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Papular dermatitis due to Leishmania infantum infection in seventeen dogs: diagnostic features, extent of the infection and treatment outcome
Parasites & Vectorsvolume 7, Article number: 120 (2014)
This study describes immunological responses, diagnostic features, follow up and treatment outcomes from seventeen dogs with papular dermatitis due to Leishmania infection diagnosed by cytology or real time-PCR.
Specific Leishmania humoral and cellular immune responses were evaluated by means of an immunofluorescence antibody test in all cases and a delayed-type hypersensitivity (DTH) reaction to leishmanin in eight cases. The extent of infection was studied in several tissues including blood, lymph node, conjunctival and oral swabs, by means of PCR, at the time of diagnosis and during follow-up. Culture was performed on nine dogs from cutaneous lesions and lymph node aspirates and molecular typing was carried out on isolates based on ITS-1, ITS-2 and Haspb gene sequencing analysis.
Cytological and molecular results from fine needle aspirates of papules were diagnostic in 8 out of 13 (61.5%) cases and in 14 out of 15 dogs (93.3%), respectively. In all dogs, specific anti-Leishmania antibody levels were low or absent. Blood and lymph node PCRs and lymph node culture were negative in all dogs. Three out of the nine dogs (33%) were positive by culture from cutaneous lesions. The three isolates were identified as ITS type A, however, polymorphism was observed in the Haspb gene (PCR products of 626 bp, 962 bp and 371 bp). DTH response was positive in all tested dogs at the time of diagnosis. The majority of dogs were successfully treated with only N-methylglucamine antimoniate, after which cutaneous lesions disappeared or were reduced to depigmented, flattened scars. All dogs remained seronegative and the majority of dogs were negative by PCR in several tissues during follow-up.
This study points out that papular dermatitis due to L. infantum is probably an underestimated benign cutaneous problem, associated with a parasite specific cell mediated immunity and a poor humoral immune response. Papular dermatitis is seen in young dogs, and appears to be a mild disease with restricted parasite dissemination and a good prognosis. PCR can be used as a non-invasive method to routinely evaluate papules if Leishmania infection is suspected in cases in which parasites are not visualized by cytology.
Leishmania parasites are the causal agents of leishmaniosis, a group of vector-borne protozoan diseases transmitted by phlebotomine sandflies to mammals, including humans. In humans, the disease manifests in different forms, which are usually divided into localized or disseminated cutaneous leishmaniosis (CL), mucocutaneous leishmaniosis and disseminated visceral leishmaniosis (VL) .
Canine leishmaniosis (CanL) due to Leishmania infantum is a major zoonotic disease endemic in more than 70 countries in the world. It is present in regions of southern Europe, Africa, Asia, South and Central America [1, 2] and the USA [3, 4]. Dogs are the main reservoir for leishmaniosis caused by L. infantum.
The clinical manifestation of L. infantum infection in dogs varies widely as a consequence of the numerous pathogenic mechanisms of the disease process, which organs are affected and the diversity of immune responses mounted by individual hosts . The opposite extremes of the broad spectrum of immune responses are characterized by protective immunity that is T cell mediated, or disease susceptibility associated with a marked humoral non-protective immune response and reduced cell mediated immunity . In addition, it is well known that a high proportion of dogs living in endemic areas are subclinically infected with Leishmania parasites, while a small proportion of dogs will develop severe disease [5, 6]. Therefore, L. infantum infection in dogs can manifest as a subclinical infection, as a self-limiting or as severe disease .
The main clinical findings based on physical examination in classical CanL includes skin lesions, generalized lymphadenomegaly, progressive weight loss, muscular atrophy, exercise intolerance, decreased appetite, lethargy, splenomegaly, polyuria and polydypsia, ocular lesions, epistaxis, onychogryphosis, lameness, vomiting and diarrhea . Skin lesions are a very common manifestation of the disease . Various cutaneous forms such as alopecia, exfoliative, ulcerative, nodular or sterile pustular dermatitis, nasal or footpad hyperkeratosis, onychogryphosis, paronychia, mucosal or mucocutaneous ulcerations, nodules or masses have been described [9–12]. A distinctive form of papular dermatitis due to L. infantum infection was described in dogs living in endemic areas [13–16]. This cutaneous manifestation of L. infantum infection is suggestive of a benign form because of the lack of systemic signs and laboratory abnormalities, a good response to therapy with no clinical relapse and on some occasions self-healing of the lesions [13–16]. In addition, papular dermatitis is associated with a Leishmania-specific immunocompetence characterized by a predominant parasite specific cellular immunity and low humoral immune response [13–15].
However, information about diagnostic parameters, extent of infection, treatment outcome and prognosis of this distinctive form of papular dermatitis due to L. infantum is limited. Therefore, the aim of this study was to further characterize papular dermatitis due to L. infantum infection in dogs at time of diagnosis and during follow-up after treatment by: (1) describing clinicopathological findings in a series of clinical cases of papular dermatitis due to L. infantum in dogs from Sicily; (2) evaluating the cellular and humoral immunological status in these dogs and the dissemination of infection by sampling several tissue samples such as blood, lymph node, conjunctival and oral swabs and testing using molecular techniques. Culture and molecular typing of isolates were also performed in some cases.
Clinical examination and sampling
Seventeen dogs (16 from Catania and one from Palermo, Italy) were enrolled in this study from September 2008 to September 2012. They were examined for the presence of chronic non-pruritic cutaneous lesions in 7 out of 17 cases (cases 3, 4, 8, 9, 10, 16 and 17) or for routine control in the other cases (cases 1, 2, 5, 6, 7, 11, 12, 13, 14 and 15). A physical examination was performed on each dog. Fine needle aspirates were taken aseptically from one to three cutaneous lesions per case (23 total cutaneous lesions sampled from all cases studied) and from lymph nodes from all dogs. Cutaneous lesions were analyzed by means of cytological examination and real-time polymerase chain reaction (RT-PCR) in 13 and 15 dogs, respectively. Distant or regional lymph nodes were analyzed by means of cytology in 9 dogs and RT-PCR in all dogs. Cytological direct smears were stained with MayGrünwald-Giemsa and evaluated by microscopy. Samples were taken for diagnostic purposes and, therefore, ethical approval was not needed.
