key: cord-0766474-6yh58vkl
authors: Chen, Ying; Liu, Mei-Qin; Luo, Yun; Jiang, Ren-Di; Si, Hao-Rui; Zhu, Yan; Li, Bei; Shen, Xu-Rui; Lin, Hao-Feng; Zhao, Kai; Hu, Ben; Shi, Zheng-Li; Yang, Xing-Lou
title: Genetic Mutation of SARS-CoV-2 during Consecutive Passages in Permissive Cells
date: 2021-04-26
journal: Virol Sin
DOI: 10.1007/s12250-021-00384-w
sha: 97e47573f04885ec4fa32bc5e3d35960bb502292
doc_id: 766474
cord_uid: 6yh58vkl

nan

The ongoing COVID-19 disease, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has led to over 112 million confirmed cases and 2.4 million deaths in more than 220 countries as of 25 February 2021 (WHO 2021) . Hospital-admitted patients show clinical features including fever, dry cough, fatigue, dyspnea, lymphopenia, and pneumonia with radiological groundglass lung opacities Guan et al. 2020) . SARS-CoV-2 was quickly isolated and could be detected in clinical samples, such as nasopharyngeal swabs, sputum, alveolar lavage fluid, and feces, as well as occasionally in seminal fluid and tears among other sources (Bhat et al. 2020; , which means that it can infect a variety of human tissues and organs.

SARS-CoV-2 is classified as a SARS-related coronavirus (SARSr-CoV) and has 79.5% and 96.2% identity, respectively, with SARS-CoV and a bat SARSr-CoV (RaTG13) at the full-genome level, indicating that it could have also originated from bats (Hu et al. 2017; Zhou et al. 2020) . Thereafter, two SARSr-CoV strains, which have 85% and 91% nt genomic sequence identities with SARS-CoV-2, were isolated from Malayan pangolins (Lam et al. 2020; Xiao et al. 2020) . To date, there is no evidence to support the direct bat or pangolin origin of SARS-CoV-2. It was reported that this virus exhibits tropism towards a wide range of cells and hosts, and a series of mutations were found in person-to-person and in vitro passages . To further investigate the genetic susceptibility of SARS-CoV-2 during the passage on different cells, we identified nine cell lines susceptible to this virus among 30 different transformed or primary cell lines; then the different SARS-CoV-2 strains isolated on Vero E6 and Huh-7 from a same patient bronchoalveolar lavage fluid (BALF) were serially passaged in Vero E6, Huh-7 and Caco-2 cell lines and continuously monitored.

Cell susceptibility was determined by an indirect immunofluorescence assay (IFA) targeting the nucleocapsid (N) protein of SARS-CoV-2 . Briefly, the SARS-CoV-2 isolated on Vero E6 cell line was cultured and titrated on Vero E6 cells. Then, different cell lines were seeded in 24 well plates and infected with SARS-CoV-2 at multiplicity of infection 1. The infected cells were washed with PBS and fixed with 4% paraformaldehyde at 24 h post-infection (hpi) overnight and then treated with TritonX-100 for cell membrane perforation. The treated cells were incubated at 4°C with a cross-reactive viral N antibody (rabbit anti-SARSr-CoV Rp3 N protein polyclonal antibody, 1:1000, made inhouse). After washing with PBS, cells were incubated with Cy3-conjugated goat-anti-rabbit IgG (1:200, Abcam, ab6939) secondary antibody for 1 h, and then, the nuclei were stained with DAPI (1:100, Beyotime). Then, the cells were observed under an AMF4300 EVOS FL cell Imaging System (Life Technologies, Carlsbad, CA, USA). Among the 30 tested cell lines, nine were positive by IFA (Fig. 1A , Supplementary Table S1). They comprised six human cell lines from various human organs, including Calu-3 (lung), HEp-2 (larynx), Huh-7 and Hep G2 (liver), Caco-2 (colon), and HaCaT (skin), two non-human primate cell lines including Vero E6 (kidney) and LLC-MK2 (kidney), and one swine cell line ST (testicle). Based on the expression of N protein, Vero E6, Caco-2, Huh-7, and Calu-3 cells were To further compare the viral replication efficiency in different cell lines that were found to be highly susceptible to SARS-CoV-2 infection, we infected Calu-3, Huh-7, Caco-2, and Vero E6 cell lines with MOIs of 0.001, 0.01, 0.1, and 1 (Fig. 1B) . Viral RNA was extracted from supernatants of infected cells at different time points using the QIAamp 96 Virus QIAcube HT Kit (Qiagen, Germany). The viral RNA copies in the supernatant were quantified with the HiScript no. II One Step qRT-PCR SYBR no. Green Kit (Vazyme, Nanjng, China) as we previously described . The primers based on the SARS-CoV-2 S gene were designed as: RBD-qF1: 5 0 -CAATGGTTTAACAGGCACAGG-3 0 ; RBD-qR1: 5 0 -CTCAAGTGTCTGTGGATCACG-3 0 . The viral loads of The mutations were observed after the isolation (pink star), 2nd (blue triangle), 5th (red triangle or rectangle), and 6th (green triangle) passage.

