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Grasscutter: The Haematology and Major Parasites

M.N. Opara
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Grasscutter contributes to both the local and export earnings of most countries in Sub-Saharan Africa. At the local market level, for example, approximately 73 tons of grasscutter meat representing more than 15, 000 animals can be sold in a year. According to recent survey, the grasscutter continues to dominate the bush meat trade. However, international trade as well as regional and continental interests in the grasscutter meat provides economic bases for the development of the grasscutter industry. The industry will be greatly enhanced through the establishment of breeding centres to provide stocks for farmers and other growers who will multiply its’ production and also provide additional source of income, desperately required in the quest to help the rural poor to meet their basic necessities and sustain their food security. Detailed information on the health and diseases of these rodents are reported here. Some of the disease agents include species of gastrointestinal helminthes (nematodes, trematodes, cestodes and acanthocephala) and haemoparasites (Trypanosoma, Babesia and Plasmodium species).

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M.N. Opara , 2010. Grasscutter: The Haematology and Major Parasites. Research Journal of Parasitology, 5: 214-223.

DOI: 10.17311/jp.2010.214.223

Received: March 19, 2010; Accepted: May 07, 2010; Published: August 07, 2010


The need for adequate cheap sources of animal protein has brought attention to the rearing of wild animals. One of the successfully reared wild animals today is the grasscutter (Akinloye, 2005).

Proper grasscutter feeding has been the major factor that determines the health of the animal apart from the environmental component in which the animal exists (Asibey, 1974).

The grasscutter meat is a favourite one and it accounts for the greater proportion of bush meat sold in most of the continent of Africa, particularly West Africa (NRC, 1991).

Studies in Ghana carried out by Ewer (1969) demonstrated that the animals could be kept in captivity (Baptist and Mensah, 1986; Ntiamo-Baidu, 1998). Their study confirmed the feasibility of rearing the grasscutter in captivity and demonstrated increased litter size as a function of good feeding.

There are several justifications for rearing the wild grasscutter when taken into captivity. Such justifications include; the grasscutter does not require an extensive area to function; it can be easily fed any other agricultural by products available in Nigeria; there is no religious taboo on the consumption of the meat; it does not require imported raw material inputs to succeed; it has a high litter size of eight per twelve months and low mortality rate of about 10% among offspring and its excretory wastes do not have offensive odour.

The domestication of grasscutter has not yet been perfectly established (Addo, 1997). Captive reared grasscutters are fed with forages and concentrates depending on the availability of the feed source, but the concentrates must be in low quantity to avoid a negative influence on the animal (Akinloye, 2005; Opara and Fagbemi, 2009).

Low production of animals is brought about by many factors in the tropics one of which is disease (Van Veen et al., 1974; Ikeme, 1977; Opara and Fagbemi, 2010a).

According to studies by Opara et al. (2006), it was reported that there was no significant difference between the haematological indices of these captive-reared grasscutters and those of the wild ones.

A previous report has also shown that the wild grasscutters harbour Trypanosoma sp., Babesia sp. and Plasmodium sp., in their blood without obvious clinical symptoms (Opara and Fagbemi, 2010b, c).

The severity of these diseases depends on the nutritional state of the animals, especially during the dry season when feed is inadequate in quality and quantity (Opara and Fagbemi, 2009).


Grasscutter is a wild herbivorous rodent found in the sub-Saharan region of Africa. It is the biggest after porcupine in the rodent class. It is referred to as Cane rat or cutting grass by many. Scientifically, it is referred to as Thryonomys swinderianus. Its sub-order is that of Hystricomorpha (porcupine relatives) and the super family is Petromuroidea (Rock rat- like), with genus Thryonomys (Wood, 1974).

Kingdom : Animalia
Phylum : Chordata
Sub-phylum : Vertebrata
Class : Mammalia
Order : Rodentia
Sub-order : Hystricomorpha
Family : Thryonomyidae
Genus : Thryonomys
Species : Thryonomys swinderianus

The Species Are of Two Types
Thryonomys swinderianus Temminck which is the giant breed and Thryonomys gregorianus (Rosevear, 1969; Simpson, 1974).


