Hostname: page-component-586b7cd67f-dsjbd Total loading time: 0 Render date: 2024-11-22T23:05:45.170Z Has data issue: false hasContentIssue false

Prevalence, seasonality, and peak age of infection of enteric adenoviruses in Japan, 1995–2009

Published online by Cambridge University Press:  20 July 2012

S. K. DEY
Affiliation:
Department of Animal and Avian Sciences, University of Maryland, College Park, MD, USA
I. HOQ
Affiliation:
Department of Microbiology, University of Chittagong, Chittagong, Bangladesh
S. OKITSU
Affiliation:
Division of Microbiology, Department of Pathology and Microbiology, Nihon University, Japan
S. HAYAKAWA
Affiliation:
Division of Microbiology, Department of Pathology and Microbiology, Nihon University, Japan
H. USHIJIMA*
Affiliation:
Division of Microbiology, Department of Pathology and Microbiology, Nihon University, Japan
*
*Author for correspondence: Dr H. Ushijima, M.D., Ph.D., Nihon University School of Medicine, 30-1 Ohyaguchi Kamimachi, Itabashiku, Tokyo 173-8610, Japan. (Email: [email protected])
Rights & Permissions [Opens in a new window]

Summary

A total of 7185 faecal specimens collected from infants and children with gastroenteritis in seven different regions of Japan during 1995–2009 were examined for adenovirus by polymerase chain reaction. Adenovirus was detected in 568 (7·9%) patients. The adenovirus activity peak was in winter and spring seasons (December–March) during the study period in the Japanese paediatric population. During the last 15 years, adenovirus 41 was the most predominant strain in Japan.

Type
Short Report
Copyright
Copyright © Cambridge University Press 2012

Human adenoviruses belong to the genus Mastadenovirus of the family Adenoviridae and are double-stranded DNA viruses without envelope. Comprehensive controlled studies revealed that the so-called ‘non-cultivable’ or ‘enteric’ adenovirus is in contrast to the conventional cultivable ‘non-enteric’ adenovirus, which is also commonly detected in faecal specimens, and is a frequent primary cause of paediatric gastroenteritis. Adenoviruses are responsible for a wide range of disease symptoms. Enteric adenovirus, however, is also considered to be a significant enteropathogen in association with sporadic cases as well as outbreaks of gastroenteritis in such settings as kindergartens, schools and hospitals [Reference Dey1Reference Atmar3]. Adenoviruses are responsible for a wide range of disease symptoms. To date, more than 51 human adenovirus serotypes have been identified and classified into six subgenera (A–F) based on their biological and genetic characteristics. Of these subgenera, subgenera F represented by two serotypes, i.e. adenovirus types 40 and 41 has been found to be associated with acute gastroenteritis [Reference Brown4, Reference Wadell5]. In Japan, there have been many studies of acute gastroenteritis in children since 1910, even before the discovery of viruses. Kasei-shoni-kolera (pseudocholera infantum) or toki-nyuyoji-gerisho (infantile winter diarrhoea) are forms of gastroenteritis with symptoms of vomiting, slight fever, dehydration, and whitish, watery stools [Reference Dey6] generally occurring in infants and young children. Seasonality of pathogens can be defined as the appearance of recurrent epidemics at defined periods of the year. Seasonality in disease incidence often reflects associations with weather factors [Reference Dey6]. Climate change is predicted to affect viral infection and may modulate epidemiological outcome, as well as morbidity and mortality of viral infectious diseases. It is predicted that viral infection is attributable to weather fluctuations; therefore climate change may influence the incidence and the spread of the infection [Reference Dey7]. Adenovirus infection may also be influenced by weather fluctuations. The objectives of this study were to determine the prevalence, seasonality, and peak age of infection of enteric adenoviruses in Japan during 1995–2009.

