Skip to main content

The epidemiology of Norovirus in the Middle East and North Africa (MENA) region: a systematic review

Abstract

Norovirus (NoV) is considered the second leading cause of viral acute gastroenteritis (AGE). To our knowledge, there are no systematic reviews assessing the role of NoV in AGE in the Middle East and North Africa (MENA) region. Consequently, we conducted an extensive systematic literature review on articles studying NoV in the 24 countries of the MENA region during the past 15 years (2000-2015). The methods and reporting were set according to the 2015 PRISMA-P and based on the elements from the international prospective register of systematic reviews (PROSPERO). We retrieved 38 studies meeting our predefined inclusion criteria and were used to extract full data. Studies reporting on NoV were conducted in 15 out of the 24 countries of the region. The reported NoV infection rates in MENA countries ranged between 0.82% and 36.84%. The majority of studies were clinical observational studies assessing NoV rates mainly among children. Participants were recruited from in- and outpatient clinics. NoV infection was reported all year round with with peaks observed mainly during cold months. GII.4 was the predominant genotype detected in stool of participants as reported by 16 out of 25 studies (64%). Overall, there is an increasing recognition of NoV as an important causative agent of AGE across all age groups in the MENA region. Further studies are needed to assess the national and the regional burden of NoV among different age groups, its molecular diversity and seasonal variability.

Background

Diarrheal disorders still mark the second highest burden among all communicable diseases [1] with an estimated 1.4 million yearly deaths and 89.5 million disability-adjusted life-years (DALYs) [1, 2]. Recently, noroviruses have been recognized as a leading cause of both sporadic and epidemic acute gastroenteritis (AGE) across all age groups seeking medical care in emergency departments, outpatient clinics and the community [3,4,5,6]. Norovirus (NoV), the second leading cause of viral AGE worldwide [7] after rotavirus, is responsible globally for substantial morbidity and mortality rates in both developed and developing countries [8,9,10]. It is estimated that 212, 000 deaths are caused by NoV yearly worldwide with 99% of these occurring in middle- and high mortality countries [11]. In the USA, NoV contributes to at least 20 million illnesses per year leading to 56,000-71,000 hospitalizations and 570-800 deaths [12]. In Europe, NoV was reported to be responsible for 5.7 million infections, 800,000 medical visits, 53,000 hospitalizations and 102 deaths among children less than 5 years between 2003 and 2013 [13]. Moreover, NoV is a major cause of gastroenteritis outbreaks accounting for at least 50% of the investigated cases [14]. NoV has been associated with diarrheal diseases among different age groups [15, 16]. In children less than 5 years old, the incidence of NoV is five times higher compared to other age groups [17] causing 18% of diarrheal diseases [18]. Global reports suggest that 70% of pediatric norovirus cases affect children in the 0-4 year age group [19] with greater infection rates in low-income countries and among inpatients.

Recently, the World Health Organization (WHO) positioned NoV in the global estimates of the burden of foodborne diseases [20] as the most common cause of morbidity and mortality and the fourth in DALYs’ burden [21]. These numbers reflected estimates for all age groups and modes of transmission and prompted researchers to report on the economic burden exerted by NoVs globally. NoV results in a global economic burden of $4.2 billion on health system costs with two-thirds affecting children less than 5 years old [22].

In recent systematic reviews assessing the role of NoV in AGE worldwide, the pooled prevalence of NoV was estimated at 18% [3] with winter seasonality [23]. The prevalence of NoV was reported to be higher in community settings (24%) followed by outpatient (20%) and inpatients settings (17%). Moreover, the introduction of rotavirus vaccine contributed to ranking NoV as the most common cause of gastroenteritis among children [24, 25]. Importantly, these reviews highlighted the lack of data from high mortality settings and low-income countries and the need for more studies to understand the role exerted by NoVs on the burden of diarrheal diseases. This is especially true since data on the regional distribution of NoV are only available from developed countries like USA, Europe and Japan [12, 17, 26,27,28]. Nineteen studies from fourteen African countries were recently reviewed by Mans et al. [29] whereby authors identified the lack of data on NoVs from diverse age groups in Africa in agreement with previous reports from low- and middle-income countries [3].

To our knowledge, there are no systematic reviews reporting on the NoV-associated AGE in the Middle East and North Africa (MENA) region. In this review, we present the reported frequencies of NoV-associated gastroenteritis in countries of the region in different age groups, the type of tests used to report NoV, the predominant circulating genotypes compared to globally reported ones as well as seasonality patterns in the region.

Methods

Search strategy and selection process

An extensive systematic literature search was carried out on articles studying NoV in the 24 countries of the MENA region during the past 15 years (2000-2015). These countries are: Algeria, Bahrain, Djibouti, Egypt, Iran, Iraq, Israel, Jordan, Kuwait, Lebanon, Libya, Mauritania, Morocco, Oman, Palestine, Qatar, Saudi Arabia, Somalia, Sudan, Syria, Tunisia, Turkey, UAE and Yemen.The methods and reporting of this systematic review were set according to the 2015 preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) [30] and based on the elements from the international prospective register of systematic reviews (PROSPERO) [31]. The search strategies were developed using the proper Medical Subject Headings (MeSH) terms and keywords related to NoV and the 24 countries listed above. To ensure the comprehensiveness and completeness of the search [32], six electronic bibliographic databases were used: Medline (OVID), PubMed, EMBASE, COCHRANE, SCOPUS and Web of Science. Moreover, in order to rule out any source of bias to the selected studies and in order to account for hard to reach material, unpublished literature in theses, dissertations and grey literature were screened through ProQuest and OpenGrey databases. The Global Health Library (GHL) was used to retrieve studies published on the regional databases namely: Index Medicus for the Eastern Mediterranean Region (IMEMR) and African Index Medicus (AIM).

All relevant studies were sent to the citation manager Endnote (version X7.1) where duplicates were removed. The titles and abstracts of the exported studies were extracted and screened by two independent reviewers for relevance according to the inclusion and exclusion criteria. Disagreements were resolved by consensus of a third reviewer.

We included the studies that reported the prevalence of NoVs in AGE in any of the 24 countries of the MENA region and published between 2000 and 2015. These studies should have reports on the total number of stool samples tested for NoV along with positive occurrences. Moreover, studies were included when the use of standardized laboratory techniques for the detection of the virus was clearly reported. These assays include enzyme immune assay (EIA), enzyme linked immunosorbent assays (ELISA), immunochromatography (IC), latex agglutination (LA), reverse transcriptase polymerase chain reaction (RT-PCR), real time RT-PCR (rRT-PCR), and sequencing.

We excluded review articles, case studies, clinical trials, animal and environmental studies. We also excluded studies that did not have English abstracts. Studies lacking the number of participants, the number of positive cases or the percentages that allowed these raw numbers to be calculated were also excluded.

