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Updated canine infection rates for Dirofilaria immitis in areas of Brazil previously identified as having a high incidence of heartworm-infected dogs

Abstract

Background

Canine heartworm infections were frequently diagnosed in Brazil before the new millennium. After the year 2000, the frequency of diagnosis showed a sharp decline; however, a few years later, new evidence indicated that the parasite was still present and that canine infection rates seemed to be increasing. Therefore, an updated survey of canine heartworm prevalence was conducted in several locations in south, southeast, and northeast Brazil.

Methods

Dogs from 15 locations having previously reported a high prevalence of heartworm infection were included in the survey according to defined criteria, including the absence of treatment with a macrocyclic lactone for at least 1 year. Blood samples from 1531 dogs were evaluated by an in-clinic immunochromatography test kit (Witness® Heartworm, Zoetis, USA) for detection of Dirofilaria immitis antigen. At each location, epidemiologic data, including physical characteristics and clinical signs reported by owners or observed by veterinarians, were recorded on prepared forms for tabulation of results by location, clinical signs, and physical characteristics.

Results

The overall prevalence of canine heartworm infection was 23.1%, with evidence of heartworm-infected dogs detected in all 15 locations studied. There was a tendency for higher prevalence rates in environmentally protected areas, despite some locations having less-than-ideal environmental temperatures for survival of vector mosquitoes. Among physical characteristics, it was noted that dogs with predominantly white hair coats and residing in areas with a high (≥20%) prevalence of heartworm were less likely to have heartworm infection detected by a commercial heartworm antigen test kit than were dogs with other coat colors. In general, dogs older than 2 years were more frequently positive for D. immitis antigen than were younger dogs. Clinical signs of heartworm infections were rare or owners were unable to detect them, and could not be used for reliable prediction of the presence of heartworm.

Conclusions

These results indicate that the prevalence of D. immitis has increased in these areas of Brazil over the past few years. Small animal practitioners in these areas should include routine screening tests for heartworm infections in every dog’s annual evaluation protocol and make sure to have uninfected dogs on prevention.

Background

Dirofilaria immitis (Leidy, 1856) Raillet & Henry, 1911, is a mosquito-borne parasite species distributed throughout all continents although in different prevalences. The prevalence of the parasite in Brazil was reported to be 8% during the 1980s [1], with hotspots that could be as high as 45% in the coastal lowlands of the state of São Paulo [2] and in the eastern lowland section of the state of Rio de Janeiro [3]. Several canine heartworm hotspots were identified in coastal areas such as Florianópolis (12%), state of Santa Catarina [4]; Guaratuba (6%) and Guaraqueçaba (21%), state of Paraná [5]; Bertioga (45%) and Guarujá (14%), state of São Paulo [2], região dos lagos (52%) and Niterói (37%), state of Rio de Janeiro [3]; Recife (12%) [6] and Itamaracá (29%) [7], state of Pernambuco; and Salvador (5.4%) and Lauro de Freitas (23.3%), state of Bahia [8]. As awareness of the disease increased following introduction of chemoprophylatic drugs in Brazil and with the increased treatment of canine tick-borne diseases, the number of heartworm-infected dogs declined. At the beginning of the new millennium (2001), the reported national prevalence of heartworm infection in Brazil was 2%, while Ehrlichia canis seroprevalence was 30% [9]. The reasons for the downward trend in D. immitis infection in Brazil included appropriate use of chemoprophylaxis, widespread use of off-label injectable ivermectin, and increased use of tetracycline (or derivatives) to control ehrlichiosis [10] that may affect the Wolbachia endosymbiont as well as the survival and reproduction of adult heartworm [11].

Following the observed decline in the prevalence of heartworm in the early years of the new millennium, the first report of a Brazilian outbreak was in the state of Rio de Janeiro, at the eastern lowland section [12]. Subsequent to this report, small animal practitioners from different areas of the country began to detect heartworm infections in dogs in their clinics during routine blood work [13]. Despite the apparent increase in reports of infected dogs, there are no updated systematic surveys conducted in Brazil. Therefore, the need for an update on canine heartworm prevalence in Brazil is unquestionable.