A total of 7185 faecal specimens were collected from infants and children with acute gastroenteritis in seven different regions from north to the south of Japan (Sapporo, Tokyo, Maizuru, Osaka, Saga, Kagawa, Kurume) during July 1995 to June 2009. In this period, adenovirus analysis was performed systematically on all stool samples by polymerase chain reaction (PCR). Adenovirus was further characterized for genotypes by a sequencing method [Reference Shimizu8]. We determined the seasonality of adenovirus-associated disease by plotting the percentage of the total number of annual cases that occurred in each month. Monthly distribution of adenovirus was defined after adjusting the epidemic curves according to a 3-month unweighted moving average (mean) [Reference Dey6, Reference Dey7]. The ‘peak’ month during the adenovirus season was then defined as that during which the greatest numbers of adenovirus-positive specimens were collected. We analysed the laboratory-confirmed adenovirus cases between 1995 and 2009. We used November as the start month of the adenovirus season for convenience, given that the annual adenovirus season commences between November and May during the study period. To ascertain any shift in the peak, the Mann–Whitney U test was used for analysis of the relationship between duration from August to the peak month (beginning of peak duration) during the 15 seasons. All calculations were performed with SPSS for Windows version 13.0 (SPSS Inc., USA), and significance was set at P<0·05 [Reference Dey6, Reference Dey7].

Between 1995 and 2009, a total of 7185 stool samples were received from patients aged <15 years with acute gastroenteritis for microbiological study. Adenovirus was detected in 565 (7·9%) patients. The annual number and percentage of detected patients with adenovirus in 1995–2009 were 10·4% (24/231), 8·1% (31/381), 15·4% (83/537), 6·5% (32/493), 13·5% (88/650), 9·4% (45/477), 6·2% (31/495), 8% (33/413), 6·5% (26/397), 11·9% (57/477), 6·2% (32/513), 5·2% (23/443), 6·2% (32/513), 2·9% (18/607), and 1·8% (10/553), respectively (Table 1). The highest detection rates of adenovirus were in December (15·6%, 88/565) followed by March (13·8%, 78/565), February (13·1%, 74/565) and January (12%, 68/565) and the lowest detection rates were in October (2·1%, 12/565) followed by August (2·3%, 13/565) and September (2·5%, 14/565). Seasonal decrease in adenovirus diarrhoea occurred annually in Japan (Table 1). Peak adenovirus activity occurred between December and March during the study period (1995–2001). A marked finding of this study was that a low number of adenovirus-positive cases occurred in the warm summer months in Japan. Another interesting feature of this study was that the number of adenovirus-positive cases decreased year by year in Japan. During the last 15 years, adenovirus 41 (Ad41) was the most predominant strain in Japan followed by Ad40, Ad5, Ad1, Ad3, and Ad2, respectively.

Table 1. Monthly distribution of adenovirus infection in Japan, 1995–2009

Epidemiological studies have detected adenoviruses in stool samples collected from infants and young children with acute gastroenteritis, in the developed and developing world [Reference Dey1, Reference Shimizu8Reference Matsushima10]. A number of research groups in Japan have confirmed that most gastroenteritis cases caused by adenovirus occurred during the winter time and were related to ambient temperature. Our analysis, based on laboratory studies during the past 15 years, shows that the adenovirus peak was observed mainly in winter and spring seasons (December–March) in Japan, with statistical significance (P=0·001), in accord with laboratory data from seven regions (Sapporo, Tokyo, Maizuru, Osaka, Saga, Kagawa, Kurume) of Japan for 1995–2009. The typical pattern of regular adenovirus epidemics that appear during cold months in other countries is similar to that observed in our region in the 1995–2009 period of this study. Seasonality in disease incidence often reflects associations with weather factors [Reference Dey1, Reference Dey6Reference Shimizu8].

Data from previously published studies from 1995 to 2009 have shown that adenovirus is a universal cause of acute gastroenteritis in Japanese infants and children [Reference Dey7Reference Matsushima10]. Ad41 was the most predominant strain in Japan. It should be noted that the overall pattern of serotypes was similar to those described in other countries of Asia [Reference Dey1].