Data extraction

Based on the pre-defined inclusion and exclusion criteria, the full-texts of potentially eligible or relevant titles and abstracts were screened. Following screening and using a standardized data sheet, two reviewers extracted the data independently from eligible studies and assessed the inclusion criteria in details. The abstracted information was checked by a third reviewer. The following information was extracted from each study when available: country, population studied, number of cases tested, positive rate, diagnostic method used, predominant genogroups or genotypes and seasonal peaks. The population studied was recoded into participants’ setting, i.e. community, outpatient or inpatient. When studies did not report the positive rates of NoV infection, we calculated the former using the sample size and the number of positive cases.

Results

Study selection and characteristics

Our literature search identified 816 articles on NoV in the MENA region. After removal of duplicates, we assessed the eligibility of 217 citations based on their titles and abstracts (Fig. 1). We retrieved 47 eligible articles out of which 9 were excluded based on our inclusion criteria. Consequently, 38 studies met our predefined inclusion criteria and were used to extract the full data. Between 2000 and 2015, studies were conducted in 15 out of the 25 countries of the MENA region (Table 1). Algeria, Bahrain, Mauritania, Oman, Palestine, Somalia, Sudan, Syria and UAE lacked studies on NoV. The largest number of studies was reported from Turkey (n = 8), followed by Iran (n = 6) and Tunisia (n = 5). The reported NoV infection rates in MENA countries ranged between 0.82% as reported in Morocco [33] and 36.84% in Tunisia [34]. When applicable, we calculated the median percentage of NoV infection in individual countries. Consequently, we report a 15.13% median percentage of positive NoV in the MENA region based on reported rates across countries (Table 1).

Fig. 1
figure 1

Flow diagram of NoV study selection in MENA countries, 2000-2015

Table 1 Norovirus infection in countries of the MENA region between 2000 and 2015

Based on the World Bank classification, our review includes studies from the following classes of countries: low-income, Yemen; lower-middle income, Djibouti, Egypt, Iran, Iraq, Jordan, Morocco, and Tunisia; upper-middle income, Lebanon, Libya and Turkey and high-income countries, Israel, Kuwait, Qatar and Saudi Arabia. The reported rates of NoV infection ranged between 10 and 37% (Table 1) in lower-middle income and upper-middle income countries. Studies from Israel, Kuwait, Qatar and Saudi Arabia, classified as high-income countries, reported variable rates of 10-17%, 8%, 28%, and 0.4%-5%, respectively (Table 1). In summary, NoV clearly contributes to similar proportion of disease in low, middle- and high-income settings of the MENA region.

The majority of studies on NoV in the MENA region were clinical observational studies aiming at assessing NoV rates mainly among children. Three studies originating from Djibouti, Iran and Qatar reported on NoVs among adults or other non-specified age groups (all ages). Seventeen studies were conducted among children less than 5 years old (15 studies specified age at less than 5 and 2 studies specified age groups at less than 1 and less than 3 years old). While children less than 5 years old constituted the majority of studied target groups, many studies reported on the association of NoV with AGE among children less than other age groups (< 6-18 years). This variability in reporting age makes it difficult to categorize studies based on age.

When looking at the setting, we noted that study participants were recruited from in- or outpatient clinics (Table 2). In summary, 10 studies included inpatients less than 5 years of age (with one study reported on age group less than 3 years). Six other studies were also conducted on in-patients from age groups less than 6, 7, 10, 14 and 17 years old and one on adults (Djibouti) without a specific age category. Two studies from Egypt and a single one from Libya reported on NoV rates among outpatient children. The variability in reporting is complicated by reporting the setting as both in- and outpatient as reported in 13 studies among different age groups. Similarly, the variability in the reported results extends to the study periods during which NoVs were detected from stool of study participants (between 2 months and 7 years) (Table 2).

Table 2 Distribution and molecular characteristics of Norovirus in countries of the MENA region (2000-2015)

Diagnostics, seasonality and variability

When assessing the diagnostics, the majority of studies (n = 30) relied on RT-PCR to detect NoV in stool of study participants. RT-PCR is the most sensitive and specific method to diagnose NoVs. Nevertheless, the use of rapid detection methods (i.e. EIA, ELISA or IC) was reported in 12 studies. Studies relying on molecular assays were able to report on the circulating genotype associated with NoV gastroenteritis (n = 25 studies). GII was reported in all the 25 studies with GII.4 predominantly detected in stool of participants as reported by 16 out of the 25 studies (64%). GII.4 circulated in Egypt, Iran, Iraq, Israel, Kuwait, Libya, Morocco, Tunisia, Turkey and Yemen followed by GII.3 (reported in 4 studies, 16.0%) isolated in Jordan and Tunisia.

A recent systematic review on the global seasonality of NoV infection [35], recognized the latter as a “winter phenomenon” especially in the northern hemisphere. In an attempt to compare regional data from MENA countries to globally reported ones, we extracted data when available on seasonality from studies conducted on NoV between 2000 and 2015. Studies extending for 12 months or more reported on the seasonal peaks of NoV (n = 15 studies). When described, NoV infection was detected all year round with detectable winter peaks in Egypt, Morocco, Tunisia and Turkey. However, summer peaks of NoV infections were also reported in Egypt, Libya, Morocco, Tunisia and Turkey. In summary, 5 studies reported detectable peaks in the fall, 8 in the winter, 2 during the spring and 1 during the summer season (Fig. 2). This variability requires further investigation due to the narrow time frame during which hospitalization due to diarrhea was reported and stool tested.

Fig. 2
figure 2

Number of studies reporting seasonal peaks of NoV infection in MENA countries (2000-2015)

We attempted to address the variability among the studies on NoV from the MENA region in relation to age, settings and diagnostic tool. Studies on participants less than 5 years old reported higher NoV rates than those of older age. This trend was clearly observed in studies from Egypt where NoV infection rates of 26% were reported among children under 5 years old compared to 13.48% and 16% in studies including children less than 18 years (Table 2). A similar trend was observed in Iran where higher rates were observed among infants less than 1 year old (32.92%) compared to the other studies reporting on older children. These results are in agreement with previously reported ones whereby NoV is a significant cause of AGE among children under age of five [19].

Two studies from Israel recruited children of similar age groups and participants’ settings and detected NoV using rRT-PCR. Thus, these studies could be safely considered comparable. The difference in NoV rates between the two studies (9.95% versus 17.28%) could be attributed to the different study periods (7 versus 3 years, respectively); however, we cannot confirm this variability. While two studies from Morocco reported NoV (using RT-PCR) from inpatients less than 5 years old, a wide range of infection rates was reported (i.e. less than 1% vs. 16%) as well as opposite seasonal peaks (winter vs. summer). Using RT-PCR, data reported from Tunisia were from similar settings (in- and out-patients, 4/5 studies), albeit among different age groups. Importantly, NoV rates were the highest among in-patients less than 6 years of age (37% vs. 9-17% among other age groups). The largest number of studies originated from Turkey during the past 15 years. These studies were extremely variable in terms of settings and age groups as shown in Table 2.