Blood EDTA tubes, syringes with fine needle used for aspiration of lymph nodes and cutaneous lesions, tubes with serum and swabs were stored at 4°C and sent to the laboratory (National Reference Centre for Leishmaniosis – Italy) up to 72 hours after sampling for Leishmania RT-PCR and in some cases for parasite culture. Real-time polymerase chain reaction for detecting Leishmania DNA [17, 18] was performed on the following specimens: one or more cutaneous lesions in 15 dogs (20 total lesions tested), peripheral blood and lymph-node aspirates in all dogs, conjunctival swabs in nine cases and oral swabs in eight cases. Sera were tested for IgG antibodies to L. infantum antigen by the immunofluorescence antibody test (IFAT) .
The IFAT was performed according to Duxbury (1964)  and Badaro (1983)  with some modifications as previously described . The cut off value was established at 1:80 . Seropositive dogs were ranked in three categories based on range of the IFAT antibody titer as follows: low (1:80–1:320), intermediate (1:640–1:1280) and high positive antibody titers (> 1:1280).
DNA extraction and Leishmania real time PCR on clinical samples
DNA extraction of cutaneous lesions, blood, lymph node, conjunctival and oral swabs and Leishmania real time PCR (RT-PCR) were performed as previously described .
Leishmanin skin test
Leishmanin skin test (LST) for the evaluation of a delayed-type hypersensitivity (DTH) reaction was carried out in five cases upon clinical presentation and in three cases during the follow up evaluation (8 to 10 months post treatment). Briefly, 100 μl solution of inactivated suspension of 3×108L. infantum promastigotes/mL in 0.4% phenol-saline (kindly provided by Carmen Cañavate Instituto de Salud Carlos III, Madrid, Spain) were intradermally injected in the skin of the groin. Skin reactions were recorded after 48 and 72 h and an induration or erythematous area > 0.5 cm in diameter was considered positive [22, 23].
Culture and molecular typing of isolates
In-vitro culture was performed on 9 dogs. Culture was carried out on 12 out of 23 cutaneous lesions sampled and on 9 out of 17 lymph-node fine needle aspirates. Parasites were grown in Tobie agar medium modified by Evans with 15% rabbit blood, 5% fetal bovine serum, 250 μg of gentamicin/mL, and 500 μg of 5-fluorocytosine/mL. The cultures were incubated at 25°C for 7 days. In samples that were negative after 7 days of incubation, 1 mL of the culture sample was subcultured in the medium for a further 10 days.
Molecular typing of isolates
DNA was obtained from Leishmania cultures using the QIAamp DNA mini kit (QIAGEN).
For molecular typing analysis, the polymorphism of two different target genes was studied: ITS1 and ITS2 (ribosomal DNA internal transcribed spacers) and haspb (k26) gene (hydrophilic acylated surface protein B).
ITS1 and ITS2 were amplified as described by Kuhls et al. (2005) . Direct sequencing of the ITS1 and ITS2 PCR products and the analysis of the data sequences were performed following the protocol described by Chicharro et al. (2013) .
Haspb (k26) gene was amplified according to the protocol previously described by Haralambous et al. (2008) . PCR products were analyzed by electrophoresis in 2% agarose gel stained with PronaSafe (CONDA) and visualized under ultraviolet light. Product size was estimated with comparison to a 100-bp DNA ladder, and adjusted according to the gene size variability attributed to the number of 42 nucleotide repeated motifs [27, 28].
Treatment and follow up
The treatment protocol that was instituted for patients with papular dermatitis was a non-standard protocol of one dose of N-methylglucamine antimoniate (100 mg/kg SC q24 h) for 25–30 days due to mild disease . Fifteen dogs were treated with N-methylglucamine antimoniate (100 mg/kg SC q24 h) for 25–30 days. Unfortunately, two owners did not agree to perform the treatment protocol mentioned above. In case 11, the treatment offered for the dog was refused by the owner and the dog was rechecked after four months. In case 12, the owner refused antimonial treatment for the dog and the dog was treated with allopurinol (20 mg/kg q24h) for six months.
All dogs were re-visited at the end of therapy (approximately one month after first visit). Unfortunately, monitoring of the dogs after treatment was not so well standardized. Dogs were presented for control visits at different times when owners decided to do a check up at a private veterinary clinic.
Thus, we obtained a long term follow-up (range 6–24 months after clinical presentation) in seven cases based on physical examination and in five of them Leishmania infection was assessed by means of IFAT and Leishmania real-time PCR on blood, lymph node, conjunctival and oral swabs and in three cases also by means of DTH.
Time of diagnosis
Signalment of seventeen dogs studied is listed in Table 1. Half of them were mongrels and their ages ranged from 3.5 to 36 months (mean ± SD 10.3 ± 7.8.months). Eleven out of 17 dogs lived outdoors, 2 indoors and 4 both indoors and outdoors.
On physical examination, solitary or multiple coalescent erythematous, firm and umbilicate non-pruritic papules (diameter 0.2 to 0.5 mm) were observed at various locations on sparsely haired skin areas (Table 1; Figures 1, 2, and 3). In fifteen dogs (88%), papules appeared from September to January and in the two other cases in May and June. In seven cases, cutaneous lesions were chronic from three weeks to six months of duration and, in the other ten cases, lesions were observed as an incidental finding during routine examination. No other abnormalities were found on physical examination, except for two cases where a mild solitary lymphadenomegaly of regional popliteal lymph nodes were noted (cases 8 and 11). PCR was negative in both cases. Cytology of the lymph node revealed reactive hyperplasia (case 8) and no abnormalities (case 11).