SARS-CoV-2 all increased more than 4 log values and showed increasing trends with an escalating MOI. Vero E6 cells showed the highest susceptibility to SARS-CoV-2, as up to 10 11 RNA viral copies/mL supernatant were detected at an MOI of 1 at 96 hpi. Huh-7, Caco-2, and Calu-3 cells showed equivalent susceptibility to SARS-CoV-2 with up to 10 7 viral RNA copies/mL. The viral loads in Calu-3 cells peaked at 48 hpi with MOIs of 1 and 0.1 or at 72 hpi with MOIs of 0.01 and 0.001. The viral loads in Huh-7 cells peaked at 48 hpi with MOIs of 1 and 0.1 or at 96 hpi with MOIs of 0.01 and 0.001. Meanwhile, the viral loads in Caco-2 cells peaked at 72 hpi with an MOI of 0.01 or at 96 hpi with MOIs of 1, 0.1, and 0.001.

Previous studies have shown that mutations in viral genes occur during virus passage in Vero and Vero E6 cells Vankadari 2020) . We further investigated whether a primary isolate could be efficiently maintained in other susceptible cell lines. SARS-CoV-2 WIV04 genome was sequenced from a patient BALF sample . Virus was isolated successfully in Vero E6 and Huh-7 cells from the same BALF sample; three and two mutations were observed in the virus genomes after isolation in Vero E6 and Huh-7 cells, respectively, compared to SARS-CoV-2 WIV04 genome (Fig. 1C, 1D) . These results suggest that there might be adaptations for SARS-CoV-2 in different cell lines. The SARS-CoV-2 isolate from Vero E6, was serially passaged in Vero E6 cell line for 11 passages; while the SARS-CoV-2 isolate from Huh-7 was serially passaged in Huh-7 and Caco-2 for 9 passages, respectively (Fig. 1C, 1D ). Supernatants were collected from every passage of each cell line, and then, next-generation sequencing (MGISEQ-2000RS FAST, Shenzhen MGI Tech Co., Ltd.) via the direct RNA sequencing was conducted to investigate the dynamics of mutations. Additional mutations were observed in N83K, R691Q, and H664Y of the spike protein from the P2, P5, and P6 passages in Vero E6, respectively. However, no more mutations were observed in Huh-7 cells over 9 consecutive passages. Notably, a 27-nucleotide deletion occurred in the spike protein resulting in a deletion of nine amino acids (77-85 IHVSGTNGT) when SARS-CoV-2 was passaged to the P6 generation in Caco-2 cells, and this deletion variant was stable in the following 3 passages.

In our study, we investigated the susceptibility, cell tropism, and viral replication efficiency of SARS-CoV-2. Results showed that nine of thirty cell lines derived from various tissues of humans (including lung, liver, colon, larynx, and skin), monkey (kidney), and swine (testicle) were susceptible to SARS-CoV-2. The virus replicated efficiently in human cell lines (Huh-7, Calu-3, Caco-2) and non-human primate cells (Vero E6) but less so in swine cells. In a previous study, it was reported that five human cell lines, including Calu-3, Caco-2, Huh-7, 293T, and U251, and six non-human cell lines, including Vero E6, FRhK4, LLC-MK2, CRFK, RK-13, and PK-15, were susceptible to SARS-CoV-2 (Chu et al. 2020) . In our study, we showed that three additional human cell lines, including HEp2 (larynx), Hep G2 (liver), and HaCaT (skin), are slightly susceptible to SARS-CoV-2 infection. Our study, together with others, demonstrates the wide cell tropism of SARS-CoV-2 in human and non-human primates in vitro. Meanwhile, the swine cell line ST (testicle) showed low susceptibility. Unexpectedly, none of the tested bat cell lines supported SARS-CoV-2 replication. Previously, we found that HeLa cells expressing ACE2 from Rhinolophus sinicus could support SARS-CoV-2 entry. This inconsistency might be due to the low or undetectable expression of ACE2 in immortal bat cell lines. We also investigated the susceptibility of other animal cell lines, including those from canine, mink, hamster, rat, and mouse; none of these cell lines could be infected with SARS-CoV-2. A possible explanation for this is that these cells do not express or have lower expression of ACE2 proteins or that SARS-CoV-2 does not use ACE2 of these cells as the cellular entry receptor .

The viral replication efficiency results showed that the Vero E6 cell line was more susceptible to SARS-CoV-2 than the Caco-2, Huh-7, and Calu-3 cell lines. Our results verified that the Vero E6 cell line is suitable for viral amplification. However, the results of our group and others suggested that the spike glycoprotein of SARS-CoV-2 is more likely to mutate during culture in this cell line. Most strikingly, no mutations were observed in Huh-7 cells during 10 consecutive passages, indicating that the virus is more stable in this cell line, which indicates that they could be applicable for investigations of pathogenicity and pathogenesis. However, as a human intestinal cell line, culture in Caco-2 cells resulted in a 27-nt deletion in the NTD of the spike glycoprotein, whereas a mutant with this deletion was not found in human clinical specimens. These results suggest that the spike glycoprotein of SARS-CoV-2 is more likely to mutate during in vitro passage, which is consistent with the reported outcomes of person-to-person transmission (Gong et al. 2020) . It remains largely unknown whether mutations acquired during in vitro passages additionally affect viral intrinsic characteristics. Continuous monitoring of SARS-CoV-2 could benefit not only biological studies of this virus but also vaccine development in the future.

Conflict of interest The authors declare that they have no conflict of interest.

Animal and Human Rights Statement This article does not contain any studies with human and animal subjects performed by any of the authors.

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