When rRT-PCR was used, higher rates of NoV infection were reported compared to those reporting the use of multiplex RT-PCR. This was confirmed in studies from Morocco (16.12% versus 0.82%) and Tunisia (36.84% versus 8.99%). The low rates reported in studies from Saudi Arabia (3.56% and 4.58%) might be an underestimation of NoV-associated gastroenteritis especially since rapid detection methods were used (ELISA and EIA); the latter are less sensitive and specific than RT- PCR [36,37,38]. Similar findings were detected in Libya where EIA was used [39] and in Turkey where IC was used as detection methods (lowest rates) [40, 41] compared to RT-PCR. We could not assess the heterogeneity in studies from Iraq, Jordan Kuwait, Lebanon, Qatar and Yemen since only one study on NoV was reported in each of these countries.

Discussion

While the status of NoV-associated AGE is well established in many parts of the world, limited data exist about the contribution of NoV to the burden of diarrheal disease in countries of the MENA region. This prompted us to perform a systematic review providing a summary of the current status of NoV across all age groups and settings in the region. The gathered data suggest that NoV imposes a burden of AGE in the MENA region among children less than 5 years old. The rate of NoV in these studies ranged between 0.82% and 32.9%. These results are compatible with data compiled from studies conducted in Latin America and Africa whereby infection rates ranged between 2.2%-43% [42] and 0.58%-22.0%, [43] respectively. While NoV is associated with AGE among children, recent studies clearly show that other age groups including elderly are at high risk due to the mode of transmission and the severity of symptoms [16]. Only 3 studies on NoV were conducted among all age groups in the MENA region. Consequently, more studies are needed to assess the burden of viral AGE among these groups as well as elderly and immunosuppressed patients at risk of several complications [44, 45]. Moreover, most of the studies included in this systematic review were conducted among in- and outpatients from hospitals. Thus, community studies are needed to assess the community prevalence rates of NoV infection. Importantly and due to living in suboptimal conditions of hygiene and sanitation, community studies assessing NoV infection among displaced populations are also important in conflict areas, many of which are located in the MENA region [46, 47].

Our review clearly shows that NoV GII.4 is predominantly associated with reports of AGE across all age groups in the MENA region (16 studies out of 39; 40%). These results are compatible with data from the Americas, Europe, Asia and Africa [48, 49] whereby GII.4 is reported to be responsible for approximately 55-85% of the gastroenteritis cases worldwide. NoV GII.4 was responsible for a number of pandemics. These pandemics occurred during 1996-1997, 2002, 2004, 2006, 2009, and 2012 [50]. Globally, the GII.4 Sydney strain was associated with outbreaks during the 2012-2013 winter season [51]. This review does not allow us to report on the similarities between the reported NoVs in studies from MENA countries and viral variants circulating or spreading worldwide during the same time periods due to the lack of reporting of sequencing data in the majority of these studies.

When assessing the seasonal pattern of NoV, data from MENA countries clearly show an all year circulation of the virus; however, NoV was mostly detected during winter season as reported by 40% of the included studies followed by fall and summer (25% each). A recent systematic review addressing the global seasonality of NoV infections reported a variable pattern with peaks observed during the winter season; i.e. December -February in the Northern Hemisphere and June - August in the Southern Hemisphere [35]. Importantly, this review used data from regional or national surveillance systems. These systems report on outbreaks from diverse settings including schools, nursing homes, hospitals and others. Countries of the MENA region are geographically located in the Northern Hemisphere where NoV AGE cases peak during the winter season. To the best of our knowledge, NoV is not included in active or passive surveillance systems of MENA countries to help in continuously monitoring incidence/prevalence of NoV associated-AGE. Consequently, we suggest a cautious interpretation of the reported seasonality in studies from MENA countries. Seasonality is impacted by changes in environmental conditions, humidity, temperature cycles, rain patterns and winds affecting NoV transmission [52]. The highly variable data shown in this systematic review, the diverse settings and the short duration of studies limit our ability to clearly identify the factors affecting NoV transmission as previously suggested [35].

Diarrheal diseases are indicators of the development scale of countries. Countries of the MENA region are of variable levels of socioeconomic status as well as sanitation infrastructure suggested to impact the transmission of noroviruses. The availability of and access to safe drinking water and sanitation are key indicators of diarrheal morbidity and mortality and determinants of integral prevention measures to reduce the burden of NoV infections [53, 54]. Our review does not capture data on sanitation and access to clean water.

Our systematic review has a number of limitations. The age groups reported in countries of the MENA region were extremely variable; consequently, the stratification of these target groups was difficult. This is especially important to draw conclusions regarding the gradient of susceptibility among different groups including older individuals. A clear gap exists for data on NoV prevalence in many high-mortality developing countries; consequently we believe that this underrepresentation has clear impact on the assessment of the burden of the disease in the region. Moreover, the comparability between studies is hampered by variability in study design including age groups and methods of detection. While GII.4 was predominantly reported, viral variants in MENA countries could not be deduced in order to assess the role played by pandemic strains in the region. Importantly, our review lacks pooled estimates of NoV prevalence due to the variability and the heterogeneity between studies and settings over time. Consequently, we are not able to generalize these reports to the population level. Further studies are needed where the target group is a close representation of the national population in relation to relevant variables.

Conclusion

Overall, this review highlights the increasing recognition of NoV as an important causative agent of AGE across all age groups in countries of the MENA region. Further studies are needed to assess the extent of NoV molecular diversity among different age groups. The continuous monitoring of infection among different age groups is important to develop estimates of the regional burden of NoV-gastroenteritis. The introduction of NoV to the panel of surveillance is important to successfully monitor the impact of the virus on the national and regional burden of disease, the diversity of viral variants and seasonal fluctuations. This knowledge is needed to support intervention strategies and to detect new circulating variants possibly associated with underrepresented increased rates of morbidity and mortality in MENA countries.

