Volume 22, Number 5—May 2016
Acute Human Inkoo and Chatanga Virus Infections, Finland
Inkoo virus (INKV) and Chatanga virus (CHATV) are 2 members of the California serogroup of orthobunyaviruses that are currently found in Finland. They are trisegmented, enveloped negative-strand RNA viruses belonging to genus Orthobunyavirus (family Bunyaviridae), which includes several recognized mosquitoborne human pathogens.
INKV was first isolated from Ochlerotatus communis and O. punctor mosquitoes in 1964 in Finland (1) and has since been found in Sweden, Norway, and Russia (2–4). The high seroprevalence in these countries suggests that INKV infections are common in these locations (5–8). Although the virus has been known to occur in Finland for decades, only 1 domestic report describes a possible association of INKV to clinical disease (9). Reports from Russia show INKV IgM or neutralizing antibodies in patients with neurologic symptoms or fever, but only 2 cases were identified as INKV infection; most often, the California serogroup virus infections were caused by Tahyna virus (TAHV), or the infecting virus could not be defined (10–12).
CHATV was isolated in Finland in 2007 (13) but is known to have circulated earlier in Russia, where the first characterized isolate was from a mosquito collected in 1987 (14). CHATV strains have ≈84% aa identity with INKV within the nucleocapsid protein but are more similar to the Snowshoe hare virus (93% nucleocapsid protein identity) that occurs in the United States. We found no previous reports of CHATV infections naturally occurring in humans or animals.
Patients with California serogroup virus infections usually remain asymptomatic or have symptoms of mild influenza-like illness, but some of these viruses may also cause encephalitis (15–17). The California serogroup viruses cross-react on many serologic tests, so neutralization assays are required to verify the specific virus. In the United States, 29–167 cases of California serogroup virus encephalitis are diagnosed annually, and most cases result from La Crosse virus (LACV) (18), which is one of the most important arboviral agents causing encephalitis in children in the United States but is rarely found in adults. This pattern contrasts with the arbovirus West Nile virus, which causes central nervous system (CNS) infections in adults more often than in children (19). LACV encephalitis can be mistaken for herpes simplex virus (HSV) or enterovirus meningoencephalitis and is often undiagnosed (15,20). Other orthobunyaviruses that cause neuroinvasive disease in the United States and Canada are California encephalitis, Jamestown Canyon, and Snowshoe hare viruses (17,21–24), although infections caused by these viruses are reported more rarely than those caused by LACV and are not as extensively studied.
The incidence of California serogroup virus infections in Europe is largely unknown because of underdiagnosing and underreporting that result from lack of alertness among healthcare workers and lack of surveillance efforts. Available data indicate that TAHV has the most widespread distribution in Europe and is mostly asymptomatic or causes febrile illness, especially in children (16,25,26).
Because pathogens that cause encephalitis during the summer months in Finland are mostly unknown (27), we attempted to study the occurrence of acute California serogroup virus infections, particularly those caused by INKV, in febrile and encephalitic patients during the mosquito season in Finland and to characterize those infections. We report our observance of INKV and CHATV infections in humans and describe the clinical characteristics of acute infections caused by these viruses.
Our analysis comprised 3 sets of patient samples (7,961 total patients). First, we retrospectively screened serum samples that were collected from patients in healthcare facilities across Finland during the summer months of 2001–2013 (Table 1) and were sent as diagnostic samples to the Department of Virology and Immunology, Helsinki University Central Hospital Laboratory, Hospital District of Helsinki and Uusimaa (institutional review board permit 119/E0/05). For patients presumed to have CNS symptoms, samples were screened for antibodies against a panel of meningoencephalitis agents (HSV, varicella zoster virus, human herpesvirus 6, enterovirus, and Mycoplasma pneumoniae bacteria); for patients presumed to have febrile illness, samples were screened for Puumala virus. For most samples, laboratory screening was negative for the viral agents studied. In addition to these 2 sample groups, we analyzed samples specifically received for screening of INKV antibodies during the study period.
Of the total 8,793 samples we tested for California serogroup virus IgM, 4,214 serum samples and 832 cerebrospinal fluid (CSF) samples had been initially sent for screening of meningoencephalitis agents; 3,574 serum samples had been initially sent for Puumala virus testing; and 173 serum samples had been sent for INKV testing. Samples were stored at −20°C; aliquots of the serum samples were stored at –70°C for PCR testing. Laboratory data and patient histories were collected from patient records for cases with confirmed California serogroup virus IgM positivity. Data on 2 previously confirmed cases with INKV infection that occurred in 1976 and 1980 were included in the analysis; these cases had been confirmed with hemagglutination inhibition and neutralization tests, and full patient histories had been described previously (9).
