key: cord-0865861-vrkbsh9d authors: Stoefs, Anke; Heyndrickx, Leo; De Winter, Jonathan; Coeckelbergh, Evelien; Willekens, Barbara; Alonso-Jiménez, Alicia; Tuttino, Anne-Marie; Geerts, Yvette; Ariën, Kevin K.; Van Esbroeck, Marjan title: Autochthonous Cases of Tick-Borne Encephalitis, Belgium, 2020 date: 2021-08-03 journal: Emerg Infect Dis DOI: 10.3201/eid2708.211175 sha: f31c26484069bc2fe17fb4c30cd85f0ced69b778 doc_id: 865861 cord_uid: vrkbsh9d We report 3 confirmed autochthonous tick-borne encephalitis cases in Belgium diagnosed during summer 2020. Clinicians should include this viral infection in the differential diagnosis for patients with etiologically unexplained neurologic manifestations, even for persons without recent travel history. (MRI) showed demyelinating lesions and encephalopathy and electroencephalography showed diffuse slow activity. Serum collected on day 5 after illness onset tested positive for TBEV IgM and IgG by immunofl uorescence assay (IFA) performed at the NRC. Several months later, the patient still had weakness of her right arm, loss of cognitive function, inability to concentrate, fatigue, and tremor. A 59-year-old man was admitted to the neurology department of a hospital in Belgium with paraparesis and meningitis. Infl uenza-like symptoms, including fever, fatigue, myalgia, and headache, had occurred a few days earlier. CSF showed an elevated leukocyte count (371 cells/µL; reference range 0-5 cells/µL). Positron emission tomography (PET) and MRI showed no signs of underlying malignancies or encephalopathy. Infectious diseases screening did not reveal the etiology. The patient recalled a tick bite after a walk in a forest in his neighborhood 2 weeks before symptom onset. Borrelia and TBEV serology were added to the differential diagnosis, and TBEV antibodies were detected by IFA performed on serum collected on day 20 after illness onset. The patient went through a severe motor polyradiculitis and was using a wheelchair at discharge. At his last clinical evaluation, 9 months after hospitalization, the patient's motor skills had clearly improved. A 58-year-old man sought medical attention 48 hours after onset of dyspnea, cough, and fever. A COVID-19 test was done and repeated a week later; results of both were negative. The symptoms subsided for a week, but then fever returned, accompanied by severe and persistent headaches, weakness, decreased appetite, and diarrhea. The patient lived in the woods and enjoyed outdoor activities, such as biking and hiking. He recalled multiple tick bites and a bite by a sick squirrel in the weeks before symptom onset. A transesophageal echocardiogram and PET scan were normal, and screening for expected infectious diseases was negative. TBE was diagnosed by IFA performed on serum collected on day 18 after We report 3 confi rmed autochthonous tick-borne encephalitis cases in Belgium diagnosed during summer 2020. Clinicians should include this viral infection in the diff erential diagnosis for patients with etiologically unexplained neurologic manifestations, even for persons without recent travel history. illness onset. Except for occasional headaches, he recovered without residual symptoms. The NRC used Flavivirus Profile 2 (EUROIM-MUN AG, https://www.euroimmun.com) mosaic IFA to detect TBEV IgM and IgG antibodies in serum from the 3 patients and in CSF from 2 of them (no CSF was available for case 3). TBEV-specific antibodies were confirmed in all patients by plaque-reduction neutralization test (PRNT) with a 90% PRNT at titer ≥1:25. Retrospective real-time reverse transcription PCR (rRT-PCR), adapted from M. Schwaiger (4), on acute-phase serum collected from case-patient 3 revealed the presence of TBEV RNA, but the viral load was too low for further analysis (Table) . We describe 3 cases of confirmed autochthonous TBE in Belgium. TBEV IgM and IgG were detected in serum samples from all 3 cases. TBE was confirmed by PRNT. Intrathecally produced TBEV IgM were detected in 2 cases. In the third case, for which no CSF was available, TBE infection was confirmed by detection of TBEV RNA in an acute-phase serum sample. Because the virus typically is not detectable in serum or CSF by the time patients undergo TBE testing, rRT-PCR was not performed on convalescent samples from the other 2 cases (4, 5) . PCR testing on urine can be useful 1-2 weeks after symptom onset (6), but urine samples were not available from these cases. The 3 cases we describe met the current European Centre for Disease Prevention and Control case definition for confirmed TBE (7) . None of the patients had been vaccinated against TBEV or other flaviviruses, and none had traveled abroad in the months before symptom onset. Belgium closed its borders during March 20 through mid-June 2020 as part of measures to contain the COVID-19 pandemic. These regulations greatly increased outdoor activities, such