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Echinococcus granulosus Infection and Options for Control of Cystic Echinococcosis in Tibetan Communities of Western Sichuan Province, China

  • Yu Rong Yang,

    Affiliations Molecular Parasitology Laboratory, Queensland Institute of Medical Research, Brisbane, Queensland, Australia, Ningxia Medical University, Yinchuan, Ningxia Hui Autonomous Region, People's Republic of China, School of the Population Health, University of Queensland, Brisbane, Queensland, Australia

  • Donald P. McManus ,

    Affiliation Molecular Parasitology Laboratory, Queensland Institute of Medical Research, Brisbane, Queensland, Australia

  • Yan Huang,

    Affiliation Institute of Parasitic Disease Control, Sichuan Centres for Disease Control, Chengdu City, Sichuan, People's Republic of China

  • David D. Heath

    Affiliation AgResearch New Zealand Limited, HopKirk Research Institute, Grasslands Research Centre, Palmerston North, New Zealand

Echinococcus granulosus Infection and Options for Control of Cystic Echinococcosis in Tibetan Communities of Western Sichuan Province, China

  • Yu Rong Yang, 
  • Donald P. McManus, 
  • Yan Huang, 
  • David D. Heath



Human cystic echinococcosis (CE) is highly endemic in the Tibetan regions of Sichuan where most families keep guard dogs and where there are considerable numbers of ownerless/stray dogs. Strong Buddhist beliefs do not allow for elimination of stray dogs, and many strays are actually fed and adopted by households or monasteries. On account of the high altitude (3900–5000 m), pasturage is the major agricultural activity in this area. The harsh mountainous climate often leads to many grazing animals dying on the pasture at the end of a hard winter. The skin and some meat are taken, and the rest of the animal is left for scavenging birds and animals. The poor sanitation and hygiene, the Buddhist doctrine of allowing old livestock to die naturally, plus the unrestricted disposal of animal viscera post-slaughter may be responsible for the high prevalence of human CE in this setting.

Methods and Findings

As part of a large collaborative control program for CE in Ganzi County, situated in the west of Sichuan Province, surveillance for Echinococcus infection in domestic dogs using a coproantigen method and necropsy of unwanted dogs was carried out prior to (in 2000) and after (in 2005) dog anthelminthic treatment (5 mg/kg oral praziquantal at 6 month intervals) to determine the efficacy of the treatment for control. The prevalence of E. granulosus only in dogs by necropsy was 27% and 22%, and prevalence of both Echinococcus spp. by necropsy was 63% and 38%; prevalence of both Echinococcus spp. by coproantigen analysis was 50% and 17%. Necropsy of sheep/goats (age <1 to 12 years) (prevalence of E. granulosus in 1–6-year-old animals was 38% and in 10–12-year-old animals was 70%) and yaks (age 4 years) (prevalence of E. granulosus was 38%) was undertaken to determine the baseline transmission pressure. Protoscoleces were only found in very old sheep/goats and yaks. Necropsy of dogs in the Datangma district indicated that there was no apparent significant change in the overall prevalence of E. granulosus in unwanted dogs after 5 years of 6-month praziquantel treatment. However, this was likely due to the number of dogs available for necropsy being too small to reflect the real situation prevailing. There was a highly significant decrease in Echinococcus prevalence after the 5-year treatment program shown by coproantigen-ELISA. This indicated a decreasing but continuing risk for re-infection of domestic and stray dogs. Genotyping of E. granulosus samples obtained from necropsied sheep/goats and yaks and from locally infected humans at surgery was carried out to determine the strain of parasite responsible for human infection. DNA genotyping indicated that only the sheep strain (G1) of E. granulosus was present in the study area.


Considerable re-infection rates of E. granulosus among dogs indicated a high infection pressure from infected livestock in this region, most likely from older animals dying on the pasture. A combination of livestock vaccination with the Eg95 vaccine, which is effective against the sheep strain of E. granulosus, and dog anthelmintic treatment, thus targeting two critical points of the parasite life-cycle, would avoid the conflicts of religion or local culture and could achieve the goal of hydatid control in the long term.

