Detection of Rotavirus Genotypes in Korea 5 Years after the Introduction of Rotavirus Vaccines

Ju-Young Chung; Min-Sung Kim; Tae Woong Jung; Seong Joon Kim; Jin-Han Kang; Seung Beom Han; Sang Yong Kim; Jung Woo Rhim; Hwang-Min Kim; Jae Hong Park; Dae Sun Jo; Sang Hyuk Ma; Hye-Sook Jeong; Doo-Sung Cheon; Jong-Hyun Kim

doi:10.3346/jkms.2015.30.10.1471

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Chung, Kim, Jung, Kim, Kang, Han, Kim, Rhim, Kim, Park, Jo, Ma, Jeong, Cheon, and Kim: Detection of Rotavirus Genotypes in Korea 5 Years after the Introduction of Rotavirus Vaccines

Original Article

Pediatrics

Journal of Korean Medical Science 2015; 30(10): 1471-1475.

Published online: 12 September 2015

DOI: https://doi.org/10.3346/jkms.2015.30.10.1471

Detection of Rotavirus Genotypes in Korea 5 Years after the Introduction of Rotavirus Vaccines

Ju-Young Chung¹

, Min-Sung Kim², Tae Woong Jung²

, Seong Joon Kim²

, Jin-Han Kang³

, Seung Beom Han³

, Sang Yong Kim⁴

, Jung Woo Rhim⁵

, Hwang-Min Kim⁶

, Jae Hong Park⁷

, Dae Sun Jo⁸

, Sang Hyuk Ma⁹, Hye-Sook Jeong¹⁰

, Doo-Sung Cheon¹⁰

, Jong-Hyun Kim²

¹Department of Pediatrics, Sanggyepaik Hospital, Inje University College of Medicine, Seoul, Korea.

²Department of Pediatrics, St. Vincent's Hospital, College of Medicine, The Catholic University of Korea, Suwon, Korea.

³Department of Pediatrics, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.

⁴Department of Pediatrics, Incheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Incheon, Korea.

⁵Department of Pediatrics, Daejeon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Daejeon, Korea.

⁶Department of Pediatrics, Wonju Severance Christian Hospital, Yonsei University Wonju College of Medicine, Wonju, Korea.

⁷Department of Pediatrics, Pusan National University Yangsan Hospital, Pusan National University School of Medicine, Yangsan, Korea.

⁸Department of Pediatrics, Chonbuk National University Hospital, Chonbuk National University Medical School, Jeonju, Korea.

⁹Department of Pediatrics, Changwon Fatima Hospital, Changwon, Korea.

¹⁰Division of Vaccine Research, Center for Infectious Diseases, National Institute of Health, Korea Centers for Disease Control and Prevention, Cheongwon, Korea.

Address for Correspondence: Jong-Hyun Kim, MD. Department of Pediatrics, St. Vincent's Hospital, College of Medicine, The Catholic University of Korea, 93 Jungbu-daero, Paldal-gu, Suwon 16247, Korea. Tel: +82.31-249-8212, Fax: +82.31-257-9111, jh00mn@catholic.ac.kr

Received 13 March 2015 Accepted 7 July 2015

(open-access):

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Rotavirus (RV) is one of the most important viral etiologic agents of acute gastroenteritis (AGE) in children. Although effective RV vaccines (RVVs) are now used worldwide, novel genotypes and outbreaks resulting from rare genotype combinations have emerged. This study documented RV genotypes in a Korean population of children with AGE 5 yr after the introduction of RVV and assessed potential genotype differences based on vaccination status or vaccine type. Children less than 5-yr-old diagnosed with AGE between October 2012 and September 2013 admitted to 9 medical institutions from 8 provinces in Korea were prospectively enrolled. Stool samples were tested for RV by enzyme immunoassay and genotyped by multiplex reverse-transcription polymerase chain reaction. In 346 patients, 114 (32.9%) were RV-positive. Among them, 87 (76.3%) patients were infected with RV alone. Eighty-six of 114 RV-positive stool samples were successfully genotyped, and their combinations of genotypes were G1P[8] (36, 41.9%), G2P[4] (12, 14.0%), and G3P[8] (6, 7.0%). RV was detected in 27.8% of patients in the vaccinated group and 39.8% in the unvaccinated group (P=0.035). Vaccination history was available for 67 of 86 cases with successfully genotyped RV-positive stool samples; RotaTeq (20, 29.9%), Rotarix (7, 10.4%), unvaccinated (40, 59.7%). The incidence of RV AGE is lower in the RV-vaccinated group compared to the unvaccinated group with no evidence of substitution with unusual genotype combinations.

