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Trematode infections in cattle in Arumeru District, Tanzania are associated with irrigation
Parasites & Vectorsvolume 7, Article number: 107 (2014)
The relationship between the environment and infection of cattle with trematodes was studied at Arumeru District, Arusha Region, northern Tanzania. Randomly selected villages were grouped into three cattle management strata, (i) zero-grazing (ZZ) (ii) communal grazing without irrigation (ZC) and (iii) communal grazing with irrigation (ZCI).
Faecal samples were collected from 241 cattle, and processed using the Flukefinder® method. Snail intermediate hosts were collected with a snail scoop from the water bodies in the study villages and identified morphologically.
The overall prevalence of F. gigantica, paramphistomes and S. bovis were 33%, 37% and 2% respectively. Prevalence for F. gigantica, paramphistomes, and S. bovis for each stratum were, zero-grazing (ZZ) (29.7%, 36.0% and 0%), communal grazing without irrigation (ZC) (6.3%, 15.0% and 3.8%) and communal grazing with irrigation (ZCI) (57.7%, 56.7% and 1.0%) respectively. The differences between strata were significant for F. gigantica (p < 0.001) and paramphistomes (p < 0.05) but not for S. bovis. Irrigation could account for the high prevalence of F. gigantica and paramphistomes in the ZCI stratum as compared to the ZZ and ZC strata. The higher prevalences of F. gigantica and paramphistomes in the ZZ stratum compared with the ZC stratum were unexpected and attributed to the practice of farmers in some ZZ stratum villages buying fodder for their cattle obtained from pastures in ZCI villages.
Trematode infections in cattle are prevalent in Arumeru District. Fasciola gigantica and paramphistomes are associated with grazing in areas with irrigation of crops. Zero-grazing of cattle does not necessarily prevent the risk of infection.
Trematode infections in cattle especially Fasciola gigantica cause severe economic losses in sub-Saharan African countries [1–3], including Tanzania . Trematode species that have been reported in Tanzania are F. gigantica, Fasciola hepatica, Schistosoma bovis, Paramphistomum species and Dicrocoelium hospes. Abattoir surveys [9–13], found trematode infections in the southern highlands zone, northern zone, Lake zone and eastern zone of Tanzania and the epidemiology and control of trematode infections in cattle has been studied in the Southern Highlands [5–7, 14]. Scanty information is available on the epidemiology in cattle in other parts of the country where trematode infections have been reported. This study was conducted in Arumeru District in northern Tanzania to investigate the epidemiology of trematode infections in cattle under different cattle management systems in order to generate base line data that will provide information for the design of effective control strategies.
Study design and sample size
A cross-sectional study was conducted from August to September 2012 to determine the prevalence of trematode infections in cattle and to identify the potential snail intermediate hosts in Arumeru District, Arusha Region, Tanzania. Study villages were selected using probability proportional to size, based on their cattle populations as reported by the local District Veterinary Office. A total of 15 study villages were selected and further divided into three strata according to their cattle management system and whether there was irrigation of crops. Generally in the wet season all villages confined cattle to avoid their consumption of growing crops and practiced zero-grazing. The three strata comprised (i) villages which confine cattle and practice zero-grazing all year-round (ZZ), (ii) those without irrigation which practice communal grazing in the dry season (ZC) and those with irrigation practicing communal grazing in the dry season (ZCI). Sample size was calculated using Bennett’s formula for cluster sample surveys to enable estimation of prevalence with ±5% absolute precision and 95% certainty .
Parasitological examination of cattle
A total of 241 cattle were selected and faecal samples were collected per rectum, using sterile surgical gloves that were then turned inside out to contain the sample, and labelled with a unique identification number encoding area, age (categorized as weaners 6–24 months and adult above 24 months) sex, date, herd identity and sample number before storing them in an ice packed cool box awaiting examination. Faecal samples were processed using a Flukefinder® (Richard Dixon, ID, US) in accordance with the manufacturer’s instructions. Flukefinder® is a kit comprising a unit made up of two 50 mm wide sieves of approximately 125 nm and 30 nm mesh. Briefly 2 g of faeces were mixed with water then poured into the Flukefinder® unit and flushed well with water. Larger faecal debris were retained by the larger diameter sieve and discarded. Faecal material retained in the smaller diameter sieve, including trematode eggs, was back washed into a 50 ml plastic cup. This was allowed to settle for five minutes then the supernatant was poured off and the remaining faecal material poured into a 50 mm petri dish. Water was added to fill the petri dish, and then the contents allowed to settle for 30 seconds before the supernatant was poured off. Three drops of methylene blue were added to the remaining faecal material which was then examined under a x4 objective stereoscopic dissecting microscope. Eggs were identified using key morphological features  and counted. All work on animals described in this manuscript was conducted in accordance with internationally recognised guidelines and approved by Sokoine University of Agriculture.
