Volume 30, Number 2—February 2024
Dispatch
Tick-Borne Encephalitis, Lombardy, Italy
Abstract
Tick-borne encephalitis was limited to northeast portions of Italy. We report in Lombardy, a populous region in the northwest, a chamois displaying clinical signs of tickborne encephalitis virus that had multiple virus-positive ticks attached, as well as a symptomatic man. Further, we show serologic evidence of viral circulation in the area.
Tick-borne encephalitis (TBE) is a considerable public health concern caused by the tick-borne encephalitis virus (TBEV), a member of the Flaviviridae family. This virus is classified into 5 genotypes; European, Siberian, and Far Eastern are the main types, each exhibiting distinct epidemiologic patterns and clinical manifestations (1). TBEV infection is mainly attributed to the bite of Ixodes ticks, most notably Ixodes ricinus in Europe (1). The virus primarily affects the central nervous system, leading to a range of neurologic symptoms and potential long-term complications, including death. Clinical manifestations of TBE consist of a first phase characterized by headache and fever and a second phase, where myelitis can cause altered consciousness, tremors, ataxia, and paresis (1).
TBEV is distributed across several regions of Europe and Asia. European TBEV is prevalent in Austria, Germany, Sweden, Switzerland, and the Russian Federation (2). This strain is endemic in northeastern Italy (3), but the rest of the country has been considered virus-free, with the exception of a single autochthonous case in Emilia-Romagna (4). A recent serologic screening of wild ungulates confirmed the absence of TBEV in the Piedmont region (5). No data on TBEV in the most populous region of Italy, Lombardy, have been published recently. Considering Lombardy’s position, bordering states (Switzerland) and regions where the pathogen is endemic, and the abundant presence of I. ricinus ticks (6,7), Lombardy represents an area at risk for expansion of TBEV.
The Experimental Zooprophylactic Institute of Lombardy and Emilia Romagna (IZSLER) is responsible for the surveillance of the wild fauna in the Lombardy region. Considering the potential risk for TBEV expansion, the Institute started molecular screening of ticks retrieved from humans in Lombardy in 2019 (8). Since 2021, serologic analysis of wild ungulates (9) was added to the surveillance program, including serum samples collected in the previous year. A total of 3,555 ticks have been subjected to molecular surveillance since the start of the program (2,556 from humans, 999 from wildlife), and none were found to be positive. Out of the 1,954 examined samples from wild ungulates, 47 samples tested positive for TBEV antibodies (Table; Figure 1). Albeit not fully conclusive, those results prompted an increased alert, with attention to possible cases of neurologic symptoms compatible with TBE in animals and humans in the region.
On November 28, 2022, a 49-year-old male hunter sought treatment at the Pope John XXIII Hospital in Bergamo, Lombardy, displaying clinical symptoms compatible with TBE. The man reported a tick bite in the previous month while in Val Brembana valley (Figure 1), with no recent history of travel outside of the region, but multiple mountain excursions in the study area. He reported clinical manifestations that included fever and fatigue, followed a few days later by neurologic symptoms (lack of coordination and equilibrium), which supported a 2-phase clinical picture compatible with TBE (1). Serologic exam for TBEV resulted in positive readings for both IgG and IgM. The patient’s clinical picture improved spontaneously, and he was discharged on December 12, 2022. Since that time, he has reported myalgia, fatigue, impairment of concentration, and memory lapses.
On May 12, 2023, in Carona, Bergamo Province, Lombardy region (Figure 1), a hunter encountered a chamois (European goat-antelope) that had neurologic symptoms of ataxia, muscle tremors, incoordination, and frequent swallowing. The chamois was killed and conferred to the IZSLER, where we performed necropsy and collected blood and organs for further examination. Postmortem examination revealed poor general condition, absence of adipose tissue, and incomplete molt. Necropsy did not reveal mechanical trauma or ingestion of poisonous food. A massive tick infestation was presen; some ticks were clustered, but others were scattered on various areas of the body. At the lung level, pleuro-costal adhesions and parasitic nodular lesions were evident. Other observations included gastrointestinal nematodes, pallor of the kidney parenchyma and cribrous appearance of the cortical surface, hypertrophy of the adrenals, and pallor of the liver, including focal irregular, whitish lesions on the surface. Histopathology revealed severe, chronic, nonpurulent meningoencephalitis, characterized by perivascular lymphohistiocytic cuffs, neuronal necrosis, and satellitosis (Figure 2, panel A). Immunohistochemical analysis showed neuronal positivity for TBEV (Figure 2, panel B). An attempt to culture the virus from brain tissue on Vero E6 cells (IZSLER Biobank code BSCL87, http://www.ibvr.org) was unsuccessful.
