Journal List > J Korean Med Sci > v.23(6) > 1020769

Koh, Baek, Shin, Chung, and Jee: Coinfection of Viral Agents in Korean Children with Acute Watery Diarrhea

Abstract

Currently, there are a few reports on viral coinfection that causes an acute watery diarrhea in Korean children. So, to evaluate the features of coinfectious viral agents in children with acute watery diarrhea, we enrolled 155 children with acute watery diarrhea from July 2005 to June 2006. Fecal samples were collected and evaluated for various viral infections such as rotavirus, norovirus, adenovirus and astrovirus. The mean (±standard deviation) age of the children was 2.71±2.37 yr. The detection rate of viral agents was most common in children between the ages of 1 and 3 yr. Rotavirus was detected in 63 children (41.3%), norovirus in 56 (36.2%), adenovirus in 11 (7.1%), and astrovirus in 1 (0.6%). Regarding rotavirus, there were 38 (60.3%) cases with monoinfection and 25 (39.7%) with coinfection. For norovirus, there were 33 (58.9%) cases with monoinfection and 23 (41.1%) with coinfection. Coinfection with rotavirus and norovirus was most common, and occurred in 20/155 cases (12.9%) including coinfection with adenovirus. So, rotavirus and norovirus were the most common coinfectious viral agents in our study population with acute watery diarrhea.

INTRODUCTION

There are more than 20 viruses known to cause acute watery diarrhea. Among them, four viral groups including group A rotavirus, norovirus, enteric adenovirus type 40/41, and astrovirus are frequently associated with acute watery diarrhea (1-3). There is limited information on coinfections in Korean children with watery diarrhea. Guerrero et al. demonstrated coinfection with another pathogen in 11 (42%) of the 26 Mexican infants with acute watery diarrhea (4). Simpson et al. also reported an incidence of causative agents (rotavirus in 28%, norovirus in 13%, sapovirus in 1%, and coinfections in 9%) in American children (5). Recently, Sanchez-Fauquier et al. showed that coinfection of rotavirus with other viral infections was detected in 6.3% of Spanish children with watery diarrhea in 2005 (6). The aim of this study was to assess the coinfectious viral agents causing watery diarrhea including age and seasonal distribution in this population.

MATERIALS AND METHODS

Subjects

The present study was conducted according to good clinical practice and was approved by our hospital ethics committee. Stool specimens were collected from 155 children with acute watery diarrhea that were admitted to Severance Children's Hospital, Seoul, Korea from July 2005 to June 2006. Acute watery diarrhea was defined as more than three liquid stools per day lasting for more than 24 hr (7).

Sample collection and analysis

For long-term preservation of the viral samples, they were stored at -70℃ until use within two weeks. Rotavirus was detected by the rapid stick test (Biocard Rotastick™, Ani Biotech Oy, Vantaa, Finland) using a sandwich type immunoassay. Adenovirus and astrovirus were detected with the Viro-Capture™ Adenovirus Detection Kit (Bioincell, Houston, TX, U.S.A.) and Amplified IDEIA™ Astrovirus Kit (Dako, Glostrup, Denmark), respectively, according to the manufacturer's instructions using polyclonal and monoclonal antibodies in a solid phase immunoassay. The stool samples were also sent to the Korean National Institute of Health for the detection of norovirus. The samples were suspended in phosphate-buffered saline to a concentration of 10-20% and were tested immediately or stored at -70℃. The stool suspensions were clarified by centrifugation at 4℃, 5,000 g for 10 min. The supernatants were mixed with an equal volume of fluorocarbon and centrifuged at 4℃, 3,500 g for 10 min; the supernatants were then collected and centrifuged at 4℃, 100,000 g for 90 min. The pellets were re-suspended in H2O and examined after negative staining with 2.0% uranyl acetate. This suspension was centrifuged at 4℃, 20,000 g for 10 min, and viral RNA was extracted from 140 µL of the supernatant using a commercial RNA extraction kit (QIAmp viral RNA extraction kit; QIAGEN, Hilden, Germany) according to the manufacturer's instructions. After treating with DNase I (Invitrogen, Carlsbad, CA, U.S.A.) at 37℃ for 5 min, the RNA sample was used for reverse-transcriptase-polymerase chain reaction (RT-PCR) immediately. Two sets of primers, NV82+SM82/NV81 (8) and Yuri22F/Yuri22R (9) were used for PCR to amplify the RNA-dependent PNA polymerase region. For nested PCR, two outer primer sets, 36/35' (10) and MR3/MR4 (11) were used for the first PCR; and then NV82, SM82/NV81, and Yuri22F/Yuri22R were used for the second PCR, respectively (12, 13).
All fresh stool specimens were cultured to isolate Salmonella, Shigella, and Campylobacter respectively. But other bacterial cultures of enteropathogens such as E.coli O-157, Clostridium difficile, Vibrio, and Yersinia were not performed before storage.

