key: cord-1029347-frqi57z5
authors: Liu, Long; Zeng, Feng; Rao, Jingjing; Yuan, Shengren; Ji, Manshan; Lei, Xu; Xiao, Xiao; Li, Zhijun; Li, Xiaohua; Du, Weixing; Liu, Yanqing; Tan, Huabing; Li, Junmin; Zhu, Jianyong; Yang, Jing; Liu, Zhixin
title: Comparison of Clinical Features and Outcomes of Medically Attended COVID-19 and Influenza Patients in a Defined Population in the 2020 Respiratory Virus Season
date: 2021-03-23
journal: Front Public Health
DOI: 10.3389/fpubh.2021.587425
sha: f2e698df09ee1b79001a6cab0ec6100d8b2ce8cc
doc_id: 1029347
cord_uid: frqi57z5

The emergence of severe acute respiratory syndrome coronavirus 2 (SARS-COV-2), which is causing the coronavirus disease-2019 (COVID-19) pandemic, poses a global health threat. However, it is easy to confuse COVID-19 with seasonal influenza in preliminary clinical diagnosis. In this study, the differences between influenza and COVID-19 in epidemiological features, clinical manifestations, comorbidities and pathogen biology were comprehensively compared and analyzed. SARS-CoV-2 causes a higher proportion of pneumonia (90.67 vs. 17.07%) and acute respiratory distress syndrome (12.00 vs. 0%) than influenza A virus. The proportion of leukopenia for influenza patients was 31.71% compared with 12.00% for COVID-19 patients (P = 0.0096). The creatinine and creatine kinase were significantly elevated when there were COVID-19 patients. The basic reproductive number (R(0)) for SARS-CoV-2 is 2.38 compared with 1.28 for seasonal influenza A virus. The mutation rate of SARS-CoV-2 ranges from 1.12 × 10(−3) to 6.25 × 10(−3), while seasonal influenza virus has a lower evolutionary rate (0.60-2.00 × 10(−6)). Overall, this study compared the clinical features and outcomes of medically attended COVID-19 and influenza patients. In addition, the S477N and N439K mutations on spike may affect the affinity with receptor ACE2. This study will contribute to COVID-19 control and epidemic surveillance in the future.

An increasing number of COVID-19 cases have caused a global health burden due to the rapid transmission throughout the human community. The pathogen SARS-COV-2 causes respiratory system and severe systemic symptoms through respiratory tract infection (1, 2) . As of February 17th, 2021, more than 100 million COVID-19 cases were confirmed, and more than 2 million deaths had occurred (3) . Although many countries are developing vaccines and racing to run clinical trials (4) , there are still many unresolved questions regarding viral invasion, pathogenesis and clinical features. In particular, the relationship between mutations and pathogenicity or transmissibility remains unknown.

The seasonal influenza epidemic is caused by strains of influenza virus, including two influenza A viruses (H1N1 and H3N2) and one influenza B virus. There have been four documented influenza pandemics in the past 100 years (in 1918, 1957, 1968, and 2009 ) (5) . The influenza case fatality rates of the 1918 and 2009 H1N1 pandemics ranged from 0.1% to 2.5% (6, 7) . The very important issue is the emergence of a new subtype or strain through uncontrollable and unpredictable mutations or antigenic drift and shift (8) . The same situation may also occur with SARS-COV-2. Some studies have reported spike mutations and attempted to clarify the transmissibility change associated with new mutations (9, 10) .

Currently, SARS-COV-2 remains a lasting threat to public health, causing mild respiratory system disease similar to that caused by seasonal influenza virus. To investigate the COVID-19 clinical progression, prognosis and SARS-COV-2 epidemic trends, we systematically contrasted the proportions or values of epidemiologic characteristics, clinical features, blood abnormalities, progressive symptoms, and hospitalization rates between influenza and COVID-19. Seasonal influenza was prevalent in winter, and COVID-19 also emerged in the last winter. The parameters of coinfection patients who presented with both COVID-19 and flu were also compared with those of COVID-19 patients. In addition, the mutants of influenza virus HA and SARS-COV-2 spike causing the epidemic were resolved and discussed. We expect that this comparative research will aid pandemic control and be beneficial to the clinical diagnosis of SARS-COV-2.

This study was approved by the Institutional Review Committee of Shiyan Renmin Hospital of Hubei University of Medicine, and no informed consent was required. This study was designed as a retrospective case analysis, with no patients directly involved in the study design, question setting, or outcome evaluation.