Cytological examination of the papules was diagnostic in 8 out of 13 (61.5%) cases. Variable numbers of intracellular and /or extracellular Leishmania amastigotes associated with neutrophilic-macrophagic and/or lymphoplasmocellullar inflammation were observed (Figure 4). In the cutaneous lesions sampled, cytology revealed the presence of Leishmania amastigotes in 14 out of 19 lesions (68.4%) (Table 2). RT-PCR performed on cutaneous lesions was positive in 14 out of 15 dogs (93.3%) with positive results in 19 out of 20 lesions (95%) sampled and a parasite load ranging from 20 to 60000 parasite/sample. The diagnosis of Leishmania infection was confirmed based on cytology or RT-PCR in all cases. Parasite isolation from cutaneous lesions was obtained only in 3 out of 9 dogs (33.3%) and 5 out of 13 cutaneous lesions sampled (38.4%).
Results of IFAT, RT-PCR and culture on other tissues are displayed in Table 3. The majority of dogs were seronegative (12 out of 17, 70.6%) and the remaining were low positive with antibody titers ranging from 1:80 to 1:320. Lymph-node cytology revealed reactive hyperplasia in two dogs (case 1 and 8), no abnormalities in five cases (case 3, 4, 6, 10 and 11) and it was non-diagnostic in the remaining two cases (case 2 and 9). Lymph-node culture was negative in all nine dogs.
LST was positive in all 5 tested cases at 48 h reading with a mean ± SD diameter of 1.50 ± 0.46 cm (range 1 – 2.25 cm) and was positive in 4/5 of the cases at 72 h reading with a mean ± SD diameter of 1.54 ± 0.40 (range 1.15 – 2 cm).
Molecular characterization was performed in five L. infantum strains isolated from three dogs with skin lesions: case 2 (two samples), case 9 (one sample) and case 10 (two samples) (Figure 5). ITS-1 and ITS-2 were sequenced and all L. infantum strains were identified as ITS type A. On the other hand, the polymorphism of the haspb (k26) sequence was determined by analysis of the size of the PCR products and adjusted according to the haspb (k26) gene present repeated motifs of 42 nucleotides. Strains isolated from cases 2, 9 and 10 revealed k26 PCR products of 626 bp, 962 bp and 371 bp, respectively. No differences were observed between strains isolated from the same dog.
The dog that was not treated (case 11) was evaluated four months later. On physical examination, the cutaneous lesion was still present but slightly flattened. In addition, antibody levels decreased from a low positive antibody titer of 1:160 at time of diagnosis to a negative antibody titer of 1:40 at recheck (4 months later). Blood, lymph node and conjunctival swab RT-PCRs were negative 4 months later as well. The dog (case 12), treated only with allopurinol for six months (January- August 2010), remained seronegative and blood, lymph-node and conjunctival swabs were also negative at three and eight months post diagnosis. The dog seroconverted at 10 months (November 2010) (IFAT 1:160) and clinical examination and full CBC and biochemistry profile showed no clinicopathological abnormalities. A treatment with allopurinol was repeated for eight more months (until August 2011). On July 2011, serology was negative. After the second course of therapy, this dog was regularly monitored every six months by IFAT and remained seronegative and clinically healthy in the following year. The last IFAT, performed on March 2012, was still negative.
All dogs treated with meglumine antimoniate were clinically evaluated after 25 days of therapy and the cutaneous lesions had disappeared or changed to a depigmented, flattened scar.
Six out of 17 dogs were only revisited after 25 days of therapy with meglumine antimoniate and then, these dogs were lost to follow up (cases 2, 5, 6, 8, 9 and 13). Five dogs were also assessed for Leishmania infection between two and five months post therapy (cases 10, 12, 14 and 16). They remained seronegative (cases 10, 12, 16) or showed a decrease in antibody titers (cases 14 and 15: a diagnostic antibody titer of 1:320 for both cases and post therapy antibody titers of 1:40 and 1:80, respectively). Moreover, blood, lymph node and conjunctival RT-PCRs were also negative. One dog was only clinically evaluated five months post therapy and the dog was in good health with a normal physical examination (case 17).
Long term follow up (6–24 months after therapy) was obtained in seven dogs (cases 1, 3, 4, 7, 12, 14 and 15). Two of them (cases 14 and 15) were assessed only by physical examination and there were no clinical abnormalities. Five dogs were also rechecked for Leishmania infection. Three dogs (cases 1, 3, 7) remained negative for both IFAT and RT-PCR performed on blood, lymph-node, conjunctival and oral swabs. One dog (case 4) showed a reactive lymph-node with positive RT-PCR results (n. 300 Leishmania/sample) and culture after 9 months but the dog was negative 4 months later by lymph node RT-PCR. A DTH test was performed in three dogs (cases 1, 3, 4) during the follow up period. A positive result was observed in all three cases with a mean ± SD diameter of 2.36 ± 0.71 cm (range 1.6-2.5 cm) at 48 h and a mean ± SD diameter of 2.25 ± 0.86 (range 1.75-3.25 cm) at 72 h.
This study describes seventeen cases of papular dermatitis due to Leishmania infection in dogs living in a highly endemic area for canine leishmaniosis (Sicily) and is the largest published case series concerning this cutaneous clinical manifestation of Leishmania infection. Nodular lesions caused by Leishmania infection were previously described to include lesions of variable size from a few millimetres to 10 cm in diameter . More recently, papular and nodular dermatitis were differentiated into two distinct dermatological forms of cutaneous lesions caused by L. infantum as described in the literature [13–15]. In fact, the lack of progression of these persistent papules to nodules characterizes clinically this benign form of dermatitis due to Leishmania infection in the present study and in previous studies [13–16]. It is noteworthy that in 58% of this case series the papular lesions were not noticed by the owner and were incidentally found during the physical examination and, therefore, these cutaneous lesions might be underdiagnosed. The young age, the distribution and evolution of papular lesions, and the clinical findings of these dogs are similar to those reported in the previous studies [13–16].
