key: cord-0842325-1e5zp4bg
authors: Singh, Amit K.; Stellrecht, Kathleen A.; Arunachalam, Thilaka; Barman, Tarani K.; Robek, Michael D.; Waxman, Michael J.; Elmendorf, Sarah L.; Metzger, Dennis W.
title: Lack of active SARS-CoV-2 virus in a subset of PCR-positive COVID-19 congregate care patients
date: 2021-06-04
journal: J Clin Virol
DOI: 10.1016/j.jcv.2021.104879
sha: f854eba3335fcfd1921e6a1d82647bce13868bc3
doc_id: 842325
cord_uid: 1e5zp4bg

Highly sensitive nucleic acid amplification tests (NAATs) designed to detect SARS-CoV-2 RNA are the standard of care for the diagnosis of COVID-19. However, the accuracy of these methods for the quantitation of active virus rather than non-infectious RNA fragments that can persist for extended periods of time has been unclear. This issue is particularly relevant for congregate care patients who are unable to return to their home residence until fully negative by NAATs. We tested paired samples from individual patients for the presence of virus at both early and later stages of disease. Culture of nasopharyngeal swab samples for 10 days in Vero E6 cells revealed active virus in only 4 out of 14 (28.6%) patients. The ability to isolate viral plaque-forming units (PFU) correlated with viral RNA loads of >6.79 log genomic copies/ml and only occurred in samples collected from patients early after symptom onset and before development of antibody. Culture in Vero E6 cells lacking the STAT1-dependent interferon signaling pathway increased the numbers of viral PFU detected but did not affect the incidence of positive cultures. We conclude that culturable virus is correlated with SARS-CoV-2 NAATs detection only during early symptom onset and with high viral titers/low antibody titers in non-immunosuppressed patients.

The ongoing global COVID-19 pandemic continues to profoundly affect individuals and communities, often overwhelming US health care institutions. (1) . One particularly pressing challenge for health care institutions is to effectively isolate infected patients to minimize transmission within the hospital and the community (2, 3) . As per Centers for Disease Control and Prevention (CDC) recommendations, nucleic acid amplification tests (NAATs) from nasopharyngeal (NP) and throat swabs are the gold standard for identifying active infection.

Most NAATs are highly sensitive methods for detecting SARS-CoV-2 RNA in both symptomatic and asymptomatic patients (3) . However, NAATs detect all SARS-CoV-2 RNA, including genomic RNA, sub-genomic fragments and messenger RNAs produced during viral replication.

Cytosolic mRNAs can be protected against nuclease-mediated decay, and thus, are not necessarily indicative of active viral replication (4) . Since, NAATs do not distinguish between replicating virions versus persisting viral genomic fragments (2, 5) , the detection of SARS-CoV-2 using these methods could result in extended and unnecessary isolation of hospitalized patients following the infectious stage (6) .

Virus culture methods combined with assays to detect viral plaque-forming units (PFU) are time-consuming and technically challenging, requiring a BSL-3 facility to culture SARS-CoV-2. However, such procedures are most appropriate for clear identification of replicating virions in human samples. Using extended culture periods as well as Vero cells lacking the STAT1dependent interferon signaling pathway, we tested paired samples from hospitalized congregate care patients at early and later stages of disease and who remained hospitalized for extended periods of time due to NAAT positivity. Our results show that infectious virus can be isolated only in a subset of early-stage patients while all samples from later stage patients failed to show evidence of culturable virus.

Patients being treated at Albany Medical Center were selected for study if they presented from a congregate care facility (skilled nursing facility or rehabilitation facility, n=14), had clinical signs and symptoms consistent with COVID-19, and had multiple PCR-positive tests separated by at least 14 days (patient demographics, Table 1 ). Many patients remained hospitalized until their SARS-CoV-2 NAAT results were negative. There were three patients (patients A1, A2, A12) with multiple visits between the hospital and nursing facility, which was counted as one hospital visit. NP swabs were placed in ~3 ml of viral transport medium and transported to the clinical lab for diagnostic testing within 4 hrs of collection.

