMLE and Super Learning yielded similar estimates (Supplementary Table 5).
Table 3:
Secondary attack rate disaggregated by covariates; mean household secondary attack rate only reported disaggregated by household level characteristics.
| Non-West Coast Strain | West Coast Strain | |||
|---|---|---|---|---|
| Positives Among Tested Contacts (%) |
Mean Household Attack Rate (95% CI) |
Positives Among Tested Contacts (%) |
Mean Household Attack Rate (95% CI) |
|
| Location | ||||
| San Francisco | 88/321 (27.4%) | 22.9% (17.2-28.8) | 113/315 (35.9%) | 37.8% (30.6-45.1) |
| Outside of San Francisco | 34/94 (36.2%) | 34% (22.1-46.2) | 48/136 (35.3%) | 32.1% (22.2-42.1) |
| Age Group | ||||
| Age ≤ 12 | 31/78 (39.7%) | - | 41/79 (51.9%) | - |
| Age > 12 | 91/337 (27%) | - | 120/372 (32.3%) | - |
| Race/Ethnicity | ||||
| Latinx/Hispanic | 107/372 (28.8%) | - | 136/378 (36%) | - |
| Not Latinx/Hispanic | 15/43 (34.9%) | - | 25/73 (34.2%) | - |
| Household Size | ||||
| 2 persons | 1/13 (7.7%) | 7.7% (0-23.1) | 12/20 (60%) | 60% (40-80) |
| 3-4 persons | 30/116 (25.9%) | 26% (17.4-35.4) | 35/101 (34.7%) | 33.9% (24.1-44.3) |
| 5+ persons | 91/286 (31.8%) | 28.1% (21.1-35.4) | 114/330 (34.5%) | 32% (25.1-39.2) |
| Household Density | ||||
| Bottom half | 43/160 (26.9%) | 23.4% (15.4-31.6) | 52/175 (29.7%) | 33.4% (24.3-42.9) |
| Top half | 76/242 (31.4%) | 27.7% (20.5-35.3) | 101/262 (38.5%) | 35.7% (27.9-43.6) |
Estimation of Reproductive Number
Using Bayesian phylogenetic analysis, we estimated the reproductive number to be 1.27 (95% CI: 1.10-1.46) for B.1.427 and 1.18 (95% CI: 1.05-1.32) for B.1.429 during the second half of 2020. These values were slightly higher than two other lineages spreading in California during the same time period: 1.12 (95% CI: 1.10-1.14) for B.1.232, and 1.02 (95% CI: 0.98-1.05) for B.1.243. As the reproductive numbers are very similar and were calculated from the median SkyGrid estimates, we cannot conclude any statistically significant differences between the lineages.
DISCUSSION
We monitored SARS-CoV-2 viral variants by genomic sequencing and integration of metadata from households at a community based “test-and-respond” program. We found that the West Coast variants (PANGO lineages B.1.427 and B.1.429) increased in prevalence relative to wild type from November to January in the San Francisco Bay Area among persons tested in the same community-based location. These data extend and confirm prior observations from convenience, outbreak, and clinical samples reporting apparent increases in relative prevalence of the West Coast variants[18].
Household secondary attack rates of the West Coast variants were modestly higher than for non-West Coast variants, suggesting the potential for increased transmissibility. The West Coast variants compromise two closely related lineages (B.1.427 and B.1.429) that share identical sets of mutations in the spike protein, but differ by additional synonymous and non-synonymous mutations in other genes, including ORF1a and ORF1b. While the frequency of both lineages increased in this study and in California more widely[18], and the estimated increase in risk of secondary household infection relative to non-West Coast variants was fairly consistent across lineages, the point estimate was somewhat higher for B.1.429. Although moderate compared to increased transmissibility of some other previously identified variants, even small increases in transmissibility could contribute to a substantial increase in cases, particularly in the context of reproductive numbers just below one. While this finding may be due to chance, future work, should continue to monitor individual lineages.
The household attack rate observed here was higher than that reported in a recent global meta analysis[23], even for the non-West Coast variants. It was similar to, or lower than attack rates reported in other US settings. Prior US reports, however, were based on substantially smaller sample sizes.
Our findings that the West Coast variants increased in relative prevalence and had higher household secondary attack rates potentially suggest higher transmissibility. However, the West Coast variant has been detected in multiple locations, and has been detected since May 2020 in California without relative expansion until the peak associated with the holiday season of November-January. Using Bayesian phylogenetic analysis, the estimated reproductive number for both West Coast lineages was found to be modestly higher than other circulating lineages. However, further studies are required to evaluate the contribution of specific mutations.
We found no significant differences in viral load (using Ct) between West Coast and non-West Coast variants (Supplementary Figure 2), and recorded hospitalizations (n=5/388) remained rare, despite the West Coast variant representing 54.9% of positive cases. This highlights the importance of studying walk-up populations, whether they are symptomatic or asymptomatic, as hospitalized populations often are confounded by co-morbidities and subject to selection bias.
At the time of this sampling, no instances of B.1.1.7, or independent N501Y mutations were detected in our sample population of 830, despite sporadic observations elsewhere in CA (approximately 3% [69/2423] of genomes reported in California during the January study period; accessed from GISAID Feb 24, 2021). This suggests that introductions of B.1.1.7 to the sample population may not yet have occurred or have been rare[24]. A single case of the P.2 variant, which carries the E484K mutation[1], was detected in this study. Surprisingly, this case did not have a travel history, highlighting the risk of cryptic transmission.
