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Article

Co-Circulation of Leishmania Parasites and Phleboviruses in a Population of Sand Flies Collected in the South of Portugal

by
Fátima Amaro
1,2,3,*,†,
Anabela Vilares
4,†,
Susana Martins
4,
Tânia Reis
4,
Hugo Costa Osório
1,2,
Maria João Alves
1,2,3 and
Maria João Gargaté
4
1
Centre for Vectors and Infectious Diseases Research, National Institute of Health Doutor Ricardo Jorge, No. 5, 2965-575 Águas de Moura, Portugal
2
Environment and Infectious Diseases Research Group, Environmental Health Institute, 1649-028 Lisboa, Portugal
3
Centre for Animal Science Studies (CECA), University of Porto, 4050-453 Porto, Portugal
4
National Reference Laboratory of Parasitic and Fungal Infections, National Institute of Health Doutor Ricardo Jorge, 1649-016 Lisboa, Portugal
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Trop. Med. Infect. Dis. 2024, 9(1), 3; https://doi.org/10.3390/tropicalmed9010003
Submission received: 21 November 2023 / Revised: 15 December 2023 / Accepted: 18 December 2023 / Published: 20 December 2023
(This article belongs to the Special Issue Leishmaniasis: Vector-Host-Pathogen Interactions in Health and Disease)
Browse Figure
Versions Notes

Abstract

:
In the Old World, phlebotomine sand flies from the genus Phlebotomus are implicated in the transmission of Leishmania spp. parasites (Kinetoplastida: Trypanosomatidae) and viruses belonging to the genus Phlebovirus (Bunyavirales: Phenuiviridae). Two of the five sand fly species known to occur in Portugal, Phlebotomus perniciosus and Ph. ariasi, the former being the most ubiquitous, are recognized vectors of Leishmania infantum, which causes visceral leishmaniasis, the most prevalent form of leishmaniasis in the country. Phlebotomus perniciosus is also the vector of the neurotropic Toscana virus, which can cause aseptic meningitis. Entomological surveillance is essential to provide fundamental data about the presence of vectors and the pathogens they can carry. As such, and given the lack of data in Portugal, an entomological survey took place in the Algarve, the southernmost region of the country, from May to October 2018. Polymerase chain reaction assays were performed in order to detect the presence of the above-mentioned pathogens in sand fly pools. Not only were both Leishmania parasites and phleboviruses detected during this study, but more importantly, it was the first time their co-circulation was verified in the same sand fly population collected in Portugal.

1. Introduction

Phlebotomine sand flies (Diptera, Psychodidae) are insects with worldwide distribution. Despite their small size, they are very important in terms of spreading infectious diseases. With few exceptions, the females require a blood meal to produce eggs. They can acquire pathogens while feeding on infected hosts and transmit them to other hosts during the next blood meal. Sand flies of the genus Phlebotomus are vectors of flagellated obligate intracellular protozoans of the genus Leishmania (Kinetoplastida: Trypanosomatidae) and of viruses belonging to the genus Phlebovirus (Bunyavirales: Phenuiviridae) in several countries of the Old World [1].
The taxonomy of the genus Leishmania has been the subject of much debate and is a controversial topic, making it difficult to differentiate between species [2]. Vickerman (1976) proposed the recognition of four species complexes within the genus: the donovani complex, the tropica complex, the mexicana complex, and the braziliensis complex (adapted later, partially by Lainson and Shaw) [3,4]. The clustering of Leishmania at the subgeneric level and the definition of “complexes” in the Leishmania classification have gained rather wide acceptance, but there are still serious challenges in terms of the genus composition. In this way, defining a Leishmania species or accepting all the described species is still not straightforward [5]. Notwithstanding, four species of Leishmania are recognized in Europe and surrounding countries: L. donovani complex species, which includes both L. infantum and L. donovani s.s.; L. tropica and L. major [6]. Leishmania infantum is distributed throughout southern European countries. To date, L. donovani s.s. has only been described in Turkey and Cyprus, and L. major and L. tropica are limited to northern Africa and in some parts of the Caucasus [6,7,8]. In addition, there is evidence of the presence of L. tropica in Crete during the first decade of the twenty-first century, implying the disease had re-emerged on that island [6,9].
Leishmaniasis is the designation for the disease caused by Leishmania parasites. It can manifest in three main forms: visceral (VL), often known as kala-azar and although less incident, the most severe form; cutaneous (CL), the most common; and mucocutaneous (MCL), the most disabling form of the disease. Visceral leishmaniasis, caused by L. infantum, is mainly transmitted by Ph. perniciosus and Ph. ariasi sand flies and is endemic in Europe and the Mediterranean basin [10,11,12,13]. The VL was mostly known as a pediatric disease, although in the last few years, a decrease in cases has been observed, while an increase in infection in adults has been noted, usually associated with HIV/AIDS. This seems to be a common trend in countries in the south of Europe, including Portugal [10,11]. Based on the World Health Organization’s (WHO) Global Health Observatory Data Repository (GHDR), after reaching a value of 0.4 from 2013 to 2016 in Portugal, the median annual incidence of VL per 100,000 inhabitants increased to 0.06 in the period 2017−2020 [6]. There are, however, discrepancies in the reported incidence between WHO sources and hospital discharge records available in some countries. In this way, and due to the underreporting of leishmaniasis cases, there is an urgent need to improve surveillance and notification systems [6].
In Portugal, there are three recognized leishmaniasis foci: the Alto Douro region in the north, the Algarve in the south, and suburban areas of Lisbon [10]. Besides being a human threat, L. infantum also poses a serious veterinary problem since canine leishmaniasis (CanL) commonly presents a fatal outcome. The CanL is increasing in Portugal and is recorded with a prevalence of 20% in endemic foci [10]. Due to the mode of infection (through sand fly bites), it is easily transmitted to other dogs or humans. Dogs are considered the main reservoirs for human VL, and, for that reason, in order to prevent the spread of human transmission, infections in these domestic animals should be contained [14,15].
Phleboviruses are single-stranded RNA viruses with a tri-segmented genome composed of small (S), medium (M), and large (L) segments [16]. The taxonomy of phleboviruses is constantly changing, and currently, the International Committee on Taxonomy of Viruses (ICTV) recognizes 67 phleboviruses species [17]. In Europe and in the Mediterranean region, the most medically important phlebovirus transmitted by sand flies is Toscana virus (TOSV) (recently renamed as Phlebovirus toscanaense), which can cause not only asymptomatic or mild flu-like syndromes but also self-limiting neuro-invasive diseases such as meningitis or meningoencephalitis. This virus has been considered the third main cause of aseptic meningitis in the Mediterranean region during the summer months and, as such, a major public health concern [18]. Furthermore, TOSV has been associated with unusual clinical manifestations, with or without permanent sequelae, and even with some cases of fatal outcomes [19,20,21]. Although human seroprevalence studies for TOSV show numbers around 10–24%, in endemic regions such as Tuscany, this value can go up to 77% [19,22].
The proven vectors of TOSV are Ph. perniciosus and Ph. perfiliewi [23]. Other circulating phleboviruses in the Mediterranean region associated with human disease, namely some members of the sand fly fever Sicilian virus (Phlebovirus siciliaense, SFSV), including Sicilian, Turkish, and Cypriot variants and the sand fly fever Naples virus species (Phlebovirus napoliense) are also transmitted by sand flies of the Larroussius group (e.g., Ph. ariasi, Ph. papatasi). These phleboviruses may cause febrile syndromes accompanied by headaches, malaise, photophobia, myalgia, and retro-orbital pain, usually known as sand fly fever, three-day fever, or pappataci fever [24]. Nowadays, it is believed that phlebovirus infections are largely underreported, and this may happen due to the number of asymptomatic or mild disease cases.
To date, at least four phleboviruses are known to circulate in Portugal: TOSV with reported isolation and serological evidence in humans and serological evidence in cats and dogs; Massilia and Alcube viruses (Phlebovirus massiliaense and Phlebovirus alcubeense, respectively), isolated and detected, up to date, only in sand flies; and the SFSV recently associated with human disease in Portugal and detected in sera samples of humans, cats, and dogs [25,26,27,28,29,30,31,32,33,34].
In the most recent study conducted to evaluate the presence of antibodies against TOSV and SFSV in a human population residing in the southwest of Portugal, seroprevalences of 5.3% and 4.3% were detected, respectively [32]. Nonetheless, phlebovirus infections are still neglected in the country.
There are five species of sand flies currently known to circulate in Portugal: Ph. ariasi, Ph. papatasi, Ph. perniciosus, Ph. sergenti, and Sergentomyia minuta. Interestingly, in this country, although Leishmania parasites have been detected several times in their natural vectors, to date, the only phleboviruses locally recognized as causes of disease (TOSV and SFSV) have never been isolated in sand flies. Moreover, data regarding this group of insects are largely limited in Portugal. If we want to be prepared for outbreaks and promptly engage in public health interventions, information about the circulating vectors and the pathogens they can carry and transmit is essential. In this way, entomological surveillance is of utmost importance and should be consistently implemented.
The aim of this work is to report the findings of an entomological survey performed in the Algarve region, Portugal, during the summer of 2018, where we found, for the first time in our country, the co-circulation of Leishmania parasites and phleboviruses in wild-caught sand flies.