The body length of Thryonomys swinderianus varies from 25-70 cm, with an average of 48 cm and their tail reaches 0.65-26 cm in length (Fitzinger, 1995). The total body weight of adult ranges between 4-12 kg. The heaviest bodies have an average weight in males of 4.5 and 3.5 kg in females (Merwe, 2000), which looks like a giant guinea pig with a short tail. The body is heavily built, small round with bristle fur and coat and a circular ear (Akinloye, 2005). The fur reflects the general colour of the animal, with brownish colour from the base to the middle of the fur, while the upper fur appears light yellow to reddish. The combination of these colours gives the animal brownish yellow/red colour. Besides these, common colours that range from grayish black to brown exist.

Image for - Grasscutter: The Haematology and Major Parasites
Fig. 1: The Grasscutter (Thryonomys swinderianus), matured adult measures 40-60 cm long; weighs 2-6 kg; mixture of reddish brown and grey fur; monogastric herbivore; quick runner; skilled swimmer; poor vision; good sense of smell; lives up to 4 years in captivity; Induced ovulator; Gestation period 150-156 days; litter size up to 6. (Opara et al., 2006)

Genetic improvement on breeding has produced other colours such as black, yellow red and white coloured animals. But the skin is always white after processing. They have rounded nose, short ears and incisors that grow continuously (Mills, 1997). The pelage is coarse, with flattened bristle- like hairs that grow in groups of five or six. The fore feet are smaller than the hind feet and have three well developed middle digits with the first and fifth digits greatly reduced. The hind feet have no first digit and all digits have heavy claws (Fitzinger, 1995). The dental formula for Thryonomys swinderianus is 1/1, 0/0. 1/1, 3/3 (Merwe, 2000). They are endothermic and bilaterally symmetrical. The arrangement of the grasscutters digits and pads on the fore feet allows a stem to be gripped in one paw only, while being fed into the mouth unlike other rodents that use both paws to hold a single stem (Fitzinger, 1995).

Despite their size and short limbs, grasscutter runs quickly when disturbed and they are reputed to be good swimmers. Their nipples are arranged in lateral position and this makes the young ones to suckle their mother from the side (Asibey, 1974). The head is broad with short flattened muzzle and with small eyes and ears. Its tail is covered with small hairs. The mammary formula is 3+3 = 6 (Asibey, 1974). The grasscutter is shown in Fig. 1.


Thryonomys swinderianus is a semi nocturnal animal and they live in colonies comprising of one male and several females in each colony and the young ones from more than one generation. Even though it possesses digits equipped with power and sharp claws, it does not crawl on vertically erect wall or object unlike African giant rat. It burrows into the ground, but can temporarily shelter in hollow made by other animals. It is sensitive to noise and almost very frightened when it senses danger (Fitzinger, 1995).

The animal always shelters itself with dry grass to provide warmth since the animals is allergic to cold weather (Abioye et al., 2008). Grasscutter cannot jump any obstacle above 3 ft. Many of the animal’s weaknesses make it prone to easy capture when spotted by hunters, capture team or predators. Nevertheless, grasscutter has the ability of freezing up while hiding under grasses without being detected when it is being hunted (Ntiamoa-Baidu, 1998). That is why hunters usually adopt the heavy use of fiend dogs to flush it out during hunting. The animal tends to always protect its home range (feeding, nesting and mating territory) against another animal of their kind. That is why grasscutter’s house and enclosure are divided into many partitions suitable for easy grouping of the animals to avoid cannibalism and fighting among animals, more especially during mating. They are also caecophagic (Asibey, 1974; Fitzinger, 1995; Abioye et al., 2008).


Thryonomys swinderianus live in groups of males and females during the breeding season. During the dry season, the males separate from the groups and live by themselves. The females live together afterwards (Fitzinger, 1995; Jori et al., 2001). The wet season of the year is usually the breeding season (Oduor-Okelo and Gombe, 1982). The females are spontaneous ovulators (Addo et al., 2001) and usually two litters are possible in a year, but the females must be flushed before refertilization for high prolificacy. Sexual maturity is attained at 6 months for males and 5 months for females. There may be slight variation due to feeding. The gestation period is 5 months (152+2 or -2 days). The average litter size is 4 in the wild but up to twelve litters size has been recorded in captivity (Addo, 2002; Abioye et al., 2008). Growth continues at old age but very slowly. The estrus cycle lasts for a period of 6.62 days and the offspring weighing about 1.29 g and relatively well developed. The offsprings are precocious, fully furred and capable of running and have their eyes open at birth. Sexual determination in the grasscutter is done at birth on the basis of the pro-genital distance, which is larger in males than in females as well as a dark brownish stain around the genital part of the mature buck (Addo et al., 2001). Flushing of doe is necessary also to allow for proper breast feeding of the kids and this can last for about three to six weeks. The doe possesses three pairs of mammary glands by the side of the belly. Apart from the anogenital colour and distance, the animal size can be a criterion for sex differentiation, where the males are larger in size than the females. Shape of the animal’s nose is also a criterion. The male has blunt and muscular nose shape, while the female has a pointed nose shape. However, the shape of the animal’s nose becomes more conspicuous when the animal is in motion or while the animal adopts a standing position. Another criterion is the peculiar sound produced by the males and females, especially during courtship (Asibey, 1974).