Author Summary

Human cystic echinococcosis (CE) is highly endemic in Tibetan regions of Sichuan. As part of a control program for CE in Datangma district, Ganzi County, necropsy of strays and coproantigen-ELISA of all dogs was carried out prior to and post-drug treatment to determine the efficacy of the treatment for control. Examination of sheep/goats and yaks was undertaken to determine the baseline transmission pressure to dogs. The necropsy results indicated no apparent significant change in the overall prevalence of E. granulosus in unwanted dogs after 5 years of 6-month treatment. In contrast, there was a highly significant decrease in Echinococcus prevalence in domestic/stray dogs after the 5-year treatment program shown by coproantigen-ELISA. This indicated a decreasing but continuing risk for re-infection of dogs resulting from high infection pressure from the numerous infected domestic animals. DNA genotyping indicated the presence only of the sheep strain (G1) of E. granulosus in the study area. A combination of livestock vaccination with the highly effective Eg95 vaccine and dog drug treatment, targeting two critical points of the parasite life-cycle, would avoid the conflicts of religion or local culture and achieve the goal of hydatid control in the long term in the area.


Cystic echinococcosis (CE), caused by ingesting the eggs of the dog tapeworm Echinococcus granulosus is distributed worldwide in both humans and ungulates [1], and is a major public health problem in western China [2],[3]. E. granulosus has a two-host carnivore-prey life cycle, which commonly involves dogs and farm livestock. A common source of infection for dogs is offal from infected livestock. Two types of hydatid cysts can be observed in the various intermediate hosts: fertile cysts, in which brood capsules containing protoscoleces are both joined to the germinal layer and are free in the hydatid fluid filling the cyst cavity, and infertile cysts, which may not produce protoscoleces or are immature and are therefore unable to continue the life cycle of the parasite [4],[5].

Tibetan communities in north-western Sichuan Province are hyper-endemic for echinococcosis [6]. Poor sanitation and hygiene, the Buddist doctrine of allowing old livestock to die naturally, plus the unrestricted disposal of animal viscera post-slaughter may be responsible for the high prevalence of human CE. As part of a large collaborative control program for CE, surveillance for Echinococcus infection in domestic dogs using a coproantigen method and necropsy of unwanted dogs was carried out in Datangma district, Ganzi County, which is situated in the west of Sichuan province, near the border with the Tibet Autonomous Region, prior to (in 2000) and post- (in 2005) 6-monthly dog anthelminthic treatment to determine the efficacy of the treatment for control. Necropsy of sheep/goats (age <1 to 12 years) and yaks (age 4 years) was undertaken to determine the baseline transmission pressure. As well, genotyping of E. granulosus samples obtained from necropsied sheep/goats and yaks and from locally infected humans at surgery was carried out to determine the genotype of parasite responsible for human infections. Previous examination of yaks ranging in age from 4 to 12 years old in the field and at local slaughter houses in Ganzi County, revealed a high prevalence of E. granulosus cysts of the common sheep-dog strain (G1 genotype) but no cysts with protoscoleces [7]. This is in contrast to other published abattoir records such as in western Iran [8] where fertile cysts were found in 75% of sheep and goats, 45% in cattle and 15% in buffaloes. Notably, the prevalence of human CE has been shown by ultrasound to be as high as 6% in Ganzi villages that are dedicated to pastoralism [9], although as no other intermediate host animals were examined for the presence of hydatid cysts during the earlier survey, it was unclear which animals were responsible for infecting dogs [7]. Among E. granulosus, there is recognised genetic heterogeneity whereby different strains have been shown to have different host preferences, morphology and other biological characteristics, likely to impact on control [10]. Although the common domestic sheep-dog strain (G1 genotype) is responsible for most human infections, there is substantial evidence to indicate that other strains also infect humans [10]. Genotyping of E. granulosus samples obtained from necropsied sheep/goats and yaks, and from locally infected humans at surgery in Datangma district was carried out to determine the strain of parasite responsible for human infection.