The damage promoted over time to pulmonary arteries, right ventricle, and to all vascular structures near the lungs by the adult worms often leads to severe disease [14], generally recognized by clinical signs, such as coughing, dyspnea, and exercise intolerance [15],[16]. Although the disease is well known in the literature, many times it is difficult to be identified by owners and veterinarians; thus, infected dogs may not receive prompt treatment for heartworm infection. Therefore, there is an urgent need to convince small animal practitioners to include heartworm testing as a routine examination for their dogs even when owners report the absence of any clinical signs that could suggest D. immitis infection.

Considering that updated data regarding the prevalence of D. immitis in areas of Brazil is warranted and that reliable clinical signs of heartworm infection in dogs are missed or underestimated by owners, the present article reports the prevalence of canine heartworm infection at different sites in the coastal area of Brazil as well as dog-owners’ perceptions regarding clinical signs of the presence of heartworm infection. These data are expected to aid veterinary practitioners for better and earlier diagnosis of canine heartworm infection in their practice.

Methods

The study was designed to include approximately 1600 dogs from areas previously identified as having high rates of heartworm infection. Dogs were selected for inclusion in the study according to the following criteria: i) dogs should have lived at the location for at least 1 year; ii) if possible, there should be no more than three dogs kept in the home; iii) dogs could have not received any treatments with macrocyclic lactones for at least 12 months; and iv) a formal consent must be signed by owners. The protocol was approved by the committee of animal use (CEUA) of the Universidade Federal Rural do Rio de Janeiro.

Along the Brazilian coast, the states Santa Catarina, Paraná, São Paulo, Rio de Janeiro, Bahia, and Pernambuco were included in the survey (Figures 1, 2 and 3). These states had previously been reported to have high rates of heartworm infection. The minimum number of samples to be obtained in each state was calculated with Epi Info 2000 (Centers for Disease Control and Prevention, Atlanta, Georgia) for determining 90% confidence intervals, considering the canine population to be 15% of the human population [17] and the estimated heartworm prevalence to be as reported previously [2],[4]-[8].

Figure 1
figure 1

Map showing the percentage of canine positive test results for heartworm antigen in southern Brazil.

Figure 2
figure 2

Map showing the percentage of canine positive test results for heartworm antigen in southeastern Brazil.

Figure 3
figure 3

Map showing the percentage of canine positive test results for heartworm antigen in northeastern Brazil.

Blood samples were obtained from dogs presented for rabies vaccination or spay and neuter campaigns. At places where no such campaigns were available, active search for homes with dogs was used, avoiding buildings that were multiple-housing units. At each locale, epidemiologic data, including each dog’s characteristics and clinical signs, were recorded on prepared survey forms. Blood samples were processed to obtain plasma to be tested by an in-clinic immunochromatography test kit (Witness® HW (heartworm) antigen test kit, Zoetis, USA) for detection of D. immitis antigen.

Test results were compiled by locale, clinical signs, and dog characteristics for determination of statistical significance by chi square or Fisher exact tests.

Results

A total of 1531 blood samples were obtained from September 2013 through March 2014, reaching the minimum sample size for a 90% confidence interval. Overall, 23.1% of the samples examined were positive for heartworm antigen (Table 1). Heartworm-infected dogs were diagnosed in all locales.