Testing was performed in the clinical laboratories at Albany Medical Center Hospital (AMCH) using one of four commercial NAATs, three of which are RT-qPCR based: (1) (Supplemental table 1 ). Samples initially tested by TMA were thawed for RT-qPCR testing using BioGX SARS-CoV-2 reagents to obtain a viral load. Likewise, samples selected for viral culture were thawed, kept on ice and immediately transferred to the Albany Medical College (AMC) BSL-3 facility.

Vero E6 wild-type (WT) (CRL-1586™) and STAT1 -/-(CCL-81VHG TM ) cell lines were purchased from the American Type Culture Collection (ATCC). Cell monolayers were prepared in 6-well tissue culture plates and maintained in DMEM that was supplemented with 10% heat inactivated fetal bovine serum (FBS) (Thermo-Scientific, USA), 2mM L-glutamine, 50 U/mL penicillin, and 50 µg/mL streptomycin. Vero E6 STAT1 -/cell monolayers were cultured in the same medium that was additionally supplemented with nonessential amino acids. The cells were infected under BSL-3 conditions for 1 hr at 37˚C with patient samples or as a positive control, supernatants from Vero cells that had been infected with the SARS-CoV-2, Isolate USA-WA1/2020 (provided by the Biodefense and Emerging Infections Repository). An aliquot of the cells was cultured for an additional 10 days in 2 ml of the DMEM culture medium. Culture supernatants were collected both at 1 hr (day 0) and 10 days post-infection and were tested by RT-qPCR (an off-label modification of the CDC assay, see below) and PFU assay. Vero E6 cells cultured without virus served as negative controls and showed no evidence of viral RNA or PFU.

Vero E6 cell monolayers were washed with DPBS and infected at 37˚C with culture supernatants that were diluted 10-fold in DMEM. At 1 hr post-infection, the cell monolayers were overlaid with DMEM supplemented with 2% FBS, penicillin-streptomycin and 1% methylcellulose (4000 centipoise viscosity) (Sigma, USA). Four days later, the cells were fixed with 10% formalin for 1 hr followed by staining with 1% crystal violet. PFU numbers were counted under 10X magnification.

Extraction of SARS-CoV-2 RNA and RT-qPCR were performed using commercially available kits and CDC recommendations. In brief, extraction of viral RNA directly from NP swabs and from cell-free culture supernatants was performed using the Qiagen QIAamp® viral RNA mini kit as per the manufacturer's instructions. RT-qPCR quantification of viral titers used a single step qPCR kit (Promega catalog #A6101) with primers designed to amplify N1 and N2 nucleic acids, and probes procured from IDT, USA. A known concentration of viral SARS-CoV-2 cDNA was used as a positive control in all experiments. This assay had an upper detection limit of approximately 10 Ct with Ct values of >40 considered negative. No nucleic acid amplification was detected in the absence of RT.

Nunc MaxiSorp 96-well plates were coated overnight at 4°C with 1 μg/ml of purified recombinant SARS-CoV-2 S1/S2 spike protein (Biolegend, catalog #794206) in carbonate/bicarbonate buffer pH=9.4. The plates were then incubated at room temperature with 1% BSA in PBS/0.05% Tween blocking solution and then with 2-fold dilutions of patient NP samples in the same buffer.

A patient serum sample with a known anti-spike antibody titer was used as a positive control and a NP sample from an uninfected patient was used as a negative control. After washing of the wells with 1% BSA in PBS/0.05% Tween, bound antibody was detected using goat antihuman Ig conjugated to horseradish peroxidase (1:5,000 dilution; Sigma, catalog #AP120P) followed by 3,3′,5,5′-Tetramethylbenzidine substrate (BD OptEIA ™ kit, BD Biosciences, USA).

After color development, titers were determined as the last dilution giving an OD value of at least 0.1 above the negative control.

Because our study was specifically requested by a public health authority during the COVID-19 pandemic, the Albany Medical Center Institutional Review Board (IRB) deemed this research to be public health research and exempt from IRB approval.