The average lifespan of a captive-reared grasscutter ranges from 7-9 years. They can live up to 12 years depending on health care given to the animals during their service lives. The total life span is measured from the period of parturition to death while the service life is the period when the animal reaches maturity to the time when it can no longer reproduce. That is the period of efficient reproductive performance of the animals.


Studies have shown that certain factors influence haematological and biochemical parameters (Weldy et al., 1964). Haematological and biochemical analyses of an animal’s blood represent a good diagnostic aid for the assessment of physiological, nutritional and pathological conditions of animals (Jain, 1986; Bush, 1991;Awah-Ndukum et al., 2001). Nutrition age, sex, genetics (breed and crossbreeding), reproduction, housing, starvation, environment factors, stress, transportation and diseases are known to affect haematological and biochemical values (Coles, 1986) and thought to play major roles in the differences in haematological and biochemical parameters observed between tropical and temperate animals (Ogunriade et al., 1981; Bush, 1991; Ogunsanmi et al., 1994; Opara and Fagbemi, 2009). Ogunsanmi et al. (2002), determined the haematological, plasma biochemical and whole blood electrolytes profile in the normal live-captive and rehabilitated adult African grasscutters. They reported no statistical evidence of sexual dimorphism in the values of these parameters of the cane rats, except plasma alanine transaminase (ALT), which was significantly higher (p<0.001) in the males than in the females. In their studies, Owolabi (2002) and Opara et al. (2006), reported a significantly (p<0.05) higher lymphocyte, eosinophil and basophil values for both the female and male wild grasscutters, compared with those of captive- reared. They equally reported a significantly higher white blood cell counts in female than male wilds grasscutters and attributed these differences to the free nature of the wild rodents which are more prone to all kinds of infections (Gotoh et al., 2001; Dinh, 2002). The significantly high levels of basophils and eosinophils among the wild grasscutters (Opara et al., 2006) were due to the presence of inhabiting parasites in the animals.


The grasscutter unlike many other livestock species such as rabbits, sheep and goats requiring an appreciable drug input, is very hardy and requires little or no drug input (Adu, 2002; Opara and Fagbemi, 2008a).

Incidence, severity and disease prevalence have been shown to vary with the management systems (Smith and van Hautert, 1984; Adu, 2002). Again, Adu (2002) reported that the major disease conditions include pulmonary congestion, septic wounds, ruptured uterus, orchitis with septicaemia, gastro-intestinal obstruction, gastroenteritis and pneumonia. The gastrointestinal obstruction and gastro enteritis may be caused by helminthes parasites (Jori et al., 2001; Awah-Ndukum et al., 2001).


The study of helminth parasites of domestic animals began as early as 1884 in America where on Act was enacted to prevent the exportation of diseased cattle and to provide means for the suppression and extirpation of diseases among domestic animals (Blood and Radostits, 1994). The idea came up as a result of hardship and large economic losses brought about by these parasitic helminthes, hence the need for control and eradication of these parasites. As a result of this, many researches on gastrointestinal helminthes parasites have been reported.

Blood and Radostits (1994), observed that the incidence of helminthes diseases varies between areas depending on the climate, nutritional status of the animal, pasture management a s well as the animals’ immunity to worm infestation. As a result, Van Veen et al. (1974) reported that environmental factors such as topography, climate and husbandry practice have led to a situation where a number of helminthes parasites common to many parts of the world are rare or do not occur at all in Nigeria and that some helminth parasites common in Nigeria have not been reported elsewhere.

The incidence, severity and disease prevalence have been shown to vary with management systems. Smith and van Hautert (1984) reported that, while infections accounted for over half of the disease conditions observed in a group of intensively managed ruminants, they were of negligible prevalence in a controlled group raised semi-intensively. In the later group, parasitic gastroenteritis was the most prevalent disease condition.