Materials and Methods

Study area and population

Datangma district, Ganzi County is in the north of Ganzi Tibetan Autonomous Prefecture, Sichuan Province, and consists of four townships (Cha-zha, Da-de, Ka-long and Cha-long) (Fig 1). Pasturage is the only agricultural activity in Datangma because of the high altitude (from 3900 m to 5000 m). Serious winter snow falls and summer flooding occur approximately every 5 years, and often lead to 50–70% loss of livestock in some villages/households. Within this study area, there are 89000 yaks, 25000 sheep, 8000 goats and 10000 horses (1999 records) which provide a primary income source for the local nomads. Most families keep at least one guard dog, and there are also large numbers of ownerless, stray dogs. The main source of water is the Daqu (moon) river that crosses the district from northwest to southeast; it provides sufficient water for human and livestock consumption, but there is no formal drinking water system. The water in the river is not clean as various items including dung, and yak, sheep and even human cadavers are thrown into it. Most of the households collect water several times a day for personal use and drink it without boiling. The population is composed primarily of transhumant herdsmen, who move their animals between winter pasturelands, now associated with fixed settlements, and higher altitude summer pasturelands not associated with fixed settlements. Hygiene and sanitation are extremely poor. In addition, people live in close proximity to both owned and unwanted domestic dogs.

Figure 1. Map of China showing Datangma district in the northwest area of Ganzi Tibetan Autonomous Prefecture, Sichuan Province, China.

Dog treatment

All owned (4263) or stray dogs (1500–2000) in the study area were to be treated with praziquantel (PZQ) twice a year from the year 2000 onwards, at the end of spring and the end of autumn. It was not difficult to treat stray dogs because they were usually close to households or monastries and were always looking for food. Each dog received a 200 mg pill in tsampa (a mixture of barley meal and ghee), and was observed to make sure that the pill was ingested. At a recommended dose of 5 mg/kg, the 200 mg pill is sufficient for a 40 kg dog, and even the large Tibetan mastiffs would not exceed this weight.

Dog coproantigen ELISA surveys

The dog coproantigen ELISA detection method used both prior to and following treatment of all dogs in the study area has been described [11]. On six occasions (Sept./2000, Sept./2003, May/2004, Oct./2004, Apr./2005, Oct./2005), faecal samples were collected from dogs from 20 selected households from each of 29 villages surveyed. They were allocated a number (1–580).

Dog necropsy procedures

Unwanted dogs were euthanized humanely by feeding them a pill that contained para-amino propiophenone (PAPP). The small intestine was removed and opened longitudinally. After visual inspection of the surface of the intestine, the areas containing worms were placed in closed bottles of 0.85% (w/v) NaCl (saline) and vigorously shaken. Released worms were fixed in 4% (v/v) of 40% (v/v) formaldehyde in saline, either before or after relaxing overnight in tap water. E. granulosus worms were identified by morphology and were differentiated from E.multilocularis using light microscopy according to WHO Guidelines [12]. Other taeniid cestodes present in the necropsied dogs were identified based on established morphological criteria [13][15]. The only two Taenia species found were Taenia serials and T. pisiformis. It is possible that T. multiceps was present and could not be differentiated from T. serialis. However, there was no record in this region of T. multiceps metacestodes in sheep or goats, and also, surprisingly, no T. hydatigena or T. ovis.

Sheep/goat/yak necropsy procedures

Yaks were observed after slaughter at Ganzi County abattoir. Sheep and goats were usually home-killed and were not available for necropsy inspection. The assistance of village and County cadres was sought in order to obtain young (4 years old) and older aged yaks (17–18 years old) or sheep and goats (aged 10–12 years). Animals were killed humanely by their owners, according to the Tibetan Buddhist custom. The head was presented, together with lungs and liver, so that an estimate could be made of the age of the animal. Yaks were aged from horn growth rings while sheep were aged by inspecting the number of incisor teeth and the degree of tooth wear. Organs were palpated and macroscopic cysts removed. The organs were then sliced at 2 mm (liver) or 4 mm (lungs) intervals to discover any small cysts. Cysts were dissected from liver or lung tissue. The cysts were then incised, and inner membranes and any brood capsules containing protoscoleces were rinsed in saline and then fixed in 95% (v/v) ethanol. Fixed samples were transported to the Australian laboratory for genotype analysis.

Parasite sample collection and DNA analysis

Echinococcus cysts from sheep, goats and yaks were obtained from the study area as described above. An individual isolate represents parasite material collected from a single hydatid cyst. Human cystic material from patients of Datangma district was collected during surgery at Ganzi County Hospital. All cystic samples were examined by microscopy and isolates from sheep, goats, yak and humans that had protoscoleces and/or germinal membranes present were analysed by DNA sequencing of the atp6 gene [16].

Statistical analysis

Chi-square values and 95% confidence intervals were calculated using Epi-Info (Centres for Disease Control and Prevention, Atlanta, GA) for analyses of prevalence. Comparisons between groups were performed using chi-square of Fisher's exact tests. The level of statistical significance was set at P = 0.05, unless otherwise stated.