2. Materials and Methods

2.1. Field Survey

The study was conducted in Algarve, south of Portugal, from May to October 2018. The area covered by the survey is characterized mainly by a temperate climate with a rainy winter (precipitation concentrated between October and April) and a hot, dry summer [35].
Sand flies were trapped with modified (ultra-fine mesh) CDC light traps (John W. Hock Company, Gainesville, FL, USA) baited with dry ice, placed at sunset, and collected after sunrise, during four consecutive nights. The traps were positioned in selected locations of known ecological preferences of the sand flies (e.g., animal facilities with organic matter and high humidity, such as kennels, rabbit, and chicken pens). After collection, the sand flies were stored at −80° until further processing in the laboratory.

2.2. Identification of Sand flies

Once in the laboratory, around 10% of the male sand flies were mounted on spot slides for morphological identification to species level in a stereomicroscope according to existing taxonomic keys [36,37]. Regarding female sand flies, when there was only one specimen per pool for the pathogen screening, they were identified by molecular methods using the cytochrome c oxidase subunit I gene of mitochondrial DNA, as previously described [38].

2.3. Phleboviruses and Leishmania spp. Detection and Sequencing

All female sand flies were processed in pools for detection of phleboviruses and Leishmania parasites. Male sand flies not used for morphological identification were also processed in pools for detection of phleboviruses.
Pools of one to 35 sand flies were organized by sex, date, and place of collection and were grounded and suspended in Hank’s solution containing 7.5% bovine albumin and antibiotics, as previously described [28]. After centrifugation of the mixture, a 400 μL aliquot of the supernatant fluid was used for pathogen detection, and the remainder was stored at −80° for further viral isolation attempts and other studies.
For detection of phleboviruses, after nucleic acid extraction (NUCLISENS® easyMAG®, bioMérieux, Marcy-l’Étoile, France), a pan-phlebo rt-PCR targeting a 370-nucleotide region of the S segment of phleboviruses was performed [39]. In the case of positive samples, pools were used to infect VERO E6 cells as previously described [39]. For the detection of Leishmania, and after nucleic acid extraction as mentioned above, pools of female sand flies were screened by nested PCR amplification of the 18S rRNA gene [13,40]. Despite whole-genome sequencing and multilocus sequence typing (MLST) being the traditional methods used to differentiate between the species of the L. donovani complex, the 18S PCR is the most sensitive for identifying Leishmania spp. The choice of this PCR marker is consistent with a study by León et al. in which the authors reported that the 18S rRNA marker exhibited the best performance in terms of analytical sensitivity and specificity for the detection of Leishmania spp. [41]. Also, it is widely acknowledged that many regions of the 18S rRNA gene are either completely conserved or partially conserved [42].
All PCR products (from the sand fly species identification and both pathogen reactions) were visualized in GelRED (Biotarget, Lisbon, Portugal)-stained 1.5% agarose gel electrophoresis, purified, and sequenced in an ABI 3130xl Genetic Analyzer (Applied Biosystems, Foster City, CA, USA).
Homology searches were performed using the BLAST algorithm [43], and partial sequences were aligned with control sequences retrieved from GenBank via Clustal W in Bioedit [44].