Table 1 Detection of antigens of Dirofilaria immitis a in canine blood samples from different areas of Brazil

The lowest area rate (13.2%) was found in the southern states, which have a milder climate. Nonetheless, even in the southern area, in less urbanized locales with better preserved natural resources, some states had rates higher than the overall prevalence in the survey (Table 1, Figure 1). Anthropization and climate seem to have had the greatest influence in the southeast, in which 26.3% of dogs tested positive. In Guarujá, a locale with mild temperatures (10.5° to 34.5°C) and which is highly impacted by industrial activities, 2.8% of the samples tested positive. In Niterói, where nature is better preserved, despite being located in a metropolitan area and temperature range from 10.1° to 41°C, 58.6% of the samples tested positive; and at Armação de Búzios, a well-preserved summer resort, 62.2% of samples tested positive (Table 1, Figure 2). The collective rate of dogs positive for heartworm in the southeast area was 26.3%. The overall regional rate of positive tests in the northeast was 29.7%, with the two biggest cities of the region (Salvador and Recife) displaying high rates (20% and 36.7%, respectively) in areas that are less anthropized (Table 1, Figure 3).

Results in areas with low prevalence

In areas where a low prevalence of heartworm infection was detected (<20%), owner perception of the density of mosquitoes and the majority of individual canine characteristics were not associated with positive test results (Table 2). Two individual characteristics that could be associated with positive results were gray coat color versus other coat colors (χ2 = 17.93; df = 4; P = 0.001) and size (weight). Small dogs (<5 kg), medium-large dogs, and large dogs (>25 kg) were less associated with positive test results than were medium-small dogs (5-15 kg) (χ2 = 19.37; df = 3; P < 0.001) (Table 2).

Table 2 Number and percentage positive for antigens of Dirofilaria immitis a in canine blood samples according to the relative prevalence in areas sampled

Results in areas with high prevalence

At locales where positive test results were high (≥20%), owner perception of mosquito density also showed no association with canine heartworm infection (χ2 = 1.23; df = 2; P = 0.540). However, hair coat length, predominant coat color, life style, age, and size all demonstrated an effect on prevalence of heartworm. Short-haired dogs were positive for heartworm antigen more often than dogs with medium coat length (χ2 = 5.46; df = 1; P = 0.027) or dogs with long hair (χ2 = 5.58; df = 1; P = 0.024). Dogs with white hair coats tested negative for heartworm antigen more often than dogs with black (χ2 = 11.5; df = 1; P < 0.001), golden (χ2 = 17.34; df = 1; P < 0.001), or brown coats (χ2 = 5.391; df = 1; P = 0.020). Outdoor animals showed higher probability of testing positive than those kept indoors most of the time (χ2 = 7.103; df = 1; P < 0.008). Younger dogs (1-2 years) were less likely to test positive than were dogs of other (older) age groups (χ2 = 8.23; df = 3; P = 0.042). The percentage of large dogs (>25 kg) that tested positive was statistically similar to that for medium-large dogs (15-25 kg) (χ2 = 2.61; df = 1; P = 0.106), and dogs in both of these two size (weight) groups tested positive significantly more often than medium-small or small dogs (χ2 = 19.46; df = 1; P < 0.001) (Table 2). Medium-small dogs and small dogs had similar percentages of positive tests (χ2 = 1.18; df = 1; P = 0.277).

Clinical signs and physical categories

Physical variables that had a significant influence on test results included age group (χ2 = 31.1; df = 3; P < 0.001); size (χ2 = 21.3; df = 3; P < 0.001), and breed (χ2 = 22.7; df = 2; P < 0.001) (Table 3).

Table 3 Percentage of positive canine tests for heartworm antigens a within physical category and according to clinical signs

Overall, presence of clinical signs reported by owners was not predictive of positive tests results for D. immitis (Table 3). However, when associating clinical signs with age or size, without regard for the test result, some correlation could be detected (Table 3): Age was correlated with frequency of coughing (χ2 = 52.2; df = 3; P < 0.001), exercise intolerance (χ2 = 60.5; df = 3; P < 0.001), and weight loss (χ2 = 33.3; df = 3; P < 0.001). Size of the animals was predictive of the presence of coughing (χ2 = 8.33; df = 3; P = 0.040) and weight loss (χ2 = 10.1; df = 3; P = 0.018); however, it was not predictive of exercise intolerance.

