key: cord-0698293-b5dw5mxf
authors: Lee, Han Sol; Lim, Sooyeon; Noh, Ji Yun; Song, Joon Young; Cheong, Hee Jin; Lee, Jung Hwa; Woo, Sung Il; Kim, Woo Joo
title: Identification of influenza C virus in young South Korean children, from October 2013 to September 2016
date: 2019-03-27
journal: J Clin Virol
DOI: 10.1016/j.jcv.2019.03.016
sha: f1afff219f11d2a1a11cc75d12db262630290569
doc_id: 698293
cord_uid: b5dw5mxf

BACKGROUND: Influenza C virus has been largely neglected, compared to influenza A orB viruses, and is not routinely tested in clinical practices. However, several studies have indicated that influenza C virus causes severe acute respiratory illness and pneumonia in all ages. OBJECTIVE: We conducted a study to identify influenza C virus among young children in South Korea.Study design. From October 2013 to September 2016, 973 young children with influenzalike illness (ILI) were enrolled at three university hospitals. We tested nasopharyngeal samples for 16 types of respiratory viruses. Among the tested samples, 564 were positive for one or more respiratory viruses. Except for the samples where 16 types of respiratory viruses were found, 409 negative samples were examined for the presence of influenza C virus, using a matrix gene specific primer set. RESULTS: Among 409 nasopharyngeal samples, five influenza C viruses were detected. The manifestation of influenza C virus infection in young children was observed acute respiratory illness, such as fever, rhinorrhea, and cough, but no pneumonia or severe respiratory illness. Nucleotide sequencing was conducted and a phylogenetic tree was generated. We found that C/Sao Paulo/387/82-like lineage viruses circulated in South Korea, and the fully sequenced virus (C/Seoul/APD462/2015) was closely related to C/Victoria/2/2012 and C/Tokyo/4/2014 strains. CONCLUSIONS: This study was the first report of influenza C virus detection in South Korea. Although severe illness was not observed in this study, we suggest the necessity for influenza C virus testing in pediatric patients with ILI, considering other reports of severe illnesses caused by influenza C virus infections.

Background: Influenza C virus has been largely neglected, compared to influenza A orB viruses, and is not routinely tested in clinical practices. However, several studies have indicated that influenza C virus causes severe acute respiratory illness and pneumonia in all ages. Objective: We conducted a study to identify influenza C virus among young children in South Korea.Study design. From October 2013 to September 2016, 973 young children with influenzalike illness (ILI) were enrolled at three university hospitals. We tested nasopharyngeal samples for 16 types of respiratory viruses. Among the tested samples, 564 were positive for one or more respiratory viruses. Except for the samples where 16 types of respiratory viruses were found, 409 negative samples were examined for the presence of influenza C virus, using a matrix gene specific primer set. Results: Among 409 nasopharyngeal samples, five influenza C viruses were detected. The manifestation of influenza C virus infection in young children was observed acute respiratory illness, such as fever, rhinorrhea, and cough, but no pneumonia or severe respiratory illness. Nucleotide sequencing was conducted and a phylogenetic tree was generated. We found that C/Sao Paulo/387/82-like lineage viruses circulated in South Korea, and the fully sequenced virus (C/Seoul/APD462/2015) was closely related to C/Victoria/2/2012 and C/Tokyo/4/2014 strains. Conclusions: This study was the first report of influenza C virus detection in South Korea. Although severe illness was not observed in this study, we suggest the necessity for influenza C virus testing in pediatric patients with ILI, considering other reports of severe illnesses caused by influenza C virus infections.

Influenza C virus generally causes mild upper respiratory illness in children or young adults [1, 2] . However, recent studies have reported that it can cause lower respiratory illness, such as pneumonia and bronchitis in infants [3] [4] [5] . Studies of influenza C virus have indicated that the virus is widely distributed throughout the world, and that the majority of the human population acquires immunity by first exposure in childhood [6] [7] [8] [9] [10] [11] [12] [13] [14] [15] [16] [17] [18] . Despite a high seropositive rate in children (40-60%) and adults (80-100%), detection and isolation of influenza C viruses have rarely been described [6] [7] [8] [9] [10] [11] .

The genome of influenza C virus consists of seven RNA segments that encode nine proteins: three polymerase proteins (P3, PB2 and PB1), hemagglutinin-esterase (HE) glycoprotein, nucleoprotein (NP), matrix protein (M), CM2 protein, and two nonstructural proteins (NS1 and NS2). In the antigenic analysis and HE gene phylogenetic analysis of influenza C viruses, the virus separated into six antigenic lineages: C/ Taylor/1233/47 (C/Taylor lineage), C/Kanagawa/1/76 (C/Kanagawa lineage), C/Mississippi/80 (C/Mississippi lineage), C/Aichi/1/81 (C/ Aichi lineage), C/Yamagata/26/81(C/Yamagata lineage), and C/Sao Paulo/378/82 (C/Sao Paulo lineage) [11, 19] . Influenza C viruses belonging to different lineages that co-circulate in a community can lead T to emergence of virus reassortment [19, 20] .

Although it has almost 70 years since the first isolation of influenza C virus, there is no information on influenza C virus in South Korea. In this study, we identified influenza C virus infection in children (< 2 years of age) with influenza-like illness (ILI) in South Korea.

