Aelurostrongylus falciformis (Schlegel 1933) is a metastrongyle lung nematode of European badgers (Meles meles) and has been reported in continental Europe 12 and Great Britain 3 but not Fennoscandia. Other lung nematodes seen in European badgers include the metastrongyles Angiostrongylus vasorum (Baillet 1866) 45, Crenosoma sp. (Molin 1861) 1234, Aelurostrongylus pridhami (Anderson 1962) 5, as well as the trichuroid nematode Capillaria aerophila (Creplin 1839) 2. A. vasorum is considered to be absent from the Scandinavian Peninsula. However, recently it has been found on the island of Sydkoster off the south west coast of Sweden 6 close to the Norwegian border. This parasite has its predilection site in the pulmonary artery and right ventricle of the heart. The diagnosis however, as for A. falciformis, is frequently based on the identification of first stage larvae (L1) in faeces or sputum 7. Crenosoma sp. and Capillaria aerophila infections can be differentiated from those of A. vasorum and A. falciformis on the basis of their typical L1 (Crenosoma sp.) and eggs (Capillaria aerophila).

Nine badgers from the Oslo and Akershus regions were sent to the National Veterinary Institute, Oslo, during 2004 and 2005 (Table 1). Routine post-mortem was carried out and revealed trauma as the cause of death in seven of the animals whereas two had been shot for humane reasons. Parasitological examination of the respiratory tract, cardiovascular system and faeces was also carried out.

The trachea and bronchi were dissected; two scrapes from the mucous membrane were taken and examined for nematode eggs and larvae. Biopsies, from each lung lobe, were fixed in 10% formalin and embedded in paraffin. They were then cut at 5μm and stained with haematoxylin and eosin for histological examination. The right side of the heart was incised and this incision extended along the pulmonary artery to look for adult A. vasorum. At least two 10 gram faecal samples per animal, from some of the badgers, were set up in Baermann apparatus for 6 hours and then examined for faecal larval burden, larvae per gram (lpg); the larvae collected were stored in 70% ethanol. Larvae from the respiratory tract and faeces were examined under magnification, those with a wavy tail were digitally photographed: length and width measurements were taken (Leica Image Manager IM50 Measurement Module, Version 4.0, Release 106). The width was measured at the widest point.

Nematode larvae with a curvy tail and a notch, suggestive of A. vasorum infection, were found for the first time in bronchial scrapes. A more advanced examination of the lungs in badger 1 was carried out. The lungs were dissected to bronchiolar level and any adult nematodes were carefully removed and placed in 70% ethanol. Larvae were extracted from the uterus of an adult female and compared to those found in the respiratory tract and faeces. The adult nematodes and larvae were examined under magnification, digitally photographed and measured. All adult nematodes fragmented during extraction, and their overall length could not be measured. Width measurements were taken just anterior to the spicules in the males and level with the uterus in the females. The length of the male spicules and accessory spicules were recorded.

A. falciformis was found in five badgers and three had Crenosoma melesi infections. Two of the badgers were simultaneously infected with both parasites. Histological examination confirmed the location of A. falciformis within the terminal airways (Figure 1). Width measurements of adult male and female nematodes, as well as the length of the male spicules (Figure 2) and accessory spicule are given in Table 2, which also shows reference values given in the literature for A. falciformis and A. vasorum. No A. vasorum was found during the dissection of the heart and pulmonary artery.

Larval burden varied considerably between the positive animals (Table 1). Morphologically, the larvae appeared identical to those obtained from an adult female. The length and width of the isolated L1 were within the reference range given for A. falciformis (Table 2). The larvae had a wavy tail with a notch (Figure 3a) and the anterior end of the larvae had what could be interpreted as a cephalic button (Figure 3b) resembling the L1 of A. vasorum 67. The parasite was identified as A. falciformis given the location of the adult nematodes in the lung tissue, the length of the male spicules, the presence of an accessory spicule, and the size and morphology of the larvae 89.

The present study is believed to be the first report of A. falciformis infection in Fenno-Scandinavian badgers. The L1 length was within the published reference range for A. falciformis, which overlaps the published L1 range for A. vasorum. A. vasorum can be found in ectopic locations 10, but the male nematodes, from the reported badger's lungs, had short spicules and an accessory chitinous piece, excluding A. vasorum from the differential list. Nevertheless, the great similarity between the L1 stages of A. falciformis and A. vasorum, in size and general morphology, needs to be considered.

The prevalence of A. falciformis found in European badgers, as well as the diagnostic criteria underlying the diagnosis, varies considerably between studies and needs further investigation. Magi et al. (1999) 1 identified adult A. falciformis and L1 in the lungs of 10 of 19 (53%) Italian badgers. In a British study of 118 badgers for tuberculosis, A. falciformis was recorded incidentally in one animal 3. In Spain, Millán et al. (2004) 4 reported A. vasorum larvae in the faeces of 24 of 26 (92%) badgers; however, they were unable to find adult nematodes in the pulmonary artery or the right ventricle of the heart. Another Spanish badger study 5 reported the presence of both A. vasorum and A. pridhami, the latter is a parasite of wild mink in North America 11, without describing the identification methods used. It may be possible that an infection with A. falciformis, particularly in areas where A. vasorum is endemic, could be misinterpreted as A. vasorum, when larval identification is the only diagnostic method used.