Abstract
To date, sand flies (Phlebotominae) are the only recognized biological vectors of Leishmania infantum, the causative agent of human visceral leishmaniasis, which is endemic in the Mediterranean basin and also widespread in Central and South America, the Middle East, and Central Asia. Dogs are the main domestic reservoir of zoonotic visceral leishmaniasis, and the role of secondary vectors such as ticks and fleas and particularly Rhipicephalus sanguineus (the brown dog tick) in transmitting L. infantum has been investigated. In the present paper, the presence of Leishmania DNA was investigated in questing Ixodes ricinus ticks collected from 4 rural areas included in three parks of the Emilia-Romagna Region (north-eastern Italy), where active foci of human visceral leishmaniasis have been identified. The analyses were performed on 236 DNA extracts from 7 females, 6 males, 72 nymph pools, and 151 larvae pools. Four samples (1.7%) (i.e., one larva pool, 2 nymph pools, and one adult male) tested positive for Leishmania kDNA. To the best of our knowledge, this is the first report of the presence of Leishmania kDNA in questing I. ricinus ticks collected from a rural environment. This finding in unfed larvae, nymphs, and adult male ticks supports the hypothesis that L. infantum can have both transstadial and transovarial passage in I. ricinus ticks. The potential role of I. ricinus ticks in the sylvatic cycle of leishmaniasis should be further investigated.
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Introduction
Leishmania infantum (Kinetoplastea, Trypanosomatida) is the causative agent of human visceral leishmaniasis, an important zoonosis endemic in the Mediterranean basin and also widespread in Central and South America, the Middle East, and Central Asia (Alvar et al. 2012). The parasite is naturally transmitted to humans by phlebotomine sand flies and, in the peridomestic cycle, the dog is traditionally recognized as a reservoir (Podaliri Vulpiani et al. 2011), for its high susceptibility to the infection and heavy skin parasitism (Dantas-Torres 2007).
Sand flies are the only recognized biological vectors for L. infantum, and their rapid geographical spread is followed by the spread of leishmaniasis into previously free areas (Dujardin et al. 2008), although secondary routes of transmission (i.e., transfusions, vertical in utero transmission, and venereal transmission) of little epidemiological relevance have been reported in dogs (de Freitas et al. 2006; Silva et al. 2009; Boggiatto et al. 2011). However, a possible role of secondary vectors such as ticks and fleas has been suggested (Coutinho et al. 2005; 2007). In particular, the brown dog tick Rhipicephalus sanguineus has received a lot of attention mainly due to its parasitic life cycle and its close relationship with dogs in both rural and urban areas, being highly adapted to live within human dwellings (Dantas-Torres 2010). Although a considerable amount of research has been carried out to investigate the presence of L. infantum in R. sanguineus collected from dogs (Colombo et al. 2010; Dantas-Torres et al. 2010a; Solano-Gallego et al. 2012; Campos and Costa 2014; Medeiros-Silva et al. 2015) and possible transmission routes (e.g., ticks bites, ingestion of infected ticks) (McKenzie 1984; Coutinho et al. 2005), their role in the transmission of L. infantum has been debated (Otranto and Dantas-Torres 2010) and is still questioned. L. infantum DNA was also detected in the castor bean tick Ixodes ricinus: particularly, Trotta et al. (2012) found it in ticks collected from dogs in Central Italy, and subsequently Salvatore et al. (2014) detected it in I. ricinus from both dogs and cats in Northern Italy, areas where human visceral leishmaniasis is endemic. To the best of our knowledge, no previous research has been performed to establish the presence of Leishmania spp. in questing ticks from rural environments. The present study is focused on the search of Leishmania spp. in I. ricinus questing ticks collected from three parks of Emilia-Romagna region (northeastern Italy), in hilly areas where human visceral leishmaniasis has long been described.
Material and methods
Sampling
The analyses were performed on DNA extracts from questing Ixodes ricinus ticks collected from April to October 2010 in 4 sites within 3 parks of the Emilia-Romagna region (Fig. 1). The parks are located along the hilly area of the Apennines, where the presence of autochthonous cases of leishmaniasis has been described in both humans and dogs (Mollicone et al. 2003; Varani et al. 2013). The area is characterized by a series of gypsum outcrops, closed valleys, cliffs, forested mountains, and gray calanques alternated with farmland. The sampling sites are natural pathways and picnic areas with habitual human attendance. Questing ticks were collected every 15 days by continuously flagging with a 1 m2 white cotton cloth, from transects of 20 m along the uphill side of the pathways, usually reported as having higher tick density than the downhill side, while the picnic areas were flagged completely as described in detail by Aureli et al. (2015). Collected ticks were preserved in 70% ethanol at room temperature. Following morphological identification performed according to Manilla (1998) and Iori et al. (2005), ticks (individual adults, and pools consisting of either 5 nymphs or 10 larvae) were processed for DNA extraction as described by Aureli et al. (2015). Overall, 236 DNA extracts from 7 females, 6 males, 72 nymphs pools (i.e., 380 nymphs) and 151 larvae pools (i.e., 1510 larvae) were analyzed.
DNA analysis
To detect the presence of Leishmania kDNA, a real-time PCR protocol was performed targeting a 71-bp region of the minicircle kinetoplast DNA using the primer pair Leish71Up (5′-CCAAACTTTTCTGGTCCTYCGGGTAG-3′) and Leish71Do (5′-TGAACGGGATTTCTGCACCCATTTTTC-3′) (Tsakmakidis et al. 2017) and following the conditions reported by Magri et al. (2022a, b).