Persistent, solitary or multiple coalescent erythematous and firm umbilicate non-pruritic papular lesions were located on sparsely haired skin areas and the majority of dogs (82%) were one year of age or less. The presence of papular lesions in young dogs might be the direct consequence of the first contact of an immunocompetent host with the parasite inoculated by sandflies in the skin. This occurred mainly from September to January potentially some months after the end of the classical sandfly season previously reported by Noli et al., (2006) . We hypothesize that the onset of cutaneous lesions at the end of or after the sandfly season might occur after a silent phase of parasite amplification, as described in mice experimentally infected by intradermal inoculation with a low dose of Leishmania major promastigotes . However, a prolonged duration of P. pernicious activity until November has been demonstrated in some Italian provinces . The two most prevalent sandfly species found in Sicily are Phlebotomus perfiliewi and P. pernicious, however, studies about seasonal activity of sandflies in Sicily are lacking [30–32]. Other studies reported papular dermatitis in summer months [13–15] as we observed in two cases in our study.
In this study, papular dermatitis was associated with no other clinical signs (excluded two cases of mild regional lymph node enlargement), absence of or low levels of humoral immunity and a predominant parasite specific cellular immunity in all dogs studied as previously reported . In addition, all dogs treated with only meglumine antimoniate that were followed-up in the long term promptly cured with antimonial therapy, did not develop any other clinical manifestations, did not seroconvert and they probably contained the parasite infection, suggesting that papular dermatitis is associated with competent specific immunity and has an excellent prognosis. The only dog treated with a six month course of therapy with allopurinol seroconverted with a low antibody level which required a second course of therapy but remained clinically healthy and reverted to a negative persistent antibody status after the second course of therapy. Thus, papular dermatitis is considered a mild clinical manifestation of this infection (stage I) when accompanied with negative or low antibody levels and no laboratory abnormalities . Similar benign forms of cutaneous leishmaniosis have been described in human beings and horses [33–35]. In human beings, this is the most common form of disease caused by L. infantum in Europe. Patients present one or more localized and ulcerated skin lesions, which may also self-cure and are mainly associated with a positive delayed type hypersensitivity (DTH) response  as reported previously in dogs with papular dermatitis  and as described in the present study in one dog which self-cured. Leishmania infantum has also been reported as a causative agent of cutaneous leishmaniosis in the horse in various European countries, including Spain, Portugal and Germany [33–35]. The skin lesions reported were solitary or multiple papules or nodules, most commonly present in the head, pinnae, scrotum, legs and neck. Even in horses self-healing from the cutaneous lesions after a short period of time there is an association with a strong Leishmania-specific cellular immunity and a low humoral response [33, 34].
As mentioned previously, papular dermatitis due to Leishmania in young dogs resembles the typical form of localized cutaneous leishmaniosis, mainly seen in children between 10 and 15 years of age. The lesion begins as a single, asymptomatic, pink or red papule, which is 3–5 mm in diameter, found at the site of the sandfly bite. However, unlike the canine species, the papule slowly evolves to a firm, inflamed, smooth nodule that enlarges progressively and eventually ulcerates, four to twelve weeks after its appearance. Five to twelve months after the initial appearance, the nodulo-ulcerative lesions begin to regress from the center and resolve completely, leaving a scar . In addition, it seems that in human localized cutaneous leishmaniosis the number of parasites present in the lesions is inversely proportional to the duration of the lesion . Unfortunately, we could not corroborate this finding in the present study due to the limited number of dogs where duration of the lesions was known.
This study evaluated, for the first time, the extent of dissemination of Leishmania infection in dogs with papular dermatitis as only clinical manifestation. In most of the dogs studied, the only evidence of parasitic infection was in the cutaneous lesions and not in other tissues sampled such as blood, lymph node, oral or conjunctival swabs, at both time of diagnosis and follow-up. Therefore, dogs with papular dermatitis and with the immunological profile described in the present study appear to contain the Leishmania infection in the skin.
Some dogs were positive by conjunctival swab PCRs even if they had a very low parasite load. PCR on conjunctival swabs has shown good sensitivity (92%) and specificity (100%) in the diagnosis of classical severe CanL [38, 39]. Experimentally infected dogs were found to be positive by PCR on conjunctival swabs as early as 45 days post infection (83%) and before seroconversion [38–40]. In addition, a previous study suggested the use of PCR on conjunctival swabs as a non-invasive alternative diagnostic method to lymph node PCR . These findings suggest that Leishmania infection in some dogs is probably not limited to the site of inoculation even in dogs that might restrict the infection and, therefore, there are other tissues where parasite infection might be present.
Only one dog was positive on oral swab PCR. The detection of Leishmania DNA in oral swabs has been described in humans with visceral leishmaniosis and in asymptomatic individuals  as well as in dogs without any evident oral lesions . A recent study performed in Europe reported low sensitivity of Leishmania PCR in oral swabs in both infected or sick dogs without oral lesions (at least stage II of disease) [17, 42], while in Brazil a good sensitivity was found . Differences between these studies might be due to the existence of other Leishmania species in Brazil that can be detected by PCR and the inclusion of sick dogs with oral or mucosal lesions in the study carried out in Brazil . Evidence to date indicates that in Europe, the sensitivity of the detection of Leishmania DNA in oral swabs for diagnosis of subclinically infected or sick dogs appears to be low and not very useful [17, 42].
