INTRODUCTION
The coronavirus pandemic has spread worldwide. Polymerase chain reaction (PCR) testing is used for diagnosis; many countries seek to expand testing [
1]. However, PCR testing is expensive and time-consuming [
2]. The nasal cavity and pharynx are sampled. Nasal cavity samples are more informative, suggesting that detailed observation of the nasal cavity is necessary. Nasal endoscopy is commonly performed by otolaryngologists to evaluate the condition of the mucosa or to determine the effectiveness of treatment. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-infected patients may have nasal symptoms such as a runny nose; nasal secretions may transmit the virus [
3]. SARS-CoV-2 propagates more readily than SARS-CoV, particularly in aerosols [
4]. We performed nasal endoscopy on an individual attending an outpatient clinic who had not been tested for the virus; he was later confirmed to have the virus. Here, we compare this patient’s nasal imaging findings with the findings of normal subjects and patients with allergic rhinitis.
METHODS
Nasal endoscopic images were analyzed using the hue, saturation, and luminance (HSL) method, which is an alternative to the red, green, and blue (RGB) color model. The HSL method was designed in the 1970s by computer graphics researchers to more closely reflect human color vision [
5]. The colors of each hue are arranged radially. Saturation indicates various depths of brightly colored paint. Values refer to mixtures of such paints with varying amounts of black or white. Matrox Design Assistant, version 5.0 (Matrox
® Imaging, Montreal, QC, Canada), was used for optical analysis.
Images were normalized using histogram equalization of the blue (B) band area; the mean brightness value of the B band in the RGB area of each nasal endoscopic image was approximately 20 to 30 (maximum possible value: 255). The minimum B band applied during histogram equalization was 0, and the maximum B band applied for image processing was 50. RGB-to-HSL conversion was performed for all images. At the time of nasal endoscopy, the patient had received no treatment nor manipulation; both inferior turbinates were analyzed.
Normal subjects and patients with allergic rhinitis were distinguished using the multiple allergen simultaneous test (MAST; an in vivo inhalation test). Normal subjects did not mount a substantial response to any antigens in MAST level I (the MAST features three levels). All subjects underwent nasal endoscopy and provided written informed consent for the MAST test prior to (possible) nasal surgery. The study was approved by the SoonChunHyang University Gumi Hospital Institutional Review Board (IRB no. 2019-22). All patients provided written informed consent.
A 29-year-old man presented with a runny nose and cough on February 18, 2020. He was diagnosed with SARS-CoV-2 infection on February 27. He had contracted the virus at a Sincheonji meeting (a religious gathering) on February 16 and had visited our clinic after the onset of symptoms. He had no history of any other illness, was not receiving any medication, and had not visited any hospital with symptoms. His body temperature during the visit to our clinic was 37.1°C and he exhibited no sinusitis on a paranasal sinus X-ray. We obtained a nasal endoscopic image during this visit.
RESULTS
Of the 15 subjects in this study, 6 were clinically normal, 8 had allergic rhinitis, and 1 had SARS-CoV-2 infection. The MAST test results confirmed the six normal subjects and eight patients with allergic rhinitis. Optical analysis of the nasal mucosa revealed differences in color and blood vessel distribution among groups. The inferior turbinate was paler and smoother in patients with allergic rhinitis than in normal subjects, but the surfaces were similarly uniform. Compared with patterning, smoothness is associated with different hue and luminance values. The nasal mucosa of the patient with SARS-CoV-2 exhibited widespread spikes or scratches (
Fig. 1), and was thus not smooth (
Fig. 2). The patterns of both inferior turbinates were similar in this patient. The luminance feature of HSL most clearly demonstrated these features. On hue analysis, the general appearance was rougher in the patient with SARS-CoV-2 than in normal subjects and patients with allergic rhinitis. Normal subjects had a total immunoglobulin E (IgE) grade of 1 (of a maximum of 3) on the MAST test, and no significant reaction to other antigens. Patients with allergic rhinitis exhibited total IgE grades of 1–3 and allergic reactions to various antigens.
DISCUSSION
The coronavirus binds to a host cell using a spike (S) protein, which features three segments, including a large ectodomain containing a receptor-binding S1 subunit and the membrane-fusion S2 subunit. The virus binds to the host cell via the S1 subunit and is then fused to the cell membrane by the S2 subunit [
6]. The viral receptor is angiotensin-converting enzyme 2. Coronavirus membrane fusion is similar to membrane fusion mediated by the hemagglutinin glycoprotein of influenza virus [
7]. The S protein is a trimeric class I protein involved in both prefusion and postfusion activities [
8]. The receptor-binding domain of the S1 subunit behaves like a hinge when bound to the host cell receptor. S1 moves up and down, and thus appears unstable [
8].
Earlier reports had found a close connection between infection and the market [
9]. Virus was cultured in human airway epithelial cells; ciliary action ceased at 96 h after inoculation. Under the electron microscope, the virus exhibited distinctive spikes and a sun-like corona [
10], perhaps explaining our hue data.
Joko et al. [
11] reported that, when analyzed through RGB, the red value with a lot of blood flow was high in AR patients at the beginning, and then gradually became pale, and the red value was low in the perennial cedar group. In another RGB analysis, it was reported that green and blue were higher in AR patients, and that the cumulative RGB value was high [
12].
In this study, HSL rather than RGB was used, which is a different point of view of color, and it is a method that can express subtle differences even in the same color.
Electron microscopy identifies viruses. However, prior culture is required. Furthermore, PCR analysis requires viral genomic amplification. Both techniques are associated with risks of viral spread. It is possible to detect the virus via nasal endoscopy. Millions of viral particles confer a distinct shape on the nasal mucosa, which presumably led to the scratches and stretching observed in this study. Shape changes can be highlighted by changing the background color or the color tone system. We found the HSL system useful in this respect. No normal subject or patient with allergic rhinitis (all of whom lacked fever and sinusitis) exhibited the pattern present in the patient with SARS-CoV-2. In patients with allergic rhinitis, the mucosal cells were more expanded than in normal subjects and thus absorbed more light.
Our test is macroscopic; it would be useful to investigate whether virus was adherent to the mucosa. However, ethical issues limited our ability to perform this investigation; non-invasive diagnosis is optimal. We studied only one patient with SARS-CoV-2; samples from additional patients are required. Variations in nasal endoscopy brightness may be of concern; in this analysis, we normalized all images. The extents of inferior turbinate scratching require further investigation using hue and luminance analyses. Nasal endoscopy may be a useful viral diagnostic tool.