Discussion

The presence of D. immitis was detected at all locales in the survey, demonstrating that the reduction, or in some areas, the supposed disappearance of heartworm observed by small animal practitioners early in the new millennium [13] has been replaced by an observed increase in the presence of the parasite in these areas of Brazil. We found the overall percentage of positive D. immitis antigen test results, despite differences in diagnostic methodologies and inclusion criteria, was higher in all three Brazilian regions compared with findings in previous studies and when the pooled prevalence (3.9%) of the three surveyed regions observed previously [9] is compared with the current result (23.1%), it is irrefutable that there is a recrudescence of heartworm in these areas.

Notwithstanding all locales being coastal, differences in landscape due to human action seem to have influenced test results in some areas. Guarujá (state of São Paulo) is a locale where, in the past, 14.2% of examined dogs were positive for heartworm infection [2] and in the current study, prevalence of heartworm was only 2.8%. Also, in Florianópolis (state of Santa Catarina), prevalence decreased from 12% reported in 1992 [4] to 2.1% in the current study. Both cities are structured. Guarujá is affected by industrial pollution from neighboring cities, and Florianópolis experienced a human population boom during the past decades. Although human densification enhances the canine population, which in turn facilitates the transmission of heartworm [18], it transforms the environment, usually making it inhospitable to the majority of mosquito-vector species [19],[20], thereby disturbing transmission.

On the other hand, at conserved estuaries, such as in the lowlands of Paraná, where the local economy is based on tourism or artisanal fishing, even though their annual mean temperatures generally range from 14° to 22°C [21], the prevalence of heartworm-infected dogs was higher than that observed in the more urbanized cities of Salvador or Lauro de Freitas, where the average temperature is much warmer (20°-28°C) [21]. Therefore, if on one hand, temperature is directly related to the number of mosquito generations produced [22]-[24] and with the speed of parasite development in the mosquito vectors [25], the level of environmental conservation seems to play a crucial role in maintaining dense mosquito populations.

The perception of dog owners regarding the presence of mosquitoes was not associated with the prevalence of heartworm detected by testing for D. immitis antigen with a reliable commercial antigen test kit. This lack of perception suggests that inhabitants in these areas are accustomed to the presence of vectors and, therefore, are unwilling to control mosquitoes, which likely contribute to enhancing D. immitis transmission.

In areas where the prevalence of infected dogs was lower than 20%, a higher percentage of dogs with gray hair coat tested positive; however, the sample size for this hair color was small (15/1531) and may have biased the results. At areas with a prevalence 20% or higher, the majority of dogs with a white hair coat tested negative for heartworm. The prevalence of heartworm infection in these dogs with a white hair coat was significantly lower than among dogs with black, golden, or brown hair color. If mosquitoes can perceive different colors, as suggested by Maranhão [26], it is possible that the white hair coat may play a protective role in areas where heartworm transmission challenge is high. In addition to hair coat color, the length of the hair coat (long), and life style (living primarily indoors) appeared to be associated with reduced heartworm infections, presumably because these characteristics interfere with the vectors’ ability to locate hosts and obtain blood meals [27]. Considering that short hair coat presumably provides mosquitoes with better access to a dog’s skin [28]-[30] and that dogs that stay primarily outdoors are exposed to the sylvatic and the more efficient mosquito vectors that are hemi-synanthropic and exophylic [29],[30], these characteristics also may have played a key role in increasing the percentage of positive test results.

Despite these findings of statistical association of certain physical characteristics, these results suggest that the relationship of canine individual characteristics (hair coat color or length, and outdoors life style) to test results is minor, mainly because it could only be detected where challenge was high. In previously surveyed areas, where the prevalence of heartworm infection was lower (10.4% and 15%), interference by these factors could not be detected [27],[31].

The fact that the length of time the dogs lived at enzootic locales did not increase the percentage of positive test results suggests that infections occur soon after the animal is introduced to a location. Also, traveling experiences did not influence the results, suggesting that dogs in the areas surveyed most likely became infected in the home region; however, it would be expected that these animals could eventually spread the infection if and when they traveled abroad, as suggested before [32].