In this study, RT-PCR has been tested as a diagnostic tool to detect Leishmania infection in fine needle aspiration of cutaneous lesions and was found more sensitive than cytological evaluation. In the past, the presence of Leishmania parasites in skin lesions was investigated using cytological examination, in vitro culture or immunohistochemistry on skin biopsy samples. The low number of amastigotes in some samples can make cytological and histopathological diagnosis difficult [14, 44, 45]. The application of immunohistochemical techniques has given better results in the diagnosis of cutaneous leishmaniosis despite the limitations of this technique due to the presence of false negative cases . In some of our cases, cytological evaluation was not diagnostic probably due to either the small size of the lesions or the hemodilution of the sample. Recently, PCR on paraffin-embedded, frozen skin biopsy specimens or dermal scraping for detection of Leishmania amastigotes in cutaneous lesions has been described in both veterinary and medical literature. PCR sensitivity ranged from 81 to 100%, when compared to the presence of Leishmania parasites in culture, cytological and histopathological examination [46–49]. In a recent study, a PCR performed on serous material collected by puncture from cutaneous lesions in human patients with CL demonstrated good concordance with parasitological results . It is worthy to mention that although a positive PCR result from a papule from a dog living in an endemic area does not necessarily mean that Leishmania is the cause of the papule, due to the high frequency of positive PCR in the skin of infected dogs . However, the list of differential diagnoses of papules in dogs is low and, therefore, when the clinical picture and cytological or histological findings are consistent with Leishmania infection, the most likely cause of papules is Leishmania infection, even if diagnosed by PCR.
There is limited information on the use of in vitro culture for the diagnosis of Leishmania infection in dogs in a clinical setting. The majority of studies have evaluated the use of culture from lymph node, bone marrow and spleen samples [51–54], while investigations on the use of culture from skin or blood samples are less common [55, 56]. Although culture is a highly specific diagnostic test, this technique is less frequently used at present for various reasons including delay in results, susceptibility to microbiological contamination and in general poor sensitivity compared to molecular techniques. In addition, molecular and/or isoenzymatic techniques are required for species identification . In the present study, only 33% of cultured cutaneous lesions were positive, confirming the low sensitivity of this technique. It is important to highlight that a positive skin culture is most likely in dogs with clinical illness , even with mild disease, as shown from results of the dogs evaluated in the present study. A positive skin culture is less likely in subclinically infected dogs .
Although in vitro culture appears not to be useful for diagnostic purposes, molecular typing of L. infantum isolates is an extremely useful taxonomic tool that contributes to better understanding of the epidemiological and pathogenetic aspects of leishmanioses. Molecular genotyping of L. infantum strains isolated from papular dermatitis showed that all five samples analysed were L. infantum ITS type A, which is a very common ITS sequence type mainly described in human isolates with VL and CL from the Mediterranean basin, including Italy [24, 25]. To the best knowledge of the authors, only two previous canine isolates (MON-108 from France and MON-77 from Spain) have undergone molecular typing by ITS sequence analysis resulting in ITS type A and type B/A, respectively . Haspb characterization revealed polymorphism in the present study with three different gene sizes (626, 962 and 371 bp) for three different dogs. The 626 bp haspb gene size is commonly described in the Mediterranean basin both in humans and dogs [25, 26]. The 962 bp haspb gene size is also reported in the Mediterranean basin in humans mainly with VL . The 385 bp haspb gene size is encountered in non MON-1 canine isolates from the Mediterranean basin including Sicily  and it is probably identical to the same fragment as the 371 bp haspb gene size described in the present study due to the fact that, in the previous study, adjustment according to the gene size variability attributed to the number of 42 nucleotide repeated motifs was not performed after electrophoresis . Multilocus enzyme electrophoresis, the classical reference method for Leishmania typing  was not performed due to the fact that it is laborious and expensive and, therefore, in the present study, it was not possible to match the MON system with the molecular typing results. Unfortunately, the number of analysed strains was very low and it was not possible to establish any type of correlation between the genotypes identified and this distinctive form of papular dermatitis in dogs.
In conclusion, papular dermatitis due to L. infantum is an underestimated clinical occurrence associated with a predominant parasite specific cellular immunity and low humoral response, seen in young dogs in endemic areas. This clinical entity is confirmed to be a mild cutaneous clinical manifestation of Leishmania infection with restricted parasite dissemination and excellent prognosis when treated for one month with antimonials. Cytological evaluation of papules in dogs living in endemic areas is a useful technique to evaluate inflammation and presence or absence of Leishmania amastigotes. However, due to the higher sensitivity of RT-PCR technique in cutaneous aspirates, RT-PCR can be used as a non- invasive method to routinely evaluate persistent papules, if Leishmania infection is suspected, in cases in which parasites are not visualized by cytology.
- haspb gene:
Hydrophilic acylated surface protein B
Immunofluorescence antibody test
Ribosomal DNA internal transcribed spacers
Leishmanin skin test
Real-time polymerase chain reaction
Disseminated visceral leishmaniosis.
Reithinger R, Dujardin JC, Louzir H, Pirmez C, Alexander B, Brooker S: Cutaneous leishmaniasis. Lancet Infect Dis. 2007, 7: 581-596. 10.1016/S1473-3099(07)70209-8.
Baneth G, Solano-Gallego L: Global aspects of leishmaniosis: canine leishmaniosis. Infectious disease of the dog and cat. Edited by: Greene CE. 2012, St. Louis: Elsevier saunders, 734-746. 4
Sellon RK, Menard MM, Meuten DJ, Lengerich EJ, Steurer FJ, Breitschwerdt EB: Endemic visceral leishmaniasis in a dog from Texas. J Vet Intern Med. 1993, 7: 16-19. 10.1111/j.1939-1676.1993.tb03163.x.
Gaskin AA, Schantz P, Jackson J, Birkenheuer A, Tomlinson L, Gramiccia M, Levy M, Steurer F, Kollmar E, Hegarty BC, Ahn A, Breitschwerdt EB: Visceral leishmaniasis in a New York foxhound kennel. J Vet Intern Med. 2002, 16: 34-44. 10.1111/j.1939-1676.2002.tb01604.x.