3. Results

3.1. Collected Sand Flies

Sixteen field stations distributed in nine parishes belonging to the counties of Loulé, Olhão, and Tavira were surveyed. Sand flies were found in 13 of 16 field stations (Figure 1).
A total of 1161 specimens were collected, comprising of 736 females and 425 males. One hundred and eighteen specimens were identified to species level, and four species were found: Ph. ariasi, Ph. perniciosus, Ph. sergenti, and Se. minuta (Table 1).

3.2. Detection of Phleboviruses and Leishmania spp.

We tested 736 females organized in 140 pools and 394 males distributed in 38 pools (Table 1).
The RNA of two phleboviruses – PoSFPhlebV/11/2018 and PoSFPhlebV/38/2018 – was detected in pools 11 and 38 (each one composed of 20 female sand flies), respectively, in a rural setting in Tavira, Santa Maria parish (Alg3), in a hennery adjacent to a kennel in May and June 2018. Isolation attempts were not successful, but partial genome sequences of the nucleoprotein gene (segment S) were obtained, and these were deposited in GenBank. For PoSFPhlebV/11/2018, a sequence of 381 nucleotides was retrieved (ON807199), phylogenetically distinct from other known phleboviruses. The other obtained sequence (530 nucleotides, ON807200) seems to belong to a Massilia virus strain. These findings were all previously published, including the sequence files and the respective phylogenetic trees, and can be found in Amaro et al. [19].
Regarding Leishmania parasites, DNA was detected in six pools: four in Tavira, Santa Maria parish (Alg3), in May and June (pools 19, 45, 57, and 61), at the exact location as above mentioned, and two in Conceição, Olhão (Alg5) in June (pools 32 and 86), near a rabbit hutch, in a pedagogical farm (Table 2). Three sequences were deposited in GenBank (accession numbers: OR783264-66). After alignment analysis, the sequences were attributed to the L. donovani complex since the sequencing of these PCR products did not allow for species discrimination. Sequencing of pools 57, 61, and 86 was not possible due to low DNA concentration, but we assumed they belonged to the same complex found in the other pools.
The co-circulation of phleboviruses and species from the L. donovani complex in the same sand fly population was detected on 16 May and 5 June, 2018 in Tavira (Alg3). The location of the surveyed sites and detected pathogens is depicted in Figure 1 (geographical coordinates are available in Supplementary Table S1). Data regarding the detections are presented in Table 2.

4. Discussion

Four of the five species of sand flies known to occur in Portugal were collected during this survey. This is in accordance with previous studies [45,46]. Phebotomus perniciosus was the most identified species in our samples and was present in all the sites where sand flies were found. This conforms with other surveys where it is referred to as the most ubiquitous species in Portugal, present from north to south [47]. Phlebotomus ariasi, another vector of L. infantum responsible for zoonotic visceral leishmaniasis in western Mediterranean countries, was collected in two localities (Santa Maria and São Sebastião). This species has been shown to be dominant in some regions of Portugal, namely in Douro [48]; however, that was not the case in our study. Phlebotomus papatasi, the only missing species in our survey (from the five known to exist in the country), is considered uncommon in Portugal [37].
Two phleboviruses were detected in our study. One of them may be an unknown phlebovirus, at least in Portugal, but it was not possible to confirm it further with genomic analysis. Nevertheless, the sequence obtained from the standard nucleotide BLAST (blastn) [43] presented similarities with Phlebovirus hediense [49], which is a largely unknown phlebovirus, previously isolated from sand flies in China, and with phleboviruses collected in Italy, with only partial sequences available in GenBank. The other detected phlebovirus seems to be a Massilia virus strain since it clustered together with other strains isolated or detected previously in the south of Portugal [19]. However, the partial phleboviruses sequences obtained in the Algarve in 2018 are too small to make a valid assumption. We would need to perform whole genome sequencing to be certain of the identity of those phleboviruses, specifically with the complete sequences of the RdRp gene (Large segment). Currently, the ICTV uses criteria to differentiate phleboviruses’ species [17]. These findings were already discussed in a previous publication [19]. Still, we can hypothesize that at least two phlebovirus species were in circulation in the same location at that time. The co-circulation of different phleboviruses is not uncommon. It was reported previously in Portugal and should not go unnoticed as recombination events may occur, given the genetic characteristics of these viruses, which could result in new strains or species with unknown pathogenic potential [29].
The sand fly pools where both phleboviruses were detected were composed of 20 female specimens each. Moreover, at that collection site (Alg3), three sand fly species were identified: Ph. ariasi, Ph. perniciosus, and Se. minuta. Although it seems that Ph. perniciosus is the most abundant species at that location, we cannot make any conjectures about the sand fly species with which the referred phleboviruses might be associated. However, the first reported isolation of the Massilia virus was achieved in pools of Ph. perniciosus sand flies collected in 2005 in Marseille, France, and this may indicate the species as the probable vector for the referred virus [50].
Concerning Leishmania detections, species of the L. donovani complex were identified. We can assume that all the isolates belong to the same complex and further hypothesize that we are in the presence of L. infantum, a fact supported by previous studies that recognized this species as the only one circulating in Portugal and the most prevalent in southern Europe [6,12,51,52,53].