The mean age of the patients was 72.57 years (range 55 to 92), with a mean peak Sequential

Organ Failure Assessment score of 5.6 (range 1 to 11). Patients were hospitalized for a mean of 37.0 days (range 25 to 60). Viral RNA was detected by PCR for a mean of 32.9 days (range 19

to 47). The median RNA viral load for the first positive NP swab collected was 5.81 log gc/mL (range 2.12 to 9.72) ( Table 1 ). Viral load decreased after clinical symptom onset (R = -0.69, 95% CI, -0.80 to -0.54). At 26 days of symptoms, no specimens had viral loads greater than 4.00 log gc/mL ( Figure 1 ).

Twelve patients came from skilled nursing facilities, one patient (patient A2) came from an adult care home, and one patient (patient A1) was homeless and later transferred to a rehabilitation facility. All patients had at least one comorbidity, with hypertension as the most common comorbidity and chronic heart disease as the second most common comorbidity. Ten patients were chronically bedbound (Patients A5-A14). All patients had respiratory symptoms, characterized by cough, congestion, and/or dyspnea. Thirteen patients exhibited findings on chest radiography consistent with a COVID-19 diagnosis. Four patients had at least a one-night stay in the ICU (Patients 2, 5, 10, 12). Fortunately, no patients expired during their hospital stay.

Exposure of Vero E6 cells to NP swab extracts for 1 hr and culture for 4 days failed to yield infectious virus as determined by PFU assay. We considered the possibility that the 4-day culture period was insensitive for detection of low amounts of active virus in the tested samples.

Thus, Vero cells exposed to patient NP swab extracts were cultured for 10 days and the PFU assays were repeated. We found that of the samples tested, four out of 14 (28.6%) showed evidence of replicating virus 10 days after culture (patients A1, A2, A6 and A7, Table 2 ). All four positive samples were obtained within 12 days of COVID-19 symptom onset (Figure 1 ).

Positivity by PFU assay correlated with greater levels of virus genomic copies (gc). A time course study of two patient samples showed that viral RNA copy numbers increased substantially within 5 days of culture but PFU were only detected after 10 days (Figure 2 ). All Figure 1 .

Interferon (IFN)-stimulated genes induced through STAT1 signaling are highly expressed during COVID-19 infection and are well-known to have anti-viral activity (7). We therefore considered the possibility that Vero cell-derived IFN might limit viral replication during in vitro culture and thus, be responsible for the lack of PFU observed in many of our cultures. To test this, we compared growth of virus from NP swab extracts in Vero WT versus STAT1 -/cells. All NP swab samples that showed no viral growth in WT Vero cells remained negative when tested with Vero STAT1 -/cells (Table 3) . However, those samples that showed viral PFU in WT Vero cells produced 10-100-fold greater numbers of PFU in Vero STAT1 -/cells (Table 3 and Figure 3 ).

Interestingly, RT-qPCR analysis of all samples showed comparable production of viral gc in both WT and STAT1 -/cells. Taken together, these results indicate that IFN signaling in host cells inhibits virus production, likely at a post-transcriptional stage of replication. Nevertheless, IFN signaling does not completely inhibit viral cytopathic effects and thus, was not the reason for failure to detect active virus in 10 out of 14 of the congregate care patient samples.

Recent studies have identified neutralizing antibodies reactive with SARS-CoV-2 spike protein in host mucosal tissues (8, 9) . Such antibodies are detectable within 6-15 days post-infection (9) . We thus evaluated the potential presence of antibodies in our patient NP samples by ELISA. Specifically, we compared samples that produced differential gc and PFU results after These results could partially explain our negative PFU results but nevertheless, indicate that the patients are noninfectious despite the presence of viral RNA.

We tested sequential NP samples from hospitalized, congregate care COVID-19 patients for the differential identification of viral nucleic acid versus actively replicating virus. Consistent with previous studies (10, 11) , Vero E6 cells were found to be susceptible to SARS-CoV-2 virus replication and damage but extended culture for 10 days was necessary to detect PFU in were derived from patients with viral loads >6.8 log 10 gc/ml, which agrees with earlier reports that found a dissociation between viral RNA production and positive viral cultures (12) . In fact, our findings are nearly identical to those of Bullard et al. (13) , who reported that 28.9% of samples from COVID-19 patients showed viral growth in Vero cells but samples from patients

with Ct values of >24 or symptom onset >8 days lacked replicating virus. Of note, our experimental approach was novel in that it directly compared sequential samples from the same patient at various stages of disease. In our study, all NAAT positive patients tested negative by viral culture at later symptom onset, although admittedly, we only examined NP swabs, and other sample sources such as sputum could conceivably contain more active virions. An explanation for the consistent disconnect between levels of viral genome copies and active virus described by us and other groups is offered by a recent finding indicating long-term production of genomic and sub-genomic fragments of RNA following SARS-CoV-2 infection of host cells (4) . The authors of this latter study suggested that sub-genomic RNAs are nuclease-resistant possibly due to protection by intracellular cell membranes. However, they did not use culture methods to directly measure infectious virus.