A study conducted by Adu et al. (1999) in Ghana reported the infestation of grasscutters by Ascaris sp., Schistosoma haematobium and Trichuris sp., including ticks of Dermacentor sp. and Rhipicephalus sp. But the Ascaris sp., encountered in the grasscutter is non-pathogenic to the domestic stock until proved otherwise since each animal species has its specific ascarid (Blood and Radostits, 1994). The observation of Schistosoma haematobium eggs in the grasscutter is very important in the spread of infection to both livestock and man and the infection can only occur when part of its life cycle passes through an intermediate fresh water mollusc host. The identification of the eggs of Trichuris trichuria is important, in that various species attack various domestic stock and possibility of infection of domestic stock would be by sharing the same pasture and by domestic stock hanging around where the wild-stock are slaughtered and faeces disposed of in the nearby bushes.

Jori et al. (2001) revealed the presence of Paralibyostrongylus hebreniticus, Trichuris sp. and Taenia sp., in the gastrointestinal tracts of the grasscutters. Matamorous et al. (1991) in Costa Rica also reported the incidence of Trichuris sp., Taenia sp., Strongyloides sp. and Ascaridia sp., as the helminthes parasites of the grasscutters.

A preliminary study conducted by Yeboah and Simpson (2004) in Ghana, reported some ecto and end-parasites of the grasscutters Four species of ticks found included Rhipicephalus simpsoni, Ixodes aulacodi Ixodes sp. and Haemaphysalis parmata. The six helminthes parasites they reported comprised of two genera of cestode and four of nematodes. The cestodes were Furhmanella transvaalensis, Railletina mahonae; while the nematodes were Longistriata spira Trachypharynx natalensis, Paralibyostrongylus vondewei and Trichuris paravispicularis.

A study carried out in Cameroon by Mpoame (1994) and Awah-Ndukum et al. (2001) had also reported the presence of a flea (Xenopsylla sp.) cestode (Hymenolopsis sp.) and Nematode (Heterakis sp.) from a dead grasscutter in captivity. Opara and Fagbemi (2008a, b) in Nigeria reported a wider array of helminthes in the wild grasscutters, which comprised of 14 nematode species (Ascaris, Bunostomum, Cooperia, Gaigaria, Gongylonema, Haemonchus, Heterakis, Mammomonogamus, Metastrongylus, Oesophagostomum, Strongyloides, Toxocara, Trichstrongylus and Trichuris sp.), 5 trematodes, (Cotylophoron, Dicrocoelium, Gastrodiscus, Paramphistomum and Schistosoma sp.), 4 cestodes (Avitellina, Moniezia, Taenia and Thysaniezia sp.) and 1 acanthocephala (Moniliformis sp.). Another study by these same authors (Opara and Fagbemi, 2010a) showed that grasscutters harbor helminth parasites while in captivity. The helminthes of interest observed in the captive-reared grasscutters included 7 nematodes (Ascaridia, Haemonchus, Mammomonogamus, Oesophagostomum, Strongyloides, Trichostrongylus and Trichuris sp.), two trematodes (Fasciola and Schistosoma sp.) and two cestodes (Taenia and Thysaniezia sp.).


There have been reports of few cases of naturally occurring blood parasites of the cane rats (Namso and Okaka, 1998), since they co-habit with other animal species. For example Ntekim and Braide (1981) reported the occurrence of Trypanosoma lewisi in the blood of wild rats, while Opara and Fagbemi (2008b) reported the natural occurrence of Trypanosoma congolense, T. vivax, T. simiae, Plasmodium and Babesia sp., among wild grasscutters and Trypanosoma congolense, T. vivax, Plasmodium and Babesia sp., in the captive-reared grasscutters.


Opara and Fagbemi (2010a) reported that the Mean Corpuscular Volume (MCV) of trypanosome infected grasscutters does not change more than for uninfected ones, while the Mean Corpuscular Haemoglobin Concentration (MCHC) significantly decreases (p>0.05) suggesting a macrocytic hypochromic anaemia). They also observed that grasscutters experimentally infected with Trypanosoma congolense and T. vivax suffered leucopenia at 7 dpi, while the uninfected ones did not. Thus, indicating that trypanosomiasis in grasscutters also leads to leucopenia (Seifert, 1996), which further reduces the animals’ immunity and thereby exposing them to other infections.