Water bodies were visited for collection of snail intermediate hosts in each study village that included: rivers, irrigation canals, swamps and water reservoirs. Collection of snails was performed by scooping [17, 18] and or hand picking conducted by two people at each site for 20 min. Snails were identified morphologically using a field guide to African freshwater snails [19, 20]. Furthermore, each of the snails was placed in a 10 ml beaker filled with 6 ml of distilled water and exposed to light overnight to stimulate shedding of the cercariae. The following morning water in each beaker was poured into the petri dish, and examined under the x4 objective stereoscopic microscope for the presence of cercariae.
Prevalence was calculated as the number of positive faecal samples over the total number of faecal samples examined at district, management, village and age strata levels. Differences in prevalence were assessed with generalised linear models with binomial errors using R- statistical software (version i386 2.15.0; the R Foundation for Statistical Computing, http://www.R-project.org). Fisher’s exact test was used for significance of differences between the three strata in terms of age profiles of cattle, because of the expected value (4.2) for the youngest age group in the ZZ stratum was less than 5.
Prevalence of trematode infections in cattle
Fasciola gigantica, paramphistome and Schistosoma bovis infections were found in all but two of the fifteen villages in Arumeru District in which cattle were examined (Table 1). The overall prevalences of Fasciola, paramphistome and Schistosoma infections in 241 cattle were 33.2%, 37.3% and 1.7% respectively. The prevalences of these three genera of trematodes in cattle in each stratum are shown in Table 2.
The differences in prevalence of F. gigantica were investigated using a generalised linear model with a quasibinomial empirical scale parameter to allow for overdispersion. Differences among strata were significant (p < 0.02), with stratum ZCI prevalence significantly greater than stratum ZC, (but neither significantly different to stratum ZZ). Compared with cattle zero-grazing all year round, prevalence of F. gigantica in cattle grazing communally during the dry season was not significantly different (p > 0.1). Cattle in villages practicing irrigation had significantly higher prevalence (57.7%) than in those that did not (16.7%). The odds ratio for risk of F. gigantica infection associated with irrigation was 6.8 (95% C.I. 1.45 – 32.0, p < 0.05), corresponding to a relative risk of 3.5 (C.I. 95% 1.3 – 9.8). Differences among management strata in prevalence of paramphistome infection were similar to those for Fasciola, but not significant (p = 0.097) and nor was the practice of irrigation (p = 0084). Numbers of cattle with Schistosoma infection were too few for meaningful statistical analysis; three cattle were infected (in two villages) in stratum ZC and one in stratum ZCI, but none in stratum ZZ.
There was no significant difference between the three strata in terms of age profiles of cattle (p = 0.38). Adult cattle had the highest prevalence of F. gigantica and paramphistomes while weaners had the highest prevalence of S. bovis (Table 3). The differences of prevalence between age groups were statistically significant for paramphistomes (p > 0.05) but not for F. gigantica or S. bovis. A total of 96 (40%) out of 241 cattle had co-infections of F. gigantica and paramphistomes, villages under ZCI stratum having the most co-infection compared to other villages. The faecal egg counts for F. gigantica, paramphistomes and S. bovis ranged from 0–167, 0–483 and 0–1 eggs per gram (epg) respectively. The majority of cattle had fewer than 10 epg.
Trematode infection in snails
A total of 761 snails were collected including 215 Lymnaea (Radix) natalensis, 545 Biomphalaria species and 1 Bulinus tropicus. The majority of the snails were collected in irrigation canals and rice fields in villages with irrigation, with the exception of 11 L. natalensis that were collected in one swampy location at a zero-grazing village (Ngyani). No snails were collected in villages that practiced communal grazing without irrigation. Seven L. natalensis were found to shed Xiphidiocercariae (not of veterinary importance).