The prevalence of heartworm infection among younger dogs (1-2 years) may have been smaller than for the older age groups due to the long prepatent period of the infection (6-7 months) [14], especially because the time dogs lived at the enzootic areas did not demonstrate an effect on test results. An association between the small size (i.e. dogs weighing <5 or 5-15 kg) and indoor life style may have been the reason for smaller animals to have fewer positive test results as compared with the prevalence among larger dogs (i.e. dogs weighing 15-25 or >25 kg), as observed previously [33],[34].

Breeds have been previously compared as purebred versus mongrels, with most reports showing no difference among different breed categories [35],[36], although one report showed purebred dogs to have more positive test results [37]. Therefore, it is difficult to interpret the lower percentage of positive test results in mixed-breed dogs compared with results in mongrels or purebred dogs, and the current results may have occurred by chance alone.

Independent of D. immitis antigen test results, testing of various characteristic variables against the reported clinical signs reported by owners indicated that older dogs presented a higher prevalence of exercise intolerance, cough, and weight loss than younger dogs. With regard to size, smaller dogs were more inclined to have a cough and lose weight more frequently, possibly due to heart or respiratory diseases associated with other etiologies [38],[39].

Conclusions

Canine D. immitis infection was detected in every region surveyed, with a tendency to have higher percentage of positive test results where nature is better conserved. In areas where heartworm was highly prevalent, there were significantly more cases of D. immitis infection in large dogs, outdoor dogs, and dogs with short hair coats. Clinical signs observed by owners did not correlate with positive test results, suggesting that clinical signs of heartworm infections are rare or, at best, subtle, and call for other methods to be used for detection of heartworm infection, particularly for light or early infections. Therefore, small animal practitioners must include heartworm routine screening tests in every Brazilian dog’s annual evaluation protocol and make sure to have uninfected dogs on prevention.

Authors’ contributions

NVL conceived of the study and participated in coordination of the study, the acquisition of data, interpretation of results, and helped to draft the manuscript. JPP participated in the study coordination and performed the statistical analysis. FMA participated in the study coordination, acquisition of data, laboratory analysis and helped to draft the manuscript. LR, CJCP, PSJ, MAO de A, and LCA participated in the study coordination, acquisition of data, and laboratory analysis. AM participated in the study design and coordination, interpretation of results, and helped to draft the manuscript. All authors read and approved the final manuscript.

References

  1. Guerrero J, Vezzoni A, Ducos-de-Lahitte , Bussieras J, Rojo FA, Ortega LM, Rodenas A, Bulman GM, Larson MH, Labarthe NV, Charles T, Bordin EL: Distribution of Dirofilaria immitis in selected areas of Europe and South America. Proceedings of Heartworm Symposium'89. Edited by: Otto GF. 1989, American Heartworm Society, Washington DC, 13-18.

    Google Scholar 

  2. Duque-Araujo AM, Labarthe NV, Luvisário SL, Reina D: Filariose canina no Estado de São Paulo-Brasil. In Proceedings of IV Congresso Ibérico de Parasitologia 1995 Santiago de Compostela, Espanha. Edited by Congresso Ibérico de Parasitologia. Congresso Ibérico de Parasitologia; 1995:93-95

    Google Scholar 

  3. Labarthe NV, Almosny NR, Guerrero J, Duque-Araujo AM: Description of the occurrence of canine dirofilariasis in the State of Rio de Janeiro, Brazil. Mem Inst Oswaldo Cruz. 1997, 92: 47-51. 10.1590/S0074-02761997000100010.

    Article  CAS  PubMed  Google Scholar 

  4. Labarthe NV, Araujo AM, Bordin EL, Larsson ME, Guerrero J: Update on the distribution of Dirofilaria immitis in dogs in Brazil. Proceedings of the WSAVA World Congress '92. 1992, 1: 287-289.