Trypanosome infected grasscutters equally experience a significant decrease in plasma glucose, which also agrees with Soulsby (1982), who reported that blood form of trypanosomes absorb nutrients such as glucose by mediated mechanism of membrane transport.

He also reported that blood protozoa increase the long chain fatty acids of plasma membrane of red blood cells, but this is not the case in the grasscutters, as this could probably be because the grasscutter has very low body fat content (Adu et al., 1999). In their work, Opara and Fagbemi (2010a) reported that grasscutters experimentally infected with T. vivax had significantly (p< 0.05) higher plasma Aspartate Amino Transferase (AST). Serum AST is however not a specific enzyme for the liver, as high levels can also be found in skeletal and cardiac muscles as well as red blood cells (Bush, 1991). Thus, increase in AST may indicate an on-going liver disease (Duncan et al., 1994) as observed at histopathology.

Temperature of grasscutters infected with T. vivax and T. congolense, showed dramatic fluctuation. Soulsby (1982) had reported that undulating temperature is a clinical feature in animals infected with trypanosomes.

Pathological lesions observed in some of the tissues of trypanosome infected grasscutters include liver and kidney vacuolar and tubular epithelial degeneration, respectively, with thrombosis in alveolar blood vessels. These are in agreement with Soulsby (1982) and Shah-Fischer and Say (1989), who also reported organ degenerative changes in animal trypanosomiasis.


The distribution of grasscutters in Africa, south of Sahara, the management system required, nutrition and reproductive performance have all been well studied. Also detailed information on health and diseases of these rodents are reported here. Furthermore, the grasscutter is known to be economically important as an agricultural pest and its’ meat is widely accepted by all classes of people. It is also a good laboratory animal for research studies.


1:  Abioye, F.O., A.C. Uda, M.N. Opara, P.C. Aju and M.C. Onyema, 2008. Adaptability of grasscutter (Thryonomys swinderianus) in natural and domestic environments. Proceedings of the Conference of Forestry Association of Nigeria, Aug. 15-20, Uyo, Akwa Ibom State, pp: 537-550

2:  Addo, P.G., 1997. Domesticating the wild grasscutter (Thryonomys swinderianus Temminck, 1827) under laboratory conditions. Ph.D. Thesis, University of Ghana, Legon, Ghana.

3:  Addo, P.A., S. Adjei, B. Awumbila and E. Awotwi, 2001. Determination of the ovulation mechanism of he grasscutter (Thryonomys swinderianus). J. Anim. Reprod. Sci., 22: 11-13.
PubMed  |  

4:  Addo, P., 2002. Detection of mating, pregnancy and imminent Parturition in the grasscutter (Thryonomys swinderianus) Livest. Res. Rural Dev., 14: 8-13.
Direct Link  |  

5:  Adu, E.K., 2002. Dexieme conference on promoting the dissemination of the breeding of the cane rats in Africa, Su Du Sahara. Experiences of a Research Institute on Grasscutter Farming in Ghana.

6:  Adu, E.K, W.S. Alhassan and F.S. Nelson, 1999. Smallholder farming of the greater cane rat Thryonomys swinderianus Temminck, in Southern Ghana: A baseline survey of Management practices. Trop. Anim. Health Prod., 31: 223-232.
CrossRef  |  

7:  Akinloye, A.P., 2005. Update on Grasscutter Rearing-Thryonomys Swinderianus (Temminck). Height Mark Printers, Ibadan, Nigeria, pp: 21-23

8:  Asibey, E.O.A., 1974. Wildlife as a source of protein in Africa South of the Sahara. Biol. Conservation, 6: 32-39.
CrossRef  |  

9:  Mills, G.L.H., 1997. The Complete Book of South African Mammals. Struik Publishers, Cape Town, Winchester, ISBN-13: 9780947430559, pp: 6-18

10:  Awah-Ndukum, J., J. Tchoumboue and J.C. Tong, 2001. Stomach impaction in grasscutter (Thryonomys swinderianus) in captivity: Case report. Trop. Vet., 19: 60-62.

11:  Baptist, R. and G.A. Mensah, 1986. Benin and West Africa: The cane rat farm animal of the future. World Anim. Rev., 60: 2-6.