On the basis of faecal egg counts, cattle in Arumeru District were found to be infected with three genera of cattle trematodes with overall prevalences of 33%, 37% and 2% for F. gigantica, paramphistomes and S. bovis respectively. While these figures are lower than those in previous studies in the southern highlands of Tanzania, which reported prevalences of 58.5%, 75.2% and 22.8% respectively for the three genera of trematode [13, 14, 21], prevalences in individual villages varied greatly, with 90-100% of tested cattle infected with F. gigantica and paramphistomes and up to 13% with S. bovis in some villages (Table 1). The differences in prevalence might be due to the variations in ecological and climatic conditions in the study areas [22, 23]. Unsurprisingly, the prevalences of F. gigantica and paramphistomes were higher in adult cattle than in weaners, reflecting their greater length of exposure to infection [5, 24, 25]. The prevalence of S. bovis was higher in weaners than in adult cattle; this was also in agreement with other studies . The lower infection rate in adult animals is probably associated with acquired immunity, which leads to resistance to re-infection . The higher prevalences of F. gigantica and paramphistomes in the ZCI stratum might be attributed to irrigation, which provides favourable ecological conditions for growth of intermediate hosts snails and development of trematode larval stages [24, 27]. Snail intermediate hosts (L. natalensis) of F. gigantica were indeed mainly found in the irrigated villages. A high proportion of infected snails in Tanzania is reported to occur at the transition from the rainy season to the dry season , and a high proportion of cattle acquire trematode infections at the end of the rainy season, reaching a peak during the dry season . Cattle grazing in the irrigation canals and associated swampy areas in the ZCI stratum during the dry season, are more likely to be highly infected with F. gigantica and paramphistomes than cattle in the non-irrigated ZC stratum which graze dryer pasture during the dry season [28, 29]. Better understanding of the transmission dynamics of F. gigantica through intermediate host snails in the irrigated areas could present opportunities for control. For instance, as L. natalensis survives poorly through periods of desiccation , cessation of irrigation for an appropriate period during the dry season, perhaps following crop harvest, might be helpful in reducing intermediate host population size.
There was considerable variation in prevalence of F. gigantica and paramphistomes among villages within strata (Table 1), especially those in the ZCI and ZZ strata. For both F. gigantica and paramphistomes, irrigated villages (ZCI stratum) fell into two groups, those with prevalences greater than 75% (Lekitatu, Makiba and Usa River), and those with prevalences less than 45% (Uwiru, Mikungani and Olkung’wado). It was noteworthy that irrigation in the high prevalence villages was much more extensive than in those with low prevalences. Unexpectedly, F. gigantica and paramphistomes were observed in cattle in two of the year round zero-grazed villages (ZZ stratum), Sing’isi and Patandi, which had prevalences of at least 50% for both trematodes. Trematode prevalences in these two villages (50% - 94%) greatly exceeded those in cattle in communally grazed cattle in the ZC stratum villages (0% - 19%), which might have been expected to be at greater risk than zero-grazed cattle . Again, it was noteworthy that farmers in Sing’isi and Patandi acquired cattle fodder from irrigation canals and swamps in Lekitatu village (ZCI stratum), which has extensive irrigation, and hence is likely to be contaminated with the infective metacercaria stage of Fasciola and Paramphistomum species. Selecting fodder from other sources might provide an opportunity for control of trematode infections in zero-grazed cattle in this region, and farmers in these villages could be educated on the importance of avoiding cattle fodder sourced from contaminated areas, and they might consider growing their own pastures to ensure safe feed for their cattle. Since L. natalensis was shown to occur in a swampy area within a zero-grazed village, care should be taken to prevent access to such areas by unconfined, small ruminants, which may also potentially host F. gigantica.
The overall prevalence of S. bovis infection in this study (2%) was very low compared to other trematodes, and infection was observed in only a few cattle in the ZC and ZCI strata. Bulinus africanus and Bulinus forskalli, the primary intermediate hosts of S. bovis, were not found in the study area. Rather B. tropicus, which becomes susceptible to S. bovis when previously infected with Paramphistomum species , was present and this might lead to limited transmission of S. bovis and hence the low level of infection observed. Moreover, adult cattle develop acquired immunity expressed as reduction of the fecundity of the female worms and resulting in reduced faecal egg counts . This might lead to some infected animals to be missed by the Flukefinder® method due to very low numbers of eggs in the faecal material. The presence of S. bovis in more cattle in communal grazing areas without irrigation (ZC stratum) than with irrigation (ZCI) was unexpected, but the numbers of infected animals were too few to be of significance. Absence of S. bovis from zero –grazing cattle (ZZ stratum) could be explained by the mode of transmission of S. bovis through cercarial skin penetration when cattle enter contaminated water bodies. This clearly cannot happen with zero-grazed animals.