Statistical analysis

SPSS version 12.0 statistical package (Chicago SPSS Inc., Chicago, IL, U.S.A.) was used for the statistical analysis of frequency, one sample t-test and cross table method.

RESULTS

Detection rates of infectious agents

There were 115/155 (74.2%) positive cases. Rotavirus was detected in 63/155 (41.3%), norovirus 56/155 (36.2%), adenovirus 11/155 (7.1%), and astrovirus 1/155 (0.6%). For the rotavirus, 38/63 (60.3%) cases had monoinfection, and 25/63 (39.7%) coinfection. For the norovirus, 33/56 (58.9%) cases had monoinfection, and 23/56 (41.1%) coinfection. One child had coinfection with Salmonella and norovirus. Among 11 cases with adenovirus, 9 (66.7%) cases had coinfection and only 2 (18.2%) cases had monoinfection. Astrovirus was detected in 1 case (Table 1).
As shown in Table 2, coinfection with another pathogen was observed in 28/155 (18.1%) cases. Coinfection with rotavirus and norovirus was the most common, and occurred in 20/155 (12.9%) including coinfection of adenovirus. In bacterial cultures, Shigella and Campylobacter were not cultured, but Salmonella was detected in only one child coinfected with norovirus.

Clinical manifestations of infectious agents

The mean age of the children with acute watery diarrhea was 2.71±2.37 yr of age with a slight male preponderance (M:F=88:67). Fever was present in 98 (63.2%) children and vomiting in 96 (61.9%). The diarrhea lasted from 3 days in 18 cases to 8 days in 10 cases. There was no significant difference between the cases with monoinfection compared to those with coinfection (data not shown).

Age and seasonal distribution of infectious agents

Thirteen (20.6%) children infected with rotavirus were less than 1 yr of age, and 35 (55.6%) were between 1 and 3 yr. Eighteen (32.1%) children infected with norovirus were less than 1 yr of age and 23 (41.1%) were between 1 and 3 yr. The peak age for both viruses was between 1 and 3 yr. Adenovirus infection was slightly higher in the children between 1 and 3 yr of age compared to other age group. However these differences were not statistically significant (Table 3).
Rotavirus outbreak was observed between December and March with its peak incidence in February. That is, 47 (74.6%) cases occurred during winter season. Norovirus had three peaks in February, June, and October without an apparent seasonal variation. Adenovirus infection showed an even occurrence throughout the year.