12:  Blood, D.C. and O.M. Radostits, 1994. Veterinary Medicine. 8th Edn., Bailliare Tindall Ltd., London

13:  Bush, B.M., 1991. Interpretation of Laboratory Results for Small Animal Clinicians. Backwell Scientific Publications, London, ISBN: 9780408108492, Pages: 515

14:  Coles, E.H., 1986. Veterinary Clinical Pathology. 4th Edn., W.B. Saunders Co., Philadelphia, London, ISBN: 978-0721618289, Pages: 486

15:  Dinh, V.O., 2002. Hematological values of macques (Macaca fascicualaris) in a mangrove forest, Vietnam. J. Zool., 10: 15-15.

16:  Duncan, J.R., K.W. Prasse and E.A. Mahaffey, 1994. Veterinary Laboratory Medicine: Clinical Pathology. 3rd Edn., Iowa State University Press, Ames, Iowa, USA.

17:  Ewer, R.F., 1969. Form and function in the grasscutter Thryonomys swinderianus Temminck (Rodentia, Thryonomyidae). Ghana J. Sci., 9: 131-149.

18:  Fitzinger, F., 1995. Cane Rats. In: Walker's Mammals of the World, Nowak, R. (Ed.). The John Hopkins University Press, Maryland, pp: 1650-1651

19:  Gotoh, S., O. Takennako, K. Watanabe, Y. Hamada and R. Kawamoto et al., 2001. Hematological values and Parasitic fauna in free ranging Macaca hecki and the Macaca tonkeana/Macaca hecki hybrid group of Salawesi Island. Indonesia Primates, 42: 27-34.
CrossRef  |  

20:  Ikeme, M.M., 1977. Helminthes of livestock and poultry: An overview. Trop. Vet., 15: 97-102.

21:  Jain, N.C., 1986. Schalm Veterinary Haematology. 4th Edn., Lea and Febiger, Philadelphia, USA

22:  Jori, F., J.E. Cooper and J. Casal, 2001. On post mortem findings in captive cane rats (Thryonomys swinderianus) in Gabon. Vet. Record, 148: 624-628.
PubMed  |  

23:  Merwe, M., 2000. Tooth successions in the greater cane rat (Thryonomys swinderianus) (Temminck, 1827). J. Zool., 251: 535-547.
Direct Link  |  

24:  Matamorous, Y., J. Velazquez and B. Pashov, 1991. Intestinal parasites of Agouti paca (Rodentia, Dasyproctidae) in costa-rica. Revista de Biologia Tropical, 39: 173-176.

25:  Mpoame, M., 1994. Gastro intestinal helminthes of the cane rat Thryonomys swinderianus, in Cameroon. Trop. Anim. Health Prod., 26: 239-240.

26:  NRC., 1991. Quail: Micolivestock-Little Known Small Animals with a Promising Economic Future. National Academy Press, Washington, DC., pp: 147-155

27:  Ntiamo-Baidu, Y., 1998. Sustainable use of bush meat. Wildlife Development Plan (1998-2003) Wildlife Department Accra, 6: 78-78.

28:  Ntekim, A. and E.I. Braide, 1981. A study of the parasites of wild Rats from the University of Calabar Poultry. Niger. J. Parasitol., 4: 20-21.

29:  Ogunriade, A., J. Fajimi and A. Adenike, 1981. Biochemical Indices in the White Fulani (Zebu) Cattle in Nigeria. Rev. Elev. Med. Pays. Trop., 34: 413-415.
PubMed  |  

30:  Ogunsanmi, A.O., S.O. Akpavie and V.O. Anosa, 1994. Serum biochemical changes in West African Dwarf sheep experimentally infected with Trypanosoma brucei. Rev. Elev. Med. Vet. Pays. Trop., 47: 195-200.
PubMed  |  

31:  Ogunsanmi, A.O., P.C. Ozegbe, D. Ogunjobi, V.O. Taiwo and J.O. Adu, 2002. Haematology, plasma biochemistry and whole blood minerals of the captive adult African grasscutter (Thryonomys Swinderianus, Temminck). Trop. Vet., 20: 27-35.

32:  Opara, M.N., K.A. Ike and I.C. Okoli, 2006. Haematology and plasma biochemistry of wild adult African crasscutter (Thryonomis swinderianus, Temminck). J. Am. Sci., 2: 17-22.
Direct Link  |  

33:  Opara, M.N. and B.O. Fagbemi, 2008. Observations on the Gastrointestinal Helminth parasites of the wild Grasscutter (Thryonomys swinderianus, Temminck) in Imo State, Nigeria. Int. J. Trop. Agric. Food Syst., 2: 105-110.

