Hostname: page-component-745bb68f8f-g4j75 Total loading time: 0 Render date: 2025-02-09T15:45:42.108Z Has data issue: false hasContentIssue false

Canine filarial infections in Tuscany, central Italy

Published online by Cambridge University Press:  04 April 2011

M. Magi
Affiliation:
Dipartimento di Patologia Animale, Profilassi e Igiene degli Alimenti, Pisa University, Viale delle Piagge 2, 56124Pisa, Italy
L. Guardone
Affiliation:
Dipartimento di Patologia Animale, Profilassi e Igiene degli Alimenti, Pisa University, Viale delle Piagge 2, 56124Pisa, Italy
M.C. Prati
Affiliation:
Scuola Normale Superiore di Pisa, Italy; INFN Sezione di Pisa, Italy
G. Tozzini
Affiliation:
Dipartimento di Patologia Animale, Profilassi e Igiene degli Alimenti, Pisa University, Viale delle Piagge 2, 56124Pisa, Italy
B. Torracca
Affiliation:
Dipartimento di Patologia Animale, Profilassi e Igiene degli Alimenti, Pisa University, Viale delle Piagge 2, 56124Pisa, Italy
G. Monni
Affiliation:
Dipartimento di Patologia Animale, Profilassi e Igiene degli Alimenti, Pisa University, Viale delle Piagge 2, 56124Pisa, Italy
F. Macchioni*
Affiliation:
Dipartimento di Patologia Animale, Profilassi e Igiene degli Alimenti, Pisa University, Viale delle Piagge 2, 56124Pisa, Italy
*
*Fax: 0502216941 E-mail: fmacchion@vet.unipi.it
Rights & Permissions [Opens in a new window]

Abstract

This study was conducted in order to investigate the epidemiology of filarial species in a region of central Italy (Tuscany) in dogs that did not undergo prophylaxis for filariasis. From 2007 to 2009, 630 blood samples were collected from 40 kennels throughout the regional territory. Samples were analysed with Knott's modified test and with an enzyme-linked immunosorbent assay (ELISA) for the detection of Dirofilaria immitis antigens, those positive for microfilariae were also subjected to histochemical staining for acid phosphatase activity to validate the identification of the species. An overall elevated prevalence of filariasis (23.2%) was found. Dirofilaria immitis and D. repens were found to be the dominant species, with similar prevalences (12.5% and 12.1% respectively), while Acanthocheilonema reconditum was less common (1.9%). Results of this study indicate that monitoring for filariasis should be kept at a high level. A constant monitoring of the canine sanitary status should also be carried out for the protection of human health, considering the zoonotic potential of filarial worms.

Type
Research Papers
Copyright
Copyright © Cambridge University Press 2011

Introduction

Dogs can be infected by several species of filarial worms; species found in Italy are Dirofilaria immitis, Dirofilaria (Nochtiella) repens, Acanthocheilonema (syn. Dipetalonema) reconditum and, less frequently, Acanthocheilonema (syn. Dipetalonema) dracunculoides and Cercopithifilaria (syn. Acanthocheilonema) grassii. These species can also infect cats and wild animals, as well as foxes and wolves, and occasionally humans. Filarial nematodes differ in the localization of adult parasites: D. immitis adult stages live in the right side of the heart and in the pulmonary artery, D. repens lives in the subcutaneous tissue, while A. reconditum, A. dracunculoides and C. grassii live in the peritoneal cavity, in adipose tissue and in intramuscular spaces, respectively. Their life cycle is indirect, with definitive vertebrate hosts and arthropods as intermediate hosts, also acting as vectors. After mating, adult female worms release microfilariae into the haematic circulation of the definitive host. Arthropods, in which first-stage larvae complete their development to the infective third stage, are mosquitoes belonging to genera Culex and Aedes for Dirofilaria spp., and fleas (Ctenocephalides spp.) and ticks (Rhipicephalus spp.) for Acanthocheilonema spp. and C. grassii.