as walking in forests, among the population in early spring 2020, probably leading to higher exposure to ticks (8) . The increased incidence of tick bites also was illustrated through the online platform TekenNet (9), a project of the Belgian Institute of Public Health that monitors tick exposure among the population by inviting citizens to voluntarily report tick bites. The 3 patients had been exposed in geographically separate regions of the country, 2 of which were adjacent to an area with known TBEV seropositivity in animals (Figure) . TBE occurs after an incubation period of a median of 8 (range 4-28) days after a bite from an infected tick (1). Serologic diagnosis of TBE is hampered by a degree of cross reactivity with the antibodies against other flaviviruses in nearly all assays (5) . The flavivirus IFA used by the NRC can determine the predominant flavivirus antibody response because it combines 8 different flavivirus substrates on different biochips. Unlike IgG, IgM responses generally are type-specific; therefore, IFA IgM is a useful tool for identification of infections during the acute phase of disease (1) . The incidence of TBE in Europe has increased in recent years, and the infection emerged in the Netherlands in 2016 and the United Kingdom in 2019 (10,11). The occurrence of autochthonous cases in the Netherlands in 2016, not far from the border with Belgium, led to a 26% increase in TBE serology inquiries at the NRC in 2017 compared with those for 2016 and a 143% increase in 2018 compared with those for 2017 (M. Van Esbroeck, unpub. data). In Belgium, the virus has been shown to circulate in animals, but human infections have been limited to a few imported cases until now (2, 12) . In 2018, two human cases of autochthonous TBE were suspected but not confirmed because both patients also spent time abroad during the incubation period (3, 13, 14) . In a study on the prevalence of pathogens in ticks collected from humans in Belgium, none of the examined ticks were infected with TBEV (14, 15) . Studies to determine the geographic spread and genetic diversity of TBEV in ticks were put on hold in 2020 due to the COVID-19 pandemic. During the 2021 tick season, ticks will be collected by flagging in areas where TBEV exposure most likely occurred for the 3 described patients. Confirmed TBE cases involving the central nervous system are reported to the European Surveillance System (3) . Because approximately two thirds of human TBEV infections are asymptomatic, TBE probably is underdiagnosed in Europe (15) . Vaccination against TBEV is not recommended for the general population (3). However, persons living in Belgium should be aware of the risk for exposure to ticks and protect themselves against tick bites when engaging in outdoor activities. Clinicians also should include TBE in the differential diagnosis in patients with etiologically unexplained neurologic manifestations, even without a recent travel history. Geographic distribution of autochthonous human cases of tick-borne encephalitis, Belgium and the Netherlands (adapted from National Institute of Public Health and Environment [10]). Grey shading indicates communities in Belgium in which antibodies against tick-borne encephalitis virus have been detected in animals (adapted from S. Roelandt [2] ). Ms. Stoefs is completing a postgraduate specialization in clinical biology at the University of Louvain and is an intern at the Institute of Tropical Medicine, Antwerp. Her current research interest includes arboviral diseases. Tick-borne encephalitis Questing for tick-borne encephalitis virus in Belgium using veterinary sentinel surveys and risk factor mapping Superior Health Council. Vaccination against tick-borne encephalitis (TBE) Development of a quantitative real-time RT-PCR assay with internal control for the laboratory detection of tick borne encephalitis virus (TBEV) RNA Diagnosis of tick-borne encephalitis Detection of tick-borne encephalitis virus RNA in urine European Centre for Disease Prevention and Control. EU case definitions: European Commission TickNet 2020: surveillance of tick bites in Belgium National Institute for Public Health and the Environment. Spread of tick-borne encephalitis virus in the Netherlands A probable case of tick-borne encephalitis (TBE) acquired in England Case report: tick-borne encephalitis (TBE) in a Belgian traveller returning from Germany Zoonoses and vector-transmitted diseases: summary annual review The TBE Book Prevalence of pathogens in ticks collected from humans through citizen science in Belgium We thank the patients for providing permission to report their clinical symptoms and disease course. We thank John Lebbink, Anne-Sophie Sauvage, Sophie de Worm, and all laboratory technicians for their contribution in generating the data for this study. We thank Jens Roux for assistance with illustration preparation.