This study has established that trematode infections including the major pathogen F. gigantica are widely prevalent in cattle in Arumeru District, an important livestock farming area of Tanzania. Infection rates with F. gigantica and paramphistomes were greatest in villages practicing irrigation of crops which appeared to increase transmission during the dry season when cattle graze freely. Intermediate host snails were also found mainly in villages practicing irrigation. Further studies on snail dynamics and infection rates in irrigated areas would be useful to inform control strategies. Some villages practicing year round zero-grazing also had high levels of trematode infection, which could be controlled by more careful sourcing of cattle fodder. Schistosoma bovis was also detected in small numbers of cattle in a few villages where cattle grazed during the dry season. Finally, in the broader context of food security, it is interesting to note how two common practices intended to make a positive contribution to agricultural productivity in this area, namely irrigation of arable crops and zero-grazing of cattle (primarily as a means of controlling ticks and tick-borne disease) may also have negative impacts on cattle health and productivity by increasing burdens of the clinically important parasite F. gigantica. This finding underlines the value of transdisciplinary research and intersectoral collaboration to agricultural development activities in sub-Saharan Africa.
Abunna F, Asfaw L, Megersa B, Regassa A: Bovine fasciolosis, coprological, abattoir survey and its economic impact due to liver condemnation at Soddo municipal abattoir, Southern Ethiopia. Trop Anim Health Pro. 2010, 42: 289-292. 10.1007/s11250-009-9419-3.
Dargie J: The impact on production and mechanism of pathogenesis of trematode infections in cattle and sheep. Int J Parasitol. 1987, 17: 453-463. 10.1016/0020-7519(87)90121-4.
Spithill TW, Smooker PM, Copeman DB: Fasciola gigantic a, epidemiology, control, immunology and molecular biology. Fasciolosis. Edited by: Dalton JP. 1999, Oxford, UK: CABI Publishing, 465-525.
Swai ES, Ulicky E: An evaluation of the economic losses resulting from condemnation of cattle livers and loss of carcass weight due to fasciolosis: a case study from Hai town abattoir, Kilimanjaro region, Tanzania. Livestock Res Rural Dev. 2009, 21:http://www.lrrd.org/lrrd21/11/swai21186.htm,
Keyyu JD, Monrad J, Kyvsgaard NC, Kassuku AA: Epidemiology of Fasciola gigantica and amphistomes in cattle on traditional, small scale dairy and large scale dairy farms in the southern highlands of Tanzania. Trop Anim Health Pro. 2005, 37: 303-314. 10.1007/s11250-005-5688-7.
Walker SM, Makundi AE, Namuba FV, Kassuku AA, Keyyu J, Hoey EM, Prodohl P, Stothard JR, Trudgett A: The distribution of Fasciola hepatica and Fasciola gigantica within southern Tanzania–constraints associated with the intermediate host. Parasitology. 2008, 135: 495-503.
Kassuku AA, Christensen NO, Monrad J, Nansen P, Knudsen J: Epidemiological studies of Schistosoma bovis in Iringa Region, Tanzania. Acta Trop. 1986, 43: 153-163.
Mahlau EA: Liver fluke survey in zebu cattle of Iringa Region, Tanzania and first finding of the small fluke Dicrocoelium hospes/Loos. Bull Epizootic Dis Afr. 1970, 18: 21-28.
Hyera JMK: Prevalence, seasonal variation and economic significance of fascioliasis in cattle as observed at Iringa abattoir between 1976–1980. Bull Anim Health Pro Afr. 1984, 32: 356-359.
Komba EVG, Komba EV, Mkupasi EM, Mbyuzi AO, Mshamu S, Luwumba D, Busagwe Z, Mzula A: Sanitary practices and occurrence of zoonotic conditions in cattle at slaughter in Morogoro Municipality, Tanzania: implications for public health. Tanzania J Health Res. 2012, 4:http://dx.doi.org/10.4314/thrb.v14i2.6,
Mellau LSB, Nonga HE, Karimuribo ED: A slaughterhouse survey of liver lesions in slaughtered cattle, sheep and goats at Arusha, Tanzania. Res J Vet Sci. 2010, 3: 179-188.
Msanga JF: Prevalence and economic importance of Fasciola gigantica and Stilesia hepatica in Sukumaland, Tanzania. Tanzania Vet Bull. 1985, 7: 9-16.
Swai ES, Mtui PF, Mbise AN, Kaaya E, Sanka P, Loomu PM: Prevalence of gastrointestinal parasite infections in Maasai cattle in Ngorongoro District, Tanzania. Livestock Res Rural Dev. 2006, 18:http://www.lrrd.org/lrrd18/8/swai18107.htm,
Makundi AE, Kassuku AA, Maselle RM, Boa ME: Distribution, prevalence and intensity of Schistosoma bovis in cattle in Iringa District, Tanzania. Vet Parasitol. 1998, 75: 59-6. 10.1016/S0304-4017(97)00179-9.