Dirofilaria immitis and D. repens are filarial species of major concern in Europe for both canine and human health (Simón et al., Reference Simón, Morchón, González-Miguel, Marcos-Atxutegi and Siles-Lucas2009). Dirofilaria immitis is the aetiological agent of canine heartworm disease and it is the most pathogenic species, as it can be lethal; in dogs D. repens is considered less dangerous and causes pruriginous dermatitis. In Italy current data on canine dirofilariasis confirms the expanding trend of parasites as observed in the rest of Europe (Genchi et al., Reference Genchi, Rinaldi, Mortasino, Genchi and Cingoli2009). Today D. immitis is present, not only in the hyperendemic area of the Po River Valley, but also in the northern part of Italy (Lombardy and Friuli Venezia Giulia), in central Italy (Umbria, Abruzzo and Tuscany), in the south (Campania, Apulia and Calabria) and in the islands (Sicily and Sardinia). Dirofilaria repens is distributed in almost all of the Italian territory.

Acanthocheilonema reconditum has a worldwide distribution in dogs (Quinn et al., Reference Quinn, Donnelly, Carter, Markey, Torgerson and Breathnach1997). In Europe it has been reported in Serbia (Tasić et al., Reference Tasić, Rossi, Tasić, Miladinović-Tasić, Ilić and Dimitrijević2008), in Spain (Aranda et al., Reference Aranda, Panyella, Eritjia and Castellà1998), in Greece (Vakalis & Himonas, Reference Vakalis and Himonas1997), in Austria (Hinaidy et al., Reference Hinaidy, Bacowsky and Hinterdorfer1987) and in Italy (Cringoli et al., Reference Cringoli, Rinaldi, Veneziano and Capelli2001). Acanthocheilonema dracunculoides has rarely been reported: in Europe it has been found in dogs in The Netherlands, Greece, Spain and Portugual (Bolio et al., Reference Bolio, Montes, Alonso, Gutiérrez, Bernal, Rodríguez-Vivas and Sauri2004). In Italy it was found in foxes in Latium and Tuscany (Cancrini, Reference Cancrini1986; Magi et al., Reference Magi, Macchioni, Dell'Omodarme, Prati, Calderini, Gabrielli, Iori and Cancrini2009) and for the first time it has been reported in a dog in Sicily (Giannetto et al., Reference Giannetto, Poglayen, Gaglio, Brianti, Ferlazzo and Giudice2003). Cercopithifilaria grassii was discovered in 1907 in a dog from Rome (Noè, Reference Noè1908), subsequent sporadic reports have occurred (India: Balasubramanian et al., Reference Balasubramanian, Anandan and Alwar1975; Greece: Vakalis & Himonas, Reference Vakalis and Himonas1997). In Italy microfilariae were found in the blood of a dog from Sicily (Giannetto et al., Reference Giannetto, Poglayen, Gaglio, Brianti, Ferlazzo and Sorgi2004) and of a cat from the Aosta Valley (Tarello, Reference Tarello2004).

All canine filarial species have the potential to infect humans; D. immitis can cause pulmonary nodules, D. repens ocular and subcutaneous nodules and pruriginous dermatitis (Pampiglione & Rivasi, Reference Pampiglione, Rivasi, Genchi, Rinaldi and Cringoli2007; González-Miguel et al., Reference González-Miguel, Rosario, Rota-Nodari, Morchón and Simón2010) and A. reconditum can affect the eye (Huynh et al., Reference Huynh, Thean and Maini2001). The aim of this study is to investigate the prevalence and the distribution of different filarial species in an area of central Italy (Tuscany).

Materials and methods

The study was carried out between April 2007 and December 2009 in Tuscany, a region with natural breeding sites for a great variety of mosquito species, such as Culex pipiensCulex modestusAnopheles maculipennis, Coquilletidia richardii and Aedes albopictus (Cancrini et al., Reference Cancrini, Magi, Gabrielli, Arispici, Tolari, Dell'Omodarme and Prati2006), which have all proved to be suitable vectors of dirofilarial nematodes (Cancrini & Gabrielli, Reference Cancrini, Gabrielli, Genchi, Rinaldi and Cringoli2007).