The animal’s blood was used for molecular and serologic investigations, which both showed evident TBEV positivity, as did a pool of organs and brain. The threshold cycle of the PCR of the organ pool was low, suggesting a high viraemia. A total of 26 ticks were found attached to the body, all identified morphologically as adult I. ricinus ticks, 12 of them male and 14 partially engorged female. All retrieved ticks were subjected to TBEV PCR; 4 male and 8 female ticks showed clear positivity. We Sanger sequenced PCR products (224 nt) from the chamois and from the ticks; sequences were all identical (Genbank accession nos. OR473050–4) so we used 1 representative for phylogenetic reconstruction (Figure 3). The phylogenetic tree shows that the novel sequence falls within sequences representing the European genotype (10).
In parallel, we performed bacteriologic examination of the viscera of the chamois and tested for Anaplasma phagocytophilum, Babesia spp., and pestiviruses. All test results were negative. We also screened the ticks for other pathogens, namely Borrelia spp., Babesia spp., Rickettsia spp., Francisella spp., Coxiella burnetii, and Anaplasma, as previously performed (11,12). All results were negative, except for 2 females found positive for Rickettsia helvetica and 1 found positive for Borrelia miyamotoi, all confirmed by Sanger sequencing.
We report TBE cases in a human and in a chamois in the Lombardy region of Italy, as well as molecular positivity in I. ricinus ticks. A clinical case in a chamois is especially noteworthy given recently reported clinical cases of TBEV in other wild and domestic animals, including ruminants (13), and the steady increase of wild ruminants in the Alps (14). The high viraemia of the chamois we studied, together with the TBEV positivity of multiple attached ticks, suggests a potential role in the maintenance of the virus, one generally not considered (13,15). Our finding of TBE-positive I. ricinus male ticks with sequences identical to female ticks is compatible with transstadial and venereal transmission; female tick positivity could also be explained by cofeeding. When considered alongside the high amount of virus detected in the chamois, the findings from our analysis of the attached ticks corroborate the existence of a complete cycle of infection and a potential role of this animal as reservoir.
Results from our investigation indicate the presence of TBE in northwestern Italy and suggest the need for increased awareness of the westward spread of TBEV, now present in most of the central Alps. The severity of the reported human case highlights the importance of raising the awareness of stakeholders and high-risk portions of the population (e.g., hunters, excursionists, and farmers) to promote vaccination and control of raw milk and traditional cheesemaking. Taking immediate preventive measures in the most at-risk areas will help prevent subsequent clinical cases of TBEV in humans.
Dr. Gaffuri is a graduate in veterinary medicine in Milan, Italy, and works at the Istituto Zooprofilattico Sperimentale della Lombardia e dell’Emilia Romagna, Bergamo. She is involved in research and surveillance in microbiology, and animal and wildlife health.
Acknowledgment
Work was funded by the Extended Partnership Project INF-ACT (PE_00000007), which is part of the National Recovery and Resilience Plan, and by the Italian Ministry of Health, Directorate–General for animal health and veterinary medicinal products (grant no. IZSLER 2021/014).
