Trichostrongylus calcaratus

 

 

Esther van Praag, Ph.D.

 

 

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Trichostrongylus parasitic worms are frequently observed infesting wild rabbits and cottontails, particularly the eastern cottontail (Sylvilagus floridanus) in the USA. These parasites are uncommon in pet rabbits. Trichostrongylus calcaratus is found in the small intestine and the colon of the rabbit. The extra-intestinal migration remains to be fully elucidated. The rabbits become infested by consuming food (hay, straw, fresh vegetables) that has been contaminated by the larvae. This parasite does not represent a public health danger.

The eggs produced by the female will pass in the feces and hatch outside the host. These measurements are typically between 80 and 90 micrometers in length. The eggs are already segmented at the time of laying and develop into infective larvae within six days. The L1 and L2 stages of the larvae are microbivores. The L3 stage, which is reached after 16-18 days, is non-feeding and infective by ingestion. The L3, L4, and L5 stages are immature adults that develop into mature forms within the digestive tract of the host. The life cycle is direct, with no intermediate hosts.

The worms are slender, with small anterior ends and no buccal cavity. Male worms are distinguished by their asymmetrical dorsal ray and two short, nearly equal spicules. The female has a vulva measuring approximately 1 millimeter near the tip of the tail. It is possible to observe the presence of spherical-shaped eggs in her body.

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Z/Trichostrongylosis/body_Trichostrongylosis_il1.htm

Trichostrongylus sp. femelle worm and egg

Several Trichostrongylus species have been observed in rabbits. The differentiation of these species is based on their size and the structure of the spicules.

Trichostrongylus affinis

This strongyle parasitic worm is found throughout the USA and has been identified in cottontails (Sylvilagus floridanus) and snowshoe hares (Lepus americanus). It is a rare occurrence in pet rabbits. This parasite infects the cecum and the large intestine.

The eggs, with an average measurement of 61 x 37 micrometers, will be excreted alongside the fecal matter. The larvae hatch and develop outside the host, becoming infective after approximately 10 days. The adult worms have an average size of 5-7.5 millimeters for males and 8.7-9.3 millimeters for females. Males are equipped with spicules, while the posterior end of the female is characterized by a vulva.

Severe infestation can lead to a loss of body weight.

Trichostrongylus retortaeformis

This parasite is endemic to Europe and the UK, and it was introduced to Australia. It is found in the small intestine of rabbits and hares (Lepus europaeus). Its life cycle is likely comparable to that of Trichostrongylus affinis. The presence of Trichostrongylus retortaeformis in a population of rabbits can affect and reduce its size.

The eggs measure approximately 87 by 33 micrometers. They are found in the portion of the herbage that experiences the least climatic changes. Their development is stopped at temperatures under 10°C. The larvae can migrate within the vegetation to moist conditions. The adult worms measure between 6.8 and 8.4 millimeters long for the males and 9.6 and 10.4 millimeters long for the females. They are characterized by the presence of thin transverse and longitudinal grooves.

The clinical test includes fecal flotation at 25°C. Higher temperatures will result in the killing of the parasite.

Trichostrongylus ransomi

Trichostrongylus ransomi has been reported in cottontails (Sylvilagus floridanus) in Louisiana, USA. This parasite is not prevalent in rabbits. It is known to infest the small intestine. The life cycle of this worm is not yet fully understood, but it is believed to be like that of T. affinis.

The eggs of this parasite measure approximately 65 by 33 micrometers. The adult worms are small, measuring 2.2–3 mm for males and 3–3.5 mm for females.

Trichostrongylus colubriformis (T. instabilis)

This cosmopolitan parasite infects the small intestine of cattle and other ruminants, as well as lagomorphs.

Clinical signs

The intrinsic pathogenic strength of these worms is weak, and most rabbits remain asymptomatic. However, severe infestation can lead to weight loss and/or anemia, as well as the exacerbation of other rabbit disorders, such as diarrhea and severe eosinophilia. In some cases, it can even result in death. The mucous layer of the intestine is often irritated, which can lead to blood loss. In certain instances, the presence of nodules may also be observed.