Ethics statement

This study was reviewed and approved by Sichuan CDC, Sichuan Provincial Ethics Committee and the Institutional Review Board of the Ethics Committee of the First Teaching Hospital of Xinjiang Medical University as well as the Tibetan community representatives. Written informed consent was obtained from all participants before commencement. All animal work was carried out with the approval of AgResearch New Zealand limited, Wallaceville Animal Research Centre Animal Ethics Committee.


Structure of the dog and livestock populations in Datangma district


Most households kept 1–2 dogs; male dogs (70%) were preferred to bitches (30%). The main food of the dogs was the same as humans (barley plus ghee). Some nomads indicated they had seen the dogs eating hares, pika and rodents, mainly Lepus oiostolus, Ochotona curzoniae and/or Microtus spp. Dogs also ate the offal and remains of slaughtered or dead livestock, especially in the slaughtering season (November) and after a harsh winter (March). The nomads from this area treat their unwanted dogs and old or wounded dogs as free animals, and they never kill dogs because of their religious beliefs. Accordingly, there were a large number of unwanted dogs present. For the coproantigen survey one dog was sampled from each of 580 households (29 villages and 20 households per village). The same household was sampled each time, and in most cases it was the same dog. Some dogs died and were replaced. For the praziquantel treatment every dog in every household in every village, and all the unwanted dogs in the vicinity of each household received the pill in a small ball of tsampa (barley meal mixed with butter oil).


In 2000, livestock in Datangma District comprised 89,000 yaks and 33,000 sheep/ goats. The yak herd structure comprised approximately 50% males, which were mostly castrated for transportation. Roughly similar numbers of males and females were in each age group ranging from 1–17 years. A few yaks were older than 17 years. Between the ages of 5 and 11 years, females might have one calf every 2 years. Most sheep/goat flocks had equal numbers of males and females with ages ranging from 1–12 years, with a few as old as 14 years. An average of 30% of females gave birth each year. The remaining females were too young or were past breeding age.

Echinococcus prevalence

Prevalence in dogs.

Dog necropsies were undertaken in 2000 and 2005. In 2000, necropsies of 22 unwanted dogs took place prior to the commencement of 6-monthly treatment of all dogs with praziquantel. The overall baseline prevalence of E. granulosus was 27% and that of E. multilocularis was 36% (Table 1). One dog had about 100,000 E. multilocularis worms, and others had 500–1000 E. multilocularis. All E. granulosus infections ranged from 10–50 worms. The prevalence of Taenia spp. (T. serialis and/or T. pisiformis) was 32%; 23% of dogs had no worms (Table 1). Two out of the 9 positive dogs had large numbers of E.multilocularis worms. The 5 dogs with E.granulosus worms had from 4–100 worms. The second series of necropsies took place at the end of 2005, 5 years after implementation of the control program; twenty-six stray dogs were necropsied, with an overall prevalence for E. granulosus of 22% and for Taenia spp. of 16% (Table 1). The prevalence of E. granulosus and the Taenia spp. decreased but the changes were not significant. Possibly, all of these were new infections, because all dogs in the region, wanted or stray, had been treated with praziquantel at the end of the previous autumn. There was a significant decrease (P<0.05) in E. multilocularis prevalence (16%) and a significantly increased percentage (54%) of dogs without worms (P<0.05).

Table 1. The prevalence of Echinococcus granulosus in dogs determined by necropsy and coproantigen surveys in 2000 prior to the commencement of a 6-monthly anthelmintic dosing program and 5 years later in 2005, Datangma district, Ganzi County.

In addition, the dog coproantigen positivity rate showed a constantly decreasing trend from 50% in 2000 prior to any treatment compared with post-treatment of 35% in September, 2003, 30% in both May and October, 2004, and 26% in April and 17% in October, 2005.

Comparing the coproantigen positivity rates, there was a highly significant difference in coproantigen positivity in dogs surveyed prior to treatment in 2000 compared with animals after 5-years of 6-monthly praziquantel treatment in 2005 (P<0.01) (Table 1).

Prevalence in intermediate hosts.