From January 23, 2020 to February 27, 2020, the confirmed COVID-19 patients and influenza patients on outpatient visits and admission to Shiyan Renmin Hospital were uniformly collected. The clinical data of 75 COVID-19 patients, 41 influenza patients and 23 coinfection patients were retrospectively collected at the same time. All patients underwent chest computed tomography (CT) scanning at admission. Flu patients were infected with the seasonal influenza A or B virus, COVID-19 patients were infected with SARS-COV-2, and coinfection patients were infected with both SARS-COV-2 and influenza A or B virus or parainfluenza virus (PIV). The clinical subtype for COVID-19 was screened according to the Diagnosis and Treatment Protocol for Novel Coronavirus Pneumonia (Trial Version 7) which was released by the National Health

Commission & National Administration of Traditional Chinese Medicine (11) . Influenza diagnosis and treatment plan (2019 version) (12) was used for screening the flu patients.

After admission to the hospital, specimens from all patients were screened for SARS-COV-2 using throat swabs. The positive result of real-time reverse transcription-polymerase chain reaction (RT-PCR) confirmed the infection. Other respiratory pathogens were detected by indirect immunofluorescent assay using IgM antibodies, including Legionella pneumophila, Coxiella burnetii, Chlamydia pneumoniae, Mycoplasma pneumoniae, adenovirus (AdV), influenza A virus, influenza B virus, parainfluenza virus (PIV type 1+2+3), and respiratory syncytial virus (RSV). Sputum or body fluids were also examined at admission for other possible infections with bacteria or fungi.

The epidemiological data, symptoms, laboratory abnormalities on admission, clinical treatments, and outcomes were recorded and collected. The examination of WBC, influenza virus antigen, joint test of nine respiratory tract pathogens, procalcitonin (PCT), hypersensitive C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), blood gas analysis, and chest computed tomography (CT) were completed in the hospital. The above information was extracted from the case database of Shiyan Renmin Hospital.

The genome sequences of SARS-COV-2 were downloaded from the GISAID database (13) . Multiple sequences were aligned using MAGE-X software (version 10.0.5), phylogenetic analysis was completed through multiple comparisons using neighbor-joining algorithms, and the number of bootstraps was 500. All spike mutations were referenced to the website of the SARS-COV-2 Sequence Analysis pipeline (14) .

To analyze the dynamic model of the spike protein, we used the PDB file 6VXX. The model 1RUZ was used to validate the HA structure of influenza. PyMOL software (version 2.3.2) was used to map the S477N and N439K domain onto the 3D structure. MM/GBVI was used to calculate the binding free energy of each conformation with receptor ACE2 (15), ACE2 (PDB ID: 1R42) was used for computation.

Statistical Analysis SPSS 22.0 software (SPSS, Inc. Chicago, USA) was used for statistical analysis of the obtained data, and the measurement data are shown as the medians and interquartile ranges (IQRs), which were compared with the Mann-Whitney U-test. The categorical variables are shown as numbers (%) and were compared with the χ² test or Fisher's exact test. 

The clinical characteristics of the patients are shown in Table 2 . Some COVID-19 patients, flu patients and coinfection patients had the common manifestation of fever and cough. A total of 69.33 and 9.33% of COVID-19 patients had fever and nasal obstruction and rhinorrhea, respectively, which were all lower rates than those for the flu patients (P = 0.0263, P = 0.0083). Fatigue reported in 36% of COVID-19 patients was higher than the rate in flu patients (P = 0.0023). Patients coinfected with SARS-COV-2 and influenza virus or PIV had a lower cough rate than COVID-19 patients (P = 0.0310). Other symptoms included headache, nausea, vomiting, and diarrhea. For routine blood tests, a higher proportion of flu patients developed leukopenia than COVID-19 patients (31.71 vs. 12.00%, P = 0.0096), while coinfection patients had a decreased proportion (4.35%) of leukopenia relative to that of the COVID-19 patients, but there was no significant difference (P = 0.2889). A total of 70.67% of COVID-19 patients had increased CRP, sharing a median of 13.63 mg/L, which was higher than that of the flu group (P = 0.0372). The median of an increased proportion of ESR was not significantly different among the three groups. The increase of ESR (48.00 vs. 53.66%) and D-dimer (37.33 vs. 36.58%) was a common phenomenon in the COVID-19 and flu patients. The creatinine was significantly increased in the COVID-19 group than flu group (P = 0.0239), while creatine kinase was elevated when there were COVID-19 patients (16.00% or 30.43 vs. 2.44%).

