Echinococcus granulosus is usually transmitted between canid definitive hosts and ungulate intermediate hosts.
Lesions found in the livers of ground squirrels, Spermophilus dauricus/alashanicus, trapped in Ningxia Hui Autonomous Region, an area in China co-endemic for both E. granulosus and E. multilocularis, were subjected to molecular genotyping for Echinococcus spp. DNA. One of the lesions was shown to be caused by E. granulosus and subsequently by histology to contain viable protoscoleces.
This is the first report of a natural infection of the ground squirrel with E. granulosus. This does not provide definitive proof of a cycle involving ground squirrels and dogs or foxes, but it is clear that there is active E. granulosus transmission occurring in this area, despite a recent past decline in the dog population in southern Ningxia.
Echinococcus granulosus and E. multilocularis are important zoonotic pathogens that cause serious disease in humans. E. granulosus can be transmitted through sylvatic cycles, involving wild carnivores and ungulates; or via domestic cycles, usually involving dogs and farm livestock. E. multilocularis is primarily maintained in a sylvatic life-cycle between foxes and rodents. As part of extensive investigations that we undertook to update available epidemiological data and to monitor the transmission patterns of both E. granulosus and E. mulilocularis in Ningxia Hui Autonomous Region (NHAR) in northwest China, we captured small mammals on the southern slopes of Yueliang Mountain, Xiji, an area co-endemic for human alveolar echinococcosis and cystic echinococcosis. Of 500 trapped small mammals (mainly ground squirrels; Spermophilus dauricus/alashanicus), macroscopic cyst-like lesions (size range 1–10 mm) were found on the liver surface of approximately 10% animals. One of the lesions was shown by DNA analysis to be caused by E. granulosus and by histology to contain viable protoscoleces. This is the first report of a natural infection of the ground squirrel with E. granulosus. We have no definitive proof of a cycle involving ground squirrels and dogs/foxes but it is evident that there is active E. granulosus transmission occurring in this area.
Citation: Yang YR, Liu T, Bai X, Boufana B, Craig PS, et al. (2009) Natural Infection of the Ground Squirrel (Spermophilus spp.) with Echinococcus granulosus in China. PLoS Negl Trop Dis 3(9): e518. doi:10.1371/journal.pntd.0000518
Editor: Hector H. Garcia, Universidad Peruana Cayetano Heredia, Peru
Received: June 24, 2009; Accepted: August 21, 2009; Published: September 22, 2009
Copyright: © 2009 Yang et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: Partial financial support came from Ningxia Provincial Science Technique Foundation (Kgx-19-07-01), The Ecology of Infectious Diseases Program NIH/NSF (EID #1565), the Japan Society for the Promotion of Science (17256002) (Japan), Foreign Experts Foundation (China), and the National Health and Medical Research Council (Australia). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
The canid adapted intestinal tapeworms, Echinococcus granulosus and E. multilocularis are important zoonotic pathogens that cause serious disease in humans ; both are endemic to Ningxia Hui Autonomous Region (NHAR) in northwest China ,. E. granulosus can be transmitted through either sylvatic cycles, involving wild carnivores and ungulates; or via domestic cycles, usually involving dogs and farm livestock. A common source of infection for dogs is hydatid infected offal from sheep, which often harbour the common G1 genotype (sheep-dog strain) responsible globally for most cases of human cystic echinococcosis (CE) ,. E. multilocularis is primarily maintained in a sylvatic life-cycle between foxes and rodents, with human infections considered as a relatively rare accidental event caused by spill-over from the wildlife cycle in European countries . Synanthropic transmission cycles are believed to be responsible for the high prevalence of human alveolar echinococcosis (AE) in Alaska and on the eastern Tibetan Plateau, whereby domestic dogs predating on rodents in and around villages are considered to be the primary source of infection causing human AE ,.
A report of E. granulosus in plateau pika (Ochotona curzoniae) in Qinghai Province  appears retrospectively almost certainly to be due to E. shiquicus, a new Echinococcus species described in 2005 that infects Tibetan foxes (Vulpes ferrilata) on the Tibetan Plateau . Work in the 1980s in NHAR indicated that the transmission modes for co-hyperendemic AE and CE involved domestic dogs/livestock (mainly sheep) for CE and foxes/rodents for AE .