    Google Scholar 

  5. Reifur L, Soccol VT, Montiani-Ferreira F: Prevalence of filariosis in dogs from the coast of Parana State Brasil: Emphasizing Dirofilaria immitis. Proceedings of the 10th Triennial Heartworm Symposium. 2001, American Heartworm Society, Batavia, IL, 243-251.

    Google Scholar 

  6. Alves LC, Cole EF, Athayde ACR: Prevalência da filariose canina no Bairro de Dois Irmãos. Rev Bras Parasitol Vet. 1993, 2: 68-

    Google Scholar 

  7. Pimentel A, Alves LC: Estudos epidemiológicos preliminares na população canina de Itamaraca-PE [abstract].Simpósio Nacional de Filariose. 1987,

    Google Scholar 

  8. Barros MTG, Santos EP, Gondim LFP, Almeida MAO: Frequencia de microfilarias de Dirofilaria immitis (Leidy,1856) em caes dos municipios de Salvador e Lauro de Freitas. Rev bras saude prod anim. 1991, 1: 70-

    Google Scholar 

  9. Labarthe N, de Campos PM, Barbarini O, McKee W, Coimbra CA, Hoskins J: Serologic prevalence of Dirofilaria immitis, Ehrlichia cani s, and Borrelia burgdorferi infections in Brazil. Vet Ther. 2003, 4: 67-75.

    PubMed  Google Scholar 

  10. Labarthe N, Guerrero J: Epidemiology of heartworm: what is happening in South America and Mexico?. Vet Parasitol. 2005, 133: 149-156. 10.1016/j.vetpar.2005.04.006.

    Article  PubMed  Google Scholar 

  11. Bandi C, Trees AJ, Brattig NW: Wolbachia in filarial nematodes: evolutionary aspects and implications for the pathogenesis and treatment of filarial diseases. Vet Parasitol. 2001, 98: 215-238. 10.1016/S0304-4017(01)00432-0.

    Article  CAS  PubMed  Google Scholar 

  12. Bendas AJR, Paiva JP, Doria MI, Mendes-de-Almeida F, Branco AS, Silvano DRB, Valle LG, Labarthe NV: Ocorrência de Dirofilaria immitis no entorno de um case diagnosticado na Zona Sul do rio de Janeiro/RJ, Brasil. Acta Sci Vet. 2007, 35: 678-679.

    Google Scholar 

  13. Labarthe NV: As filarias estão de volta. Prepare-se. Nosso Clinico. 2009, 62: 68-

    Google Scholar 

  14. Knight DH: Heartworm infection. Textbook of Respiratory Disease in Dogs and Cats. Edited by: King LG. 2004, Saunders, St. Louis, 517-525. 10.1016/B978-0-7216-8706-3.50074-8.

    Chapter  Google Scholar 

  15. Grandi G, Zivicnjak R, Beck R: Pathogenesis of Dirofilaria spp. infections. Mappe parassitologiche-Dirofilaria: Dirofilaria immitis and D. repens in dog and cat and human infections. Edited by: Genchi C, Rinaldi L, Cringoli G. 2014, Rolando Editore, Naples, 59-66.

    Google Scholar 

  16. Venco L: Heartworm (Dirofilaria immitis) disease in dogs. Mappe parassitologiche-Dirofilaria: Dirofilaria immitis and D. repens in dog and cat and human infections. Edited by: Genchi C, Rinaldi L, Cringoli G. 2007, Rolando Editore, Naples, 117-125.

    Google Scholar 

  17. IBGE. 2010., [http://censo2010.ibge.gov.br]

  18. Walters LL: Rick factors for heartworm infection in northern California. Proceedings of the Heartworm Symposium '95. Edited by: Soll MD, Knight DH. 1995, American Heartworm Society, Batavia, IL, 5-26.

    Google Scholar 

  19. Paula MB, Gomes AC: Culicidae (Diptera) in a dam construction area in the state of São Paulo, Brazil. Rev Saúde Públ. 2007, 41: 284-289. 10.1590/S0034-89102006005000018.