Baneth G, Koutinas AF, Solano-Gallego L, Bourdeau P, Ferrer L: Canine leishmaniosis - new concepts and insights on an expanding zoonosis: part one. Trends Parasitol. 2008, 24: 324-330. 10.1016/j.pt.2008.04.001.
Solano-Gallego L, Morell P, Arboix M, Alberola J, Ferrer L: Prevalence of Leishmania infantum infection in dogs living in an area of canine leishmaniasis endemicity using PCR on several tissues and serology. J Clin Microbiol. 2001, 39: 560-563. 10.1128/JCM.39.2.560-563.2001.
Solano-Gallego L, Koutinas A, Miro G, Cardoso L, Pennisi MG, Ferrer L, Bourdeau P, Oliva G, Baneth G: Directions for the diagnosis, clinical staging, treatment and prevention of canine leishmaniosis. Vet Parasitol. 2009, 165: 1-18. 10.1016/j.vetpar.2009.05.022.
Ciaramella P, Oliva G, Luna RD, Gradoni L, Ambrosio R, Cortese L, Scalone A, Persechino A: A retrospective clinical study of canine leishmaniasis in 150 dogs naturally infected by Leishmania infantum. Vet Rec. 1997, 141: 539-543. 10.1136/vr.141.21.539.
Ferrer L, Rabanal R, Fondevila D, Ramos JA, Domingo M: Skin lesions in canine leishmaniasis. J Small Anim Pract. 1988, 29: 381-388. 10.1111/j.1748-5827.1988.tb02298.x.
Blavier A, Keroack S, Denerolle P, Goy-Thollot I, Chabanne L, Cadore JL, Bourdoiseau G: Atypical forms of canine leishmaniosis. Vet J. 2001, 162: 108-120. 10.1053/tvjl.2000.0556.
Font A, Roura X, Fondevila D, Closa JM, Mascort J, Ferrer L: Canine mucosal leishmaniasis. J Am Anim Hosp Assoc. 1996, 32: 131-137.
Koutinas AF, Scott DW, Kantos V, Lekkas S: Skin lesions in canine leishmaniasis (Kala-Azar): a clinical and histopathological study on 22 spontaneous cases in Greece. Vet Dermatol. 1992, 3: 121-130. 10.1111/j.1365-3164.1992.tb00158.x.
Bottero E, Poggi M, Viglione M: Lesioni papulari indotte da Leishmania spp. in 8 cani giovani. Veterinaria. 2006, 1: 33-36.
Noli C, Cornegliani L: Leishmaniosi bottorniforme. Descrizione di cinque casi italiani e confronto con la letteratura. Quaderni di dermatologia. 2006, 11: 23-26.
Ordeix L, Solano-Gallego L, Fondevila D, Ferrer L, Fondati A: Papular dermatitis due to Leishmania spp. infection in dogs with parasite-specific cellular immune responses. Vet Dermatol. 2005, 16: 187-191. 10.1111/j.1365-3164.2005.00454.x.
Catarsini O, Pugliese A, Niutta PP, Pantano V, Domina F, Pennisi MG, Lombardo A: Canine leishmaniasis: description of unusual lesions. Atti della società italiana di scienze veterinarie vol. 45. 1991, 1371-1374.
Lombardo G, Pennisi MG, Lupo T, Migliazzo A, Capri A, Solano-Gallego L: Detection of Leishmania infantum DNA by real-time PCR in canine oral and conjunctival swabs and comparison with other diagnostic techniques. Vet Parasitol. 2012, 184: 10-17. 10.1016/j.vetpar.2011.08.010.
Vitale F, Reale S, Vitale M, Petrotta E, Torina A, Caracappa S: TaqMan-based detection of Leishmania infantum DNA using canine samples. Ann N Y Acad Sci. 2004, 1026: 139-143. 10.1196/annals.1307.018.
Reale S, Maxia L, Vitale F, Glorioso NS, Caracappa S, Vesco G: Detection of Leishmania infantum in dogs by PCR with lymph node aspirates and blood. J Clin Microbiol. 1999, 37: 2931-2935.
Duxbury RE, Sadun EH: Fluorescent antibody test for the serodiagnosis of visceral leishmaniasis. Am J Trop Med Hyg. 1964, 13: 525-529.
Badaro R, Reed SG, Carvalho EM: Immunofluorescent antibody test in American visceral leishmaniasis: sensitivity and specificity of different morphological forms of two Leishmania species. Am J Trop Med Hyg. 1983, 32: 480-484.
Pinelli E, Killick-Kendrick R, Wagenaar J, Bernadina W, del Real G, Ruitenberg J: Cellular and humoral immune responses in dogs experimentally and naturally infected with Leishmania infantum. Infect Immun. 1994, 62: 229-235.
Solano-Gallego L, Llull J, Ramos G, Riera C, Arboix M, Alberola J, Ferrer L: The Ibizian hound presents a predominantly cellular immune response against natural Leishmania infection. Vet Parasitol. 2000, 90: 37-45. 10.1016/S0304-4017(00)00223-5.
Kuhls K, Mauricio IL, Pratlong F, Presber W, Schonian G: Analysis of ribosomal DNA internal transcribed spacer sequences of the Leishmania donovani complex. Microbes Infect. 2005, 7: 1224-1234. 10.1016/j.micinf.2005.04.009.