Extensive investigations that we undertook in 2001–2007 to update available epidemiological data and to monitor the transmission patterns of both E. granulosus and E. mulilocularis in NHAR, indicated that owned dogs were a risk factor for human AE (involving a dog/rodent cycle) as well as CE (involving a dog/domestic livestock cycle) ,. An increase in susceptible rodent populations due to deforestation and over use of farmland for agriculture have been emphasised as important zoonotic risk factors for human AE in NHAR and in other Chinese settings ,. As part of these ongoing studies, we captured small mammals on the southern slopes of Yueliang Mountain, Xiji County (Figure 1) (E, 105°64′–105°89′; N, 36°03′–36°18; altitude ranging from 2000–2200 m) in July, 2007. This is an area known to be co-endemic for both human AE and CE , and where high seroprevalence for echinococcosis among village-children has been recorded . Of 500 trapped small mammals (mainly ground squirrels; Spermophilus dauricus/alashanicus referred to also as S. dauricus, Myospalax fontanieri and Mus musculus), macroscopic cyst-like lesions (size range 1–10 mm) were found on the liver surface of approximately 10% animals. Lesions were subjected to molecular genotyping and histopathological examination. None were attributable to E. multilocularis but one lesion was identified unambiguously as E. granulosus, subsequently shown by histology to contain viable protoscoleces. This is the first report of a natural infection of the ground squirrel with E. granulosus.
Materials and Methods
This study was reviewed and approved by the Ethics Committee of Ningxia Medical University. All small mammals were humanely euthanized soon after being trapped. Animals were identified, dissected and the obtained livers fixed in absolute ethanol for DNA analysis and histology.
Prior to histopathology, involving sectioning, haematoxylin/eosin staining and microscopic examination by standard procedures, liver lesions were transported to the Cestode Zoonoses Laboratory (University of Salford, U.K.) for molecular genotyping. Genomic DNA was extracted from these lesions using the DNeasy tissue kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions and used as a template for the amplification of a fragment within the mitochondrial 12S rRNA gene ,. Amplified cestode-specific DNA was gel purified using the PureLink™ quick gel extraction kit (Invitrogen, Paisely, U.K.) and commercially sequenced (Cogenics, Takeley, U.K.). The identity of one of these samples was confirmed in another laboratory (Department of Parasitology, Asahikawa Medical College, Asahikawa) by partial sequencing of the mitochondrial cox1 gene as described .
Comparison of the generated sequence data with those held on the NCBI database (www.ncbi.nlm.nih.gov) through the use of BLAST program revealed one sample had 100% homology (254 bp) with the mitochondrial 12S rRNA gene of E. granulosus genotype G1 (common sheep-dog strain) (accession nos. DQ408422, AF297617, AB031350, AB024515). Compared with previously published gene sequences (AF297617, E. granulosus G1 (common sheep-dog strain); AB 018440, E. multilocularis), cox1 sequence (789 bp) for the sample was nearly identical to that of the published E. granulosus G1 sequence with the exception that three transitional changes were present at positions 243 (G/A), 530 (C/T) and 594 (T/C) for the isolate. The sequence shared only 80% identity with the published E. multilocularis cox1 gene sequence.
Subsequent histological examination of this ground squirrel liver lesion revealed the presence of a thick laminated layer, thin germinal layer and presence of brood capsules containing viable E. granulosus protoscoleces (Figure 2).
Figure 2. Histopathologic section (haematoxylin and eosin stain) of the liver lesion from a ground squirrel (Spermophilus dauricus/alashanicus).
Left panel shows the typical appearance of a fertile Echinococcus granulosus cyst with laminated and germinal layers, brood capsules and numerous viable protoscoleces; right panel is an enlarged part of the section showing two viable protoscoleces (×1000).doi:10.1371/journal.pntd.0000518.g002
There are numerous previous reports of small mammal species infected with E. multilocularis in China and Europe ,. It is well accepted that microtine rodent species are the main reservoir hosts of E. multilocularis, though other rodent groups and even lagomorphs (hares and pikas) may also be naturally infected ,. However as far as we know, apart from experimental infection of rodents using either protoscolex or oncosphere injection ,, or oral administration of viable eggs , this is the first report of a rodent species naturally infected with the metacestode stage of E. granulosus. Other non rodent small mammals harbouring lesions of E. granulosus (identified morphologically) have been described in hares in Argentina  and rabbits in Australia ,. The current observation has shown, for the first time, the rodent, Spermophilus dauricus, is susceptible and can be infected naturally with E. granulosus that can become viable, producing fertile cysts.