    Article  Google Scholar 

  20. Teodoro U, Guilherma ALF, Lazaovei AL, La Salvia FV, Fukushigue Y, Spinosa R, Ferreira AMEMC, Lima EM: Culicídeos do lago de Itaipu, no rio Paraná, sul do Brasil. Rev Saúde Públ. 1995, 29: 6-14. 10.1590/S0034-89101995000100003.

    Article  CAS  Google Scholar 

  21. Cactáceas Brasileiras. 2014., [http://www.brcactaceae.org/p_index.html]

  22. Calado DC, Silva MAN: Avaliação da influencia da temperatura sobre o desenvolvimento de Aedes albopicturs. Rev Saúde Públ. 2002, 36: 173-179. 10.1590/S0034-89102002000200009.

    Article  Google Scholar 

  23. Cônsoli RAGB, Lourenço-de-Oliveira R: Principais mosquitos de importância sanitária no Brasil. 1994, FIOCRUZ, Rio de Janeiro

    Google Scholar 

  24. Roiz D, Ruiz S, Soriguer R, Figuerola J: Climatic effects on mosquito abundance in Mediterranean wetlands. Parasit Vectors. 2014, 7: 333-10.1186/1756-3305-7-333.

    Article  PubMed Central  PubMed  Google Scholar 

  25. McTier TL, McCall JW, Supakorndej N: Features of adult heartworm antigen test kits. Proceedings of the Heartworm Symposium '95. Edited by: Soll MD, Knight DH. 1995, American Heartworm Society, Batavia, IL, 115-120.

    Google Scholar 

  26. Maranhão ZC: Entomologia Geral. 1976, Nobel, São Paulo, SP, Brazil

    Google Scholar 

  27. Almeida MAO, Barros MTG, Santos EP, Ayres MCC, Guimaraes JE, Gondim LFP: Parasitismo de cães por microfilárias Dirofilaria immitis: influência da raça, sexo e idade. Rev Bras Aaude Prod Anim. 2001, 2: 59-64.

    Google Scholar 

  28. Forantinni OP, Gomes AC, Natal D, Kakitani I, Marucci D: Frequência domiciliar e endofilia de mosquitos Culicidae no Vale do Ribeira, São Paulo, Brasil. Rev Saúde Públ. 1987, 21: 188-192. 10.1590/S0034-89101987000300003.

    Article  Google Scholar 

  29. Forantinni OP, Gomes AC, Natal D, Kakitani I, Marucci D: Preferências alimentares de mosquitos Culicidae no Vale do Ribeira, São Paulo, Brasil. Rev Saúde Públ. 1987, 21: 171-187. 10.1590/S0034-89101987000300002.

    Article  Google Scholar 

  30. Forantinni OP, Kakitani I, Massad EM, Marucci D: Studies on mosquitoes (Diptera: Culicidae) and anthropic environment. 9-Synathropyc and epidemiological vector roles of Aedes scapularis in south-eastern Brazil. Rev Saúde Públ. 1995, 29: 199-207. 10.1590/S0034-89101995000300007.

    Article  Google Scholar 

  31. Araujo RT, Marcondes CB, Bastos LC, Sartor DC: Canine dirofilariasis in the region of Conceicao Lagoon, Florianopolis, and in the Military Police kennel, Sao Jose, State of Santa Catarina, Brazil. Vet Parasitol. 2003, 113: 239-242. 10.1016/S0304-4017(03)00077-3.

    Article  CAS  PubMed  Google Scholar 

  32. Rinaldi L, Musella V, Marzatico G, Mortarino M, Genchi C, Cringoli G: Mapping and modeling Dirofilaria infections in Europe. Parasit Vectors. 2014, 7 (Suppl 1): O20-10.1186/1756-3305-7-S1-O20.

