Clinical Significance of a High SARS-CoV-2 Viral Load in the Saliva

Jin Gu Yoon, Jung Yoon, Joon Young Song, Soo Young Yoon, Chae Seung Lim, Hye Seong, Ji Yun Noh, Hee Jin Cheong, Woo Joo Kim, Jin Gu Yoon, Jung Yoon, Joon Young Song, Soo Young Yoon, Chae Seung Lim, Hye Seong, Ji Yun Noh, Hee Jin Cheong, Woo Joo Kim

Abstract

Background: Patients with coronavirus disease 2019 (COVID-19) can unknowingly spread the virus to several people during the early subclinical period.

Methods: We evaluated the viral dynamics in various body fluid specimens, such as nasopharyngeal swab, oropharyngeal swab, saliva, sputum, and urine specimens, of two patients with COVID-19 from hospital day 1 to 9. Additional samples of the saliva were taken at 1 hour, 2 hours, and 4 hours after using a chlorhexidine mouthwash. The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) viral load was determined by real-time reverse transcriptase polymerase chain reaction (rRT-PCR).

Results: SARS-CoV-2 was detected from all the five specimens of both patients by rRT-PCR. The viral load was the highest in the nasopharynx (patient 1 = 8.41 log10 copies/mL; patient 2 = 7.49 log10 copies/mL), but it was also remarkably high in the saliva (patient 1 = 6.63 log10 copies/mL; patient 2 = 7.10 log10 copies/mL). SARS-CoV-2 was detected up to hospital day 6 (illness day 9 for patient 2) from the saliva of both patients. The viral load in the saliva decreased transiently for 2 hours after using the chlorhexidine mouthwash.

Conclusion: SARS-CoV-2 viral load was consistently high in the saliva; it was relatively higher than that in the oropharynx during the early stage of COVID-19. Chlorhexidine mouthwash was effective in reducing the SARS-CoV-2 viral load in the saliva for a short-term period.

Keywords: COVID-19; Chlorhexidine; SARS-CoV-2; Saliva; Viral Load.

Conflict of interest statement

The authors have no potential conflicts of interest to disclose.

© 2020 The Korean Academy of Medical Sciences.

Figures

Fig. 1. Viral dynamics of severe acute…
Fig. 1. Viral dynamics of severe acute respiratory syndrome coronavirus 2 in patient 1 (A) and 2 (B): viral load from serial nasopharyngeal, oropharyngeal, saliva, sputum, and urine samples.
NP = nasopharynx, OP = oropharynx.
Fig. 2. Impact of chlorhexidine mouthwash on…
Fig. 2. Impact of chlorhexidine mouthwash on the severe acute respiratory syndrome coronavirus 2 viral load in the saliva.
HD = hospital day.

References

    1. Ministry of Health and Welfare, Korea Centers for Disease Control and Prevention. Updates on 2019 Novel Coronavirus: for Press Release. Cheongju: Korea Centers for Disease Control and Prevention; 2020.
    1. Song JY, Yun JG, Noh JY, Cheong HJ, Kim WJ. Covid-19 in South Korea - Challenges of subclinical manifestations. N Engl J Med. 2020;382(19):1858–1859.
    1. Pan Y, Zhang D, Yang P, Poon LL, Wang Q. Viral load of SARS-CoV-2 in clinical samples. Lancet Infect Dis. 2020;20(4):411–412.
    1. Huang C, Wang Y, Li X, Ren L, Zhao J, Hu Y, et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet. 2020;395(10223):497–506.
    1. To KK, Tsang OT, Chik-Yan Yip C, Chan KH, Wu TC, Chan JM, et al. Consistent detection of 2019 novel coronavirus in saliva. Clin Infect Dis. 2020:ciaa149.
    1. Guan WJ, Ni ZY, Hu Y, Liang WH, Ou CQ, He JX, et al. Clinical characteristics of coronavirus disease 2019 in China. N Engl J Med. 2020;382(18):1708–1720.
    1. Corman VM, Landt O, Kaiser M, Molenkamp R, Meijer A, Chu DK, et al. Detection of 2019 novel coronavirus (2019-nCoV) by real-time RT-PCR. Euro Surveill. 2020;25(3):2000045
    1. Duguid JP. The size and the duration of air-carriage of respiratory droplets and droplet-nuclei. J Hyg (Lond) 1946;44(6):471–479.
    1. Choi WS, Kang CI, Kim Y, Choi JP, Joh JS, Shin HS, et al. Clinical presentation and outcomes of Middle East respiratory syndrome in the Republic of Korea. Infect Chemother. 2016;48(2):118–126.
    1. Lee N, Hui D, Wu A, Chan P, Cameron P, Joynt GM, et al. A major outbreak of severe acute respiratory syndrome in Hong Kong. N Engl J Med. 2003;348(20):1986–1994.
    1. Letko M, Marzi A, Munster V. Functional assessment of cell entry and receptor usage for SARS-CoV-2 and other lineage B betacoronaviruses. Nat Microbiol. 2020;5(4):562–569.
    1. Widagdo W, Begeman L, Schipper D, Run PR, Cunningham AA, Kley N, et al. Tissue distribution of the MERS-Coronavirus receptor in bats. Sci Rep. 2017;7(1):1193.
    1. Liu L, Wei Q, Alvarez X, Wang H, Du Y, Zhu H, et al. Epithelial cells lining salivary gland ducts are early target cells of severe acute respiratory syndrome coronavirus infection in the upper respiratory tracts of rhesus macaques. J Virol. 2011;85(8):4025–4030.
    1. To KK, Yip CC, Lai CY, Wong CK, Ho DT, Pang PK, et al. Saliva as a diagnostic specimen for testing respiratory virus by a point-of-care molecular assay: a diagnostic validity study. Clin Microbiol Infect. 2019;25(3):372–378.
    1. Kim YG, Yun SG, Kim MY, Park K, Cho CH, Yoon SY, et al. Comparison between saliva and nasopharyngeal swab specimens for detection of respiratory viruses by multiplex reverse transcription-PCR. J Clin Microbiol. 2016;55(1):226–233.
    1. Sheahan TP, Sims AC, Leist SR, Schäfer A, Won J, Brown AJ, et al. Comparative therapeutic efficacy of remdesivir and combination lopinavir, ritonavir, and interferon beta against MERS-CoV. Nat Commun. 2020;11(1):222.

Source: PubMed

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