In 2003, 15 goat and 19 sheep livers and lungs from animals up to the age of 6 years were examined; 3/15 goats and 10/19 sheep were infected (Table 2). The maximum diameter of cysts was 15 mm, but most had diameters of 2 to 3 mm. None of the cysts contained protoscoleces. E. granulosus prevalence appeared to increase with age. In 2004, seventeen sheep/goats aged 10–12 years were necropsied (Table 2). Within this older-age group, there were 6 animals with infertile cysts and 6 animals with fertile cysts having protoscoleces. There was an average of 5.8 cysts per infected animal.

Table 2. Hydatid prevalence in sheep/goats by age in Datangma district, Ganzi County.

Regarding larval E. granulosus infection in yaks, 100 four-year-old yaks were surveyed in the field and 38% had cysts. Of the infected yaks, there was an average of 8 cysts per infected animal (Table 3). Under macroscopic observation, both “apparently multilocular” and unilocular cysts were often found in the same host. Both these cyst types had been genotyped previously by atp6 gene sequence analysis as G1 [7]. The “apparently multilocular” cysts were actually overgrown germinal membrane filling a space enclosed by a thick cyst wall. Different cyst sizes were also often observed in the same host. Among 305 cysts, the majority (79%, 241/305) were in the size range from 2 to 20 mm in diameter (Table 3). The “potentially-fertile” cysts were only found with cyst diameters larger than 21 mm, and the frequency of the “potentially-fertile” cysts increased with cyst sizes (Table 3). A “potentially-fertile” cyst is defined as one containing clear fluid, an intact germinal membrane that was not convoluted, and a thin host-derived adventitial membrane. Yak 2 (17 years old) (Table 4) had 2 lung cysts of 14 and 8 cm diameter. Both cysts contained large numbers of protoscoleces.

Table 3. The characteristics of hydatid cysts in yak by cyst type and size among 100 four-year-old necropsied animals, Datangma District, Ganzi County.

Table 4. Substitutions in the atp6 gene of the E. granulosus common sheep/dog strain (G1 genotype) isolates investigated in this study.

Sequence analysis of the atp6 gene

Except for one yak isolate (yak 3; small (2 cm) cyst diameter, with no germinal membrane or protoscoleces present), all samples collected from animal intermediate hosts (sheep, goats and yaks) and humans were amenable to DNA typing by mitochondrial atp6 gene sequencing. If protoscoleces were not present, the typing was done on DNA extracted from germinal membrane. All samples were typed as the G1 genotype of E. granulosus; some minor mutations in the sequences obtained were apparent as shown in Table 4. These substitutions were distributed across the length of the 513 bp fragment examined. The sequence analysis allowed the definition of 8 different types of atp6 sequence represented by variation at 13 different nucleotide positions listed in Table 4. Of these, there were 6 isolates with variation at position 360 of the atp6 gene. Seven isolates had substitutions at positions 23, 24, 26, 43, 45, 50, 73, 75, 86, 265 and 243. Isolates with a silent substitution at position 360 originated only from animal hosts; none of the human isolates had the mutation. All the E. granulosus atp6 sequences obtained were translated into open reading frames thus eliminating the presence of pseudogenes.


The most reliable method for diagnosis of Echinococcus spp. in definitive hosts is by necropsy, because worm burdens can be accurately estimated and parasites collected for identification [17]. However, necropsy usually results in a biased sample, in that only unwanted dogs can be necropsied. Coproantigen detection of Echinococcus spp. in canine hosts has shown great promise [11] and provides a complementary method for diagnostic and surveillance purposes. Necropsy results prior to the start of the control program undertaken in the Datangma district study area in 2000 showed that only 23% of dogs had no worms, with prevalences for E. multilocularis and E. granulosus being 36% and 27%, respectively. Two Taenia species (T. pisiformis and T.serialis) with a similar transmission life-cycle to E. multilocularis (hares necropsied around townships often had E. multilocularis cysts in their liver), were found in 32% of dogs, and these were probably acquired by animals eating infected hares or rodents.

