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240


Jaeyoung Moon et al


Fig. 1. Phylogenetic analysis based on partial nucleotide sequences of M and S segments of severe fever with thrombocytopenia syndrome virus (SFTSV) strains using the maximum likelihood (ML) method and the Kimura 2-parameter model. Numbers on branches indicate bootstrap percentages based on 1,000 replications, and the scale bar indicates nucleotide substitutions per site. The index patient and case 1 are marked with closed circles.


showed leukopenia, thrombocytopenia, and elevated levels of aspartate transaminase, alanine transaminase, and creatine phosphokinase. On September 29, he rapidly deteriorated with hypersomnia and dis- orientation. He was transferred into the intensive care unit (ICU). On September 30, incidental epistaxis and oral bleeding appeared. The patient was intubated for mechanical ventilation following a seizure attack with hypoxemia. On October 1, he expired from progression of multiorgan failure. Confirmatory RT-PCR test revealed that he was positive for SFTSV, with 1.9×106 copies/mL of viral titer at admis- sion. During ICU hospitalization, standard and contact precautions were implemented with suspicion of SFTS. Epidemiologic investigation revealed that a total of 14 HCP


contacted the index patient during his hospitalization (Table 1). Of these, 2 were confirmed or suspected to have SFTS, including a 31-year-old male doctor who tried endotracheal intubation for the index patient (case 1) and a 26-year-old male mortuary beautician (case 2). Case 1 was admitted with fever of 39.3°C and chills on October 10. SFTS was confirmed by detecting SFTSV RNA (6.6×104 copies/mL) from his serum and ≥4-fold increase in antibody titers. He had short contact (within 10 minutes) with the index patient during endotracheal intubation, wearing a fluid- shield mask and gloves. During intubation, frequent oro-tracheal suctions were done to ensure visibility due to patient’s naso-oral bleeding. Case 2 had contact with the index corpse without gloves or mask. He felt malaise without documented fever 1 week after contact. He had a 2-fold increase in serial IgG titer from 1:128 to 1:256 in sera collected at 25 days and 60 days after contact, respectively, without detection of SFTSV RNA. He denied any


recent history of outdoor activity. The remaining 12 HCP were negative for SFTSV by IFA. PCR sequencing was performed for the index patient and case 1.


Sequences ofMand S segments from case 1 shared 100% nucleotide identities with the index patient. Phylogenetic analysis for sequences of M and S segments from the isolated virus were classified as genotype D and clustered with sequences of PCR products from case 1 and the index patient (Fig. 1).


Discussion


We have documented a cluster of nosocomial SFTS using epi- demiologic and viral genomic evidence. The index patient and case 1 were classified as genotype D, although genotype B strains of SFTS were predominant in Korea during 2013–2017.9 Genotype D was isolated from only 1 case in 2014. Both M and S segments showed 100% homology in nucleotide sequences, confirming the same origin of SFTS infection between the index patient and case 1. Epidemiological investigation showed that all HCP wore fluid- shield mask and gloves during potential exposure period. How- ever, these PPEs cannot protect conjunctiva or upper respiratory tract against aerosols containing the pathogen. Case 1 might be infected through aerosols generated from suctions of oral bleeding during endotracheal intubation. Previous studies reported that doctors contracted this disease after performing endotracheal intubation2,3,5 and suggested droplet or possible aerosol trans- mission.3,5 We believe that case 2 was infected through direct


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