DISCUSSION

Acute watery diarrhea is a common disease resulting in high morbidity worldwide, especially during early childhood (14-16). Cubitt et al. reported that 28% of children with gastroenteritis had rotavirus, 6% adenovirus, 3% astrovirus, and 3% calicivirus in a 1985 study conducted in London (17). In France Bon et al. showed that the rotavirus group A was detected in 61% of cases, calicivirus in 14%, astrovirus in 6%, and enteric adenovirus in 3% in 1999 (2). Chung et al. demonstrated that isolation rates of rotavirus, norovirus, adenovirus, and astrovirus of acute gastroenteritis in Korean children were 16.9%, 11.6%, 4.0%, and 4.0%, respectively (18). Recently, Lee et al. studied the etiologic agents in 962 Korean children hospitalized with gastroenteritis that rotavirus, norovirus, adenovirus and astrovirus were detected in 25.7%, 13.7%, 3.0%, and 1.1% of the study population, respectively (19). In this study, rotavirus was detected in 41.3%, norovirus 36.2%, adenovirus 7.1% and astrovirus 0.6%. Therefore, results of the present study were somewhat consistent with previous reports.
In 1998, Guerrero et al. reported that astrovirus was detected in 26/510 (5%) of Mexican infants with diarrhea and the coinfection with another pathogen occurred in 11/26 (42%), including 1 rotavirus, 2 Campylobacter spp., and 4 enterotoxigenic E. coli (4). Torres et al. showed that in Uruguay coinfection with two or more agents was detected in more than one-third of children with diarrhea, and E. coli enteric virotypes, especially enteropathogenic E. coli, were shown to be prevalent (20). Simpson et al. in America demonstrated that rotavirus was detected in 28%, norovirus in 13%, Sapporo virus in 1%, and coinfections in 9% in 2003 (5). Rosenfeldt et al. documented one patient that had coinfection with rotavirus and astrovirus conducted in Denmark. They also identified Campylobacter jejuni in 2 patients and Clostridium difficile in 5 patients among the coinfected young children (14). Yan et al. reported that norovirus, sapovirus and astrovirus were detected in 42, 16, and 4 of the 62 positive samples, respectively, but no coinfection was found among these samples from Japanese pediatric patients (21). However, Roman et al. showed that the most frequent mixed infections were rotavirus-astrovirus, and rotavirus-adenovirus in Spanish children (22). In addition, Li et al. demonstrated that a total of 3,577 fecal specimens were collected from children with acute gastroenteritis in Japan, Korea and Vietnam during the period of 1998 to 2001. Among the three countries, the detection rate of adenovirus was highest in Korea (8.7%) (23). Recently, Chung et al. studied in 812 Korean children with acute gastroenteritis that coinfection of viral agents was confirmed in 2.7% of the study population, most commonly with rotavirus and norovirus and with rotavirus and human astrovirus (18). In our study, coinfections were observed in 28/155 (18.1%). This finding showed that rotavirus and norovirus were the most common combinations occurring in 20/155 (12.9%) cases. Therefore, coinfection with rotavirus and norovirus was more frequent in this population. Furthermore, the present study reported that astrovirus infection occurred less frequently than reported in other studies and especially the cases of coinfected adenovirus were larger than those of monoinfected. The differences among studies reporting viral infections in different countries might be explained by the different age group, seasonal variations at the time of sampling, and the viral detection methods used. However, all studies, including ours, agreed that rotavirus was the most common etiological agent.
Rotavirus most commonly affects children from 6 months to 2 yr of age. Surveillance in Japan between 1994 and 1999 showed that the most frequent etiology of acute watery diarrhea was rotavirus in children younger than 3, and norovirus in children older than 3 yr of age (24). Lee et al. in Malaysia also reported that rotavirus infection was most frequent in the less than 3 yr age group in 2006 (25) similar to the results of our study.
The limitations of this study included the following: 1) not all specimens were confirmed by RT-PCR or gene amplification although the detection rate by immunoassay was relatively high, 2) specimens were not cultured for all bacterial pathogens such as E. coli, Vibrio, Yersinia and Clostridium species using specific agar.
In conclusion, the results of this study showed that rotavirus and norovirus were the most common coinfectious agents responsible for acute watery diarrhea in Korean children. The incidence of coinfection among various viral agents was relatively high in this population presenting with acute watery diarrhea.

Figures and Tables

Table 1
Incidence of viral infections in children with acute watery diarrhea
jkms-23-937-i001
Table 2
Coinfectious viral agents and its incidence
jkms-23-937-i002
Table 3
Infectious agents and age distribution of patients
jkms-23-937-i003