Land cover in the southern mountainous areas of NHAR has undergone important changes since the second half of the 20th century. The area was largely deforested in the 1970s–80s, and in the rolling hills around the southern Liupan Shan, total tree clearance was completed in the mid 90s. Now, the landscape consists entirely of fields for production of wheat, potatoes, beans, alfalfa, etc. During the late 1970s valleys and lower slopes were generally used for agricultural crop production while the upper slopes and hill tops were reserved for grazing. At the time there were no livestock restrictions and grazing pressure was intense. In the late 90s, massive reforestation campaigns carried out to prevent soil erosion led to extensive re-planting of trees and restrictions in sheep numbers allowable per family. The landscape changes had a subsequent major effect on small mammal communities  and may have played a role modifying cestode transmission patterns involving small mammals. For instance the opening of the landscape during the deforestation process may have increased the area of habitats favourable to Spermophilus dauricus . On the other hand, the dog population has been recovering after the banning of indiscriminate rodenticide use in NHAR from 2002 . The high susceptibility of various host species present together with high parasite prevalence may have increased the infection of definitive and intermediate hosts for both E. granulosus and E. multilocularis. It is possible that free roaming dogs not only could get infected with E. granulosus after feeding on discarded sheep offal containing larval E. granulosus but also perhaps through predation on Spermophilus dauricus. This large rodent species is one of the commonest in the area and largely occurs in fields, fallows and in the early stages of re-forestation. The red fox (Vulpes vulpes) which mostly feeds on small mammals is also a potential candidate for E. granulosus transmission in this area of NHAR since this canid species has been shown to be susceptible by experimental infection , although it usually harbours smaller worm burdens than dogs, and it has been found naturally infected in Australia and Europe –.
Although we have no definitive proof of a cycle involving ground squirrels and dogs/foxes, it is clear there is active E. granulosus transmission occurring in this area, despite the recent past decline in the dog population in southern Ningxia ,. Possible misidentification of morphological specimens of Echinococcus obtained from small mammals may have occurred in the past . Therefore, in further epizootiological surveillance of echinococcosis, it would be useful to apply DNA typing of metacestodes from small mammals and copro-DNA techniques  for unambiguous identification of fox or dog infections in order to provide accurate baseline data on transmission and to inform a model , for future integrated control options.
We acknowledge all the staff from Ningxia Medical University, who participated in the project. We particularly thank Professors Tao Sun, Jing Teng and Zheng Zhi Li for their help and support throughout.
Conceived and designed the experiments: YRY TL PSC AI PG DPM. Performed the experiments: YRY TL XB BB MN AI JZZ. Analyzed the data: YRY TL XB BB PSC MN AI JZZ PG DPM. Contributed reagents/materials/analysis tools: MN JZZ. Wrote the paper: YRY BB PSC AI PG DPM.
- 1. Yang YR, Rosenzvit MC, Zhang LH, Zhang JZ, McManus DP (2005) Molecular study of Echinococcus in west-central China. Parasitology 131: 547–555.
- 2. Yang YR, Sun T, Li Z, Li X, Zhao R, et al. (2005) Echinococcosis, Ningxia, China. Emerg Infect Dis 11: 1314–1316.
- 3. Yang YR, Sun T, Li Z, Zhang J, Teng J, et al. (2006) Community surveys and risk factor analysis of human alveolar and cystic echinococcosis in Ningxia Hui Autonomous Region, China. Bull World Health Organ 84: 714–721.
- 4. Yang YR, Sun T, Zhang JZ, McManus DP (2006) Molecular confirmation of a case of multiorgan cystic echinococcosis. J Parasitol 92: 206–208.
- 5. Vuitton DA, Zhou H, Bresson-Hadni S, Wang Q, Piarroux M, et al. (2003) Epidemiology of alveolar echinococcosis with particular reference to China and Europe. Parasitology 127: (Suppl)S87–107.
- 6. Rausch RL, Wilson JF, Schantz PM (1990) A programme to reduce the risk of infection by Echinococcus multilocularis: the use of praziquantel to control the cestode in a village in the hyperendemic region of Alaska. Ann Trop Med Parasitol 84: 239–250.
- 7. 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.
- 8. Guo Z, He D, Li Y (1994) Infection of Echinococcus specises in wild animals in Qinghai province. Chinese J Parasitol Parasitic Dis 12: 135–137.
- 9. Xiao N, Qiu J, Nakao M, Li T, Yang W, et al. (2006) Echinococcus shiquicus, a new species from the Qinghai-Tibet plateau region of China: discovery and epidemiological implications. Parasitol Int 55: (Suppl)S233–236.
- 10. Li WX, Huang GC, Li Z, Li M, Zhang G, Wang J (1989) The Investigations on Echinococcus species in various host origins in Ningxia Hui Autonomous Region. In: Cai J, Li WX, editors. The Chinese National Hydatidology Workshop in Xinjiang. Urumqi, Xinjiang: Endemic Disease Bulletin. pp. 35–48.
- 11. Giraudoux P, Pleydell D, Raoul F, Quere JP, Wang Q, et al. (2006) Transmission ecology of Echinococcus multilocularis: what are the ranges of parasite stability among various host communities in China? Parasitol Int 55: (Suppl)S237–246.
- 12. Pleydell DR, Yang YR, Danson FM, Raoul F, Craig PS, et al. (2008) Landscape composition and spatial prediction of alveolar echinococcosis in southern Ningxia, China. PLoS Negl Trop Dis 2(9): e287. doi:10.1371/journal.pntd.0000287.