The pools found positive for Leishmania parasites were all composed of a unique sand fly specimen. Although Ph. ariasi is also one of the vectors of the L. donovani complex reported as naturally infected with Leishmania in Portugal [51], and specimens of this species were identified during this study, all the sand flies found positive for this pathogen were identified as Ph. perniciosus. Given that L. infantum has been mostly detected in the latter species of sand fly in our country, this result is not surprising [46,51]. In fact, Ph. perniciosus was considered the primary vector of Leishmania parasites in the region in a former study because, similarly to the present work, it was not only the one species found infected with L. infantum but also the one that presented the highest abundance and distribution [52].
The co-circulation of L. infantum and phleboviruses in sand fly populations in the Mediterranean region has been reported in preceding studies. Fares et al. documented the endemic co-circulation of TOSV and that parasite in a zoonotic VL focus in Central Tunisia [54]. Moreover, Ergunay and colleagues, in research conducted in the eastern Thrace region of Turkey and Northern Cyprus, found a pool of Ph. tobbi co-infected with TOSV and L. infantum [55]. Different sand fly pools were found infected with both the Massilia virus and L. infantum at the same trapping site in an urban area in Marseille [56]. Furthermore, Calzolari and colleagues reported the detection of Leishmania and phleboviruses in the same pools, namely, Fermo virus (14 pools), Ponticelli virus (1 pool), and Corfou virus (1 pool) [57]. All these findings lead us to hypothesize that contemporaneous infections in local sand fly populations may be translated into the transmission of both pathogens.
In this study, we report, for the first time in Portugal, the circulation of Leishmania and phleboviruses in wild-caught sand fly populations. However, we did not find both pathogens in the same insect pool. Even though Dincer et al. assume that there is a low probability of double infections in sand flies [58], we believe that, to date, there are not enough data to exclude the possibility of co-infected sand flies transmitting both agents. As such, further investigation is required, and experimental co-infections of vector sand flies reared in laboratory colonies may further help to unravel some of these questions.
The co-infection of hosts with phleboviruses and Leishmania, on the other hand, has been the subject of several laboratory studies. Rossi and colleagues reported the findings of an exacerbated murine leishmaniasis disease when laboratory mice were co-infected with L. guyanensis and TOSV [59]. The latter virus favored the parasite’s persistence and spreading. In 2019, Rath et al. reported the use of Phlebovirus icoaraciense, isolated from the rodent Nectomys sp., which is also a sylvatic reservoir of L. amazonensis, and demonstrated that the co-infection of both pathogens boosted the parasite load, both in vivo and in vitro [60]. Likewise, Heirwegh and colleagues (2021), using wild-type and knock-out mouse models, determined that co-infection with L. major and SFSV influenced disease severity, inducing aggravated skin lesions and higher parasite numbers [61].
Regarding natural co-infections of vertebrate hosts, Dincer et al. documented for the first time the co-infection of TOSV and L. infantum in two dogs in Adana province, Turkey [58]. These dogs presented clinical symptoms compatible with canine leishmaniasis, namely anorexia, wasting, muscle atrophy, epistaxis, and mucosal bleeding. Furthermore, several serological studies demonstrated the presence of antibodies against Leishmania and phleboviruses, and it has been suggested that dogs infected with L. infantum are extremely appealing to Ph. perniciosus when compared to healthy ones [62]. For that reason, they may serve as sand fly magnets and promote a substantial increment in the contact between the vector and infected dogs. Moreover, in a study aimed at investigating TOSV infections in healthy and infected dogs with Leishmania following natural exposition to sand fly bites in Northern Tunisia, the authors demonstrated for the first time that, in addition to their role as the main reservoir hosts of L. infantum, dogs are competent reservoirs for the transmission of TOSV to sand fly vectors in natural settings [63]. Likewise, in Portugal, in a seroprevalence study in two different districts in the south, a significant association was observed between the presence of antibodies to L. infantum and SFSV in sheltered dogs [64].
Concerning human co-infections, Bichaud and colleagues were able to find a significant correlation between the seropositivity of L. infantum and TOSV in a retrospective serological screening in southern France and delivered the first strong indication for the existence of an epidemiological relationship between both infections [65]. Following this line of thought, Heirwegh et al., while studying severe cases of CL, pointed out that to improve patient outcomes and the time to disease clearance, the possibility of phleboviral co-infections should be considered and the disease treated accordingly [61]. Even if there is presently no evidence of co-infection in the vectors, the proven co-circulation of the pathogens in the same population of sand flies is enough to raise our attention and supports the idea that co-infections should be considered in vertebrate hosts. Regarding the Mediterranean region in particular, further research is essential in order to understand the implications of L. infantum and phleboviruses’ co-infections.

