Open Access
Issue
Parasite
Volume 18, Number 2, May 2011
Page(s) 197 - 201
DOI https://doi.org/10.1051/parasite/2011182197
Published online 15 May 2011

© PRINCEPS Editions, Paris, 2011, transferred to Société Française de Parasitologie

Licence Creative CommonsThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Giardiasis, a common intestinal protozoan infection caused by Giardia duodenalis (syn. G. intestinalis, G. lamblia), is considered a neglected disease in both developed and developing countries (Savioli et al., 2006). It is well documented that in developing countries, infections are associated with poor sanitary conditions, poor water quality and overcrowding (Younas et al., 2008), whereas in developed countries cases are usually associated with international travel and immigration (Ekdahl & Andersson, 2005). Findings in stool specimens suggest a prevalence of 20-30 % in the developing countries, and of 2-5 % in the developed world (Ortega & Adam, 1997). In addition, giardiasis affects domestic and wild animals, and thus causes major public and veterinary health concerns worldwide.

Clinical presentations of giardiasis vary from asymptomatic carriage to acute diarrhoea as well as chronic disease, and at present, Giardia is recognized as the most common parasitological cause of diarrhoea, with 280 million infections per year. Most epidemiological studies of giardiasis indicated waterborne, food-borne, and person-to-person (or, to a lesser extent, animalto- person) transmission, depending on the study population (Cacció et al., 2005). Person-to-person transmission is well recognized in crowded populations and in environments where hygiene levels may be compromised such as day care centres or schools (Thompson, 2008). Giardiasis usually occurs sporadically, although outbreaks have been reported. Waterborne outbreaks of giardiasis have been described many times in developed countries including the USA (Daly et al., 2010) and Europe (Nygård et al., 2006). In developing countries, the major risk factors include low personal hygiene, poor sanitation and urban overcrowding.

Despite the pan-European public health importance of giardiasis (Hörman et al., 2004; Sagebiel et al., 2009), data on the national incidence and prevalence in Western Balkan Countries (WBC), including Serbia, Bosnia and Herzegovina, Croatia, Montenegro and FYR Macedonia, are scarce. Moreover, waterborne outbreaks of giardiasis have not been reported in any of these countries, while the relative contribution of person-to-person, animal-to-person, waterborne and food-borne transmission to sporadic human giardiasis is still unknown. This article reviews the available data on the epidemiological characteristics of asymptomatic and symptomatic human infection in Serbia, to define the importance and risk for public health caused by Giardia.

Asymptomatic Infection

To determine the epidemiological characteristics of asymptomatic Giardia infection in Serbia, several prevalence studies have been performed between 1985 and 2005 (Nikolić et al., 2009). These studies involved a total of 6,645 asymptomatic schoolchildren, 7-11 years of age, representing 10 % of the total age-matched population (N = 69,232), from 115 settlements within 20 regions (Belgrade, Kragujevac, LuČani, Bor, Žagubica, Sjenica, Novi Pazar, Valjevo, Aleksandrovac, Pirot, Bosilegrad, Ivanjica, Golubac, Užice, Kladovo, Negotin, Kraljevo, Gornji Milanovac, Kruševac and ČaČak) throughout central Serbia. The results are presented in Fig. 1A. The study population, like in many others, comprised schoolchildren because they are an age group the most exposed to intestinal parasites, and are generally accessible. The results showed Giardia infection in all examined regions of Serbia, with an overall prevalence of 6.1 %, and highly significant (p = 0.001) differences among regions (3.2-14.2 %). According to the World Health Organization criteria (WHO, 1987) by which Giardia infection is considered sporadic at a prevalence below 1 %, endemic between 1-10 % and hyperendemic above 10 %, even 16 regions were endemic and four hyperendemic for giardiasis. These findings are important as understanding the spatial distribution may help to develop programmes for giardiasis control that combine chemotherapy (Nikolić et al., 1995) and preventive measures.

thumbnail Fig. 1.