    Article  PubMed Central  Google Scholar 

  33. Ortega-Mora LM, Gomez-Bautista M, Rojo-Vazqueza F, Roidenasb A, Guerrero J: A survey of the prevalence of canine filariasis in Spain. Prev Vet Med. 1991, 11: 63-68. 10.1016/S0167-5877(05)80045-5.

    Article  Google Scholar 

  34. Theis JH, Franti C, Lambert L, Giammattei V, Parker V, Lee G: Risk factors for heartworm infection in dogs living in Sierra Nevada foothills and Sacramento Valley counties; public health implications. California Vet. 1984, 38: 13-17.

    Google Scholar 

  35. Rajamanickam C, Wiesenhutter E, Zin FM, Hamid J: The incidence of canine haematozoa in Peninsular Malaysia. Vet Parasitol. 1985, 17: 151-157. 10.1016/0304-4017(85)90101-3.

    Article  CAS  PubMed  Google Scholar 

  36. Diagnostico da dirofilariose através da detecção de antigenos circulantes em cães do estado do Rio de Janeiro. MSc thesis. 1992, Universidade Federal Rural do Rio de Janeiro, Instituto de Veterinária

  37. Kan SP, Rajah KV, Dissanaike AS: Survey of dirofilariasis among dogs in Serembam, Malaysia. Vet Parasitol. 1977, 3: 177-181. 10.1016/0304-4017(77)90034-6.

    Article  Google Scholar 

  38. Gompf RE: A historia e o exame fisico. Manual de cardiologia para câes e gatos. Edited by: Goodwin JK, Tilley LP. 2002, Roca, São Paulo, 3-14.

    Google Scholar 

  39. Kittleson MD: Signal, history and physical examination. Small animal cardiovascular medicine. Edited by: Kittleson MD, Kienle RD. 1998, Mosby, St. Louis, 36-46.

    Google Scholar 

Download references

Acknowledgements

The authors acknowledge Livia Abdalla for producing the maps; Carolina Athar, Carolina Haje, Daniel Marques, Eunice Maria Moreira Juliani, José Carlos Roble Júnior, José Marinho, Liliane Willi Monteiro, Maria Carolina Faria, Mariana Carvalho, Mário dos Santos Filho, Matheus Bahia, Mayron Tobias da Luz, Thiago Pinto, Centro de Zoonoses de Lauro de Freitas/BA, Centro de Zoonoses de Salvador/BA, Clínica Vida Animal, and Secretaria de Saúde de Mangaratiba/RJ for assisting authors during data and sample collection or sample analysis. The authors thank Kathleen Newcomb, Nathalie, VA, USA for editorial assistance in the preparation of this manuscript. The authors also acknowledge Dr. Juliana Caroline Ávila Queiróz, director of health surveillance of the Secretaria de Saúde of Paraná state, for supporting the study and providing contact with the staff of the health surveillance system from different coastal municipalities of the same state.

Funding for this study and the publication of the results was provided by Zoetis.

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Correspondence to Norma Vollmer Labarthe.

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Competing interests

Norma Labarthe is a consultant for Bayer Animal Health, Idexx Laboratories, and Zoetis in Brazil.

Flavya Mendes-de-Almeida is a consultant for Bayer Animal Health and Idexx Laboratories.

Jonimar Paiva is a consultant for Zoetis in Brazil.

Leucio Camara Alves is a consultant for Merial Saúde Animal LTDA, Ouro Fino Saúde Animal LTDA and MSD Saúde Animal.

Alexandre Merlo is a current employee of Zoetis in Brazil.

Larissa Reifur, Carlos José Carvalho Pinto, Paulo Sérgio Juliani and Maria Angela Ornelas de Almeida have no competing interests.

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Labarthe, N.V., Pereira Paiva, J., Reifur, L. et al. Updated canine infection rates for Dirofilaria immitis in areas of Brazil previously identified as having a high incidence of heartworm-infected dogs. Parasites Vectors 7, 493 (2014). https://doi.org/10.1186/s13071-014-0493-7

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