5. Conclusions

The co-circulation of Leishmania parasites and phleboviruses in the same population of sand flies is documented here for the first time in Portugal. More research is needed to better understand the impact of these co-infections, not only in the vector populations but also in the susceptible hosts who may develop the disease.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/tropicalmed9010003/s1, Table S1, Geographical coordinates of the surveyed sites.

Author Contributions

Conceptualization, F.A. and A.V.; methodology, F.A., A.V., S.M., T.R. and H.C.O.; validation, F.A., A.V., M.J.G. and M.J.A.; formal analysis, F.A. and A.V.; writing—original draft preparation, F.A., A.V. and M.J.G.; writing and editing, all authors.; funding acquisition, F.A. and M.J.A. All authors have read and agreed to the published version of the manuscript.

Funding

This research was partially supported by the Portuguese Foundation for Science and Technology (FCT) through the project: “Phleboviruses in Portugal—vectors, pathogenesis and co-infections” (PTDC/DTP-SAP/0859/2014).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data are contained within the article and Supplementary Materials.

Acknowledgments

We would like to thank Natacha Milhano for the revision of the manuscript.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

References

  1. European Center for Disease Prevention and Control. Phlebotomine Sand Flies. Factsheet for Experts. Available online: https://www.ecdc.europa.eu/en/disease-vectors/facts/phlebotomine-sand-flies (accessed on 28 March 2023).
  2. Ramírez, J.D.; Hernández, C.; León, C.M.; Ayala, M.S.; Flórez, C.; González, C. Taxonomy, diversity, temporal and geographical distribution of Cutaneous Leishmaniasis in Colombia: A retrospective study. Sci. Rep. 2016, 6, 28266. [Google Scholar] [CrossRef] [PubMed]
  3. Vickerman, K. The diversity of the kinetoplastid flagellates. In Biology of the Kinetoplastida; Lumsden, W.H.R., Evans, D.A., Eds.; Academic Press: London, UK, 1976; pp. 1–34. [Google Scholar]
  4. Lainson, R.; Shaw, J.J. Leishmaniasis of the New World: Taxonomic problems. Br. Med. Bull. 1972, 28, 44. [Google Scholar] [CrossRef] [PubMed]
  5. Akhoundi, M.; Kuhls, K.; Cannet, A.; Votýpka, J.; Marty, P.; Delaunay, P.; Sereno, D. A Historical Overview of the Classification, Evolution, and Dispersion of Leishmania Parasites and Sandflies. PLoS Negl. Trop. Dis. 2016, 10, e0004349. [Google Scholar] [CrossRef] [PubMed]
  6. European Centre for Disease Prevention and Control. Surveillance, Prevention and Control of Leishmaniases in the European Union and Its Neighbouring Countries; ECDC: Stockholm, Sweden, 2022; p. 60. [Google Scholar]
  7. Özbilgin, A.; Harman, M.; Karakuş, M.; Bart, A.; Töz, S.; Kurt, Ö.; Çavuş, İ.; Polat, E.; Gündüz, C.; Van Gool, T.; et al. Leishmaniasis in Turkey: Visceral and cutaneous leishmaniasis caused by Leishmania donovani in Turkey. Acta Trop. 2017, 173, 90–96. Available online: https://www.ncbi.nlm.nih.gov/pubmed/28587839 (accessed on 6 December 2023). [CrossRef] [PubMed]
  8. Antoniou, M.; Haralambous, C.; Mazeris, A.; Pratlong, F.; Dedet, J.P.; Soteriadou, K. Leishmania donovani leishmaniasis in Cyprus. Lancet Infect. Dis. 2008, 8, 6–7. [Google Scholar] [CrossRef] [PubMed]
  9. Ntais, P.; Sifaki-Pistola, D.; Christodoulou, V.; Messaritakis, I.; Pratlong, F.; Poupalos, G.; Antoniou, M. Leishmaniases in Greece. Am. J. Trop. Med. Hyg. 2013, 89, 906–915. [Google Scholar] [CrossRef]
  10. Campino, L.; Maia, C. Epidemiology of leishmaniases in Portugal. Acta Med. Port. 2010, 23, 859–864. [Google Scholar]
  11. Martins, S.; Vilares, A.; Ferreira, I.; Reis, T.; Gargaté, M. Leishmaníase: Confirmação laboratorial de casos clínicos suspeitos de infeção entre 2008 e 2013. Bol. Epi. 2014, 3 (Suppl. S3), 23–25. [Google Scholar]
  12. Cortes, S.; Maurício, I.L.; Kuhls, K.; Nunes, M.; Lopes, C.; Marcos, M.; Cardoso, L.; Schönian, G.; Campino, L. Genetic diversity evaluation on Portuguese Leishmania infantum strains by multilocus microsatellite typing. Infect. Genet. Evol. 2014, 26, 20–31. [Google Scholar] [CrossRef]
  13. Remadi, L.; Farjallah, D.; Chargui, N.; Belgacem, S.; Baba, H.; Zrieq, R.; Alzain, M.A.; Babba, H.; Haouas, N. Blood meal analysis and molecular detection of mammalian Leishmania DNA in wild-caught Sergentomyia spp. from Tunisia and Saudi Arabia. Parasitol. Res. 2023, 122, 2181–2191. [Google Scholar] [CrossRef]
  14. Morales-Yuste, M.; Martín-Sánchez, J.; Corpas-Lopez, V. Canine Leishmaniasis: Update on Epidemiology, Diagnosis, Treatment, and Prevention. Vet. Sci. 2022, 9, 387. [Google Scholar] [CrossRef] [PubMed]
  15. Reguera, R.M.; Morán, M.; Pérez-Pertejo, Y.; García-Estrada, C.; Balaña-Fouce, R. Current status on prevention and treatment of canine leishmaniasis. Vet. Parasitol. 2016, 227, 98–114. [Google Scholar] [CrossRef] [PubMed]
  16. Bouloy, M. Molecular biology of phleboviruses. In Bunyaviridae Molecular and Cellular Biology; Plyusnin, A., Elliott, R.M., Eds.; Caister Academic Press: Norfolk, UK, 2011; pp. 95–128. [Google Scholar]
  17. International Committee on Taxonomy of Viruses. Virus Taxonomy: 2022 Release. Email Ratification March 2023 (MSL #38). Available online: https://talk.ictvonline.org/taxonomy/ (accessed on 1 June 2023).
  18. Charrel, R.N.; Bichaud, L.; de Lamballerie, X. Emergence of Toscana virus in the Mediterranean area. World J. Virol. 2012, 5, 135–141. [Google Scholar] [CrossRef] [PubMed]