Asymptomatic human Giardia infection in Central Serbia: (A) map with prevalence (%) in 20 study regions and (B) distribution of prevalence in 115 settlements throughout Central Serbia.

Compared to other studies, the 6 % prevalence in Serbia is much higher than those reported in European countries such as Poland – 0.7 % (Bitkowska et al., 2004) and UK – 1.3 % (Davies et al., 2009), but lower than in Albania – 11.2 % (Spinelli et al., 2006) and Turkey – 18.1 % (Ak et al., 2006). There are no published data for giardiasis for other WBC, which obviously implies lack of awareness of this infection in the Balkans. High as it may seem, even the 6 % prevalence established in our studies is likely to be an underestimate, since the excretion of Giardia cysts is known to be intermittent, and examination of a single stool sample identifies no more than 75-85 % of all actually infected (Naik et al., 1978; Hiatt et al., 1995). However, the nature of epidemiological field studies does not allow for the examination of more than one stool sample (by several methods) and such a diagnostic approach has been widely accepted (rev. in Nikolić et al., 1998).

Of the 115 settlements examined, only 21 were Giardia-free (Fig. 1B). The prevalence rates in the 94 Giardia-positive settlements varied from as low as 1.2 %, to a maximum of 22.7 %. Thus, infection with Giardia ranged from sporadic in 28, to endemic in 47 and hyperendemic in even 19 settlements. In the capital city of Belgrade, a highly urban setting, the detected prevalence of 5.1 % (Nikolić et al., 1998) seems much higher compared to, for instance, the 1.6 % prevalence in asymptomatic individuals in Melbourne, Australia (Hellard et al., 2000). Moreover, of all intestinal parasites detected in Serbia (Entamoeba histolytica, E. hartmanni, E. coli, Iodamoeba bütschlii, Hymenolepis nana, Enterobius vermicularis, Ascaris lumbricoides, Trichuris trichiura), Giardia was the single one, which was more prevalent (although insignificantly), in urban environments than in rural areas (7.0 % vs 6.5 %, respectively) (Nikolić et al., 1996). These findings support the significance of overcrowding in highly urban areas and living in close contact with infected persons for the spread of Giardia, and indicate that person-to-person transmission is an important means of spread of the infection in the community. Low median income was a risk factor for giardiasis in Serbia (Nikolić et al., 2002), which is in accordance with reports from other countries (Quihui et al., 2006; Ostan et al., 2007). The influence of income on infection may be associated with differences in human behaviour and living and environmental conditions that increase the risk of infection (Wilkinson et al., 1992).

The differences in the rates of giardiasis in different settings in Serbia (urban vs rural, developed vs developing regions) indicate that the nature of giardiasis transmission depends on the population analyzed. Hence, control strategies of giardiasis should be based on epidemiological information for each particular population.

Symptomatic Infection

National giardiasis surveillance should provide data to assess the epidemiological characteristics and estimate the disease burden by monitoring demographic parameters (sex, age), seasonality, and geographic variation (Furness et al., 2000). While in countries such as USA and Canada human giardiasis is a notifiable disease, among members of the European Union reporting varies from voluntary in ones to mandatory in other member states. In Serbia, reporting is mandatory, and we here summarize the national giardiasis surveillance data as reported from January 2005 through December 2008 by the Institute of Public Health of Serbia (Health Statistical Yearbook, 2005, 2006, 2007 and 2008), and analyze the epidemiological trends.

A total of 1,193 symptomatic cases were reported over this 4-year period. The number of cases has somewhat differed among the years, ranging from a high of 346 cases in 2005 (incidence 4.61 % per 100,000 population) to a low of 264 (incidence 3.55 %) in 2007, a decrease by 31 %, followed by a slight increase in 2008 (Fig. 2A). Whether the observed fluctuations reflect changes in reporting patterns or a real change in infection dynamics and disease caused by Giardia is unclear. Although giardiasis affects all age-groups, the number of reported cases was highest among adults aged 20-59 years (74.4 %), similar to findings in Germany where 83 % were age 20 or older (Espelage et al., 2010). No sex-specific differences were observed i.e. the percentage of cases among males and females were 53 % and 47 %, respectively (p > 0.05).

thumbnail Fig. 2.