Abbreviations

AGE:

Acute gastroenteritis

DALY:

Disability-adjusted life years

EIA:

Enzyme immune assay

ELISA:

Enzyme-linked immunosorbent assay

IC:

Immunochromatography

LA:

Latex agglutination

MENA:

Middle East and North Africa

NoV:

Norovirus

PRISMA-P:

Preferred reporting items for systematic review and meta-analysis protocols

PROSPERO:

International prospective register of systematic reviews

rRT-PCR:

real time RT-PCR

RT-PCR:

Reverse transcriptase polymerase chain reaction

RV:

Rotavirus

WHO:

World Health Organization

References

  1. Murray CJ, Vos T, Lozano R, Naghavi M, Flaxman AD, Michaud C, et al. Disability-adjusted life years (DALYs) for 291 diseases and injuries in 21 regions, 1990-2010: a systematic analysis for the global burden of disease study 2010. Lancet. 2012;380(9859):2197–223. Epub 2012/12/19. doi: 10.1016/s0140-6736(12)61689-4. PubMed PMID: 23245608

    Article  PubMed  Google Scholar 

  2. Lozano R, Naghavi M, Foreman K, Lim S, Shibuya K, Aboyans V, et al. Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the global burden of disease study 2010. Lancet. 2012;380(9859):2095–128. Epub 2012/12/19. doi: 10.1016/s0140-6736(12)61728-0. PubMed PMID: 23245604

    Article  PubMed  Google Scholar 

  3. Ahmed SM, Hall AJ, Robinson AE, Verhoef L, Premkumar P, Parashar UD, et al. Global prevalence of norovirus in cases of gastroenteritis: a systematic review and meta-analysis. Lancet Infect Dis. 2014;14(8):725–30. Epub 2014/07/02. doi: 10.1016/s1473-3099(14)70767-4. PubMed PMID: 24981041

    Article  PubMed  Google Scholar 

  4. Malekzadeh F, Sepanlou SG, Poustchi H, Naghavi M, Forouzanfar MH, Shahraz S, et al. Burden of gastrointestinal and liver diseases in Iran: estimates based on the global burden of disease, injuries, and risk factors study, 2010. Middle East J Dig Dis. 2015;7:138–54. Epub 2015/09/24. PubMed PMID: 26396716; PubMed Central PMCID: PMCPmc4560628

    PubMed  PubMed Central  Google Scholar 

  5. Melhem NM. Norovirus vaccines: correlates of protection, challenges and limitations. Hum Vaccin Immunother. 2016:1–17. Epub 2016/02/03. doi: 10.1080/21645515.2015.1125054. PubMed PMID: 26836766

  6. Pringle K, Lopman B, Vega E, Vinje J, Parashar UD, Hall AJ. Noroviruses: epidemiology, immunity and prospects for prevention. Future Microbiol. 2015;10(1):53–67. Epub 2015/01/20. doi: 10.2217/fmb.14.102. PubMed PMID: 25598337

    Article  CAS  PubMed  Google Scholar 

  7. Patel MM, Widdowson MA, Glass RI, Akazawa K, Vinje J, Parashar UD. Systematic literature review of role of noroviruses in sporadic gastroenteritis. Emerg Infect Dis. 2008;14(8):1224–31. Epub 2008/08/06. doi: 10.3201/eid1408.071114. PubMed PMID: 18680645; PubMed Central PMCID: PMCPmc2600393

    Article  PubMed  PubMed Central  Google Scholar 

  8. Ayukekbong JA, Mesumbe HN, Oyero OG, Lindh M, Bergstrom T. Role of noroviruses as aetiological agents of diarrhoea in developing countries. J Gen Virol. 2015;96(8):1983–99. Epub 2015/05/24. doi: 10.1099/vir.0.000194. PubMed PMID: 26002299

    Article  CAS  PubMed  Google Scholar 

  9. Fischer Walker CL, Perin J, Aryee MJ, Boschi-Pinto C, Black RE. Diarrhea incidence in low- and middle-income countries in 1990 and 2010: a systematic review. BMC Public Health. 2012;12:220. Epub 2012/03/23. doi: 10.1186/1471-2458-12-220. PubMed PMID: 22436130; PubMed Central PMCID: PMCPmc3323412

    Article  PubMed  PubMed Central  Google Scholar 

  10. Glass RI, Parashar UD, Estes MK. Norovirus gastroenteritis. N Engl J Med. 2009;361(18):1776–85. Epub 2009/10/30. doi: 10.1056/NEJMra0804575. PubMed PMID: 19864676; PubMed Central PMCID: PMCPmc3880795

    Article  CAS  PubMed  Google Scholar 

  11. Pires SM, Fischer-Walker CL, Lanata CF, Devleesschauwer B, Hall AJ, Kirk MD, et al. Aetiology-specific estimates of the global and regional incidence and mortality of diarrhoeal diseases commonly transmitted through food. PLoS One. 2015;10(12):e0142927. doi: 10.1371/journal.pone.0142927. PubMed PMID: 26632843; PubMed Central PMCID: PMC4668836

    Article  PubMed  PubMed Central  Google Scholar 

  12. Hall AJ, Lopman BA, Payne DC, Patel MM, Gastanaduy PA, Vinje J, et al. Norovirus disease in the United States. Emerg Infect Dis. 2013;19(8):1198–205. Epub 2013/07/24. doi: 10.3201/eid1908.130465. PubMed PMID: 23876403; PubMed Central PMCID: PMCPmc3739528

    Article  PubMed  PubMed Central  Google Scholar 

  13. Kowalzik F, Riera-Montes M, Verstraeten T, Zepp F. The burden of norovirus disease in children in the European Union. Pediatr Infect Dis J. 2015;34(3):229–34. Epub 2015/03/06. doi: 10.1097/inf.0000000000000546. PubMed PMID: 25742072; PubMed Central PMCID: PMCPmc4338478

    Article  PubMed  PubMed Central  Google Scholar 

  14. CDC. Updated norovirus outbreak management and disease prevention guidelines. MMWR Recomm Rep. 2011;60(Rr-3):1–18. Epub 2011/03/04. PubMed PMID: 21368741

    Google Scholar 

  15. Corcoran MS, van Well GT, van Loo IH. Diagnosis of viral gastroenteritis in children: interpretation of real-time PCR results and relation to clinical symptoms. Eur J Clin Microbiol Infect Dis. 2014;33(10):1663–73. Epub 2014/05/16. doi: 10.1007/s10096-014-2135-6. PubMed PMID: 24828003

    Article  CAS  PubMed  Google Scholar 

  16. Lindsay L, Wolter J, De Coster I, Van Damme P, Verstraeten T. A decade of norovirus disease risk among older adults in upper-middle and high income countries: a systematic review. BMC Infect Dis. 2015;15:425. Epub 2015/10/16. doi: 10.1186/s12879-015-1168-5. PubMed PMID: 26467099; PubMed Central PMCID: PMCPmc4606836

    Article  PubMed  PubMed Central  Google Scholar 

  17. Phillips G, Tam CC, Conti S, Rodrigues LC, Brown D, Iturriza-Gomara M, et al. Community incidence of norovirus-associated infectious intestinal disease in England: improved estimates using viral load for norovirus diagnosis. Am J Epidemiol. 2010;171(9):1014–22. Epub 2010/04/03. doi: 10.1093/aje/kwq021. PubMed PMID: 20360244