Blood samples were collected from 630 dogs; 40 kennels were involved in the study (see table 1). The sample size was chosen so that the number of subjects enrolled in each municipality was roughly proportional to the surface area of the municipality itself. Animals were housed in outdoor kennels located in different towns in every district of Tuscany. They were all autochthonous, older than 6 months of age and had not undergone any prophylactic treatment for filariasis. Dogs were sampled in kennels, as most privately owned dogs currently undergo chemoprophylaxis. Individual data about sex, age, breed, living habitat and geographical origin were recorded. Each blood sample was divided into two fractions: 1 ml of whole blood was mixed with 9 ml of 2% formaldehyde solution for the detection of circulating microfilariae; and at least 2 ml were collected in tubes with anticoagulant, in order to obtain plasma for D. immitis antigen detection. Samples were submitted to the Department of Animal Pathology, Prophylaxis and Food Hygiene of Pisa University.

Table 1 Dogs classified according to districts and detected filarial species; k=number of kennels sampled; n=number of dogs sampled.

The identification of microfilariae species was carried out using modified Knott's technique (Lindsey, Reference Lindsey1965). In order to confirm the morphometric identification, blood samples which were Knott's positive were further analysed using the naphthol AS-TR-phosphate method for acid phosphatase activity as described by Barka (Reference Barka and Thompson1966). This staining distinguishes microfilariae of D. immitis, D. repens, A. reconditum (Chalifoux & Hunt, Reference Chalifoux and Hunt1971; Balbo & Abate, Reference Balbo and Abate1972) and A. dracunculoides (Ortega-Mora et al., Reference Ortega-Mora, Gomez-Bautista and Rojo-Vazquez1989) by four different patterns, depending on the different activity of the acid phosphatase enzyme: D. immitis microfilariae have two red areas corresponding to the excretory pore and the anal pore; D. repens microfilariae only have one red area corresponding to the anal pore; A. reconditum microfilariae show a reddish colour on the whole body and A. dracunculoides microfilariae show a very intense red colour on the central part of the body, at the anal pore and at the excretory pore.

Samples were also subjected to an enzyme-linked immunosorbent assay (ELISA) for the detection of antigens of D. immitis with the Canine Heartworm Antigen kit (DiroCHEK®, Synbiotics, Kansas City, Missouri, USA). The procedure was conducted following instructions contained in the kit.

Results were subjected to statistical analysis, using the χ2 test, and were considered significant if P < 0.05.

Results and discussion

Amongst 630 samples tested, 146 were positive for filariasis (prevalence 23.2%; 95% confidence interval: 19.9–26.5%). Dirofilaria immitis was found in 79 cases (12.5%), D. repens in 76 (12.1%) and A. reconditum in 12 (1.9%). Several cases of double infestations were found; the detailed situations in each district are summarized in table 1. The difference amongst the prevalence of the first two species in the various districts is highly significant (P < 0.0001). No sex- and age-related differences were observed.

Filarial infections in Italy have, in recent years, shown an expanding trend, as reported for all Europe (Genchi et al., Reference Genchi, Rinaldi, Cascone, Mortarino and Cringoli2005). The prevalence (23.2%) of filariasis in untreated dogs found in this study, shows that in Tuscany the parasitic pressure and the risk of infestation are high. Dirofilaria immitis and D. repens were the dominant species, showing widespread diffusion throughout the region and similar prevalence values (12.5% and 12.1%, respectively), whereas A. reconditum (1.9%) was less common and was found in only three districts (Firenze, Pisa and Livorno). Different intermediate hosts and the easy control of fleas and ticks in contrast to dirofilariasis vectors could explain the lower prevalence of A. reconditum. The widespread diffusion in Tuscany of mosquito species, potential vectors of dirofilariae (Cancrini et al., Reference Cancrini, Magi, Gabrielli, Arispici, Tolari, Dell'Omodarme and Prati2006), including Ae. albopictus, might have played a determining role in the presence of dirofilariasis. The identification of species achieved with the modified Knott's technique was validated by the acid phosphatase histochemical staining.