Results and discussion
Out of the 236 I. ricinus DNA extracts, 4 (1.7%) tested positive for Leishmania sp. in 2 of the four sites examined: 2 nymph pools (5.4%) and 1 adult male (33.3%) from Monteveglio Abbey Park and 1 larva pool (2.3%) from Carné Park (Table 1).
Previous research mainly investigated the brown dog tick as a possible vector of L. infantum, and several studies showed the presence of L. infantum DNA in R. sanguineus collected from dogs affected by canine leishmaniasis (Coutinho et al. 2005; Paz et al. 2010; Campos and Costa 2014; Medeiros-Silva et al. 2015; Viol et al 2016) and from seronegative dogs living in endemic areas (Solano-Gallego et al. 2012). Nevertheless, the finding of Leishmania DNA in R. sanguineus ticks could be expected, given their blood feeding habits. Further work speculated that brown ticks can transmit canine leishmaniasis: Dantas-Torres et al. (2010a) reported the presence of L. infantum kDNA in the salivary glands of R. sanguineus ticks, corroborating the hypothesis that ticks could inject Leishmania parasites while blood feeding. Colombo et al. (2010) found viable Leishmania by RNA analysis in ticks 7 to 10 days after their removal from the dogs, showing that the parasite could survive for a long period in ticks, even after ecdysis had occurred in laboratory conditions. Dantas-Torres et al (2010b) demonstrated the transovarial passage of L. infantum kDNA in artificially infected R. sanguineus, and a subsequent study (Dantas-Torres et al. 2011) reported the detection and quantification of L. infantum DNA in field-collected engorged females and in their eggs and larvae. The transstadial and transovarian transmission of L. infantum in R. sanguineus was further confirmed by Dabaghmanesh et al. (2016). Medeiros-Silva et al. (2015), isolated Leishmania spp. in cultures from salivary glands and intestines of ticks collected from dogs; interestingly, it was possible to culture the parasite also from pools of unfed male ticks suggesting that Leishmania could persist in the brown tick after blood digestion (Medeiros-Silva et al. 2015). L. infantum DNA was also reported from questing Rhipicephalus spp. from Israel (Mumcuoglu et al. 2022). Finally, further studies demonstrated the capability of R. sanguineus nourished on infected dogs to transmit the parasites to hamsters (Almeida et al. 2016). Based on these findings, although sand flies are the recognized vectors of Leishmania, a minor role of the dog brown tick could not be excluded.
Concerning tick species other than R. sanguineus, also I. ricinus collected from dogs in central Italy was found positive for L. infantum (Trotta et al. 2012). Moreover, Salvatore et al (2014) found Leishmania kDNA in I. ricinus ticks removed from 4 dogs and 1 cat living in areas of northeastern Italy where canine leishmaniasis is endemic, although no anamnestic data related to infection in these animals were reported.
In the Argentine Patagonia, Millan et al. (2016) observed the presence of Leishmania DNA in the gray fox Pseudalopex griseus and in pools of Amblyomma tigrinum ticks collected from both positive and negative foxes, in a remote non-endemic area of South America, where dogs are scarce and sand flies are not known to be present, supporting the hypothesis that L. infantum could maintain a sylvatic cycle in the studied area, not involving dogs or sand flies.
Interestingly, in the same areas where the present study was carried out, a high positivity rate for L. infantum (33.3%) was observed in the roe deer Capreolus capreolus (Magri et al. 2022a, b), and blood meal preference for this species was found in sand flies (Calzolari et al. 2022), suggesting the possible involvement of C. capreolus (frequently hosts of the adult stages of I. ricinus) in the epidemiology of leishmaniasis in the area under study.
Conclusions
To the best of our knowledge, this is the first description of Leishmania DNA in questing I. ricinus ticks collected from a rural environment. This finding in unfed larvae, nymphs and males support the hypothesis that, even in this tick species, L. infantum could have both transstadial and transovarial transmission. The percentage (1.7%) of ticks positive to Leishmania DNA obtained in our study appears lower than the one reported in sand flies in other research (2.9–57.1%), stressing the fact that phlebotomine flies are the sole Leishmania efficient proven vector (Aransay et al. 2000; Gómez-Saladín et al. 2005; Ergunay et al. 2014; González et al. 2017; Latrofa et al. 2018). Nevertheless, a role of I. ricinus in a sylvatic cycle, albeit minor, could not be excluded in the endemic areas under study.
Data availability
Data supporting the conclusions of this article are included within the article and its supplementary tables.
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The authors wish to thank Dr Perla Tedesco for the English revision.
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Conceptualization: Roberta Galuppi; methodology: Alice Magri and Monica Caffara; formal analysis and investigation: Alice Magri and Monica Caffara; writing — original draft preparation: Alice Magri and Roberta Galuppi; writing — review and editing: Monica Caffara and Marialetizia Fioravanti; supervision: Marialetizia Fioravanti.
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Magri, A., Caffara, M., Fioravanti, M. et al. Detection of Leishmania sp. kDNA in questing Ixodes ricinus (Acari, Ixodidae) from the Emilia-Romagna Region in northeastern Italy. Parasitol Res 121, 3331–3336 (2022). https://doi.org/10.1007/s00436-022-07655-9
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DOI: https://doi.org/10.1007/s00436-022-07655-9