References

1. Gallimore CI, Cubitt DW, Richards AF, Gray JJ. Diversity of enteric viruses detected in patients with gastroenteritis in a tertiary referral paediatric hospital. J Med Virol. 2004. 73:443–449.
crossref
2. Bon F, Fascia P, Dauvergne M, Tenenbaum D, Planson H, Petion AM, Pothier P, Kohli E. Prevalence of group A rotavirus, human calicivirus, astrovirus, and adenovirus type 40 and 41 infections among children with acute gastroenteritis in Dijon, France. J Clin Microbiol. 1999. 37:3055–3058.
crossref
3. Chikhi-Brachet R, Bon F, Toubiana L, Pothier P, Nicolas JC, Flahault A, Kohli E. Virus diversity in a winter epidemic of acute diarrhea in France. J Clin Microbiol. 2002. 40:4266–4272.
crossref
4. Guerrero ML, Noel JS, Mitchell DK, Calva JJ, Morrow AL, Martinez J, Rosales G, Velázguez FR, Monroe SS, Glass RI, Pickering LK, Ruiz-Palacios GM. A prospective study of astrovirus diarrhea of infancy in Mexico City. Pediatr Infect Dis J. 1998. 17:723–727.
crossref
5. Simpson R, Aliyu S, Iturriza-Gómara M, Desselberger U, Gray J. Infantile viral gastroenteritis: on the way to closing the diagnostic gap. J Med Virol. 2003. 70:258–262.
crossref
6. Sánchez-Fauguier A, Montero V, Moreno S, Solé M, Colomina J, Iturriza-Gomara M, Revilla A, Wilhelmi I, Gray J. Gegavi/VIGESS-Net Group. Human rotavirus G9 and G3 as major cause of diarrhea in hospitalized children, Spain. Emerg Infect Dis. 2006. 12:1536–1541.
7. Clark B, McKendrick M. A review of viral gastroenteritis. Curr Opin Infect Dis. 2004. 17:461–469.
crossref
8. Sugieda M, Nakajima K, Nakajima S. Outbreaks of Norwalk-like virus-associated gastroenteritis traced to shellfish: coexistence of two genotypes in one specimen. Epidemiol Infect. 1996. 116:339–346.
crossref
9. Saito H, Saito S, Kamada K, Harata S, Sato H, Morita M, Miyajima Y. Application of RT-PCR designed from the sequence of the local SRSV strain to the screening in viral gastroenteritis outbreaks. Microbiol Immunol. 1998. 42:439–446.
crossref
10. Wang J, Jiang X, Madore HP, Gray J, Desselberger U, Ando T, Seto Y, Oishi I, Lew JF, Green KY. Sequence diversity of small round-structured viruses in the Norwalk virus group. J Virol. 1994. 68:5982–5990.
crossref
11. Lew JF, Petric M, Kapikian AZ, Jiang X, Estes MK, Green KY. Identification of Minireovirus as a Norwalk-like virus in pediatric patients with gastroenteritis. J Virol. 1994. 68:3391–3396.
crossref
12. Hamano M, Kuzuya M, Fujii R, Ogura H, Yamada M. Epidemiology of acute gastroenteritis outbreaks caused by Noroviruses in Okayama, Japan. J Med Virol. 2005. 77:282–289.
crossref
13. Kojima S, Kageyama T, Fukushi S, Hoshino FB, Shinohara M, Uchida K, Natori K, Takeda N, Katayama K. Genogroup-specific PCR primers for detection of Norwalk-like viruses. J Virol Methods. 2002. 100:107–114.
crossref
14. Rosenfeldt V, Vesikari T, Pang XL, Zeng SQ, Tvede M, Paerregaard A. Viral etiology and incidence of acute gastroenteritis in young children attending day-care centers. Pediatr Infect Dis J. 2005. 24:962–965.
crossref
15. Middleton PJ. Viruses that multiply in the gut and cause endemic and epidemic gastroenteritis. Clin Diagn Virol. 1996. 6:93–101.
crossref
16. Kapikian AZ. Overview of viral gastroenteritis. Arch Virol. 1996. 12:7–19.
crossref
17. Cubitt WD. Historical background and classification of caliciviruses and astroviruses. Arch Virol Suppl. 1996. 12:225–235.
crossref
18. Chung JY, Huh K, Kim SW, Shin BM, Han TH, Lee JI, Song MO. Molecular epidemiology of human astrovirus infection in hospitalized children with acute gastroenteritis. Korean J Pediatr Gastroenterol Nutr. 2006. 9:139–146.
crossref
19. Lee JI, Chung JY, Han TH, Song MO, Hwang ES. Detection of human bocavirus in children hospitalized because of acute gastroenteritis. J Infec Dis. 2007. 196:994–997.
crossref
20. Torres ME, Pírez MC, Schelotto F, Varela G, Parodi V, Allende F, Falconi E, Dell'Acqua L, Gaione P, Méndez MV, Ferrari AM, Montano A, Zanetta E, Acuña AM, Chiparelli H, Ingold E. Etiology of children's diarrhea in Montevideo, Uruguay: associated pathogens and unusual isolates. J Clin Microbiol. 2001. 39:2134–2139.
crossref
21. Yan H, Yagyu F, Okitsu S, Nishio O, Ushijima H. Detection of norovirus (GI, GII), Sapovirus and astrovirus in fecal samples using reverse transcription single round multiplex PCR. J Virol Methods. 2003. 114:37–44.
22. Román E, Wilhelmi I, Colomina J, Villar J, Cilleruelo ML, Nebreda V, Del Alamo M, Sánchez-Fauquier A. Acute viral gastroenteritis: proportion and clinical relevance of multiple infections in Spanish children. J Med Microbiol. 2003. 52:435–440.
crossref
23. Li L, Phan TG, Nguyen TA, Kim KS, Seo JK, Shimizu H, Suzuki E, Okitsu S, Ushijima H. Molecular epidemiology of adenovirus infection among pediatric population with diarrhea in Asia. Microbiol Immunol. 2005. 49:121–128.
crossref
24. Inouye S, Yamashita K, Yamadera S, Yoshikawa M, Kato N, Okabe N. Surveillance of viral gastroenteritis in Japan: Pediatric cases and outbreaks incidents. J Infect Dis. 2000. 181:Suppl 2. S270–S274.
25. Lee WS, Rajasekaran G, Pee S, Karunakaran R, Hassan HH, Puthucheary SD. Rotavirus and other enteropathogens in childhood acute diarrhoea: a study of two centres in Malaysia. J Paediatr Child Health. 2006. 42:509–514.
crossref
TOOLS
Similar articles