    Article  PubMed  Google Scholar 

  18. Belliot G, Lopman BA, Ambert-Balay K, Pothier P. The burden of norovirus gastroenteritis: an important foodborne and healthcare-related infection. Clin Microbiol Infect. 2014;20(8):724–30. Epub 2014/06/20. doi: 10.1111/1469-0691.12722. PubMed PMID: 24943671

    Article  CAS  PubMed  Google Scholar 

  19. Shioda K, Kambhampati A, Hall AJ, Lopman BA. Global age distribution of pediatric norovirus cases. Vaccine. 2015;33(33):4065–8. Epub 2015/06/09. doi: 10.1016/j.vaccine.2015.05.051. PubMed PMID: 26051514; PubMed Central PMCID: PMCPmc4612353

    Article  PubMed  PubMed Central  Google Scholar 

  20. Havelaar AH, Kirk MD, Torgerson PR, Gibb HJ, Hald T, Lake RJ, et al. World Health Organization global estimates and regional comparisons of the burden of Foodborne disease in 2010. PLoS Med. 2015;12(12):e1001923. Epub 2015/12/04. doi: 10.1371/journal.pmed.1001923. PubMed PMID: 26633896; PubMed Central PMCID: PMCPmc4668832

    Article  PubMed  PubMed Central  Google Scholar 

  21. Kirk MD, Pires SM, Black RE, Caipo M, Crump JA, Devleesschauwer B, et al. Correction: World Health Organization estimates of the global and regional disease burden of 22 Foodborne bacterial, Protozoal, and viral diseases, 2010: a data synthesis. PLoS Med. 2015;12(12):e1001940. Epub 2015/12/25. doi: 10.1371/journal.pmed.1001940. PubMed PMID: 26701262; PubMed Central PMCID: PMCPmc4689409

    Article  PubMed  PubMed Central  Google Scholar 

  22. Bartsch SM, Lopman BA, Ozawa S, Hall AJ, Lee BY. Global economic burden of Norovirus gastroenteritis. PLoS One. 2016;11(4):e0151219. Epub 2016/04/27. doi: 10.1371/journal.pone.0151219. PubMed PMID: 27115736; PubMed Central PMCID: PMCPmc4846012

    Article  PubMed  PubMed Central  Google Scholar 

  23. Patel MM, Hall AJ, Vinje J, Parashar UD. Noroviruses: a comprehensive review. J Clin Virol. 2009;44(1):1–8. Epub 2008/12/17. doi: 10.1016/j.jcv.2008.10.009. PubMed PMID: 19084472

    Article  CAS  PubMed  Google Scholar 

  24. Koo HL, Neill FH, Estes MK, Munoz FM, Cameron A, DuPont HL, et al. Noroviruses: the most common Pediatric viral enteric pathogen at a large university hospital after introduction of rotavirus vaccination. J Pediatr Infect Dis Soc. 2013;2(1):57–60. Epub 2013/05/21. doi: 10.1093/jpids/pis070. PubMed PMID: 23687584; PubMed Central PMCID: PMCPmc3656546

    Article  Google Scholar 

  25. Payne DC, Vinje J, Szilagyi PG, Edwards KM, Staat MA, Weinberg GA, et al. Norovirus and medically attended gastroenteritis in U.S. children. N Engl J Med. 2013;368(12):1121–30. Epub 2013/03/22. doi: 10.1056/NEJMsa1206589. PubMed PMID: 23514289; PubMed Central PMCID: PMCPmc4618551

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Thomas MK, Murray R, Flockhart L, Pintar K, Fazil A, Nesbitt A, et al. Estimates of foodborne illness-related hospitalizations and deaths in Canada for 30 specified pathogens and unspecified agents. Foodborne Pathog Dis. 2015;12(10):820–7. Epub 2015/08/11. doi: 10.1089/fpd.2015.1966. PubMed PMID: 26259128; PubMed Central PMCID: PMCPMC4601674

    Article  PubMed  PubMed Central  Google Scholar 

  27. Thongprachum A, Khamrin P, Maneekarn N, Hayakawa S, Ushijima H. Epidemiology of gastroenteritis viruses in Japan: prevalence, seasonality, and outbreak. J Med Virol. 2016;88(4):551–70. Epub 2015/09/22. doi: 10.1002/jmv.24387. PubMed PMID: 26387663

    Article  PubMed  Google Scholar 

  28. Verhoef L, Koopmans M, VANP W, Duizer E, Haagsma J, Werber D, et al. The estimated disease burden of norovirus in The Netherlands. Epidemiol Infect. 2013;141(3):496–506. Epub 2012/05/19. doi: 10.1017/s0950268812000799. PubMed PMID: 22595489

    Article  CAS  PubMed  Google Scholar 

  29. Mans J, Armah GE, Steele AD, Taylor MB. Norovirus epidemiology in Africa: a review. PLoS One. 2016;11(4):e0146280. Epub 2016/04/27. doi: 10.1371/journal.pone.0146280. PubMed PMID: 27116615; PubMed Central PMCID: PMCPmc4846019

    Article  PubMed  PubMed Central  Google Scholar 

  30. Shamseer L, Moher D, Clarke M, Ghersi D, Liberati A, Petticrew M, et al. Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015: elaboration and explanation. BMJ. 2015;349:g7647. Epub 2015/01/04. doi: 10.1136/bmj.g7647. PubMed PMID: 25555855

    Article  Google Scholar 

  31. Booth A, Clarke M, Ghersi D, Moher D, Petticrew M, Stewart L. Establishing a minimum dataset for prospective registration of systematic reviews: an international consultation. PLoS One. 2011;6(11):e27319. Epub 2011/11/24. doi: 10.1371/journal.pone.0027319. PubMed PMID: 22110625; PubMed Central PMCID: PMCPmc3217945

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. McGowan J, Sampson M, Salzwedel DM, Cogo E, Foerster V, Lefebvre C. PRESS peer review of electronic search strategies: 2015 guideline statement. J Clin Epidemiol. 2016 Epub 2016/03/24. doi: https://doi.org/10.1016/j.jclinepi.2016.01.021. PubMed PMID: 27005575

  33. Benmessaoud R, Jroundi I, Nezha M, Moraleda C, Tligui H, Seffar M, et al. Aetiology, epidemiology and clinical characteristics of acute moderate-to-severe diarrhoea in children under 5 years of age hospitalized in a referral paediatric hospital in Rabat, Morocco. J Med Microbiol. 2015;64(Pt 1):84–92. doi: http://dx.doi.org/10.1099/jmm.0.079830-0. PubMed PMID: 25432162

    Article  PubMed  Google Scholar 

  34. Ayouni S, Estienney M, Sdiri-Loulizi K, Ambert-Balay K, de Rougemont A, Aho S, et al. Relationship between GII.3 norovirus infections and blood group antigens in young children in Tunisia. Clin Microbiol Infect. 2015;21(9):874.e1–8. Epub 2015/05/25. doi: 10.1016/j.cmi.2015.05.015. PubMed PMID: 26003283

    Article  CAS  Google Scholar 

  35. Ahmed SM, Lopman BA, Levy K. A systematic review and meta-analysis of the global seasonality of norovirus. PLoS One. 2013;8(10):e75922. Epub 2013/10/08. doi: 10.1371/journal.pone.0075922. PubMed PMID: 24098406; PubMed Central PMCID: PMCPmc3788804

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  36. Kheyami A. Viral diarrhea in children in Saudi Arabia. J Antivirals Antiretrovirals. 2014;2014:135.