Bennett S, Woods T, Liyanage WM, Smith DL: A simplified general method for cluster-sample surveys of health in developing countries. World Health Stat Quart. 1991, 44: 98-106.
Soulsby EJL: Helminths, arthropods & protozoa of domesticated animals 7th Ed. 1982, London: Baillere Tindall
Madsen H, Coulibaly G, Furu P: Distribution of freshwater snails in the river Niger basin in Mali with special reference to the intermediate hosts of schistosomes. Hydrobiologia. 1987, 146: 77-88. 10.1007/BF00007580.
Ndifon GT, Ukoli FMA: Ecology of freshwater snails in south-western Nigeria, I: distribution and habitat preferences. Hydrobiologia. 1989, 171: 231-253. 10.1007/BF00008146.
Brown DS: Freshwater snails of africa and their medical importance. 1994, London: Taylor and Francis, 2
DBL-WHO: A field guide to African freshwater snails. Danish bilharziasis laboratory. 1998, Charlottenlund, Denmark: WHO collaborating Centre for Applied Malacology
Keyyu JD, Kassuku AA, Msalilwa LP, Monrad J, Kyvsgaard NC: Cross-sectional prevalence of helminth infections in cattle on traditional, small-scale and large-scale dairy farms in Iringa District, Tanzania. Vet Res Commun. 2006, 30: 45-55.
Lemma B, Fesseha G, Tadele S: Studies on fasciolosis in four selected sites in Ethiopia. Ethiop Vet Parasitol. 1985, 18: 29-37. 10.1016/0304-4017(85)90005-6.
Tesfaheywet Z, Negash K: Prevalence of ovine fasciolosis in Oda Bultum Woreda, western Hararghe, Ethiopia. Global Veterinaria. 2012, 9: 530-534.
Pfukenyi DM, Mukaratirwa S, Willingham AL, Monrad J: Epidemiological studies of Fasciola gigantic infections in cattle in the highveld and lowveld communal grazing areas of Zimbabwe. Onderstepoort J Vet Res. 2006, 73: 37-51.
Waruiru RM, Kyvsgaard NC, Thamsborg SM, Nansen P, Bøgh HO, Munyua WK, Gathuma JM: The prevalence and intensity of helminth and coccidial infections in dairy cattle in central Kenya. Vet Res Commun. 2000, 24: 39-53. 10.1023/A:1006325405239.
Vercruysse J, Gabriel S: Immunity to schistosomiasis in animals, an update. Parasite Immunol. 2005, 27: 289-295. 10.1111/j.1365-3024.2005.00766.x.
Traore A: Incidence and control of fascioliasis around Niono, central Mali. ILCA Bull. 33:http://www.ilri.org/InfoServ/Webpub/fulldocs/Bulletin33/incide.htm,
Malone JB, Gommes R, Hansen J, Yilma JM, Slingenberg J, Snijders F, Nachtergaele F, Ataman E: A geographic information system on the potential distribution and abundance of Fasciola hepatica and F. gigantica in East Africa based on Food and Agriculture Organization databases. Vet Parasitol. 1998, 78: 87-101. 10.1016/S0304-4017(98)00137-X.
Mungube EO, Sila DM, Kariuki CW, Bauni SM, Tenhagen BA, Wamae L, Nginyi J, Omondi GA: A cross-sectional survey on fasciolosis in selected settlements of Taveta Division, Coast Province, Kenya. Livestock Res Rural Dev. 2012, 24:http://www.lrrd.org/lrrd24/4/mung24058.htm,
Southgate VR, Brown DS, Rollison D, Ross GC, Knowles RJ: Bulinus tropicus from central Kenya acting as host for Schistosoma bovis. Z Parasitenkd. 1985, 71: 61-69. 10.1007/BF00932919.
Authors acknowledge funding from Leverhulme-Royal Society African Award Scheme which enabled the research to be undertaken. They are grateful to local staff within the District Veterinary Office and Veterinary Investigation Centre in Arusha and to farmers in Arumeru district for their cooperation in this study. Field and technical assistance from Mr. D.S. Mwangoka and L.P. Msalilwa is highly appreciated.
The authors declare that they have no competing interests.
This work will form part of the PhD thesis of JN. The study was designed by JN, AK, GC and ME. Field and laboratory work was carried out by JN, AK with guidance from JS, GC and ME. Data analysis was undertaken by JN with the help of ME. The manuscript was drafted by JN, and revised, read and approved in final version by all authors.