Among the 75 confirmed COVID-19 patients, 45 showed typical signs of viral pneumonia on chest CT. The other 23 patients showed lung infections but no typical signs on chest CT. In total, 90.67% of COVID-19 patients developed pneumonia, which is much higher than the proportion of influenza patients with pneumonia (17.07%, P < 0.0001) ( Table 3) , and this proportion increased to 95.65% in coinfection patients. The lesions for COVID-19 pneumonia were mostly in the subpleural area, with patchy or lumpy appearance ( Figure 1A) . The density of the lesions was commonly ground-glass opacities (GGOs), and there were real changes and thickened leaflet intervals. Influenza pneumonia showed GGOs with fewer solid components ( Figure 1B) . Twenty-one COVID-19 patients (28%) were diagnosed with underlying diseases ( Table 3) , and the top three were hypertension (13.33%), diabetes (8%), and coronary heart disease (5.33%). The proportion and order of underlying diseases in the flu group and coinfection group were consistent. A total of 18.67% of COVID-19 patients developed complications of liver injury, which was a higher rate than that of flu patients (4.88%, P = 0.0395). No flu patient had a complication of acute respiratory distress syndrome (ARDS), with a proportion of 12% in the COVID-19 group (P = 0.0209). In the coinfection group, ARDS was the most common complication (17.39%), followed by liver injury (13.04%) and kidney injury (8.70%).

The median hospitalization period of COVID-19 patients was 19 days, while flu patients after admission required only 4 days to discharge (P < 0.0001) ( Table 4 ). According to the Diagnosis and Treatment Protocol for COVID-19 (11), all COVID-19 patients received broad-spectrum antiviral treatment, including interferon-α sprays, arbidol hydrochloride, or lopinavir and ritonavir (16). Antibiotics, including cephalosporins, carbapenem, quinolones and so on, and antifungal drugs were used when appropriate. By the end of the study period, all patients were being treated in the hospital, and 98.67% of COVID-19 patients were cured and survived; only one patient died (1.33%). All flu and coinfection patients were cured and discharged.

Influenza virus belongs to the family Orthomyxoviridae, whose genome contains eight RNA segments. SARS-COV and SARS-COV-2 belong to the β-coronavirus (CoV) genus in the Coronaviridae family (17) . SARS-COV-2 showed a high nucleotide sequence identity (79.5%) with SARS-COV (18) . Recent reports have shown that SARS-COV-2 enters susceptible cells through binding with the receptor angiotensin-converting enzyme 2 (ACE2), which is the same as SARS-COV (19) (20) (21) . All ages of people are susceptible to influenza A virus (22), while SARS-COV and SARS-COV-2 primarily infect adults (23). 

Haemagglutinin (HA) on influenza virus and spike on SARS-COV-2 are both responsible for binding to the receptors on permissive cells. HA and spike are both homotrimers, where each monomer comprising two subunits, HA1 and HA2 or S1 and S2 (Figures 2A,B) . Several important adaptive mutations occur in HA, including E190D and G225D for H1N1 and Q226L and G228S for H2N2 and H3N2 (31) . Some mutations in the polymerase subunits PB1, PB2, and PA are critical for increasing polymerase activity and viral virulence (32) . As of 2 June 2020, more than ten thousand mutant sequences of SARS-COV-2 were uploaded to the GISAID database (13) . There were 18,539 nonsynonymous mutations on the spike protein, the D614G mutation was unusually enriched and present in more than 8,000 strains. Up to February 1st 2021, nearly 300,000 strains containing D614G variation, A222V and L18F were the second and third mutations ( Figure 2C) . N439K, S477N and N501Y which located in the receptor-binding domain may affect the immunogenicity or vaccination. Our result showed S477N and N439K mutations have the capability to enhance the affinity with receptor (Figures 2D,E) . Additional studies are needed to elucidate the effect of mutations in which are not located in the receptor-binding domain (pocket) on influenza virus and SARS-COV-2 infection and their epidemiological outcomes.

To date, most epidemiological reports have clarified the case disparities in clinical manifestations, routine blood tests, and immunity factors of COVID-19 (33) (34) (35) . However, the dual epidemics of COVID-19 and influenza makes the diagnosis, treatment, and vaccination face greater challenges, even though some studies have assessed the differences between influenza and COVID-19 in terms of clinical characteristics or outcomes (36, 37) . Both are respiratory virus infections, and influenza and COVID-19 have many of the same symptoms, including respiratory system and gastrointestinal system symptoms. Severe cases also have loss of taste or smell, difficulty breathing, or shortness of breath (38) . COVID-19 may cause gastrointestinal problems, such as diarrhea, vomiting, and abdominal pain (39) . Both the SARS-COV-2 receptor ACE2 and cellular serine protease transmembrane protease serine 2 (TMPRSS2) are critical for the fusion of viral and cellular membranes, which are not only expressed in lung alveolar type 2 cells and gland cells but also highly expressed in the ileum and colon (40, 41) , suggesting that the virus can invade the digestive tract and intestine, and viral RNA can be detected in patients' stool. Certain risk factors predispose patients to increased morbidity and mortality following exposure to the influenza A virus or SARS-COV-2. Age is the most significant risk factor for influenza and COVID-19-related mortality (42, 43) . Age may also have different effects on the results of influenza virus infection between males and females (44) . For COVID-19, the sex difference is a significant factor for mortality. Recently reported data showed that the male mortality rate is 2.4 times that of females (70.3 vs. 29.7%) (43) , and there were 1641 men among the 2248 confirmed COVID-19 patients, which was 2.6 times the proportion of women (73 vs. 27%) (45) . Chronic respiratory diseases and cardiovascular diseases are the two major comorbidities for influenza patients (5) , and other comorbidities associated with poor influenza outcomes include diabetes and obesity. In our study, the most common underlying diseases in both flu and COVID-19 patients were hypertension, diabetes, and coronary heart disease. There was a significant difference in the progressive symptoms and complications of pneumonia between influenza and COVID-19 illness, including concurrency and CT radiology features. Only 17% of flu patients developed pneumonia, while the number increased to 90.67% in COVID-19 patients. In the early stage of flu pneumonia, X-ray imaging showed thickened and blurred lung texture and small patchy shadows. The advanced stage (onset 3-7 days) is dominated by GGOs and consolidation (46) . COVID-19 pneumonia shows limited patchy shadows in the early stage, diffuse lung abnormalities, and multiple consolidations when the lesions are severe (47) .