    Google Scholar 

  37. Tayeb HT, Dela Cruz DM, Al-Qahtani A, Al-Ahdal MN, Carter MJ. Enteric viruses in pediatric diarrhea in Saudi Arabia. J Med Virol. 2008;80(11):1919–29. doi: http://dx.doi.org/10.1002/jmv.21291. PubMed PMID: 18814232

    Article  CAS  PubMed  Google Scholar 

  38. Meqdam MM, Thwiny IR. Prevalence of group a rotavirus, enteric adenovirus, norovirus and astrovirus infections among children with acute gastroenteritis in Al-Qassim, Saudi Arabia. Pak J Med Sci. 2007;23(4):551–5.

    Google Scholar 

  39. Rahouma A, Klena JD, Krema Z, Abobker AA, Treesh K, Franka E, et al. Enteric pathogens associated with childhood diarrhea in Tripoli-Libya. Am J Trop Med Hyg. 2011;84(6):886–91. doi: http://dx.doi.org/10.4269/ajtmh.2011.11-0116. PubMed PMID: 21633024; PubMed Central PMCID: PMCPMC3110355

    Article  PubMed  PubMed Central  Google Scholar 

  40. Bicer S, Col D, Erdag GC, Giray T, Gurol Y, Yilmaz G, et al. A retrospective analysis of acute gastroenteritis agents in children admitted to a university hospital pediatric emergency unit. Jundishapur J Microbiol. 2014;7(4):e9148. Epub 2014/08/26. doi: 10.5812/jjm.9148. PubMed PMID: 25147694; PubMed Central PMCID: PMCPmc4138623

    PubMed  PubMed Central  Google Scholar 

  41. Col D, Bicer S, Ugras M, Kucuk O, Giray T, Gurol Y, et al. Relative frequency of norovirus infection in children with acute gastroenteritis. Minerva Pediatr. 2015;67(1):19–24. Epub 2015/01/21. PubMed PMID: 25602748

    CAS  PubMed  Google Scholar 

  42. da Silva Polo T, Peiro JR, Mendes LC, Ludwig LF, de Oliveira-Filho EF, Bucardo F, et al. Human norovirus infection in Latin America. J Clin Virol 2016;78:111-119. Epub 2016/03/29. doi: https://doi.org/10.1016/j.jcv.2016.03.016. PubMed PMID: 27018574.

  43. Kabue JP, Meader E, Hunter PR, Potgieter N. Human Norovirus prevalence in Africa: a review of studies from 1990 to 2013. Tropical Med Int Health. 2016;21(1):2–17. Epub 2015/10/06. doi: 10.1111/tmi.12617. PubMed PMID: 26436862

    Article  Google Scholar 

  44. Green KY. Norovirus infection in immunocompromised hosts. Clin Microbiol Infect. 2014;20(8):717–23. Epub 2014/07/22. doi: 10.1111/1469-0691.12761. PubMed PMID: 25040790

    Article  CAS  PubMed  Google Scholar 

  45. White MB, Rajagopalan S, Yoshikawa TT. Infectious Diarrhea: Norovirus and Clostridium Difficile in older adults. Clin Geriatr Med. 2016;32(3):509–22. Epub 2016/07/10. doi: 10.1016/j.cger.2016.02.008. PubMed PMID: 27394020

    Article  PubMed  Google Scholar 

  46. Melhem N, Kreidieh K, Ramia S. The Syrian refugees crisis brings challenges to the health authorities in Europe: hepatitis a virus is a case in point. Eur J Epidemiol. 2016;31(7):711–4. Epub 2016/05/20. doi: 10.1007/s10654-016-0163-5. PubMed PMID: 27194123

    Article  PubMed  Google Scholar 

  47. Sharara SL, Kanj SS. War and infectious diseases: challenges of the Syrian civil war. PLoS Pathog. 2014;10(10):e1004438. Epub 2014/11/14. doi: 10.1371/journal.ppat.1004438. PubMed PMID: 25393545; PubMed Central PMCID: PMCPmc4231133

    Article  PubMed  PubMed Central  Google Scholar 

  48. Ramani S, Atmar RL, Estes MK. Epidemiology of human noroviruses and updates on vaccine development. Curr Opin Gastroenterol. 2014;30(1):25–33. Epub 2013/11/16. doi: 10.1097/mog.0000000000000022. PubMed PMID: 24232370; PubMed Central PMCID: PMCPMC3955997

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  49. Robilotti E, Deresinski S, Pinsky BA. Norovirus. Clin Microbiol Rev. 2015;28(1):134–64. Epub 2015/01/09. doi: 10.1128/cmr.00075-14. PubMed PMID: 25567225; PubMed Central PMCID: PMCPmc4284304

    Article  PubMed  PubMed Central  Google Scholar 

  50. Hoa Tran TN, Trainor E, Nakagomi T, Cunliffe NA, Nakagomi O. Molecular epidemiology of noroviruses associated with acute sporadic gastroenteritis in children: global distribution of genogroups, genotypes and GII.4 variants. J Clin Virol. 2013;56(3):185–93. Epub 2012/12/12. doi: 10.1016/j.jcv.2012.11.011. PubMed PMID: 23218993

    Article  CAS  PubMed  Google Scholar 

  51. Karst SM, Baric RS. What is the reservoir of emergent human norovirus strains? J Virol. 2015;89(11):5756–9. Epub 2015/03/20. doi: 10.1128/jvi.03063-14. PubMed PMID: 25787285; PubMed Central PMCID: PMCPMC4442419

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  52. Rohayem J. Norovirus seasonality and the potential impact of climate change. Clin Microbiol Infect. 2009;15(6):524–7. Epub 2009/07/17. doi: 10.1111/j.1469-0691.2009.02846.x. PubMed PMID: 19604277