  19. Amaro, F.; Zé-Zé, L.; Alves, M.J. Sandfly-Borne Phleboviruses in Portugal: Four and Still Counting. Viruses 2022, 14, 1768. [Google Scholar] [CrossRef]
  20. Bartels, S.; de Boni, L.; Kretzschmar, H.A.; Heckmann, J.G. Lethal encephalitis caused by the Toscana virus in an elderly patient. J. Neurol. 2012, 259, 175–177. [Google Scholar] [CrossRef] [PubMed]
  21. Popescu, C.P.; Cotar, A.I.; Dinu, S.; Zaharia, M.; Tardei, G.; Ceausu, E.; Badescu, D.; Ruta, S.; Ceianu, C.S.; Florescu, S.A. Emergence of Toscana Virus, Romania, 2017–2018. Emerg. Infect. Dis. 2021, 27, 1482–1485. [Google Scholar] [CrossRef]
  22. Valassina, M.; Valentini, M.; Pugliese, A.; Valensin, P.E.; Cusi, M.G. Serological survey of Toscana virus infections in a high-risk population in Italy. Clin. Diag. Lab. Immunol. 2003, 10, 483–484. [Google Scholar] [CrossRef]
  23. European Centre for Disease Prevention and Control. Toscana Virus Infection. Available online: https://www.ecdc.europa.eu/en/toscana-virus-infection (accessed on 28 March 2023).
  24. Depaquit, J.; Grandadam, M.; Fouque, F.; Andry, P.E.; Peyrefitte, C. Arthropod-borne viruses transmitted by Phlebotomine sandflies in Europe: A review. Euro Surveill. 2010, 15, 19507. [Google Scholar] [CrossRef]
  25. Ehrnst, A.; Peters, C.J.; Niklasson, B.; Svedmyr, A.; Holmgren, B. Neurovirulent Toscana virus (a sandfly fever virus) in Swedish man after visit to Portugal. Lancet 1985, 1, 1212–1213. [Google Scholar] [CrossRef]
  26. Amaro, F.; Luz, T.; Parreira, P.; Marchi, A.; Ciufolini, M.G.; Alves, M.J. Serological evidence of Toscana virus infection in Portuguese patients. Epidemiol. Infect. 2012, 140, 1147–1150. [Google Scholar] [CrossRef]
  27. Amaro, F.; Zé-Zé, L.; Luz, M.T.; Alves, M.J. Toscana Virus: Ten Years of Diagnostics in Portugal. Acta Med. Port. 2021, 34, 677–681. [Google Scholar] [CrossRef] [PubMed]
  28. Amaro, F.; Hanke, D.; Zé-Zé, L.; Alves, M.J.; Becker, S.C.; Höper, D. Genetic characterization of Arrabida virus, a novel phlebovirus isolated in South Portugal. Virus Res. 2016, 214, 19–25. [Google Scholar] [CrossRef] [PubMed]
  29. Amaro, F.; Zé-Zé, L.; Alves, M.J.; Börstler, J.; Clos, J.; Lorenzen, S.; Becker, S.C.; Schmidt-Chanasit, J.; Cadar, D. Co-circulation of a novel phlebovirus and Massilia virus in sandflies, Portugal. Vir. J. 2015, 12, 174. [Google Scholar] [CrossRef]
  30. Filipe, A.R. Serological survey for antibodies to arboviruses in the human population of Portugal. Trans. R. Soc. Trop. Med. Hyg. 1974, 68, 311–314. [Google Scholar] [CrossRef] [PubMed]
  31. Guerra, A.B.; Gouveia, C.; Zé-Zé, L.; Amaro, F.; Ferreira, G.C.; Brito, M.J. Prolonged Febrile Illness Caused by Sicilian Virus Infection in Portugal. In Proceedings of the 36th Annual Meeting of the European Society for Paediatric Infectious Diseases, Malmo, Sweden, 28 May–2 June 2018. [Google Scholar]
  32. Maia, C.; Ayhan, N.; Cristovão, J.M.; Pereira, A.; Charrel, R. Human seroprevalence of Toscana virus and Sicilian phlebovirus in the southwest of Portugal. Eur. J. Clin. Microbiol. Infect. Dis. 2022, 41, 137–141. [Google Scholar] [CrossRef] [PubMed]
  33. Pereira, A.; Ayhan, N.; Cristovão, J.M.; Vilhena, H.; Martins, A.; Cachola, P.; Henriques, J.; Coimbra, M.; Catarino, A.; Lestinova, T.; et al. Antibody response to Toscana Virus and Sandfly Fever Sicilian Virus in cats naturally exposed to phlebotomine Sand Fly bites in Portugal. Microorganisms 2019, 7, 339. [Google Scholar] [CrossRef]
  34. Alwassouf, S.; Maia, C.; Ayhan, N.; Coimbra, M.; Cristovão, J.M.; Richet, H.; Bichaud, L.; Campino, L.; Charrel, R.N. Neutralization-based seroprevalence of Toscana virus and sandfly fever Sicilian virus in dogs and cats from Portugal. J. Gen. Virol. 2016, 97, 2816–2823. [Google Scholar] [CrossRef]
  35. Instituto Português do Mar e da Atmosfera. Área Educativa—Clima de Portugal Continental. Available online: https://www.ipma.pt/pt/educativa/tempo.clima/ (accessed on 28 March 2023).
  36. Maroli, M.; Feliciangeli, M.D.; Arias, J. Metodos de Captura, Conservacion y Montaje de los Flebotomos (Diptera: Psychodidae); Organización Panamericana de la Salud: Washington, DC, USA, 1997; p. 72. [Google Scholar]
  37. Pires, C. Os Flebótomos (Diptera, Psychodidae) dos Focos Zoonóticos de Leishmanioses em Portugal. Ph.D. Thesis, Instituto de Higiene e Medicina Tropical, Universidade Nova de Lisboa, Lisboa, Portugal, 2000; p. 228. (In Portuguese). [Google Scholar]
  38. Folmer, O.; Black, M.; Hoeh, W.; Lutz, R.; Vrijenhoek, R. DNA primers for amplification of mitochondrial Cytochrome C oxidase subunit I from diverse metazoan invertebrates. Mol. Mar. Biol. Biotechnol. 1994, 3, 294–299. [Google Scholar]
  39. Lambert, A.J.; Lanciotti, R.S. Consensus amplification and novel multiplex sequencing method for S segment species identification of 47 viruses of the Orthobunyavirus, Phlebovirus, and Nairovirus genera of the family Bunyaviridae. J. Clin. Microbiol. 2009, 4, 2398–2404. [Google Scholar] [CrossRef]
  40. Cruz, I.; Cañavate, C.; Rubio, J.M.; Morales, M.A.; Chicharro, C.; Laguna, F.; Jiménez-Mejías, M.; Sirera, G.; Videla, S.; Alvar, J. Spanish HIV-Leishmania Study Group. A nested polymerase chain reaction (Ln-PCR) for diagnosing and monitoring Leishmania infantum infection in patients co-infected with human immunodeficiency virus. Trans. R. Soc. Trop. Med. Hyg. 2002, 96 (Suppl. S1), S185–S189. [Google Scholar] [CrossRef]