Chicharro C, Llanes-Acevedo IP, Garcia E, Nieto J, Moreno J, Cruz I: Molecular typing of Leishmania infantum isolates from a leishmaniasis outbreak in Madrid, Spain, 2009 to 2012. Euro Surveill. 2013, 18: 20545-
Haralambous C, Antoniou M, Pratlong F, Dedet JP, Soteriadou K: Development of a molecular assay specific for the Leishmania donovani complex that discriminates L. donovani/Leishmania infantum zymodemes: a useful tool for typing MON-1. Diagn Microbiol Infect Dis. 2008, 60: 33-42. 10.1016/j.diagmicrobio.2007.07.019.
Zackay A, Nasereddin A, Takele Y, Tadesse D, Hailu W, Hurissa Z, Yifru S, Weldegebreal T, Diro E, Kassahun A, Hailu A, Jaffe CL: Polymorphism in the HASPB repeat region of East African Leishmania donovani strains. PLoS Negl Trop Dis. 2013, 7: e2031-10.1371/journal.pntd.0002031.
Bhattacharyya T, Boelaert M, Miles MA: Comparison of visceral leishmaniasis diagnostic antigens in African and Asian Leishmania donovani reveals extensive diversity and region-specific polymorphisms. PLoS Negl Trop Dis. 2013, 7: e2057-10.1371/journal.pntd.0002057.
Belkaid Y, Mendez S, Lira R, Kadambi N, Milon G, Sacks D: A natural model of Leishmania major infection reveals a prolonged “silent” phase of parasite amplification in the skin before the onset of lesion formation and immunity. J Immunol. 2000, 165: 969-977.
Rossi E, Bongiorno G, Ciolli E, Di Muccio T, Scalone A, Gramiccia M, Gradoni L, Maroli M: Seasonal phenology, host-blood feeding preferences and natural Leishmania infection of Phlebotomus perniciosus (Diptera, Psychodidae) in a high-endemic focus of canine leishmaniasis in Rome province, Italy. Acta Trop. 2008, 105: 158-165. 10.1016/j.actatropica.2007.10.005.
Gomez-Saladin E, Doud CW, Maroli M: Short report: surveillance of Leishmania sp. among sand flies in Sicily (Italy) using a fluorogenic real-time polymerase chain reaction. Am J Trop Med Hyg. 2005, 72: 138-141.
Torina A, Sole M, Reale S, Vitale F, Caracappa S: Use of phlebotomine sand flies as indicator of Leishmania prevalence in an endemic area. Ann N Y Acad Sci. 2008, 1149: 355-357. 10.1196/annals.1428.017.
Solano-Gallego L, Fernandez-Bellon H, Serra R, Gallego M, Ramis A, Fondevila D, Ferrer L: Cutaneous leishmaniosis in three horses in Spain. Equine Vet J. 2003, 35: 320-323.
Fernandez-Bellon H, Solano-Gallego L, Bardagi M, Alberola J, Ramis A, Ferrer L: Immune response to Leishmania infantum in healthy horses in Spain. Vet Parasitol. 2006, 135: 181-185. 10.1016/j.vetpar.2005.09.007.
Koehler K, Stechele M, Hetzel U, Domingo M, Schonian G, Zahner H, Burkhardt E: Cutaneous leishmaniosis in a horse in southern Germany caused by Leishmania infantum. Vet Parasitol. 2002, 109: 9-17. 10.1016/S0304-4017(02)00246-7.
Akilov OE, Khachemoune A, Hasan T: Clinical manifestations and classification of Old World cutaneous leishmaniasis. Int J Dermatol. 2007, 46 (2): 132-142. 10.1111/j.1365-4632.2007.03154.x.
Jara M, Adaui V, Valencia BM, Martinez D, Alba M, Castrillon C, Cruz M, Cruz I, Van der Auwera G, Llanos-Cuentas A, Dujardin JC, Arevalo J: Real-time PCR assay for detection and quantification of Leishmania (Viannia) organisms in skin and mucosal lesions: exploratory study of parasite load and clinical parameters. J Clin Microbiol. 2013, 51 (6): 1826-1833. 10.1128/JCM.00208-13.
Pilatti MM, Ferreira Sde A, de Melo MN, de Andrade AS: Comparison of PCR methods for diagnosis of canine visceral leishmaniasis in conjunctival swab samples. Res Vet Sci. 2009, 87: 255-257. 10.1016/j.rvsc.2009.02.005.
Strauss-Ayali D, Jaffe CL, Burshtain O, Gonen L, Baneth G: Polymerase chain reaction using noninvasively obtained samples, for the detection of Leishmania infantum DNA in dogs. J Infect Dis. 2004, 189: 1729-1733. 10.1086/383281.
Di Muccio T, Veronesi F, Antognoni MT, Onofri A, Piergili Fioretti D, Gramiccia M: Diagnostic value of conjunctival swab sampling associated with nested PCR for different categories of dogs naturally exposed to Leishmania infantum infection. J Clin Microbiol. 2012, 50: 2651-2659. 10.1128/JCM.00558-12.
Vaish M, Mehrotra S, Chakravarty J, Sundar S: Noninvasive molecular diagnosis of human visceral leishmaniasis. J Clin Microbiol. 2011, 49: 2003-2005. 10.1128/JCM.00130-11.
Solano-Gallego L, Kyriacou C, Yasur D, Villanueva-Saz S, Eyal O, Baneth G: A cross-sectional study on Leishmania infantum infection by serology and non-invasive PCR in sick and clinically healthy dogs from Cyprus. 8th CVBD world forum proceedings. 2013, 42-
Ferreira Sde A, Almeida GG, Silva Sde O, Vogas GP, Fujiwara RT, de Andrade AS, Melo MN: Nasal, oral and ear swabs for canine visceral leishmaniasis diagnosis: new practical approaches for detection of Leishmania infantum DNA. PLoS Negl Trop Dis. 2013, 7: e2150-10.1371/journal.pntd.0002150.
Ferrer L, Rabanal RM, Domingo M, Ramos JA, Fondevila D: Identification of Leishmania donovani amastigotes in canine tissues by immunoperoxidase staining. Res Vet Sci. 1988, 44: 194-196.