References
- Chiffi G, Grandgirard D, Leib SL, Chrdle A, Růžek D. Tick-borne encephalitis: A comprehensive review of the epidemiology, virology, and clinical picture. Rev Med Virol. 2023;33:
e2470 . DOIPubMedGoogle Scholar - Wondim MA, Czupryna P, Pancewicz S, Kruszewska E, Groth M, Moniuszko-Malinowska A. Epidemiological trends of trans-boundary tick-borne encephalitis in Europe, 2000–2019. Pathogens. 2022;11:704. DOIPubMedGoogle Scholar
- Alfano N, Tagliapietra V, Rosso F, Ziegler U, Arnoldi D, Rizzoli A. Tick-borne encephalitis foci in northeast Italy revealed by combined virus detection in ticks, serosurvey on goats and human cases. Emerg Microbes Infect. 2020;9:474–84. DOIPubMedGoogle Scholar
- Barp N, Cappi C, Meschiari M, Battistel M, Libbra MV, Ferri MA, et al. First human case of tick-borne encephalitis in non-endemic region in Italy: a case report. Pathogens. 2022;11:854. DOIPubMedGoogle Scholar
- Garcia-Vozmediano A, Bellato A, Rossi L, Hoogerwerf MN, Sprong H, Tomassone L. Use of wild ungulates as sentinels of TBEV circulation in a naïve area of the Northwestern Alps, Italy. Life (Basel). 2022;12:1888. DOIPubMedGoogle Scholar
- Cafiso A, Olivieri E, Floriano AM, Chiappa G, Serra V, Sassera D, et al. Investigation of tick-borne pathogens in Ixodes ricinus in a peri-urban park in Lombardy (Italy) reveals the presence of emerging pathogens. Pathogens. 2021;10:732. DOIPubMedGoogle Scholar
- Otranto D, Dantas-Torres F, Giannelli A, Latrofa MS, Cascio A, Cazzin S, et al. Ticks infesting humans in Italy and associated pathogens. Parasit Vectors. 2014;7:328. DOIPubMedGoogle Scholar
- Schwaiger M, Cassinotti P. Development of a quantitative real-time RT-PCR assay with internal control for the laboratory detection of tick borne encephalitis virus (TBEV) RNA. J Clin Virol. 2003;27:136–45. DOIPubMedGoogle Scholar
- Lelli D, Moreno A, Zanoni M, Pezzoni G, Sozzi E, Brocchi E, et al. Tick-borne encephalitis (TBE): development of a serological test for the detection of specific antibodies in animal sera [D10:132]. Presented at: Epizone 7th Annual Meeting; Brussels, Belgium; October 1–4, 2013.
- Formanová P, Černý J, Bolfíková BČ, Valdés JJ, Kozlova I, Dzhioev Y, et al. Full genome sequences and molecular characterization of tick-borne encephalitis virus strains isolated from human patients. Ticks Tick Borne Dis. 2015;6:38–46. DOIPubMedGoogle Scholar
- Maioli G, Pistone D, Bonilauri P, Pajoro M, Barbieri I, Mulatto P, et al. Etiological [corrected] agents of rickettsiosis and anaplasmosis in ticks collected in Emilia-Romagna region (Italy) during 2008 and 2009. Exp Appl Acarol. 2012;57:199–208. DOIPubMedGoogle Scholar
- Pajoro M, Pistone D, Varotto Boccazzi I, Mereghetti V, Bandi C, Fabbi M, et al. Molecular screening for bacterial pathogens in ticks (Ixodes ricinus) collected on migratory birds captured in northern Italy. Folia Parasitol (Praha). 2018;65:2018.008.
- Da Rold G, Obber F, Monne I, Milani A, Ravagnan S, Toniolo F, et al. Clinical tick-borne encephalitis in a roe deer (Capreolus capreolus L.). Viruses. 2022;14:300. DOIPubMedGoogle Scholar
- Paulsen KM, das Neves CG, Granquist EG, Madslien K, Stuen S, Pedersen BN, et al. Cervids as sentinel-species for tick-borne encephalitis virus in Norway - A serological study. Zoonoses Public Health. 2020;67:342–51. DOIPubMedGoogle Scholar
- Michelitsch A, Wernike K, Klaus C, Dobler G, Beer M. Exploring the reservoir hosts of tick-borne encephalitis virus. Viruses. 2019;11:669. DOIPubMedGoogle Scholar
Figures
Table
Cite This ArticleTable of Contents – Volume 30, Number 2—February 2024
EID Search Options |
---|
Advanced Article Search – Search articles by author and/or keyword. |
Articles by Country Search – Search articles by the topic country. |
Article Type Search – Search articles by article type and issue. |
Please use the form below to submit correspondence to the authors or contact them at the following address:
Davide Sassera, Department of Biology and Biotechnology, University of Pavia, Via Ferrata 9, 27100 Pavia (PV), Italy; Email:davide.sassera@unipv.it
Top