Graphical Abstract

Keywords: Rotavirus, Vaccine, Genotype, Children, Gastroenteritis, Feces

INTRODUCTION

Rotavirus (RV) is one of the most important viral agents causing acute gastroenteritis (AGE) in children, although the importance of norovirus (NV) as a causative agent for AGE is increasing (1 2). Recently, two RV vaccines (RVVs), Rotarix® (GlaxoSmithKlein Co., Middlesex, UK) and RotaTeq® (Merck Sharp & Dohme Co., NJ, USA) were developed. Based on the results of several clinical efficacy studies, these vaccines have been used in young infants to prevent RV infection (3 4 5). Postmarketing surveillance studies revealed that the introduction of RVVs has resulted in a significant decrease in AGE due to RV infection in children (6 7 8 9). In Korea, the RVV is optional and not covered by health insurance. G1, G9, and G3 genotypes have been shown to be predominant in previous Korea studies, with variations observed according to region and study period (10 11 12). In Brazil, the possibility of immune selection due to mass vaccination has been suggested (13), although there are still ongoing debates concerning possible genotypic differences after introduction of RVVs (14 15 16 17 18 19). However, the emergence of novel genotypes and outbreaks of rare combinations of genotypes have been observed in recent years (13 20 21 22), suggesting the necessity for continued monitoring of RV strains to ensure vaccine efficacy.

The purpose of this study was to investigate RV genotypes five years after introduction of RVVs and to determine the differences in genotype distributions according to vaccination status and vaccine type.

MATERIALS AND METHODS

Study population

A total of 448 children hospitalized with AGE between October 2012 and September 2013 at 9 medical institutions from 8 provinces: Sanggyepaik Hospital (117 cases in North Seoul, Inje University College of Medicine); Seoul St. Mary's Hospital in South Seoul, 27; Incheon St. Mary's Hospital in Incheon, 18; St. Vincent's Hospital in Suwon, 38; Daejeon St. Mary's Hospital, Catholic University of Korea in Daejeon, 71; Wonju Severance Christian Hospital, Yonsei University Wonju College of Medicine in Wonju, 55; Pusan National University Yangsan Hospital, Yangsan, 53; Chonbuk National University Hospital in Jeonju, 33; Changwon Fatima Hospital in Changwon, 42.

The definition of AGE was as follows: 1) loose or watery stool three or more times within 24 hr; 2) abnormal stool associated with fever, severe abdominal pain, or vomiting; and 3) onset of symptoms within 7 days, with the above symptoms being absent 2 weeks before admission. The exclusion criteria for AGE symptoms were as follows: abnormal stool associated with 1) previously diagnosed diseases such as pneumonia or acute otitis media, 2) underlying chronic gastrointestinal diseases, and 3) nosocomial infections (with acute vomiting or diarrhea beginning 48 h after admission). At admission, information for RV immunization status and RVV type were collected from the patient's parents and verified by vaccination cards.

Sample collection and preparation

Stool samples were collected from 417 of 448 hospitalized children with AGE with informed and written consent from the patient's parents. Of 417 stool samples, 346 samples (83.0%) were included in this study, and 71 samples were excluded for the following reasons: other diagnosis (2 cases), age over 5 yr (12 cases), and incomplete case report form (57 cases). Stool samples were stored at -70℃. For experimental use, 1 g of stool was thawed, diluted 1:10 in phosphate-buffered saline (9 mL), vortexed, and centrifuged at 3,200 rpm for 20 min at 4℃. Supernatants were collected for subsequent experiments.

Enzyme-linked immunosorbent assay (ELISA) for identification of RV

RV was initially identified using a BioTracer Rotavirus ELISA kit (Bio Focus Co., Uiwang, Korea) according to the manufacturer's instructions. Stool supernatants (100 µL) and enzyme-conjugated antibodies (100 µL) were added to the plate and incubated for 60 min at 37℃. The positive control was 100 µL of the prepared sample in the ELISA kit, and the negative control was 100 µL PBS. After washing the plate five times with 200 µL PBS using an ELISA washing machine, 100 µL of reagent was added in a dark room for 15 min at room temperature, and 50 µL of stop solution was then added. Sample optical density was measured with an ELISA plate reader at a wavelength of 450 nm and analyzed according to the manufacturer's instructions.