Changes in incidence of symptomatic human Giardia infections in Serbia vs (A) Vojvodina and Central Serbia and (B) other Western Balkan Countries (Bosnia and Herzegovina, Croatia, Montenegro and FYR Macedonia) between 2005 and 2008.

Importantly, occurrence of symptomatic giardiasis in Serbia was associated with significant seasonality (seasonality χ2 = 41.576, p < 0.0001), with the highest number of cases reported between August and November (n = 470, 39.4 %) and the lowest number in the winter months (December – February) (n = 234, 19.6 %). Similar seasonal variation with most cases reported during late summer and early fall indicating that transmission occurred during summer has also been noted in the U.S. national surveillance data for giardiasis (Yoder & Beach, 2007; Yoder et al., 2010). The peaks of incidence coincide with increased outdoor and water activities, and increased water consumption during hot weather.

Giardiasis is spread throughout Serbia. However, the northern province of Vojvodina consistently reported more cases annually per 100,000 population than Central Serbia (Fig. 2A). These data indicate that the diagnosis or transmission of giardiasis may be higher in the north. However, because differences in giardiasis surveillance systems among different areas can affect the capability to detect cases, whether this finding is of true biologic significance or is only the result of differences in case detection and/or reporting is difficult to determine.

The incidence of Giardia infection varies not only among regions within Serbia, but between Serbia and other WBC as well (Fig. 2B). According to the data reported to the WHO, Serbia reported the greatest number of cases per 100,000 population for each of the four years of the reporting period compared to all other WBC (WHO/Europe, CISID, WHO/Europe, 2005-2008) (Fig. 3). However, this is likely to be at least in part due to insufficient reporting or monitoring systems (or both) among the WBC, as virtually no cases were reported in FYR Macedonia in 2006 and in Bosnia and Herzegovina in 2008, and some countries did not submit any giardiasis reports for some years (Croatia for 2006 and 2008, FYR Macedonia for 2007 and 2008, Montenegro for 2005). We believe that the reported giardiasis disease burden between 2005 and 2008 in the WBC is an underestimation, due to irregular reporting of Giardia infection on the national levels, as well as underreporting of diarrhoeal diseases in general.

thumbnail Fig. 3.

Total monthly counts of giardiasis for the four-year study period (2005-2008) in Serbia.

Conclusion

Human Giardia infection rates detected in Serbia over the last decades are high, both in symptomatic and asymptomatic populations. Although in Europe the prevalence of Giardia is lower in asymptomatic than in symptomatic populations (Hörman et al., 2004), in Serbia asymptomatic cases of Giardia represent a major proportion of the total cases of infection and so giardiasis mostly occurs sporadically. However, the occurrence of outbreaks may not be ruled out. Person-to-person transmission of giardiasis is difficult to interrupt, particularly in groups such as schoolchildren. Thus, measures to reduce the high prevalence of giardiasis in Serbia should include adherence to appropriate infection control (e.g., hand washing, chemotherapy of all infected individuals), while more targeted intervention measures require further studies to identify other risk factors for asymptomatic and symptomatic infections.

Acknowledgments

This work was supported by Grant No. 145002 from the Ministry of Science and Technological Development, Republic of Serbia.