    Article  CAS  PubMed  Google Scholar 

  53. Arias A, Emmott E, Vashist S, Goodfellow I. Progress towards the prevention and treatment of norovirus infections. Future Microbiol. 2013;8(11):1475–87. Epub 2013/11/10. doi: 10.2217/fmb.13.109. PubMed PMID: 24199805; PubMed Central PMCID: PMCPmc3904215

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  54. Parashar UD, Nelson EA, Kang G. Diagnosis, management, and prevention of rotavirus gastroenteritis in children. BMJ. 2013;347:f7204. Epub 2014/01/01. doi: 10.1136/bmj.f7204. PubMed PMID: 24379214

    Article  PubMed  Google Scholar 

  55. Maslin J, Nicand E, Ambert-Balay K, Fouet C, Kaplon J, Haus R, et al. Detection and characterization of human caliciviruses associated with sporadic acute diarrhea in adults in Djibouti (horn of Africa). Am J Trop Med Hyg. 2008;78(3):522–6. PubMed PMID: 18337354

    PubMed  Google Scholar 

  56. El-Nady GM, Badr RI, Salama MF, Shouman B, El-Bayoumi MA. Norovirus genogroup ii predominance in infants & young children with acute gastroenteritis in mansoura university children's hospital - Egypt. Pediatr Crit Care Med. 2014;15(4):142.

    Article  Google Scholar 

  57. Zaghloul MZ, El-Sahn SF, Galal ZA. Coinfection of rotavirus group a, norovirus and adenovirus in Egyptian children with gastroenteritis. Life Sci J. 2013;10(2):848–52.

    Google Scholar 

  58. El-Mohammady H, Mansour A, Shaheen HI, Henien NH, Motawea MS, Raafat I, et al. Increase in the detection rate of viral and parasitic enteric pathogens among Egyptian children with acute diarrhea. J Infect Dev Ctries. 2012;6(11):774–81. doi: http://dx.doi.org/10.3855/jidc.2349. PubMed PMID: 23277502

    Article  PubMed  Google Scholar 

  59. Kamel AH, Ali MA, El-Nady HG, de Rougemont A, Pothier P, Belliot G. Predominance and circulation of enteric viruses in the region of greater Cairo, Egypt. J Clin Microbiol. 2009;47(4):1037-1045. doi: https://doi.org/10.1128/JCM.01381-08. PubMed PMID: 19193841; PubMed Central PMCID: PMCPMC2668344.

  60. Sharifi-Rad J, Hoseini Alfatemi SM, Sharifi-Rad M, Miri A. Frequency of adenoviruses, rotaviruses and noroviruses among diarrhea samples collected from infants of zabol, southeastern iran. Jundishapur J Microbiol. 2015;8(3):e15440. Epub 2015/04/04. doi: 10.5812/jjm.15440. PubMed PMID: 25834718; PubMed Central PMCID: PMCPmc4377170

    Article  PubMed  PubMed Central  Google Scholar 

  61. Najafi A, Iranpour D, Najafi S. Epidemiological surveillance of norovirus diarrhea in hospitalized children with acute gastroenteritis in south of Iran. Jundishapur J Microbiol. 2013;6(4) https://doi.org/10.5812/jjm.7866.

  62. Roodsari SR, Bitajian F, Gachkar L, Jadali F, Adabian S, Sajadi Nia RS, et al. Detection of noroviruses isolated from children with acute gastroenteritis by Rt-PCR in Iran. Arch Pediatr Infect Dis. 2013;1(2):57–60. https://doi.org/10.5812/pedinfect.7619.

    Article  Google Scholar 

  63. Romani S, Mohebbi SR, Hosseini SM, Azimzadeh P, Vahedi M, Derakhshan F, et al. Prevalence of norovirus infection in children and adults with acute gastroenteritis, Tehran, Iran, 2008-2009. Food Environ Virol. 2012;4(1):1–5. doi: http://dx.doi.org/10.1007/s12560-011-9071-8. PubMed PMID: 23412762

    Article  PubMed  Google Scholar 

  64. Jalilian S, Samarbaf-Zadeh AR, Mozhgani SHR, Makvandi M, Parsa-Nahad M, Pirmoradi R, et al. Relative frequency of Norovirus infection in children suffering from gastroenteritis and referred to Aboozar hospital, Ahvaz. Iran Jundishapur J Microbiol. 2012;5(1):355–8. https://doi.org/10.5812/kowsar.20083645.2370.

    Google Scholar 

  65. Fazeli Bavandpour Z, Moradi A, Baghaie N, Nadji SA. Hospital-based phylogenetic analysis of noroviruses isolated from children with acute gastroenteritis in Iran. Clin Microbiol Infect. 2010;16:S324.

    Google Scholar 

  66. Al-Mashhadani MN, Nakagomi O, Dove W, Ahmed H, Nakagomi T, Hart CA, et al. Norovirus gastroenteritis among children in Iraqi Kurdistan. J Med Virol. 2008;80(3):506–9. doi: http://dx.doi.org/10.1002/jmv.21099. PubMed PMID: 18205231

    Article  CAS  PubMed  Google Scholar 

  67. Leshem E, Givon-Lavi N, Vinje J, Gregoricus N, Parashar U, Dagan R. Differences in Norovirus-associated hospital visits between Jewish and Bedouin children in southern Israel. Pediatr Infect Dis J. 2015;34(9):1036–8. Epub 2015/06/25. doi: 10.1097/inf.0000000000000786. PubMed PMID: 26107344

    Article  PubMed  Google Scholar 

  68. Muhsen K, Kassem E, Rubinstein U, Schachter Y, Kremer A, Goren S, et al. Incidence and characteristics of sporadic norovirus gastroenteritis associated with hospitalization of children less than 5 years of age in Israel. Pediatr Infect Dis J. 2013;32(6):688–90. doi: http://dx.doi.org/10.1097/INF.0b013e318287fc81. PubMed PMID: 23411623

    Article  PubMed  Google Scholar 

  69. Kaplan NM, Kirby A, Abd-Eldayem SA, Dove W, Nakagomi T, Nakagomi O, et al. Detection and molecular characterisation of rotavirus and norovirus infections in Jordanian children with acute gastroenteritis. Arch Virol. 2011;156(8):1477–80. doi: http://dx.doi.org/10.1007/s00705-011-0996-x. PubMed PMID: 21503643

    Article  CAS  PubMed  Google Scholar 

  70. Al-Rashidi A, Chehadeh W, Szucs GG, Albert MJ. Different norovirus genotypes in patients with gastroenteritis in Kuwait. J Med Virol. 2013;85(9):1611–8. doi: http://dx.doi.org/10.1002/jmv.23645. PubMed PMID: 23852687

    Article  PubMed  Google Scholar 

  71. Al-Ali RM, Chehadeh W, Hamze M, Dabboussi F, Hlais S, Mallat H. First description of gastroenteritis viruses in Lebanese children: a pilot study. J Infect Public Health. 2011;4(2):59–64. doi: http://dx.doi.org/10.1016/j.jiph.2011.01.002. PubMed PMID: 21663874

    Article  PubMed  Google Scholar 

  72. Abugalia M, Cuevas L, Kirby A, Dove W, Nakagomi O, Nakagomi T, et al. Clinical features and molecular epidemiology of rotavirus and norovirus infections in Libyan children. J Med Virol. 2011;83(10):1849–56. doi: http://dx.doi.org/10.1002/jmv.22141. PubMed PMID: 21837804

    Article  PubMed  Google Scholar 

  73. El Qazoui M, Oumzil H, Baassi L, El Omari N, Sadki K, Amzazi S, et al. Rotavirus and norovirus infections among acute gastroenteritis children in Morocco. BMC Infect Dis. 2014;14:300. doi: https://doi.org/10.1186/1471-2334-14-300. PubMed PMID: 24894194; PubMed Central PMCID: PMCPMC4057912.