  41. León, C.M.; Muñoz, M.; Hernández, C.; Ayala, M.S.; Flórez, C.; Teherán, A.; Cubides, J.R.; Ramírez, J.D. Analytical performance of four polymerase chain reaction (PCR) and real time PCR (qPCR) assays for the detection of six Leishmania species DNA in Colombia. Front. Microbiol. 2007, 8, 1907. [Google Scholar] [CrossRef] [PubMed]
  42. Baverstock, P.R.; Illana, S.; Christy, P.E.; Robinson, B.S.; Johnson, A.M. srRNA evolution and phylogenetic relationships of the genus Naegleria (Protista: Rhizopoda). Mol. Biol. Evol. 1989, 6, 243–257. [Google Scholar] [CrossRef] [PubMed]
  43. Altschul, S.F.; Gish, W.; Miller, W.; Myers, E.W.; Lipman, D.J. Basic local alignment search tool. J. Mol. Biol. 1990, 215, 403–410. [Google Scholar] [CrossRef] [PubMed]
  44. Hall, T.A. BioEdit: A user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucl. Acids Symp. Ser. 1999, 41, 95–98. [Google Scholar]
  45. Schrey, C.F.; Pires, C.A.; Macvean, D.W. Distribution of phlebotomine sandflies and the rate of their infection with Leishmania promastigotes in the Algarve, Portugal. Med. Vet. Entomol. 1989, 3, 125–130. [Google Scholar] [CrossRef] [PubMed]
  46. Maia, C.; Dionísio, L.; Afonso, M.O.; Neto, L.; Cristóvão, J.M.; Campino, L. Leishmania infection and host-blood feeding preferences of phlebotomine sandflies and canine leishmaniasis in an endemic European area, the Algarve Region in Portugal. Mem. Inst. Oswaldo Cruz 2013, 108, 481–487. [Google Scholar] [CrossRef] [PubMed]
  47. Zé-Zé, L.; Amaro, F.; Osório, H.C.; Giovanetti, M.; Lourenço, J.; Alves, M.J. Molecular Identification and Ecology of Portuguese Wild-Caught Phlebotomine Sandfly Specimens. Zoonotic Dis. 2022, 2, 19–31. [Google Scholar] [CrossRef]
  48. Alves-Pires, C.; Ribeiro, H. The phlebotomine sandflies of Portugal. V—Observations of the ecology of the vectors of leishmaniasis in the Alto-Douro region. Parasitologia 1991, 33, 63–68. [Google Scholar]
  49. Xu, Z.; Fan, N.; Hou, X.; Wang, J.; Fu, S.; Song, J.; Shi, M.; Liang, G. Isolation and Identification of a Novel Phlebovirus, Hedi Virus, from Sandflies Collected in China. Viruses 2021, 13, 772. [Google Scholar] [CrossRef]
  50. Charrel, R.N.; Moureau, G.; Temmam, S.; Izri, A.; Marty, P.; Parola, P.; da Rosa, A.T.; Tesh, R.B.; de Lamballerie, X. Massilia virus, a novel Phlebovirus (Bunyaviridae) isolated from sandflies in the Mediterranean. Vector Borne Zoonotic Dis. 2009, 9, 519–530. [Google Scholar] [CrossRef]
  51. Pires, C.A. Les Phlébotomes du Portugal. I—Infestation naturelle de Phlebotomus ariasi Tonnoir, 1921 et Phlebotomus perniciosus Newstead, 1911, par Leishmania dans le foyer zoonotique de Arrábida (Portugal) [Phlebotomus of Portugal. I-Natural infestation of Phlebotomus ariasi Tonnoir, 1921 and Phlebotomus perniciosus Newstead, 1911, by Leishmania in the zoonotic focus of Arrábida (Portugal)]. Ann. Parasitol. Hum. Comp. 1984, 59, 521–524. [Google Scholar] [PubMed]
  52. Maia, C.; Afonso, M.O.; Neto, L.; Dionísio, L.; Campino, L. Molecular detection of Leishmania infantum in naturally infected Phlebotomus perniciosus from Algarve region, Portugal. J. Vector Borne Dis. 2009, 46, 268–272. [Google Scholar] [PubMed]
  53. Branco, S.; Alves-Pires, C.; Maia, C.; Cortes, S.; Cristovão, J.M.; Gonçalves, L.; Campino, L.; Afonso, M.O. Entomological and ecological studies in a new potential zoonotic leishmaniasis focus in Torres Novas municipality, Central Region, Portugal. Acta Trop. 2013, 125, 339–348. [Google Scholar] [CrossRef] [PubMed]
  54. Fares, W.; Dachraoui, K.; Barhoumi, W.; Cherni, S.; Chelbi, I.; Zhioua, E. Co-circulation of Toscana virus and Leishmania infantum in a focus of zoonotic visceral leishmaniasis from Central Tunisia. Acta Trop. 2020, 204, 105342. [Google Scholar] [CrossRef] [PubMed]
  55. Ergunay, K.; Kasap, O.E.; Orsten, S.; Oter, K.; Gunay, F.; Yoldar, A.Z.; Dincer, E.; Alten, B.; Ozkul, A. Phlebovirus and Leishmania detection in sandflies from eastern Thrace and Northern Cyprus. Parasit. Vectors. 2014, 7, 575. [Google Scholar] [CrossRef] [PubMed]
  56. Faucher, B.; Bichaud, L.; Charrel, R.; Mary, C.; Izri, A.; de Lamballerie, X.; Piarroux, R. Presence of sandflies infected with Leishmania infantum and Massilia virus in the Marseille urban area. Clin. Microbiol. Infect. 2014, 20, 340–343. [Google Scholar] [CrossRef] [PubMed]
  57. Calzolari, M.; Romeo, G.; Callegari, E.; Bonilauri, P.; Chiapponi, C.; Carra, E.; Rugna, G.; Taddei, R.; Lelli, D.; Dottori, M. Co-Circulation of Phleboviruses and Leishmania Parasites in Sand Flies from a Single Site in Italy Monitored between 2017 and 2020. Viruses 2021, 13, 1660. [Google Scholar] [CrossRef]
  58. Dincer, E.; Gargari, S.; Ozkul, A.; Ergunay, K. Potential animal reservoirs of Toscana virus and coinfections with Leishmania infantum in Turkey. Amer J. Trop. Med. Hyg. 2015, 92, 690–697. [Google Scholar] [CrossRef]
  59. Rossi, M.; Castiglioni, P.; Hartley, M.A.; Eren, R.O.; Prével, F.; Desponds, C.; Utzschneider, D.T.; Zehn, D.; Cusi, M.G.; Kuhlmann, F.M.; et al. Type I interferons induced by endogenous or exogenous viral infections promote metastasis and relapse of leishmaniasis. Proc. Natl. Acad. Sci. USA 2017, 114, 4987–4992. [Google Scholar] [CrossRef]
  60. Rath, C.T.; Schnellrath, L.C.; Damaso, C.R.; de Arruda, L.B.; da Costa Vasconcelos, P.F.; Gomes, C.; Laurenti, M.D.; Calegari Silva, T.C.; de Carvalho Vivarini, Á.; Fasel, N.; et al. Amazonian Phlebovirus (Bunyaviridae) potentiates the infection of Leishmania (Leishmania) amazonensis: Role of the PKR/IFN1/IL-10 axis. PLoS Negl. Trop. Dis. 2019, 13, e0007500. [Google Scholar] [CrossRef]