- 13. Yang YR, Craig PS, Vuitton DA, Williams GM, Sun T, et al. (2008) Serological prevalence of echinococcosis and risk factors for infection among children in rural communities of southern Ningxia, China. Trop Med Int Health 13: 1086–1094.
- 14. von Nickisch-Rosenegk M, Silva-Gonzalez R, Lucius R (1999) Modification of universal 12S rDNA primers for specific amplification of contaminated Taenia spp. (Cestoda) gDNA enabling phylogenetic studies. Parasitol Res 85: 819–825.
- 15. Dinkel A, Njoroge EM, Zimmermann A, Walz M, Zeyhle E, et al. (2004) A PCR system for detection of species and genotypes of the Echinococcus granulosus-complex, with reference to the epidemiological situation in eastern Africa. Int J Parasitol 34: 645–653.
- 16. Xiao N, Qiu J, Nakao M, Nakaya K, Yamasaki H, et al. (2003) Short report: Identification of Echinococcus species from a yak in the Qinghai-Tibet plateau region of China. Am J Trop Med Hyg 69: 445–446.
- 17. Guislain MH, Raoul F, Giraudoux P, Terrier ME, Froment G, et al. (2008) Ecological and biological factors involved in the transmission of Echinococcus multilocularis in the French Ardennes. J Helminthol 82: 143–151.
- 18. Rausch RL (1995) Life-cycle patterns and geographic distribution of Echinococcus species. In: Thompson RCA, Lymbery AJ, editors. Echinococcus and hydatid disease. Wallingford: Cab International. pp. 89–119.
- 19. Dempster RP, Berridge MV, Harrison GB, Heath DD (1991) Echinococcus granulosus: development of an intermediate host mouse model for use in vaccination studies. Int J Parasitol 21: 549–554.
- 20. Zhang W, You H, Zhang Z, Turson G, Hasyet A, McManus DP (2001) Further studies on an intermediate host murine model showing that a primary Echinococcus granulosus infection is protective against subsequent oncospheral challenge. Parasitol Int 50: 279–283.
- 21. Heath DD (1971) The migration of oncospheres of Taenia pisiformis, T. serialis and Echinococcus granulosus within the intermediate host. Int J Parasitol 1: 145–152.
- 22. Schantz PM, Lord RD (1972) Echinococcus in the South American red fox (Dusicyon culpaeus) and the European hare (Lepus europaeus) in the Province of Neuquen, Argentina. Ann Trop Med Parasitol 66: 479–485.
- 23. Jenkins DJ, Macpherson CN (2003) Transmission ecology of Echinococcus in wild-life in Australia and Africa. Parasitology 127: (Suppl)S63–72.
- 24. Jenkins DJ, Thomson RC (1995) Hydatid cyst development in an experimentally infected wild rabbit. Vet Rec 137: 148–149.
- 25. Raoul F, Pleydell D, Quere J, Vaniscotte A, Rieffel R, et al. (2008) Small-mammal assemblage response to deforestation and afforestation in central China. Mammalia 72: 320–332.
- 26. Gemmell MA (1959) The fox as a definitive host of Echinococcus and its role in the spread of hydatid disease. Bull World Health Organ 20: 87–99.
- 27. Matoff K, Yanchev Y (1965) The fox as definitive host of Echinococcus granulosus. Acta Vet Acad Sci Hung 15: 155–160.
- 28. Thompson RC (1983) The susceptibility of the European red fox (Vulpes vulpes) to infection with Echinococcus granulosus of Australian sheep origin. Ann Trop Med Parasitol 77: 75–82.
- 29. Thompson RC, Nicholas WL, Howell MJ, Kumaratilake LM (1985) Echinococcus granulosus in a fox. Aust Vet J 62: 200–201.
- 30. Jenkins DJ, Morris B (2003) Echinococcus granulosus in wildlife in and around the Kosciuszko National Park, south-eastern Australia. Aust Vet J 81: 81–85.
- 31. Smith GC, Gangadharan B, Taylor Z, Laurenson MK, Bradshaw H, et al. (2003) Prevalence of zoonotic important parasites in the red fox (Vulpes vulpes) in Great Britain. Vet Parasitol 118: 133–142.
- 32. Abbasi I, Branzburg A, Campos-Ponce M, Abdel Hafez SK, Raoul F, et al. (2003) Copro-diagnosis of Echinococcus granulosus infection in dogs by amplification of a newly identified repeated DNA sequence. Am J Trop Med Hyg 69: 324–330.
- 33. Ishikawa H (2006) Mathematical modeling of Echinococcus multilocularis transmission. Parasitol Int 55: (Suppl)S259–261.
- 34. Torgerson PR (2006) Mathematical models for the control of cystic echinococcosis. Parasitol Int 55: (Suppl)S253–258.