  74. Al-Thani A, Baris M, Al-Lawati N, Al-Dhahry S. Characterising the aetiology of severe acute gastroenteritis among patients visiting a hospital in Qatar using real-time polymerase chain reaction. BMC Infect Dis. 2013;13:329. doi: http://dx.doi.org/10.1186/1471-2334-13-329. PubMed PMID: 23865805; PubMed Central PMCID: PMCPMC3734054

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  75. Ben Salem-Ben Nejma I, Hassine Zaafrane M, Hassine F, Sdiri-Loulizi K, Ben Said M, Aouni M, et al. Etiology of acute diarrhea in tunisian children with emphasis on diarrheagenic escherichia coli: prevalence and identification of E. Coli virulence markers. Iran J Public Health. 2014;43(7):947–60. https://doi.org/10.1186/1471-2334-11-266.

    PubMed  PubMed Central  Google Scholar 

  76. Hassine-Zaafrane M, Sdiri-Loulizi K, Kaplon J, Salem IB, Pothier P, Aouni M, et al. Prevalence and genetic diversity of norovirus infection in Tunisian children (2007-2010). J Med Virol. 2013;85(6):1100–10. doi: http://dx.doi.org/10.1002/jmv.23552. PubMed PMID: 23532785

    Article  CAS  PubMed  Google Scholar 

  77. Sdiri-Loulizi K, Ambert-Balay K, Gharbi-Khelifi H, Sakly N, Hassine M, Chouchane S, et al. Molecular epidemiology of norovirus gastroenteritis investigated using samples collected from children in Tunisia during a four-year period: detection of the norovirus variant GGII.4 hunter as early as January 2003. J Clin Microbiol. 2009;47(2):421–9. doi: http://dx.doi.org/10.1128/JCM.01852-08. PubMed PMID: 19109464; PubMed Central PMCID: PMCPMC2643701

    Article  CAS  PubMed  Google Scholar 

  78. Sdiri-Loulizi K, Gharbi-Khelifi H, de Rougemont A, Chouchane S, Sakly N, Ambert-Balay K, et al. Acute infantile gastroenteritis associated with human enteric viruses in Tunisia. J Clin Microbiol. 2008;46(4):1349-1355. doi: https://doi.org/10.1128/JCM.02438-07. PubMed PMID: 18287312; PubMed Central PMCID: PMCPMC2292941.

  79. Bozkurt D, Selimoglu MA, Otlu B, Sandikkaya A. Eight different viral agents in childhood acute gastroenteritis. Turk J Pediatr. 2015;57(1):68–73. Epub 2015/11/28. PubMed PMID: 26613223

    PubMed  Google Scholar 

  80. Mitui MT, Bozdayi G, Ahmed S, Matsumoto T, Nishizono A, Ahmed K. Detection and molecular characterization of diarrhea causing viruses in single and mixed infections in children: a comparative study between Bangladesh and Turkey. J Med Virol. 2014;86(7):1159–68. doi: http://dx.doi.org/10.1002/jmv.23744. PubMed PMID: 24105741

    Article  CAS  PubMed  Google Scholar 

  81. Altindis M, Yuksek S, Alpay F, Kalayci R, Yoldas Y. Rotavirus, norovirus and adenovirus gastroenteritis in hospitalised children Turkey. Clin Microbiol Infect. 2012;18:219.

    Google Scholar 

  82. Ozkul AA, Kocazeybek BS, Turan N, Reuter G, Bostan K, Yilmaz A, et al. Frequency and phylogeny of norovirus in diarrheic children in Istanbul, Turkey. J Clin Virol. 2011;51(3):160–4. doi: http://dx.doi.org/10.1016/j.jcv.2011.03.004. PubMed PMID: 21592853

    Article  CAS  PubMed  Google Scholar 

  83. Altindis M, Lewis DC, Hale A, Koken R, Kalayci R, Yoldas Y. Survey of viral gastroenteritis in childhood in Turkey using multiplex RT PCR methods. Clin Microbiol Infect. 2010;16:S660.

    Google Scholar 

  84. Altindis M, Banyai K, Kalayci R, Gulamber C, Koken R, Yoldas Y, et al. Frequency of norovirus in stool samples from hospitalized children due to acute gastroenteritis in Anatolia, Turkey, 2006-2007. Scand J Infect Dis. 2009;41(9):685–8. doi: http://dx.doi.org/10.1080/00365540903071342. PubMed PMID: 19544225

    Article  CAS  PubMed  Google Scholar 

  85. Kirby A, Al-Eryani A, Al-Sonboli N, Hafiz T, Beyer M, Al-Aghbari N, et al. Rotavirus and norovirus infections in children in Sana'a, Yemen. Tropical Med Int Health. 2011;16(6):680–4. doi: http://dx.doi.org/10.1111/j.1365-3156.2011.02756.x. PubMed PMID: 21392189

    Article  Google Scholar 

Download references

Acknowledgements

We thank Ms. Aida Farha who helped in the identification of the databases and the search terms.

Funding

No funding was involved in the preparation of this review.

Availability of data and materials

Data sharing is not applicable to this article as no datasets were generated or analyzed during the current study.

Author information

Authors and Affiliations

Authors

Contributions

KK and RC collected and extracted the data for this review. KK performed the analysis and contributed to the drafting of the manuscript. GD critically reviewed the manuscript. NMM designed the study, supervised the entire work and wrote the final version of the manuscript.

All authors read and approved the final version of the manuscript.

Corresponding author

Correspondence to Nada M. Melhem.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Kreidieh, K., Charide, R., Dbaibo, G. et al. The epidemiology of Norovirus in the Middle East and North Africa (MENA) region: a systematic review. Virol J 14, 220 (2017). https://doi.org/10.1186/s12985-017-0877-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12985-017-0877-3

Keywords