Reverse transcription polymerase chain reaction (RT-PCR) for identification of RV

Total RNA was extracted from stool samples with the QIAamp viral RNA kit (Qiagen GmbH, Hilden, Germany). Multiplex RT-PCR was performed for RV-positive stool samples screened by ELISA, with primers for G-type (G1-G4, G8, and G9) and P-type (P1A[8], P1B[4], P2[6], P3[9], P4[10]), as described previously (23)].

Detection of other enteric viral agents

NV was identified by real-time RT-PCR and conventional nested RT-PCR, as described previously (24). Enteric adenovirus (AdV) was detected with the BioTracer Adenovirus ELISA kit (Bio Focus Co.) according to the manufacturer's instructions. The supernatant conjugate (100 µL) was mixed in each microwell plate and reacted for 1 hr at 37℃. One hundred microliters of test sample from the kit was used as a positive control, and PBS was used as a negative control. The microwell was washed five times with 200 µL PBS. After adding 100 µL of substrate to each microwell and incubating at 20-30℃ for 15 min, 50 µL of stop solution was added to each microwell. Absorbance was read with an ELISA reader at 450 nm.

Astrovirus (AsV) and sapovirus (SV) were detected with the AccuPower Astro-Sapovirus Real Time RT-PCR Kit (BIONEER, Daejeon, Korea). Twenty microliters of RNA sample was added to a PCR tube and centrifuged. Reactions were carried out with an initial reverse transcription step at 48℃ for 40 min, followed by 45 cycles of amplification (30 sec at 94℃, 30 sec at 58℃, and 60 sec at 72℃), and a final extension of 7 min at 72℃. PCR products were run on a 1% agarose gels, stained with ethidium bromide, and visualized under ultraviolet light.

Ethics statement

The study protocol was approved by the institutional review board of the Catholic Medical Center of the Catholic University of Korea (approval number XC12TNMI0024KOVD) and the other 8 participating hospitals. Informed consent was obtained from all parents of the subjected patients.

RESULTS

RV detection

The age distribution of the 346 children in this study was as follows: under 2 months of age in 6.9% (24 cases), 2-5 months of age in 8.1% (28), 6-23 months of age in 53.5% (185), and 24-59 months of age in 30.6% (106). The sex ratio was 1.23 (male to female), 191 males and 155 females. Of 346 stool samples, enteric viral agents were detected in 66.2% (229 cases). RV was detected in 87 cases (38.0%), NV was detected in 95 (41.5%), enteric AdV was detected in 10 (4.4%), AsV was detected in five (2.2%), SV was detected in two (0.9%), and mixed infection was detected in 30 (13.1%; Table 1).

Among the 114 children identified as RV positive by ELISA, single infection of RV occurred in 87 cases (76.3%) while mixed infection with other viruses occurred in 27 (23.7%). The average age of RV-infected patients with AGE was 19.8±13.6 months (median, 16 months). When comparing the ratio of RV-infected patients with AGE to all patients with AGE, there was no statistically significant difference between age groups: 20.3% (27/133) in patients ages 0-11 months, 34.6% (37/107) in patients ages 12-23 months, 29.8% (17/57) in patients ages 24-35 months, 31.0% (9/29) in patients ages 36-47 months, and 25% (5/20) in patients ages 48-59 months. During the study period, RV detection peaked in March and April, but rapidly decreased in May. Mixed infections were frequently observed in October and December.

Vaccination history

Out of 346 children, vaccination history was available in only 272; vaccinated 144 (52.9%), unvaccinated 128 (47.1%). In the 144 vaccinated children, Rotarix was used for 55 (38.2%), RotaTeq in 73 (50.7%), and an unknown type of RVV in 16 (11.1%). The vaccination rate with RVVs according to age was as follows: 0-11 months, 55.9% (62/111); 12-23 months, 51.9% (42/81); 24-35 months, 54.8% (23/42); 36-47 months, 56.0% (14/25); and 48-59 months, 23.1% (3/13), as shown in Table 2. RV was detected in 27.8% (40/144) of children in the vaccinated group and 39.8% of (51/128) of children in the unvaccinated group (P=0.035).