The ELISA test for D. immitis antigens was positive for 65 dogs, 42 of these were also found to be positive using Knott's modified test, while 23 were negative for the presence of D. immitis microfilariae (occult filariasis): this could be due to a unisex infection, a prepatent period or an immune-mediated clearance of microfilariae. On the other hand, 10 animals were found to be positive for D. immitis microfilariae using Knott's method and acid phosphatase staining but negative for antigen detection; this could be explained by the immune-mediated clearance of antigen–antibody complexes.

This study shows that the monitoring of filariasis should be kept at a high level because, despite the common use of prophylaxis, parasites are widespread. Dogs' sanitary status should be constantly monitored, for the protection of both animal and human health, taking into consideration the zoonotic potential of filarial worms, in particular D. repens. A complete diagnosis with the correct species identification is needed in order not to underestimate the presence of species that are not detectable using serological tools. Finally, awareness of prophylaxis, accurate diagnosis and correct treatment by veterinary surgeons are important.

Acknowledgements

We would like to thank all veterinary surgeons who kindly collaborated during the sampling.

References

Aranda, C., Panyella, O., Eritjia, R. & Castellà, J. (1998) Canine filariasis. Importance and transmission in the Baix Llobregat area, Barcelona (Spain). Veterinary Parasitology 77, 267275.CrossRefGoogle ScholarPubMed
Balasubramanian, G., Anandan, R. & Alwar, V.S. (1975) The occurrence of Dipetalonema grassii (Noé, 1907) in Indian dogs. Indian Veterinary Journal 52, 513516.Google Scholar
Balbo, T. & Abate, O. (1972) Histochemical differentiation of microfilariae of Dirofilaria immitis, Dirofilaria repens and Dipetalonema spp. Parassitologia 14, 239244.Google Scholar
Barka, T. (1966) Naphthol AS-TR-Phosphate method for acid phosphatase. pp. 644645in Thompson, S.W. (Ed.) Selected histochemical and histopathological methods. Springfield Illinois, Charles C. Thomas.Google Scholar
Bolio, M.E., Montes, A.M., Alonso, F.D., Gutiérrez, C., Bernal, L.J., Rodríguez-Vivas, R.I. & Sauri, C.H. (2004) Prevalence of Dipetalonema dracunculoides in dogs in Murcia, Spain. The Veterinary Record 154, 726727.CrossRefGoogle ScholarPubMed
Cancrini, G. (1986) Filariasi in Vulpes vulpes della provincia di Roma. Parassitologia 28, 210211.Google Scholar
Cancrini, G. & Gabrielli, S. (2007) Vectors of Dirofilaria nematodes' biological behaviour and the relationship with the host/parasites. pp. 4958in Genchi, C., Rinaldi, L. & Cringoli, G. (Eds) Dirofilaria immitis and D. repens in dog and cat and human infections. Napoli, Ronaldo Editore.Google Scholar
Cancrini, G., Magi, M., Gabrielli, S., Arispici, M., Tolari, F., Dell'Omodarme, M. & Prati, M.C. (2006) Natural vectors of dirofilariasis in rural and urban areas of the Tuscan region (Central Italy). Journal of Medical Entomology 43, 574579.CrossRefGoogle Scholar
Chalifoux, L. & Hunt, R.D. (1971) Histochemical differentiation of Dirofilaria immitis and Dipetalonema reconditum. Journal of the American Veterinary Medical Association 158, 601605.Google ScholarPubMed
Cringoli, G., Rinaldi, L., Veneziano, V. & Capelli, G. (2001) A prevalence survey and risk analysis of filariasis in dogs from the Mt. Vesuvius area of southern Italy. Veterinary Parasitology 102, 243252.CrossRefGoogle Scholar