Roura X, Fondevila D, Sanchez A, Ferrer L: Detection of Leishmania infection in paraffin-embedded skin biopsies of dogs using polymerase chain reaction. J Vet Diagn Invest. 1999, 11: 385-387. 10.1177/104063879901100420.
Medeiros AC, Rodrigues SS, Roselino AM: Comparison of the specificity of PCR and the histopathological detection of Leishmania for the diagnosis of American cutaneous leishmaniasis. Braz J Med Biol Res. 2002, 35: 421-424. 10.1590/S0100-879X2002000400002.
Ampuero J, Rios AP, Carranza-Tamayo CO, Romero GA: Genus-specific kinetoplast-DNA PCR and parasite culture for the diagnosis of localised cutaneous leishmaniasis: applications for clinical trials under field conditions in Brazil. Mem Inst Oswaldo Cruz. 2009, 104: 992-997.
Belli A, Rodriguez B, Aviles H, Harris E: Simplified polymerase chain reaction detection of new world Leishmania in clinical specimens of cutaneous leishmaniasis. Am J Trop Med Hyg. 1998, 58: 102-109.
Lemrani M, Hamdi S, Laamrani A, Hassar M: PCR detection of Leishmania in skin biopsies. J Infect Dev Ctries. 2009, 3: 115-122.
Hajjaran H, Vasigheh F, Mohebali M, Rezaei S, Mamishi S, Charedar S: Direct diagnosis of Leishmania species on serosity materials punctured from cutaneous leishmaniasis patients using PCR-RFLP. J Clin Lab Anal. 2011, 25: 20-24. 10.1002/jcla.20377.
Maia C, Ramada J, Cristovao JM, Goncalves L, Campino L: Diagnosis of canine leishmaniasis: conventional and molecular techniques using different tissues. Vet J. 2009, 179: 142-144. 10.1016/j.tvjl.2007.08.009.
de Fatima Madeira M, de O Schubach A, Schubach TM, Pereira SA, Figueiredo FB, Baptista C, Leal CA, Melo CX, Confort EM, Marzochi MC: Post mortem parasitological evaluation of dogs seroreactive for Leishmania from Rio de Janeiro, Brazil. Vet Parasitol. 2006, 138: 366-370. 10.1016/j.vetpar.2006.01.059.
Rosypal AC, Troy GC, Duncan RB, Zajac AM, Lindsay DS: Utility of diagnostic tests used in diagnosis of infection in dogs experimentally inoculated with a North American isolate of Leishmania infantum infantum. J Vet Intern Med. 2005, 19: 802-809. 10.1892/0891-6640(2005)19[802:UODTUI]2.0.CO;2.
Reis LE, Coura-Vital W, Roatt BM, Bouillet LE, Ker HG, de Brito RC F, Resende Dde M, Carneiro M, Giunchetti RC, Marques MJ, Carniero CM, Reis AB: Molecular diagnosis of canine visceral leishmaniasis: a comparative study of three methods using skin and spleen from dogs with natural Leishmania infantum infection. Vet Parasitol. 2013, 197: 498-503. 10.1016/j.vetpar.2013.07.006.
de Almeida AB, Sousa VR, Sorte Eda C, Figueiredo FB, de Paula DA, Pimentel MF, Dutra V, Madeira Mde F: Use of parasitological culture to detect Leishmania (Leishmania) chagasi in naturally infected dogs. Vector Borne Zoonotic Dis. 2011, 11: 1555-1560. 10.1089/vbz.2011.0723.
Chargui N, Haouas N, Gorcii M, Lahmar S, Guesmi M, Ben Abdelhafidh A, Mezhoud H, Babba H: Use of PCR, IFAT and in vitro culture in the detection of Leishmania infantum infection in dogs and evaluation of the prevalence of canine leishmaniasis in a low endemic area in Tunisia. Parasite. 2009, 16: 65-69. 10.1051/parasite/2009161065.
Fernandez-Bellon H, Solano-Gallego L, Rodriguez-Cortes A, Ferrer L, Gallego M, Alberola J, Ramis A: Little evidence of seasonal variation of natural infection by Leishmania infantum in dogs in Spain. Vet Parasitol. 2008, 155: 32-36. 10.1016/j.vetpar.2008.04.009.
Rioux JA, Lanotte G, Serres E, Pratlong F, Bastien P, Perieres J: Taxonomy of Leishmania. Use of isoenzymes. Suggestions for a new classification. Ann Parasitol Hum Comp. 1990, 65: 111-125.
The authors thank Dr. Carmen Cañavate (Instituto de Salud Carlos III, Madrid, Spain) for kindly providing L. infantum promastigotes for leishmanin skin test; Laura Perillo for her collaboration in cytopathology; Antonino Lombardo (Studio Veterinario Lombardo, Mascalucia, CT, Italy) for his collaboration in collecting the clinical cases. The authors are grateful to Francesca Soutter (Royal Veterinary College) for the English revision of the manuscript. The authors are also grateful to technicians of the CreNaL laboratory, IZS, Sicily for their technical help. The authors also thank the reviewers for the constructive critical revision of the manuscript.
Laia Solano-Gallego holds a Ramón y Cajal senior researcher contract awarded by the Spanish Ministerio de Economia y Competitividad and the European Social Fund.
Publication of the CVBD9 thematic series has been sponsored by Bayer HealthCare - Animal Health division.
The authors declare that they have no competing interests.
GL designed the study, collected the cases, contributed with data analysis and interpretation and wrote the manuscript. TL performed serological, molecular analysis and culture. CC performed molecular typing of isolates and contributed with data analysis and interpretation. MGP contributed with data analysis and interpretation and performed a critical revision of the manuscript. LSG designed the study, contributed with data analysis and interpretation and wrote the manuscript. All authors read and approved the final version of the manuscript.