From October 2013 to September 2016, 973 young children (< 2 years of age) with ILI were enrolled at the emergency rooms of three university hospitals through a Hospital-based Influenza Morbidity and Mortality (HIMM) surveillance system [21] . ILI was defined as an acute respiratory illness with fever (measured body temperature of ≥38 ℃) and at least one of the following symptoms, cough, sore throat, or rhinorrhea/nasal congestion, and an onset within the previous seven days. After written informed consent was obtained from the legal representatives of enrolled subjects, we obtained nasopharyngeal swabs from children, and placed them into viral transport media (VTM). Clinical information of subjects, including symptoms and underlying diseases were recorded on the clinical report form. We tested the nasopharyngeal samples for 16 types of respiratory viruses using Any-plexTM II RV16 detection kit (Seegene, Seoul, Korea). Among the tested samples, 564 were positive for one or more respiratory viruses and which 383 were positive for influenza A and / or B virus (Table 1) . Excluding the RV16 positive samples, 409 negative samples were examined for the presence of influenza C virus using M gene specific primer set containing TaqManTM probes [22] . Using influenza C virus positive samples, Madin-Darby canine kidney (MDCK) cells were inoculated with VTM samples and cultured for 72 h.

Viral RNA was extracted and transcribed into complementary DNA (cDNA) with a 3′end of influenza C viral RNAs (5′-AGCAGAAGC AGG-3′), using the Primescript 1 st strand cDNA synthesis kit (Takara, Shiga, Japan). Individual segments of influenza C virus were amplified by gene-specific primer sets [16] . After amplification, sequencing was performed using the ABI BigDye Terminator v3.1 cycle sequencing kit (Applied Biosystems, Foster City, CA) and 3730xl DNA analyzer. The sequence readouts of the PCR products were analyzed with BioEdit and MEGA software [23] . The nucleotide sequences obtained from this study were submitted to GenBank under the accession numbers MK050092-MK050104.

Collected samples were tested for influenza A and B, respiratory syncytial virus A and B, adenovirus, parainfluenza virus 1, 2, 3, and 4, bocavirus, metapneumovirus, rhinovirus, coronavirus 229E, NL63 and OC43, and enterovirus, using the AnyplexTM II RV16 detection kit (Seegene, Seoul, Korea). A total of 409 samples negative for 16 respiratory viruses were examined for detection of influenza C virus. Five samples were positive for influenza C virus, including four samples from 2015 and one sample from 2016 (Table 1) . Unfortunately, we only isolated C/Seoul/APD462/2015 virus. Sequence of viral genes showed only the C/Seoul/APD462/2015 virus was fully sequenced for seven segments. The phylogenetic analysis of individual genes was performed using the reference sequences from the influenza research database (IRD). As shown in the HE phylogenetic tree, C/Seoul/APD401/2015, C/Seoul/APD462/2015 and C/Cheongju/GPD805/2015 fell into the C/ Sao Paulo lineage (Fig. 1) . Interestingly, phylogenetic analyses of individual genes revealed a close proximity of C/Seoul/APD462/2015 to C/Tokyo/4/2014 and C/Victoria/2/2012 strains.

The sequence identity score for each pair was calculated by the Sequence Demarcation Tool (SDTv1.2) program. All encoded protein sequence identity of C/Seoul/APD462/2015 strain with C/Tokyo/4/ 2014 or C/Victoria/2/2012 strains showed high identity of 99.6% (Fig. 2) . Comparison of the amino acid sequences of each segment of C/ Seoul/APD462/2015 with C/Victoria/2/2012 revealed several changes in amino acids ( Table 2 

Influenza A and B viruses are well studied in the world, including South Korea [24, 25] . In contrast, influenza C virus is not well known. In this study, we identified influenza C virus infection in five (1.22%) of 409 respiratory samples negative for sixteen respiratory viruses from young children with ILI. According to several reports, influenza C virus commonly causes mild acute respiratory illness and/or pneumonia in pediatric populations [3] [4] [5] . In this study, young children with influenza C virus infections had acute respiratory illnesses, such as fever, rhinorrhea, and cough, but no pneumonia or severe respiratory illness was observed (Supplementary data 1). Thielen BK, et al. reported that influenza C virus was detected among 0.58% of hospitalized patients with severe acute respiratory infection, and 0.48% of outpatients, in Minnesota from 2013 to 2016 [18] . They found that influenza C viruses were most frequent among young children, but occurred in all ages. Influenza C viruses in our study were detected from March to May (Supplementary data 2). This result is consistent with Japanese studies that reported influenza C viruses are mostly isolated between January and June, and usually occur after peaks of influenza A epidemics [11] .

Although there is antigenic variation among influenza C viruses, the C/Kanagawa and C/Sao Paulorelated lineage strains have been dominant strains in Japan, the Philippines, the United States, and France since 2005 [13, [17] [18] [19] . In this study, we confirmed that influenza C viruses belonging to the C/Sao Paulo antigenic group were detected in South Korea. In addition, a re-assortment event was observed in the C/Seoul/APD462/2015 strain, which contains HE, PB1 and PB2 genes belonging to the C/Sao Paulo related lineage, and NP and P3 genes belonging to the C/Mississippi related lineage. Particularly, all segments of C/Seoul/APD462/2015 strain showed high homology to C/ Tokyo/4/2014 and C/Victoria/2/2102 ( Figs. 1 and 2) . Interestingly, Odagiri et al. reported that viruses isolated from the Philippines in 2011 to 2013 were related to C/Victoria/2/2012 [17] . Therefore, these strains are considered to be derived from a common ancestor and spread to South Korea.

In conclusion, this study reports the first identification of influenza C virus among young children and phylogenetic characteristics of a C/ Seoul/APD462/2015 strain isolated in South Korea. Approximately 1.22% of young children with ILI negative for sixteen respiratory viruses during the influenza season were identified with influenza C 

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