Genchi, C., Rinaldi, L., Cascone, C., Mortarino, M. & Cringoli, G. (2005) Is heartworm disease really spreading in Europe? Veterinary Parasitology 133, 137148.CrossRefGoogle ScholarPubMed
Genchi, C., Rinaldi, L., Mortasino, M., Genchi, M. & Cingoli, G. (2009) Climate and Dirofilaria infection in Europe. Veterinary Parasitology 163, 286292.CrossRefGoogle ScholarPubMed
Giannetto, S., Poglayen, G., Gaglio, G., Brianti, E., Ferlazzo, M. & Giudice, E. (2003) Dipetalonema dracunculoides (Nematoda: Onchocercidae): first report for Italian dogs. Parasite 10, 188.Google Scholar
Giannetto, S., Poglayen, G., Gaglio, G., Brianti, E., Ferlazzo, M. & Sorgi, C. (2004) Le cinque filarie del cane. Obiettivi e Documenti Veterinari 3, 2028.Google Scholar
González-Miguel, J., Rosario, L., Rota-Nodari, E., Morchón, R. & Simón, F. (2010) The identification of the immunoreactive proteins of Dirofilaria immitis and D. repens recognized by the sera from patients with pulmonary and subcutaneous dirofilariasis. Parasitology International 59, 248256.CrossRefGoogle Scholar
Hinaidy, H.K., Bacowsky, H. & Hinterdorfer, M. (1987) Introduction of Dirofilaria immitis and Dipetalonema reconditum in Austrian dogs. [in German]. Journal of Veterinary Medicine, Series B 34, 326332.CrossRefGoogle Scholar
Huynh, T., Thean, J. & Maini, R. (2001) Dipetalonema reconditum in the human eye. British Journal of Ophthalmology 85, 13911392.CrossRefGoogle ScholarPubMed
Lindsey, L.R. (1965) The identification of canine microfilariae. Journal of the American Veterinary Medical Association 146, 11061114.Google ScholarPubMed
Magi, M., Macchioni, F., Dell'Omodarme, M., Prati, M.C., Calderini, P., Gabrielli, S., Iori, A. & Cancrini, G. (2009) Endoparasites in red foxes (Vulpes vulpes) in Central Italy. Journal of Wildlife Diseases 45, 881885.CrossRefGoogle ScholarPubMed
Noè, G. (1908) Il ciclo evolutivo della Filaria grassi, mihi, 1907. Atti della Reale Accademia dei Lincei, Roma 17, 282293.Google Scholar
Ortega-Mora, L.M., Gomez-Bautista, M. & Rojo-Vazquez, F.A. (1989) The acid phosphatase activity and the morphological characteristic of Dipetalonema dracunculoides (Cobbold, 1870) microfilariae. Veterinary Parasitology 33, 187190.CrossRefGoogle ScholarPubMed
Pampiglione, S. & Rivasi, F. (2007) Human dirofilariasis due to Dirofilaria (Nochtiella) repens: an update of world literature from 1995 to 2000. pp. 81116in Genchi, C., Rinaldi, L. & Cringoli, G. (Eds) Dirofilaria immitis and D. repens in dog, cat and human infections. Napoli, Ronaldo Editore.Google Scholar
Quinn, P.J., Donnelly, W.J.C., Carter, M.E., Markey, B.K.J., Torgerson, P.R. & Breathnach, R.M.S. (1997) Microbial and parasitic diseases in cats and dogs. 269 pp. London, W.B. Saunders.Google Scholar
Simón, F., Morchón, R., González-Miguel, J., Marcos-Atxutegi, C. & Siles-Lucas, M. (2009) What's new in animal and human dirofilariosis? Trends in Parasitology 25, 404409.CrossRefGoogle Scholar
Tarello, W. (2004) The identification and treatment of Dipetalonema grassii microfilarie in a cat from Central Italy. The Veterinary Record 155, 565566.CrossRefGoogle Scholar
Tasić, A., Rossi, L., Tasić, S., Miladinović-Tasić, N., Ilić, T. & Dimitrijević, S. (2008) A survey of canine dirofilariasis in Vojvodina, Serbia. Parasitology Research 103, 12971302.CrossRefGoogle ScholarPubMed
Vakalis, N.C. & Himonas, C.A. (1997) Human and canine dirofilariasis in Greece. Parassitologia 39, 389391.Google ScholarPubMed
Figure 0

Table 1 Dogs classified according to districts and detected filarial species; k=number of kennels sampled; n=number of dogs sampled.