Genotyping of RV

Eighty-six of 114 RV-positive stool samples were successfully genotyped. The most common combinations of genotypes were G1P[8] (36 cases, 41.9%), G2P[4] (12, 14.0%), and G3P[8] (6, 7.0%). Vaccination histories of RVV were available in only 67 of 86 RV genotyped children (Rotarix in seven cases, RotaTeq in 20, and unvaccinated in 40). In 67 RV-genotyped children with known vaccination history, the most common genotypes were G1P[8] (34 cases, 43.3%), G2P[4] (8, 11.9%), G3P[8] (6, 8.9%), and G9P[8] (4, 5.9%). In both vaccinated and unvaccinated children, the most predominant G and P genotypes were G1 and P[8], respectively (Table 3). The most common combination of G/P genotypes was G1P[8]: 57.1% in Rotarix-vaccinated children, 45% in RotaTeq-vaccinated children, and 40% in unvaccinated children (Table 4). In children under 2 months of age which was RV (16.6%, 4/24 cases), the detected genotype was as follows: G1P[8] in 2 cases, G1P[6]P[8] in 1, and G3P[8] in 1.

DISCUSSION

In this study, 32.9% (114/346) of the study population was RV positive. This result was similar to that (29.3%) of a recent Korean study (11). The detection rate of RV in vaccinated group children was significantly lower than that in unvaccinated children, which was consistent with the results of previous studies showing the effects of vaccination on prevention of severe RV-dependent AGE (7 8 9 25). In Korea, RotaTeq was introduced in June 2007, while Rotarix was introduced in March 2008. After the introduction of these vaccines in Korea, the vaccination rate was reported to be about 30% in 2009, reaching 50.2% [Rotarix-34.1%, RotaTeq-26.1%] in 2012 (26 27). Among patients in this study, the RV vaccination rate was 52.9% (144/272), a notable increase in the vaccination rate compared to that in previous studies (26 27). It is unclear whether the RV vaccination rate in Korea has actually increased or whether the observed increase in this study may reflect population differences, specifically in residents in major cities, between this study and a report of the vaccination rate in 2012 (27). The most commonly detected RV genotypes in humans are G1-G4, G9, and P[8], and rare combinations of G/P genotypes (G2P[6], G8P[14], and G9P[10]) are frequently observed in undeveloped countries (28 29), suggesting that prevalent genotypes vary depending on the year, region, and country of origin. Emergence of the previously rare G9P[4] genotype was reported in Latin America in 2009-2010, suggesting genetic re-assortment (13 22), but further epidemiological studies are required to confirm this finding. The predominance of G2P[4] after the introduction of Rotarix was regarded initially as a possible case of the immune escape phenomenon, although this is still debatable (14 15 17 18 19). In this study, G1P[8] (41.9%) and G2P[4] (14.0%) were the predominant strains among the 86 genotyped RV strains. These data suggested that the prevalent genotypes of RV have not changed after introduction of vaccines in Korea. Furthermore, the G9P[4] genotype was not observed, although some unusual genotype combinations, including P[6] with G2, G3, or G9, were detected. In this study, mixed infections were found (10%) in unvaccinated group. This finding might be a cause of strain diversity of circulating RV, which was suggested in a recent study in India (30 31). The limitations of this study include the small size of the study population, the unknown genotypes of excluded cases, and the method of genotyping (multiplex RT-PCR not including G10 and G12).

In conclusion, the RV infection season was delayed by approximately 2-4 months after the introduction of RVVs. The distribution of RV genotypes between vaccinated and unvaccinated groups, however, was not different. These results suggest that RV vaccination may not have driven the emergence of variant RV genotypes by substitution due to immune pressure in Korea during 2012-2013; however, the limitation of this study, including the small sample size and the restricted time-frame, should be considered when analyzing these results.

Figures and Tables

Table 1

Causative viral agents in inpatient children less than 5 yr with acute gastroenteritis

Single infection	No. of positive	Mixed infection	No. of positive
Rotavirus	87	Rotavirus + Norovirus	18
Norovirus	95	Rotavirus + Adenovirus	8
Adenovirus	10	Rotavirus + Astrovirus	1
Astrovirus	5	Norovirus + Adenovirus	1
Sapovirus	2	Norovirus + Astrovirus	1
Sapovirus	2	Adenovirus + Sapovirus	1
Negative	117
Total			346

Table 2

Status of rotavirus vaccination according to age of children with acute gastroenteritis

Group	No.(%) of patients after vaccine introduction
Group	0-11 mo (n=133)	12-23 mo (n = 107)	24-35 mo (n = 57)	36-47 mo (n = 29)	48-59 mo (n = 20)	Total (n=346)
Vaccinated	62 (46.6)	42 (39.3)	23 (40.4)	14 (48.3)	3 (15.0)	144 (41.6)
Unvaccinated	49 (36.8)	39 (36.4)	19 (33.3)	11 (37.9)	10 (50.0)	128 (36.9)
Unknown	22 (16.5)	26 (24.3)	15 (26.3)	4 (13.8)	7 (35.0)	74 (21.4)