References

  1. Ak M., Keleş E., Karacasu F., Pektaş B., Akkafa F., Ozgür S.,et al. The distribution of the intestinal parasitic diseases in the Southeast Anatolian (GAP=SEAP) region of Turkey. Parasitol. Res., 2006, 99, 146–152. [CrossRef] [PubMed] [Google Scholar]
  2. Bitkowska E., Wnukowska N., Wojtyniak B. & Dzbenski T.H.. Occurrence of intestinal parasites among first grade students in Poland in years 2002/2003. Przegl. Epidemiol., 2004, 58, 295–302. [PubMed] [Google Scholar]
  3. Cacció S.M., Thompson R.C.A., Mclauchlin J. & Smith H.V. Unravelling Cryptosporidium and Giardia epidemiology. Trends Parasitol., 2005, 21, 430–437. [Google Scholar]
  4. Daly E.R., Roy S.J., Blaney D.D., Manning J.S., Hill V.R., Xiao L., et al. Outbreak of giardiasis associated with a community drinking-water source. Epidemiol. Infect., 2010, 138, 491–500. [CrossRef] [PubMed] [Google Scholar]
  5. Davies A.P., Campbell B., Evans M.R., Bone A., Roche A. & Chalmers R.M. Asymptomatic carriage of protozoan parasites in children in day care centers in the United Kingdom. Pediatr. Infect. Dis. J., 2009, 28, 838–840. [CrossRef] [PubMed] [Google Scholar]
  6. Ekdahl K. & Andersson Y. Imported giardiasis: impact of international travel, immigration, and adoption. Am. J. Trop. Med. Hyg., 2005, 72, 825–830. [Google Scholar]
  7. Espelage W., an der Heiden M., Stark K. & Alpers K.. Characteristics and risk factors for symptomatic Giardia lamblia infections in Germany. BMC Public Health, 2010, 10, 41. [CrossRef] [PubMed] [Google Scholar]
  8. Furness B.W., Beach M.J. & Roberts J.M. Giardiasis surveillance – United States, 1992–1997. MMWR Surveill. Summ., 2000, 49, 1–13. [Google Scholar]
  9. Hellard M.E., Sinclair M.I., Hogg G.G. & Fairley C.K. Prevalence of enteric pathogens among community based asymptomatic individuals. J. Gastroenterol. Hepatol., 2000, 15, 290–293. [CrossRef] [PubMed] [Google Scholar]
  10. Hiatt R.A., Markell E.K. & Ng E. How many stool examinations are necessary to detect pathogenic intestinal protozoa? Am. J. Trop. Med. Hyg., 1995, 53, 36–39. [PubMed] [Google Scholar]
  11. Hörman A., Korpela H., Sutinen J., Wedel H. & Hänninen M.L. Meta-analysis in assessment of the prevalence and annual incidence of Giardia spp. and Cryptosporidium spp. infections in humans in the Nordic countries. Int. J. Parasitol., 2004, 34, 1337–1346. [CrossRef] [PubMed] [Google Scholar]
  12. Institute of Public Health of Serbia “DR Milan Jovanovic Batut”. Health Statistical Yearbook, 2005, 2006, 2007 and 2008. [Google Scholar]
  13. Naik S.R., Rau N.R. & Vinayak V.K. A comparative evaluation of three stool samples, jejunal aspirate, and jejunal mucosal impression smears in the diagnosis of giardiasis. Ann. Trop. Med. Parasitol., 1978, 72, 491–492. [PubMed] [Google Scholar]
  14. Nikolić A., Djurković-Djaković O., Petrović Z., Bobić B. & Vuković D. Effects of age-targeted treatment of intestinal parasite infections in Serbia. J. Chemotherapy, 1995, 7, 55–57. [Google Scholar]
  15. Nikolić A., Djurković-Djaković O., Bobić B. & Vuković D. Intestinal parasitism in schoolchildren in Serbia. Significance of rural vs. urban environment. Arch. Gastroenterohepatol., 1996, 15, 89–91. [Google Scholar]
  16. Nikolić A., Djurković-Djaković O. & Bobić B. Intestinal parasitic infections in Serbia. Srp. Arh. Celok. Lek., 1998, 126, 1–5. [PubMed] [Google Scholar]
  17. Nikolić A., Durković-Daković O. & Bobić B. Impact of the level of economic development on intestinal parasitism in Serbia. Acta Infectol. Iugosl., 2002, 7, 25–30. [Google Scholar]