Dynamic changes in routine blood parameters refer to the evaluation of treatment or examination of the disease by observing the quantity change and shape distribution in blood cells. The total count of WBCs, neutrophils, lymphocytes, and monocytes progressively decreased, which may be related to the direct invasion of the virus into hematopoietic cells (48) . The initial CRP of severe COVID-19 patients increased prior to CT findings (49) , and the CRP value increased rapidly after admission, indicating a strong inflammatory response; the virus is prevalent in patients' bodies at this stage. ESR, elevated by the acute-phase response, can be used as an important indicator to distinguish patients with severe COVID-19 in the early stage (50) . Severe COVID-19 illness is associated with a prominent elevation in ESR, which may provide additional information on disease progression. The BUN and blood creatinine levels rise rapidly before death in severe COVID-19 patients, this is consistent with our study (51) . The inadequate sample size may limit the conclusion of our study, further studies are needed to analyze the dynamic changes in immune factors for COVID-19 progression and prognosis.

Several adaptation mutations have been identified in different segments of influenza A virus, and thoroughly researched mutations, including E627K and D701N on PB2 of avian flu virus and other subtypes, promote polymerase activity and adaption to act cooperatively with humans (52, 53) . Adaptive mutations in SARS-COV-2 have also been reported, and the most important mutation in spike is D614G, which has attracted global attention (54, 55) . The D614G mutant began to spread in Europe in early February 2020 and became the mainstream strain worldwide by May 2020, accounting for nearly 70% of samples in Europe and North America (56). Zhang et al. (57) latest research showed that small genetic mutations in the SARS-COV-2 variants are prevalent throughout Europe and the United States, which may increase the number of spike proteins on virions, and it will greatly improve the viral infectivity by 9-10 times. The N439K variants can maintain fitness but can evade the antibody-mediated immunity (58) , it is unclear what the S477N mutation will bring to the vaccines and epidemics. More studies are needed to compare the clinical outcomes and prevalence between adaptive mutants and wild type.

This study provides new insight into the differences in clinical outcomes, laboratory abnormalities, comorbidities and hospitalization between influenza and COVID-19 patients and discusses the relationship between viral adaptive mutations and protein function, which will provide a reference for clinical differential diagnosis and epidemic surveillance.

The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author/s.

Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.

COVID-19 remains one of the key threats to public health. SARS-COV-2 causes a mild respiratory system disease, which has symptoms similar to those of seasonal influenza virus. COVID-19 and seasonal influenza both emerged in the respiratory virus season. Comparison of clinical features and outcomes of medically attended COVID-19 and influenza A patients will help us to better diagnose and treat the infection caused by SARS-COV-2. In this study, we systematically contrasted the proportions or values of epidemiologic characteristics, clinical features, blood abnormalities, progressive symptoms, and hospitalization between influenza and COVID-19. The parameters of coinfection patients who presented with both COVID-19 and flu were also compared with the COVID-19 cases. In addition, mutants of influenza virus HA and SARS-COV-2 spike causing the epidemic were resolved and discussed according to the literature or computation. This comparative research aims to aid pandemic control and be beneficial to clinical diagnosis. Epidemic Emergency Research Foundation (2020XGFYZR07 and 2020XGFYZR08). The funder has no function in the study design, data collection and analysis, manuscript writing and submission.

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The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.Copyright © 2021 Liu, Zeng, Rao, Yuan, Ji, Lei, Xiao, Li, Li, Du, Liu, Tan, Li, Zhu, Yang and Liu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.