Table 3

Distribution of children with gastroenteritis by P and G genotypes of rotavirus according to status and vaccine types

Genotypes	No.(%) of children by vaccine
Genotypes	Rotarix® (n = 7)	Rotateq® (n = 20)	Unvaccinated (n = 40)
P type
P[4]	1 (14.3)	3 (15.0)	10 (25.0)
P[6]	0	1 (5.0)	2 (5.0)
P[8]	6 (85.7)	15 (75.0)	23 (57.5)
P[4]+P[8]	0	1 (5.0)	4 (10.0)
P[6]+P[8]	0	0	1 (2.5)
G type
G1	4 (57.1)	10 (50)	20 (50.0)
G2	1 (14.3)	4 (20)	9 (22.5)
G3	0	4 (20)	3 (7.5)
G4	0	0	1 (2.5)
G9	0	0	3 (7.5)
G1+G2	1 (14.3)	0	3 (7.5)
G1+G3	0	1 (5)	0
G1+G9	1 (14.3)	0	0
G2+G9	0	1 (5)	1 (2.5)

Table 4

Combination of G and P types of rotavirus according to the status of rotavirus vaccination and type of vaccine

Genotypes	No. of vaccinated children		No. of unvaccinated children (n=40)	Total
Genotypes	Rotarix® (n = 7)	Rotateq® (n = 20)	No. of unvaccinated children (n=40)	Total
G9P[8]	0	0	3 (7.5%)	3
G3P[8]	0	3 (15%)	3 (7.5%)	6
G2P[8]	1 (14.3%)	2 (10%)	0	3
G1+G9P[8]	1 (14.3%)	0	1 (2.5%)	2
G1+G3P[8]	0	1 (5%)	0	1
G1P[8]	4 (57.1%)	9 (45%)	16 (40.0%)	29
G3P[6]	0	1 (5%)	0	1
G4P[6]	0	0	1 (2.5%)	1
G2P[6]	0	0	1 (2.5%)	1
G1P[6]+P[8]	0	0	1 (2.5%)	1
G2+G9P[4]	0	1 (5%)	0	1
G2P[4]	0	1 (5%)	7 (17.5%)	8
G1+G2P[4]	1 (14.3%)	0	2 (5.0%)	3
G1P[4]	0	1 (5%)	1 (2.5%)	2
G2P[4]+P[8]	0	1 (5%)	1 (2.5%)	2
G1+G2P[4]+P[8]	0	0	1 (2.5%)	1
G1P[4]+P[8]	0	0	2 (5.0%)	2

Notes

^Funding This study was supported by the Research Fund (No. 2013-E42001-00) of the Korea Center for Diseases Control and Prevention.

^DISCLOSURE The authors declare that they have no competing interests.

^{AUTHOR CONTRIBUTION} Conception and design of the study: Kim JH, Chung JY. Data acquisition: Kim MS, Jung TW, Chung JY, Kang JH, Han SB, Kim SY, Rhim JW, Kim HM, Park JH, Jo DS, Ma SH, Jeong HS, Cheon DS. Data review: Chung JY, Kim MS, Kim SJ, Jung TW, Kim JH. Manuscript preparation: Chung JY, Kim MS, Kim JH. Manuscript approval: all authors.

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ORCID iDs

Ju-Young Chung
https://orcid.org/http://orcid.org/0000-0003-4162-5317

Tae Woong Jung
https://orcid.org/http://orcid.org/0000-0002-0160-5242

Seong Joon Kim
https://orcid.org/http://orcid.org/0000-0002-3130-9495

Jin-Han Kang
https://orcid.org/http://orcid.org/0000-0003-1610-6742

Seung Beom Han
https://orcid.org/http://orcid.org/0000-0002-1299-2137

Sang Yong Kim
https://orcid.org/http://orcid.org/0000-0001-8360-0586

Jung Woo Rhim
https://orcid.org/http://orcid.org/0000-0002-0227-3809

Hwang-Min Kim
https://orcid.org/http://orcid.org/0000-0002-0329-1371

Jae Hong Park
https://orcid.org/http://orcid.org/0000-0002-5274-7064

Dae Sun Jo
https://orcid.org/http://orcid.org/0000-0002-3141-9539

Hye-Sook Jeong
https://orcid.org/http://orcid.org/0000-0003-2027-006X

Doo-Sung Cheon
https://orcid.org/http://orcid.org/0000-0002-0317-7122

Jong-Hyun Kim
https://orcid.org/http://orcid.org/0000-0001-8641-7904

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