Praziquantel is currently the most effective anthelmintic available for echinococcosis control in carnivores [18],[19]. Mathematical models have been developed to describe the transmission dynamics and more recently to simulate control options [20],[21]. The lengthening of the treatment intervals to beyond the pre-patent period for Echinococcus spp. can be effective because the mean time to re-infection is often considerably longer than six weeks [20],[21]. Necropsy of dogs in the Datangma district indicated there was no apparent significant change in the overall prevalence of E. granulosus in unwanted dogs after 5 years of 6-monthly praziquantel treatment. The intensities of infection also did not appear to differ between the two sampling periods. However, this was likely due to the number of dogs available for necropsy being too small to reflect the real situation prevailing. The highly significant difference in Echinococcus prevalence after the 5-year treatment program shown by the coproantigen-ELISA indicated a decreasing but continuing risk for re-infection of domestic and stray dogs, and therefore of livestock.

In intermediate hosts, cysts of E. granulosus are usually detected at post-mortem abattoir examination of the viscera. Although this can provide important epidemiological data, which can be used to define likely echinococcal infection pressure [22][24], the main disadvantage of the approach is that samples obtained at slaughterhouses are potentially biased because this material is not generally accessible to dogs. In Tibetan areas, some animals are slaughtered (usually late autumn) for meat, but most old animals are allowed to die naturally. It is very difficult to necropsy these animals so that information about the E. granulosus infection status of very old animals is hard to obtain due to the strong Buddhist religion and life-style.

Interruption of the echinococcal parasite lifecycle in intermediate hosts has been shown to be important [25]. A vaccine for animal intermediate hosts with the Eg95 vaccine has been shown to be highly effective as an intervention against the dog/sheep (G1 genotype) strain [26][29]. The hydatid isolates examined here and previously from Ganzi indicated that only the G1 strain of E. granulosus is present and is responsible for human CE prevalence in this and other hyperendemic regions of North West China [3],[6],[7],[9],[16],[30]. Some minor genetic polymorphism in the atp6 sequence was evident in a number of the isolates, with the most frequent change being a substitution (G/A) at position 360 compared with the G1 reference sequence in isolates collected from the majority of hosts except humans. Whether these polymorphisms in the atp6 sequence reflect any biological or public health relevance for control may require further investigation on a larger scale, since genetic variation may affect infectivity and pathogenicity of E. granulosus [10],[31],[32].

The genotyping results are highly relevant in terms of control as livestock vaccination with the Eg95 vaccine would not only be beneficial in increasing the value of livestock production, but would also prevent the transmission of the parasite to dogs. The vaccine only prevents new infections and does not eliminate cysts already present. Thus, it would take a number of years before all the previously infected livestock were removed from the population. A modelling study has suggested a high probability of success even if anthelmintic treatment is only given every 6 months to 60% dogs with as few as 60% of sheep vaccinated [25]. This illustrates the cumulative effect of controlling the parasite at more than one point in its life cycle and may indicate the most promising means of control for this region. A control strategy consisting of a combination of livestock vaccination by using Eg95 and routine anthelmintic dog treatment would be particularly useful in this low income rural area where CE is so highly endemic, where resources are scarce and continual reintroduction of E. granulosus through sylvatic cycles or from neighbouring counties, provinces or even countries are constant threats. Unfortunately the study environment also has high transmission of E. multilocularis, which accounts for approximately 50% of human infections. The Eg95 vaccine would not affect the transmission of E. multilocularis. This will make overall control of echinococcosis more difficult. Control of E. multilocularis will require greater attention to hygiene and to more frequent treatment of dogs with praziquantel. Also, until the coproantigen test can be made specific, surveillance using this test will include both species of Echinococcus. Nevertheless, there did appear to be some encouraging progress made during the 5 years of 6-monthly dog treatments in Datangma district.

Many studies have illustrated that the development rate of E. granulosus cysts corresponds with the longevity of the intermediate host and that large cysts, 10–20 cm in diameter, are generally fertile [33]. In our observations, the frequencies of “potential-fertile” cysts increased in lesions with a diameter>21 mm in 100 four-year old yak necropsied. In the Tibetan region E. granulosus also appears to mature towards the end of the natural lifetime of its intermediate hosts. The fertile cysts were only found in sheep/goats around the age of 10–12 years (Table 2) and in very old yaks, possibly because the drop in immunity associated with aging allows the cysts to mature and develop protoscoleces. This finding is significant for future hydatid control in Tibetan areas and it might seem logical to begin a control program by removing all old or unproductive animals. Such a recommendation, however, though good for the economics of pastoralism, may change the farming practices that Tibetans have established over a thousand years of grazing animals on the high plateau. The combination of livestock vaccination with dog anthelmintic treatment might be a more acceptable strategy than removal of stray dogs and old livestock. In this way, a control program would avoid the conflicts of religion or local culture, but could still achieve the goal of hydatid control in the long term. However, now that new epidemiological information has become available there are already suggestions that a program of hydatid control should include removal of old and unproductive animals [34] and ownerless stray dogs.