  18. Nikolić A., Klun I., Bobić B., Ivović V., Vujanić M., Živković T. et al. Current status of human zoonotic parasite infections in Serbia. Parasitic Zoonoses in Present Day Europe. Focus on South-East. Project Conference (FP6-INCO-CT-043702-SERBPARZOON), 2009, Belgrade, Serbia, 18-20.11. Abstract book, p. 56 [Google Scholar]
  19. Nygård K., Schimmer B., Søbstad Ø., Walde A., Tveit I., Langeland N., et al. A large community outbreak of waterborne giardiasis – delayed detection in a non-endemic urban area. BMC Public Health, 2006, 6, 141. [CrossRef] [PubMed] [Google Scholar]
  20. Ortega Y.R. & Adam R.D. Giardia: overview and update. Clin. Infect. Dis., 1997, 25, 545–549. [CrossRef] [PubMed] [Google Scholar]
  21. Ostan I., Kilimcioğlu A.A., Girginkardeşler N., Ozyurt B.C., Limoncu M.E. & Ok U.Z. Health inequities: lower socioeconomic conditions and higher incidences of intestinal parasites. BMC Public Health, 2007, 7, 342. [CrossRef] [PubMed] [Google Scholar]
  22. Quihui L., Valencia M.E., Crompton D.W., Phillips S., Hagan P., Morales G., et al. Role of the employment status and education of mothers in the prevalence of intestinal parasitic infections in Mexican rural schoolchildren. BMC Public Health, 2006, 6, 225. [CrossRef] [PubMed] [Google Scholar]
  23. Sagebiel D., Weitzel T., Stark K. & Leitmeyer K. Giardiasis in kindergartens: prevalence study in Berlin, Germany, 2006. Parasitol. Res., 2009, 105, 681–687. [CrossRef] [PubMed] [Google Scholar]
  24. Savioli L., Smith H. & Thompson A. Giardia and Cryptosporidium join the “Neglected Diseases Initiative”. Trends Parasitol., 2006, 22, 203–208. [Google Scholar]
  25. Spinelli R., Brandonisio O., Serio G., Trerotoli P., Ghezzani F., Carito V., et al. Intestinal parasites in healthy subjects in Albania. Eur. J. Epidemiol., 2006, 21, 161–166. [CrossRef] [PubMed] [Google Scholar]
  26. Thompson R.C.A. Giardiasis: modern concepts in control and management. Ann. Nestlé (Engl), 2008, 66, 23–29. [CrossRef] [Google Scholar]
  27. Wilkinson R.G. Income distribution and life expectancy. Br. Med. J., 1992, 304, 165–168. [CrossRef] [PubMed] [Google Scholar]
  28. WHO/Europe. Centralized Information System for Infectious Diseases (CISID), 2005–2008. http://data.euro.who.int/ cisid/?TabID=243838. [Google Scholar]
  29. WHO. Prevention and control of intestinal parasitic infections. WHO Technical Report Series, 1987, 379, 1–47. [Google Scholar]
  30. Yoder J.S. & Beach M.J.. Giardiasis surveillance – United States, 2003–2005. MMWR Surveill. Summ., 2007, 56, 11–18. [PubMed] [Google Scholar]
  31. Yoder J.S., Harral C. & Beach M.J.. Giardiasis surveillance – United States, 2006–2008. MMWR Surveill. Summ., 2010, 59, 15–25. [PubMed] [Google Scholar]
  32. Younas M., Shah S. & Talaat A. Frequency of Giardia lamblia infection in children with recurrent abdominal pain. J. Pak. Med. Assoc., 2008, 58, 171–174. [PubMed] [Google Scholar]

All Figures

thumbnail Fig. 1.

Asymptomatic human Giardia infection in Central Serbia: (A) map with prevalence (%) in 20 study regions and (B) distribution of prevalence in 115 settlements throughout Central Serbia.

In the text
thumbnail Fig. 2.

Changes in incidence of symptomatic human Giardia infections in Serbia vs (A) Vojvodina and Central Serbia and (B) other Western Balkan Countries (Bosnia and Herzegovina, Croatia, Montenegro and FYR Macedonia) between 2005 and 2008.

In the text
thumbnail Fig. 3.

Total monthly counts of giardiasis for the four-year study period (2005-2008) in Serbia.

In the text

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