In addition to the mutations associated with spike L452R in the West Coast variants, we observed, at lower frequencies, other mutations of interest, including those in spike at positions 677, and 681, both of which have been reported previously on their own, or in the case of 681, in the context of other mutations such as N501Y[6].
This study has several limitations. First, testing was conducted at a walk-up testing site, and thus these are inherently convenience samples; however, this would not be expected to impose a differential selection bias for those with or without any particular variant. Second, clear classification of the index case was not always possible, particularly when multiple adults from a household tested positive on the same date; further, secondary household attack rate calculations do not account for potential external sources of infection other than the index case. However, the relative risk of secondary infection from household exposure to West Coast versus non-West Coast variants was similar among children, a group less likely to have been misclassified as non-index or to be exposed to external infection. Third, household testing coverage was incomplete; this might contribute to an over (or under) estimate of secondary attack rate, and while we again have no reason to suspect differential ascertainment by strain, this could bias estimates of relative risk.
The occurrence of variants in SARS-CoV-2 was always expected; however, it is often difficult to understand the importance of any given single or co-occurring mutations. While further epidemiological and laboratory experiments will be required to fully understand the community impact and mechanistic underpinnings of each variant, it is clear that enhanced genomic surveillance, paired with community engagement, testing, and response capacity is an important tool in the arsenal against this pandemic.
Supplementary Material
Supplementary Figure 1: Nextclade Phylogeny. Radial tree phylogeny as visualized via Nextclade [26] using full length genomes (n=614) from the Jan 10th - 29th sampling period and the San Francisco public reference tree (downloaded Feb 17, 2021). For the purpose of visualization, six genomes were removed due to excessive private mutations. Colored nodes correspond to specific mutations as indicated in the figure legend.
Supplementary Figure 2: Viral load by Ct value. No significant differences in mean viral load as measured by RT-qPCR Cts was measured between West Coast and non-West Coast variants in (A) the subset of samples that had only spike gene sequenced (95% CI: −1.97-1.29, p-value = 0.68), (B) the subset of samples that had undergone whole genome sequencing thus allowing for determination of West Coast variant PANGO lineage of either B.1.427 (95% CI: −1.84-0.25, p-value = 0.18) or B.1.429 (95% CI: −0.49-1.76, p-value = 0.38), (C) all samples sequenced in this study (95% CI: −0.63-0.83, p-value = 0.79).
ACKNOWLEDGMENTS
We would like to thank the hundreds of academic labs and public health institutions that have been sequencing and publicly depositing genomic sequences, analysis tools, and epidemiological data throughout the pandemic. We thank Bevan Dufty and the BART team, Jeff Tumlin and the San Francisco MUNI, Supervisor Hillary Ronen, Mayor London Breed, Dr. Grant Colfax and the Department of Public Health, Salu Ribeiro and Bay Area Phlebotomy and Laboratory services, PrimaryBio COVID testing platform, and our community ambassadors and volunteers. We would like to thank the Chan Zuckerberg Initiative, Greg and Lisa Wendt, Anne-Marie and Wylie Peterson, Gwendolyn Holcombe, Kevin and Julia Hartz, and Carl Kawaja for their critical support and input. We also thank Jack Kamm, Peter Kim, Don Ganem, Sandy Schmidt, Cori Bargmann, Norma Neff, and Christopher Hoover for technical assistance and discussion.
FUNDING
This work was supported by the UCSF COVID Fund [to JD, DH, JL, and ML], the National Institutes of Health [UM1AI069496 to JD and F31AI150007 to SS], the Chan Zuckerberg Biohub [to JD and DH], the Chan Zuckerberg Initiative [to JD and DH], and a group of private donors. The BinaxNOW cards were provided by the California Department of Public Health.
Footnotes
POTENTIAL CONFLICTS
Dr. DeRisi is a member of the scientific advisory board of The Public Health Company, Inc., and is a scientific advisor for Allen & Co. Dr. Havlir reports non-financial support from Abbott, outside the submitted work. None of other authors has any potential conflicts.
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Associated Data
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Supplementary Materials
Supplementary Figure 1: Nextclade Phylogeny. Radial tree phylogeny as visualized via Nextclade [26] using full length genomes (n=614) from the Jan 10th - 29th sampling period and the San Francisco public reference tree (downloaded Feb 17, 2021). For the purpose of visualization, six genomes were removed due to excessive private mutations. Colored nodes correspond to specific mutations as indicated in the figure legend.
Supplementary Figure 2: Viral load by Ct value. No significant differences in mean viral load as measured by RT-qPCR Cts was measured between West Coast and non-West Coast variants in (A) the subset of samples that had only spike gene sequenced (95% CI: −1.97-1.29, p-value = 0.68), (B) the subset of samples that had undergone whole genome sequencing thus allowing for determination of West Coast variant PANGO lineage of either B.1.427 (95% CI: −1.84-0.25, p-value = 0.18) or B.1.429 (95% CI: −0.49-1.76, p-value = 0.38), (C) all samples sequenced in this study (95% CI: −0.63-0.83, p-value = 0.79).