Author Contributions

Conceived and designed the experiments: YRY DPM YH DDH. Performed the experiments: YRY YH DDH. Analyzed the data: YRY DPM YH DDH. Contributed reagents/materials/analysis tools: YRY YH DDH. Wrote the paper: YRY DPM YH DDH.


  1. 1. McManus DP, Zhang W, Li J, Bartley PB (2003) Echinococcosis. Lancet 362: 1295–1304.
  2. 2. Ito A, Wandra T, Sato MO, Mamuti W, Xiao N, et al. (2006) Towards the international collaboration for detection, surveillance and control of taeniasis/ cysticercosis and echinococcosis in Asia and the Pacific. Southeast Asian J Trop Med Public Health 37: S82–S90.
  3. 3. Wang Z, Wang X, Liu X (2008) Echinococcosis in China, a review of the epidemiology of Echinococcus spp. Ecohealth 5: 115–126.
  4. 4. Kamenetzky L, Canova SG, Guarnera EA, Rosenzvit MC (2000) Echinococcus granulosus: DNA extraction from germinal layers allows strain determination in fertile and nonfertile hydatid cysts. Exp Parasitol 95: 122–127.
  5. 5. Lahmar S, Debbek H, Zhang LH, McManus DP, Souissi A, et al. (2004) Transmission dynamics of the Echinococcus granulosus sheep-dog strain (G1 genotype) in camels in Tunisia. Vet Parasitol 121: 151–156.
  6. 6. Craig PS, Li T, Qiu J, Zhen R, Wang Q, et al. (2008) Echinococcosis and Tibetan communities. Emerg Infect Dis 14: 1674–1675.
  7. 7. Heath DD, Zhang LH, McManus DP (2005) Short report: inadequacy of yaks as hosts for the sheep dog strain of Echinococcus granulosus or for E. multilocularis. Am J Trop Med Hyg 72: 289–290.
  8. 8. Dalimi A, Motamedi G, Hosseini M, Mohammadian B, Malaki H, et al. (2002) Echinococcosis/hydatidosis in western Iran. Vet Parasitol 105: 161–171.
  9. 9. Tiaoying L, Jiamin Q, Wen Y, Craig PS, Xingwang C, et al. (2005) Echinococcosis in Tibetan populations, western Sichuan Province, China. Emerg Infect Dis 11: 1866–1873.
  10. 10. McManus DP, Thompson RC (2003) Molecular epidemiology of cystic echinococcosis. Parasitology 127l: S37–S51.
  11. 11. Huang Y, Yang W, Qiu J, Chen X, Yang Y, et al. (2007) A modified coproantigen test used for surveillance of Echinococcus spp. in Tibetan dogs. Vet Parasitol 149: 229–238.
  12. 12. Eckert J, Deplazes P, Craig PS, Gemmell MA, Gottstein B, et al. (2001) Echinococcosis in animals: clinical aspects, diagnosis and treatment. In: Eckert J, Gemmell MA, Meslin F-X, Pawlowski ZS, editors. WHO/OIE Manual on Echinococcosis in Humans and Animals: A Public Health Problem of Global Concern. Paris: World Organisation for Animal Health (Office International des Epizooties) and World Health Organization. pp. 73–100.
  13. 13. Verster A (1969) A toxonomic revision of the genus Taenia Linnaeus, 1758 S. str. Onderstepoort. J Vet Res 36: 3–58.
  14. 14. Beveridge I, Gregory GG (1976) The identification of Taenia species from Australian carnivores. Aust Vet J 52: 369–373.
  15. 15. Edwards GT, Herbert IV (1981) Some quantitative characters used in the identification of Taenia hydatigena, T. ovis, T. pisiformis and T. multiceps adult worms, and T. multiceps metacestodes. J Helminthol 55: 1–7.
  16. 16. Yang YR, Rosenzvit MC, Zhang LH, Zhang JZ, McManus DP (2005) Molecular study of Echinococcus in west-central China. Parasitology 131: 547–555.
  17. 17. Eckert J (1997) Epidemiology of Echinococcus multilocularis and E. granulosus in central Europe. Parassitologia 39: 337–344.
  18. 18. Andersen FL, Tolley HD, Schantz PM, Chi P, Liu F, et al. (1991) Cystic echinococcosis in the Xinjiang/Uygur Autonomous Region, People's Republic of China. II. Comparison of three levels of a local preventive and control program. Trop Med Parasitol 42: 1–10.