  61. Heirwegh, E.; MacLean, E.; He, J.; Kamhawi, S.; Sagan, S.M.; Olivier, M. Sandfly Fever Sicilian Virus-Leishmania major co-infection modulates innate inflammatory response favoring myeloid cell infections and skin hyperinflammation. PLoS Negl. Trop. Dis. 2021, 15, e0009638. [Google Scholar] [CrossRef] [PubMed]
  62. Chelbi, I.; Maghraoui, K.; Zhioua, S.; Cherni, S.; Labidi, I.; Satoskar, A.; Hamilton, J.G.C.; Zhioua, E. Enhanced attraction of sand fly vectors of Leishmania infantum to dogs infected with zoonotic visceral leishmaniasis. PLoS Negl. Trop. Dis. 2021, 15, e0009647, Erratum in PLoS Negl. Trop. Dis. 2021, 15, e0009947. [Google Scholar] [CrossRef]
  63. Dachraoui, K.; Chelbi, I.; Labidi, I.; Ben Osman, R.; Sayadi, A.; Ben Said, M.; Cherni, S.; Abbas, M.A.S.; Charrel, R.; Zhioua, E. The Role of the Leishmania infantum Infected Dogs as a Potential Reservoir Host for Toscana Virus in a Zoonotic Visceral Leishmaniasis Focus of Northern Tunisia. Viruses 2023, 15, 1012. [Google Scholar] [CrossRef] [PubMed]
  64. Maia, C.; Alwassouf, S.; Cristóvão, J.M.; Ayhan, N.; Pereira, A.; Charrel, R.N.; Campino, L. Serological association between Leishmania infantum and sand fly fever Sicilian (but not Toscana) virus in sheltered dogs from southern Portugal. Parasit Vectors. 2017, 10, 92. [Google Scholar] [CrossRef]
  65. Bichaud, L.; Souris, M.; Mary, C.; Ninove, L.; Thirion, L.; Piarroux, R.P.; Piarroux, R.; De Lamballerie, X.; Charrel, R.N. Epidemiologic relationship between Toscana virus infection and Leishmania infantum due to common exposure to Phlebotomus perniciosus sandfly vector. PLoS Negl. Trop. Dis. 2011, 5, e1328. [Google Scholar] [CrossRef]
Tropicalmed 09 00003 g001
Figure 1. Surveyed sites and collection of sand flies; the location of the co-circulation sites (Leishmania and phleboviruses) are also shown.
Figure 1. Surveyed sites and collection of sand flies; the location of the co-circulation sites (Leishmania and phleboviruses) are also shown.
Tropicalmed 09 00003 g001
Table 1. Sand flies collected and identified by sampled site and month of collection.
Table 1. Sand flies collected and identified by sampled site and month of collection.
Collection SiteParish, Municipality/MonthNumber of Collected Sand FliesTotal Number of Studied Pools (f/m)Identified Species
Alg1Quelfes, Olhão/May0--
Alg2Santiago, Tavira/May137 (6/1)Ph. perniciosus (3f; 1m)
Alg3Santa Maria, Tavira/May, June43857 (48/9)Ph. ariasi (2f; 2m), Ph. perniciosus (25f; 7m) Se. minuta (1f)
Alg4Conceição, Olhão/June5012 (1/11)Ph. perniciosus (7f)
Alg5Conceição, Olhão/June5712 (9/3)Ph. perniciosus (5f; 1m)
Alg6Loulé, Loulé/July32 (0/2)Ph. perniciosus (1f)
Alg7São Sebastião, Loulé/July7816 (13/3)Ph. ariasi (1f), Ph. perniciosus (7f; 2m)
Alg8Santa Bárbara de Nexe, Loulé/July318 (12/6)Ph. perniciosus (1f)
Alg9Moncarapacho, Olhão/August8516 (10/6)Ph. perniciosus (3f; 3m), Ph. sergenti (1f)
Alg10Quelfes, Olhão/August, October22925 (17/8)Ph. perniciosus (10f; 8m)
Alg11Quelfes, Olhão/August153 (2/1)Ph. perniciosus (1m)
Alg12Olhão, Olhão/September0--
Alg13Quelfes, Olhão/September0--
Alg14Conceição, Olhão/September988 (6/2)Ph. perniciosus (2f; 4m)
Alg15Tôr, Loulé/October248 (6/2)Ph. perniciosus (3f; 2m), Ph. sergenti (1f)
Alg16Moncarapacho, Olhão/September, October6810 (8/2)Ph. perniciosus (5f; 1m)
f—female; m—male.
Table 2. Collection stations, sampling dates, and pathogen identification in the sand fly pools.
Table 2. Collection stations, sampling dates, and pathogen identification in the sand fly pools.
Collection StationSampling Date in 2018Pool Size (f)/#Pool Number DNA BarcodingIdentified Pathogen/GenBank Accession NumberReference
Alg316 May20/#11-New phlebovirus?/ON807199[19]
Alg316 May1/#19Ph. perniciosusL. donovani complex OR783264This work
Alg55 June1/#32Ph. perniciosusL. donovani complex OR783265This work
Alg35 June20/#38-Massilia phlebovirus/ON807200[19]
Alg35 June1/#45Ph. perniciosusL. donovani complex * OR783266 This work
Alg37 June13/#57-L. donovani complex *This work
Alg37 June1/#61Ph. perniciosusL. donovani complex *This work
Alg57 June1/#86Ph. perniciosusL. donovani complex *This work
f—female; *—Sequencing was not possible due to low DNA concentration.
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Amaro, F.; Vilares, A.; Martins, S.; Reis, T.; Osório, H.C.; Alves, M.J.; Gargaté, M.J. Co-Circulation of Leishmania Parasites and Phleboviruses in a Population of Sand Flies Collected in the South of Portugal. Trop. Med. Infect. Dis. 2024, 9, 3. https://doi.org/10.3390/tropicalmed9010003

AMA Style

Amaro F, Vilares A, Martins S, Reis T, Osório HC, Alves MJ, Gargaté MJ. Co-Circulation of Leishmania Parasites and Phleboviruses in a Population of Sand Flies Collected in the South of Portugal. Tropical Medicine and Infectious Disease. 2024; 9(1):3. https://doi.org/10.3390/tropicalmed9010003

Chicago/Turabian Style

Amaro, Fátima, Anabela Vilares, Susana Martins, Tânia Reis, Hugo Costa Osório, Maria João Alves, and Maria João Gargaté. 2024. "Co-Circulation of Leishmania Parasites and Phleboviruses in a Population of Sand Flies Collected in the South of Portugal" Tropical Medicine and Infectious Disease 9, no. 1: 3. https://doi.org/10.3390/tropicalmed9010003

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