References

Barçante TA, Barçante JM, Dias SR, Lima Wdos S Angiostrongylus vasorum (Baillet, 1866) Kamensky, 1905: emergence of third-stage larvae from infected Biomphalaria glabrata snails. Parasitol Res. 2003; 91:471-5

Böhm C, Schnyder M, Thamsborg SMS Assessment of the combination of spinosad and milbemycin oxime in preventing the development of canine Angiostrongylus vasorum infections. Vet Parasitol. 2014; 199:(3–4)272-7 https://doi.org/https://doi.org/10.1016/j.vetpar.2013.10.024

Bolt G, Monrad J, Frandsen F, Henriksen P, Dietz HH The common frog (Rana temporaria) as a potential paratenic and intermediate host for Angiostrongylus vasorum. Parasitol Res. 1993; 79:428-30

Brennan SF, McCarthy G, McAllister H, Bassett H, Jones BR Clinical signs, diagnosis and treatment of three dogs with angiostrongylosis in Ireland. Ir Vet J. 2004; 57:1-7 https://doi.org/https://doi.org/10.1186/2046-0481-57-2-103

Chapman PS, Boag AK, Guitian J, Boswood A Angiostrongylus vasorum infection in 23 dogs (1999-2002). J Small Anim Pract. 2004; 45:435-40

Cobb MA, Fisher MA Crenosoma vulpis infection in a dog. Vet Rec. 1992; 130:(20)

Conboy G Helminth parasites of the canine and feline respiratory tract. Vet Clin North Am Small Anim Pract. 2009; 39:1109-26 https://doi.org/https://doi.org/10.1016/j.cvsm.2009.06.006

Elsheikha HM, Holmes SA, Wright I, Morgan ER, Lacher DW Recent advances in the epidemiology, clinical and diagnostic features, and control of canine cardio-pulmonary angiostrongylosis. Vet Res. 2014; 45 https://doi.org/https://doi.org/10.1186/s13567-014-0092–9

Epe C Intestinal nematodes: biology and control. Vet Clin North Am Small Anim Pract. 2009; 39:1091-107 https://doi.org/https://doi.org/10.1016/j.cvsm.2009.07.002

Helm J, Gilleard JS, Jackson M, Redman E, Bell R A case of canine Angiostrongylus vasorum in Scotland confirmed by PCR and sequence analysis. J Small Anim Pract. 2009; 50:255-9 https://doi.org/https://doi.org/10.1111/j.1748-5827.2009.00741.x

Hodžić A, Bruckschwaiger P, Duscher GG, Glawischnig W, Fuehrer HP High prevalence of Eucoleus boehmi (syn. Capillaria boehmi) in foxes from western Austria. Parasitol Res. 2016; 115:3275-8 https://doi.org/https://doi.org/10.1007/s00436-016-5145–8

Lebon W, Tielemans E, Rehbein S Monthly administrations of milbemycin oxime plus afoxolaner chewable tablets to prevent Angiostrongylus vasorum infection in dogs. Parasit Vectors. 2016; 9

Manning SP Ocular examination in the diagnosis of angiostrongylosis in dogs. Vet Rec. 2007; 160:(18)625-7

Mozzer LR, Lima WS Gallus gallus domesticus: Paratenic host of Angiostrongylus vasorum. Vet Parasitol. 2015; 20781-84

Rinaldi L, Pennacchio S, Musella V, Maurelli MP, La Torre F, Cringoli G Helminth control in kennels: is the combination of milbemycin oxime and praziquantel a right choice?. Parasit Vectors. 2015; 1-7

Schnyder M, Deplazes P Cross-reactions of sera from dogs infected with Angiostrongylus vasorum in commercially available Dirofilaria immitis test kits. Parasite Vectors. 2012; 5 https://doi.org/https://doi.org/10.1186/1756-3305-5–258

Schnyder M, Fahrion A, Ossent P Larvicidal effect of imidacloprid/moxidectin spot-on solution in dogs experimentally inoculated with Angiostrongylus vasorum. Vet Parasitol. 2009; 166:(3-4)326-32 https://doi.org/https://doi.org/10.1016/j.vetpar.2009.09.004

Wessmann A, Lu D, Lamb CR Brain and spinal cord haemorrhages associated with Angiostrongylus vasorum infection in four dogs. Vet Rec. 2006; 158:(25)858-6

Willesen JL, Kristensen AT, Jensen AL, Heine J, Koch J Efficacy and safety of imidacloprid/moxidectin spot-on solution and fenbendazole in the treatment of dogs naturally infected with Angiostrongylus vasorum (Baillet, 1866). Vet Parasitol. 2007; 147:(3-4)258-64 https://doi.org/https://doi.org/10.1016/j.vetpar.2007.05.001

Canine angiostrongylosis: an increasing concern

02 October 2017
8 mins read
Volume 8 · Issue 8

Abstract

Canine angiostrongylosis is a snail-borne parasitic infection caused by the nematode Angiostrongylus vasorum. This metastrongyloid nematode poses a significant threat to canine populations. It is capable of infecting wild and domestic canines as their definitive host, using gastropods as intermediate hosts. Recent data strongly suggest an increased geographic expansion of this parasite in wildlife animals that can serve as a reservoir. Once localised to the southern UK, A. vasorum now represents a tangible threat to dogs throughout the country, presenting asymptomatically or causing a wide range of clinical signs including dyspnoea and haemorrhage. Veterinary professionals have a range of efficacious anthelmintics that, when used correctly, can significantly reduce mortality, clinical illness and associated health complications. Effective control of this disease, however, entails more understanding of the role of wildlife in spreading A. vasorum. Combined with this is the need for an appropriate framework for engaging and educating pet owners, improved management of adverse health effects of infection in dogs, guidelines on precautions to be adopted in order to minimise risk of infection, and the rational use of preventatives to control this disease. This review focuses on current knowledge about A. vasorum — which affects the respiratory system of dogs — and covers diagnostics, treatment and a brief account of other species of canine lungworms.

Canine angiostrongylosis is one of the most important vector-borne parasitic diseases in dogs and is caused by the cardiorespiratory nematode Angiostrongylus vasorum (superfamily: Metastrongyloidea). Dogs become infected after ingesting the third larval stage (L3), usually within an intermediate gastropod host or a paratenic host, such as the common frog (Rana temporaria) or chicken (Gallus gallus domesticus) (Bolt et al, 1993; Mozzer and Lima, 2015). Infected snails, of the species Biomphalaria glabrata, shed L3 into the environment, creating a free-living reservoir of infection (Barçante et al, 2003). Rising numbers of confirmed cases of angiostrongylosis have thrown A. vasorum under the global spotlight, driving research into its epidemiology, diagnosis and risk factors. It is well-established that A. vasorum has spread from its original southern hotspots and can now be found throughout mainland UK, with cases reported as far north as Scotland (Helm et al, 2009). However, this parasite's territory has expanded faster than our knowledge of its epidemiology and control. Therefore, the present review provides the following:

Register now to continue reading

Thank you for visiting The Veterinary Nurse and reading some of our peer-reviewed content for veterinary professionals. To continue reading this article, please register today.