The presence of Trichostrongylus worms is diagnosed by fecal flotation for the presence of strongyle-type eggs in the feces. The cultivation of these eggs to the L3 stage is essential for accurate species identification. Adults can be distinguished by their anatomical structure and appendices.

Treatment

Benzimidazoles

fenbendazole

10-20 mg/kg, PO, repeat in 10-14 days

thiabendazole

100-200 mg/kg, PO

albendazole

10 mg/kg

Macrolide

ivermectin

0.2 - 0.4 mg/kg, PO, SC, repeat in 10-14 days

Further Information

Anderson RC (2000) Nematode Parasites of Vertebrates. Their Development and Transmission. 2nd Ed. CABI Publishing, Oxon, UK.

Andrews CL, Davidson WR. Endoparasites of selected populations of cottontail rabbits (Sylvilagus floridanus) in the southeastern United States. J Wildl Dis. 1980; 16(3):395-401.

Audebert F, Cassone J, Hoste H, Durette-Desset MC. Morphogenesis and distribution of Trichostrongylus retortaeformis in the intestine of the rabbit. J Helminthol. 2000; 74(2):95-107.

Audebert F, Hoste H, Durette-Desset MC. Life cycle of Trichostrongylus retortaeformis in its natural host, the rabbit (Oryctolagus cuniculus). J Helminthol. 2002; 76(3):189-92.

Boag B. The incidence of helminth parasites from the wild rabbit Oryctolagus cuniculus (L.) in eastern Scotland. J Helminthol. 1985; 59(1):61-9.

Boag B, Iason G. The occurrence and abundance of helminth parasites of the mountain hare Lepus timidus (L.) and the wild rabbit Oryctolagus cuniculus (L.) in Aberdeenshire, Scotland. J Helminthol. 1986; 60(2):92-8.

Ciordia H BIZZELL WE, Porter DA, Dixon CF. The effect of culture temperature and age on the infectivity of the larvae of Trichostrongylus axei and T. colubriformis in rabbits and guinea pigs. J Parasitol. 1966; 52(5):866-70.

Duwel D, Brech K. Control of oxyuriasis in rabbits by fenbendazole. Lab Anim. 1981; 15(2):101-5.

Hoste H, Reilly M. Scanning electron microscopy of the jejunal and ileal mucosa of rabbits infected with Trichostrongylus colubriformis. Ann Rech Vet. 1988; 19(2):123-8.

Hoste H, Mallet S. Effects of size of Trichostrongylus colubriformis infections on histopathology of the mucosa along the whole small intestine in rabbits.
J Comp Pathol. 1990; 103(4):457-65.

Hoste H, Mallet S, Koch C. Trichostrongylus colubriformis infection in rabbits: persistence of the distal adaptive response to parasitism after anthelmintic treatment. J Comp Pathol. 1995; 113(2):145-53.

Iason GR, Boag B. Do intestinal helminths affect condition and fecundity of adult mountain hares? J Wildl Dis. 1988; 24(4):599-605.

Molina X, Casanova JC, Feliu C. Influence of host weight, sex and reproductive status on helminth parasites of the wild rabbit, Oryctolagus cuniculus, in Navarra, Spain. J Helminthol. 1999; 73(3):221-5.

Prasad D, The effects of temperature and humidity on the free-living stages of Trichostrongylus retortaeformis. Can. J. Zool. 1959; 37: 305-316.

Purvis GM, Sewell MM. The host-parasite relationship between the domestic rabbit and Trichostrongylus colubriformis. Vet Rec. 1971; 89(5):151-2.

Strohlein DA, Christensen BM. Metazoan parasites of the eastern cottontail rabbit in western Kentucky. J Wildl Dis. 1983; 19(1):20-3.

Wiggins JP, Cosgrove M, Rothenbacher H.Gastrointestinal parasites of the eastern cottontail (Sylvilagus floridanus) in central Pennsylvania.
J Wildl Dis. 1980; 16(4):541-4.

 

  

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