  19. 19. Wei J, Cheng F, Qun Q, Nurbek , Xu SD, et al. (2005) Epidemiological evaluations of the efficacy of slow-released praziquantel-medicated bars for dogs in the prevention and control of cystic echinococcosis in man and animals. Parasitol Int 54: 231–236.
  20. 20. Budke CM, Campos-Ponce M, Qian W, Torgerson PR (2005) A canine purgation study and risk factor analysis for echinococcosis in a high endemic region of the Tibetan plateau. Vet Parasitol 127: 43–49.
  21. 21. Budke CM, Jiamin Q, Craig PS, Torgerson PR (2005) Modeling the transmission of Echinococcus granulosus and Echinococcus multilocularis in dogs for a high endemic region of the Tibetan plateau. Int J Parasitol 35: 163–170.
  22. 22. Cabrera PA, Parietti S, Haran G, Benavidez U, Lloyd S, et al. (1996) Rates of reinfection with Echinococcus granulosus, Taenia hydatigena, Taenia ovis and other cestodes in a rural dog population in Uruguay. Int J Parasitol 26: 79–83.
  23. 23. Ming R, Tolley HD, Andersen FL, Chai J, Chang Q (1992) Frequency distribution of Echinococcus granulosus in dog populations in the Xinjiang Uygur Autonomous Region, China. Vet Parasitol 43: 233–241.
  24. 24. Torgerson PR, Williams DH, Abo-Shehada MN (1998) Modelling the prevalence of Echinococcus and Taenia species in small ruminants of different ages in northern Jordan. Vet Parasitol 79: 35–51.
  25. 25. Torgerson PR, Heath DD (2003) Transmission dynamics and control options for Echinococcus granulosus. Parasitology 127: S143–S158.
  26. 26. Heath DD, Jensen O, Lightowlers MW (2003) Progress in control of hydatidosis using vaccination–a review of formulation and delivery of the vaccine and recommendations for practical use in control programmes. Acta Trop 85: 133–143.
  27. 27. Lightowlers MW, Lawrence SB, Gauci CG, Young J, Ralston MJ, et al. (1996) Vaccination against hydatidosis using a defined recombinant antigen. Parasite Immunol 18: 457–462.
  28. 28. Lightowlers MW, Jensen O, Fernandez E, Iriarte JA, Woollard DJ, et al. (1999) Vaccination trials in Australia and Argentina confirm the effectiveness of the EG95 hydatid vaccine in sheep. Int J Parasitol 29: 531–534.
  29. 29. Gauci C, Vural G, Oncel T, Varcasia A, Damian V, et al. (2008) Vaccination with recombinant oncosphere antigens reduces the susceptibility of sheep to infection with Taenia multiceps. Int J Parasitol 38: 1041–1050.
  30. 30. Li T, Ito A, Nakaya K, Qiu J, Nakao M, et al. (2008) Species identification of human echinococcosis using histopathology and genotyping in northwestern China. Trans R Soc Trop Med Hyg 102: 585–90.
  31. 31. McManus DP (2002) The molecular epidemiology of Echinococcus granulosus and cystic hydatid disease. Trans R Soc Trop Med Hyg 96: S151–S157.
  32. 32. Campbell G, Garcia HH, Nakao M, Ito A, Craig PS (2006) Genetic variation in Taenia solium. Parasitol Int 55: S121–S126.
  33. 33. Rausch RL (1993) The Biology of Echinococcus granulosus. In: Andersen FL, Chai JJ, Liu FJ, editors. Compendium of Cystic Echinococcosis with Special Reference to the Xinjiang Uygur Autonomous Region, the Peoples Republic of China. Provo (Utah): Brigham Young University Print Services. pp. 27–56.
  34. 34. Torgerson PR, Ziadinov I, Aknazarov D, Nurgaziev R, Deplazes P (2009) Modelling the age variation of larval protoscoleces of Echinococcus granulosus in sheep. Int J Parasitol. In press.