34:  Opara, M.N. and B.O. Fagbemi, 2008. Occurrence and prevalence of gastrointestinal helminthes in the captive-reared grasscutter (Thryonomys swinderianus, Temminck), from Southeast Nigeria. Life Sci. J., 5: 50-56.

35:  Opara, M.N. and B.O. Fagbemi, 2008. Haematological and plasma biochemistry of the adult wild african grasscutter (Thryonomys swinderianus): A zoonosis factor in the tropical humid rain Forest of Southeast Nigeria. Ann. N. Y. Acad. Sci., 1149: 394-397.
CrossRef  |  

36:  Opara, M.N. and B.O. Fagbemi, 2009. Dietary influences of feed types on the haematological indices of captive-reared grasscutters experimentally infected with Trypanosoma congolense. Proceeding of the 10th Biennial Conference of the Society for Tropical Veterinary Medicine, June 28-July 3, Lubeck, Germany, pp: 63-67

37:  Opara, M.N. and B.O. Fagbemi, 2010. Therapeutic effect of Berenil R in experimental murine trypanosomiasis using stocks isolated from apparently healthy captive - reared grasscutters (Thryonomys swinderianus). Nature Sci., 8: 106-110.

38:  Opara, M.N. and B.O. Fagbemi, 2010. Prevalence of gastrointestinal helminthes of grasscutters intensively reared in Imo State, Nigeria. Anim. Prod. Res. Adv.,

39:  Opara, M.N. and B.O. Fagbemi, 2010. Patho-physiological effects of experimental Trypanosoma congolense and Trypanosoma vivax infections in the grasscutter (Thryonomys swinderianus, Temminck). Nature Sci., 8: 88-101.

40:  Owolabi, O.O., 2002. Wildlife contributions to meat protein consumption of the rural communities in South Western Nigeria. Proceeding of the 27th Annual Conference of Nigeria, March, 17-21, Society Animal Production, Federal University of Technology Akure, pp: 406-409

41:  Rosevear, D.R., 1969. The Rodents of West Africa. British Museum Publications., London

42:  Van Veen, T.W.S., R.A.O. Shonekan and J.P. Fabiyi, 1974. A host-parasite checklist of helminth parasites of domestic animals in Northern Nigeria. Bull. Anim. Health Prod. Afr., 23: 269-288.

43:  Seifert, H.S.H., 1996. Tropical Animal Health. Kluwer Academic Publishers, Boston, London, UK., pp: 44

44:  Shah-Fischer, M. and R.R. Say, 1989. Manual of Tropical Veterinary Parasitology. CAB, Wallingford

45:  Simpson, G.G., 1974. Chairman's Introduction: Taxonomy Symposium. Academic Press, London

46:  Smith, D.B. and M.J.F. van Hautert, 1984. Health aspects of intensive management of West African dwarf goats in the humid forest zone. Proceeding of the National Conference on Diseases of Ruminants, Oct. 3-6, Nigeria, pp: 8-13

47:  Soulsby, E.J.L., 1982. Helminths, Arthropods and Protozoa of Domesticated Animals. 7th Edn., Bailliere Tindall, London, UK., ISBN-13: 9780702008207, Pages: 809

48:  Wood, A.E., 1974. The Evolution of the Old World and New World Hystricomorphs. Plenum Press, New York, pp: 21-60

49:  Oduor-Okelo, D. and S. Gombe, 1982. Placentation in the canerat, (Thryonomys swinderianus). Afr. J. Ecol., 20: 49-66.
CrossRef  |  

50:  Weldy, J.R., R.E. Medowell, P.J. Vansoest and J. Bond, 1964. Influence of Heat stress on Nimen Acid Levels and some Blood constituents in cattle. J. Anim. Sci., 23: 147-153.

51:  Yeboah, S. and P.K. Simpson, 2004. A preliminary survey of ecto and endoparasites of the grasscutter (Thryonomys swinderianus Temminck); case study in Ekumfi central region of Ghana. J. Ghana Sci. Assoc., 3: 2-5.

52:  Namso, M.E. and C.E. Okaka, 1998. A survey of naturally occurring parasites of cane rats. Niger. J. Parasitol., 28: 28-29.

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