We further tested whether IFN-mediated host immunity in Vero cells could be responsible for an inability to detect active virus after an extended hospital stay. Thus, we determined viral growth in STAT1 -/-Vero E6 cells, which lack the intrinsic IFN signaling pathway known to inhibit viral replication, including replication of SARS-CoV-2 (14, 15) . Notably, all samples that were PFUnegative remained negative after extended culture in these cells. Conversely, the positive samples remained positive but yielded ~10-100-fold more PFU than the same samples grown in WT cells. In addition, the actual plaques were larger and better defined compared to those developed in WT Vero cells. It is unclear whether type I (16) or type III (17) IFN was responsible for these inhibitory effects, especially since Vero E6 cells are known to be deficient in type I IFN responsiveness (17, 18) . In either case, we conclude that IFN produced by Vero cells can limit viral replication but is not ultimately responsible for culture negativity. The mechanism that mediates IFN-dependent inhibition of virus growth is unknown, particularly since IFN is known to upregulate expression of the ACE2 virus receptor, which would be predicted to increase infectivity (19) . It is likely that IFN-mediated virus inhibition occurs posttranscriptionally since virus PFU-negative cultures still contained viral RNA.

We also tested for the possible presence of anti-spike antibody in the patient NP samples to determine whether such antibodies might influence our ability to successfully obtain culture- The obvious implication is that virus may be present during early stages of infection in patients that have a low level of anti-spike antibody, but after production of larger amounts of antibody later during disease the virus is effectively neutralized and the patient becomes noninfectious.

In conclusion, we have used sequential NP swab samples to demonstrate that hospitalized congregate care patients showed active virus only during early symptom onset even though the patients remained RNA positive for weeks after initial infection. This was not due to lack of assay sensitivity nor inhibitory IFN production by the host cells but is likely related to the presence of anti-spike protein antibody. 

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Real-time RT-PCR in COVID-19 detection: issues affecting the results

SARS-CoV-2 genomic and subgenomic RNAs in diagnostic samples are not an indicator of active replication

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Virological assessment of hospitalized patients with COVID-2019

Attenuated Interferon and Proinflammatory Response in SARS-CoV-2-Infected Human Dendritic Cells Is Associated With Viral Antagonism of STAT1 Phosphorylation

IgA dominates the early neutralizing antibody response to SARS-CoV-2

Systemic and mucosal antibody responses specific to SARS-CoV-2 during mild versus severe COVID-19

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Isolation and characterization of SARS-CoV-2 from the first US COVID-19 patient

Understanding viral shedding of severe acute respiratory coronavirus virus 2 (SARS-CoV-2): Review of current literature

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Transcriptomic analysis reveals a mechanism for a prefibrotic phenotype in STAT1 knockout mice during severe acute respiratory syndrome coronavirus infection

Type I Interferon Susceptibility Distinguishes SARS-CoV-2 from SARS-CoV

Critical Role of Type III Interferon in Controlling SARS-CoV-2 Infection in Human Intestinal Epithelial Cells

New World hantaviruses activate IFNlambda production in type I IFN-deficient vero E6 cells

The genome landscape of the african green monkey kidney-derived vero cell line

CoV-2 Receptor ACE2 Is an Interferon-Stimulated Gene in Human Airway Epithelial Cells and Is Detected in Specific Cell Subsets across Tissues

We thank the Department of Immunology and Microbial Disease BSL-3 facility for assistance in the viral culture assays. 

M. Robek reports financial relationships with CaroGen Corp. and research funding from Gilead Sciences, outside of this work. The other authors declare no competing financial interests.