In this study we found that adenovirus has been mostly associated with gastroenteritis in infants and children aged <3 years. Over a 15-year period, the present study collected information on diagnosed cases of adenovirus infection and their epidemiological features in a specific geographical area and a well-defined population, i.e. children aged <5 years.

The data from our study demonstrated the cold weather predominance of adenovirus-associated disease in Japan. This finding was independent of the study setting (data not shown), the age of the patients, or the detection methods used and has many implications concerning the route of adenovirus transmission. Winter seasonal transmission is a key epidemiological feature of rotavirus and norovirus, important gastrointestinal pathogens for which airborne transmission has been postulated [Reference Dey7]. Some investigators postulated that the winter peak of viruses may be related to airborne spread [Reference Dey7]. We assumed that winter seasonality of adenovirus-associated disease may also be associated with airborne spread as a secondary route.

In conclusion, the prevalence of adenovirus infection in Japan was significantly high (7·9%). Therefore, adenovirus is considered to be an important enteropathogen responsible for viral gastroenteritis in infants and children in Japan. Although the importance of adenovirus gastroenteritis as a prime cause of morbidity and mortality is well recognized, very few studies have been conducted to evaluate the prevalence and seasonality of adenovirus-related gastroenteritis in infants and children. This paper may provide some important clues to the aetiology of viral gastroenteritis in the Japanese paediatric population.

ACKNOWLEDGEMENTS

We are grateful to Shuichi Nishimura, Hideaki Kikuta, Kumiko Sugita, Tsuneyoshi Baba, and Atsuko Yamamoto for collection of faecal specimens. This study was supported by Grants-in-Aid from the Ministry of Education, Culture, Sports, Sciences and Technology, and the Ministry of Health, Labour and Welfare, Japan. In addition, this research was supported in part by a Grant-in-Aid for Scientific Research under the JSPS Postdoctoral Fellowship.

DECLARATION OF INTEREST

None.

References

REFERENCES

1.Dey, SK, et al. Molecular epidemiology of adenovirus infection among infants and children with acute gastroenteritis in Dhaka City, Bangladesh. Infection, Genetics and Evolution 2009; 9: 518522.CrossRefGoogle ScholarPubMed
2.Akihara, S, et al. Identification of sapovirus infection among Japanese infants in a day care center. Journal of Medical Virology 2005; 77: 595601.CrossRefGoogle Scholar
3.Atmar, RL, et al. Diagnosis of noncultivatable gastroenteritis viruses, the human calicivirus. Clinical Microbiology Review 2001; 14: 1537.CrossRefGoogle Scholar
4.Brown, M, et al. Structural features unique to enteric adenoviruses. Archives of Virology (Suppl.) 1996; 12: 301317.Google ScholarPubMed
5.Wadell, G, et al. Manual of Clinical Microbiology. Washington: ASM Press, 1999, pp. 970982.Google Scholar
6.Dey, SK, et al. Seasonal trend and serotype distribution of rotavirus infection in Japan, 1981–2008. Pediatric Infectious Diseases Journal 2010; 9: 166167.CrossRefGoogle Scholar
7.Dey, SK, et al. Seasonal pattern and genotype distribution of sapovirus infection in Japan, 2003–2009. Epidemiology and Infection 2012; 40: 7477.CrossRefGoogle Scholar
8.Shimizu, H, et al. An outbreak of adenovirus serotype 41 infection in infants and children with acute gastroenteritis in Maizuru City, Japan. Infection, Genetics and Evolution 2007; 7: 279284.CrossRefGoogle ScholarPubMed
9.Okimoto, S, et al. Association of viral isolates from stool samples with intussusception in children. International Journal of Infectious Diseases 2011; 15: e641645.CrossRefGoogle ScholarPubMed
10.Matsushima, Y, et al. Genomic characterization of a novel human adenovirus type 31 recombinant in the hexon gene. Journal of General Virology 2011; 92: 27702775.CrossRefGoogle ScholarPubMed
Figure 0

Table 1. Monthly distribution of adenovirus infection in Japan, 1995–2009