Serum samples were screened with an indirect INKV-IgM immunofluorescence (IFA) test described previously (5). In brief, IFA slides contained Vero E6 cells (green monkey kidney cells, American Type Culture Collection, CRL-1586, Manassas, VA, USA); 30% of the cells were infected with INKV. Samples (serum diluted at 1:20 ratio; CSF undiluted) were incubated on slides overnight and then washed with phosphate-buffered saline; anti–human IgM fluorescein isothiocyanate conjugate was then added, and samples were incubated for 1 hour. After being washed with phosphate-buffered saline, slides were dried and examined with a fluorescence microscope. IgM-positive samples were retested with IgM IFA after removal of IgG by using Gullsorb treatment (Meridian Bioscience, Inc., Cincinnati, OH, USA) for the serum samples. To ensure that diagnostic criteria of acute infection were met, as previously described, IgM-positive samples were confirmed with IgG IFA testing (5) and studied with INKV prototype strain KN3641 (1), CHATV Möhkö strain M07–1 (13), and TAHV prototype strain Bardos 92 (28) plaque-reduction neutralization test (PRNT) (13). PRNT was performed because of the occurrence of cross-reactions.
Reverse Transcription PCR
When possible (i.e., when sufficient sample remained after serologic testing), IgM-positive samples were tested with reverse transcription PCR (RT-PCR) to study the presence and kinetics of viremia and to obtain information on the viral sequences. RNA extraction was performed by using the QIAamp Viral RNA Mini Kit (QIAGEN, Valencia, CA, USA) according to the manufacturer’s instructions. The extracted RNA was reverse transcribed to cDNA with ERT-Ro Roche Expand Reverse Transcriptase (Roche, Indianapolis, IN, USA). PCR methods, as described previously (29,30), were modified to work with the Phusion Flash High-Fidelity PCR Master Mix (Thermo Scientific, Grand Island, NY, USA). The mixture included 1.25 µL of each primer (10 µmol/L), 12.5 µL of the Phusion Flash 2X buffer, and 8 µL of sterile distilled deionized water, producing a total volume of 25 µL, which included 2 µL of cDNA.
Our hospital diagnostic laboratory received 7,961 serum and 832 CSF samples from 7,961 patients in Finland during 2001–2013 (Table 1). Samples were initially submitted to determine antibodies against either a panel of agents causing neurologic infections (4,214 serum and 832 CSF samples), Puumala virus (3,574 serum samples), or INKV (173 serum samples) (Table 1). Most (4,299 [54%]) serum samples were from healthcare settings in southern Finland. Children <10 years of age had the smallest number of samples; adults 50–59 years of age had the largest number of samples. A slight preponderance (52%) of sampled patients were male.
Including the 2 previously confirmed cases, a total of 17 serum samples and no CSF samples were found IgM positive for California serogroup viruses. Serum samples were IgM positive among 0.21% of patients with CNS symptoms, 0.14% of patients with suspected Puumala virus infection, and 0.58% of patients with suspected INKV infection (Table 1). Frequency of IgM positivity was similar for different years of sample collection. The age range of patients with positive results was 7–81 years; 8 patients were female and 9 were male. California serogroup viruses IgM was found most commonly in patients <19 or 50–59 years of age (Table 2). Most (88%) IgM-positive cases were detected during or after late August. Fourteen (82%) of the 17 patients showed the highest neutralizing antibody titers (up to 1,280) against INKV, whereas 3 patients showed the highest titers (up to 20,480) against CHATV. Neutralization tests for 2 of the 3 CHATV patients resulted in titers >4 times those for other studied California serogroup viruses, which met the diagnostic criterion for confirmed CHATV infection; the third CHATV patient with a lower titer likely had CHATV infection (Table 3). The earliest that IgM was detectable was day 3 of symptom onset (fever); 1 patient still had detectable IgM 3 weeks after symptom onset (Table 4). IgM titers varied generally between 1:30 and 1:160, and exceeded 1:320 in only 3 patients. IgG in IFA was detected in most IgM-positive patients. No patient had detectable California serogroup virus RNA.
Clinical histories were collected for all patients whose samples had a positive INKV IgM result (Table 3). Patients could be divided into 2 groups: those with a known reason (other than INKV infection) for seeking medical care (10/17) and those for whom the cause of acute infection was unknown (7/17) (Table 3). The latter group of patients were evaluated for California serogroup virus infection because their medical records showed no other cause for their symptoms (i.e., no underlying disease or laboratory findings that implied another infection) (Table 4). All 4 children (<16 years of age) with an unknown infection had acute INKV infection, whereas 2 adults with an unidentified infection had CHATV infection. These 6 patients were hospitalized. All had fever and other symptoms such as sore throat, nausea and vomiting, and neurologic conditions such as disorientation, nuchal rigidity, headache, and drowsiness. Small changes in electroencephalography were observed in 2 patients, and 1 patient had seizures (Tables 4, 5). All patients fully recovered from the infections.
Of the 17 California serogoup virus infection IgM-positive patients, 11 were not hospitalized for that infection. Four of these 11 patients visited a physician only once; 6 others were treated for another indication because their symptoms were interpreted as resulting from causes other than INKV infection. Ten (91%) of the 11 patients who were not hospitalized were >40 years of age. Six (55%) of the 11 outpatients had a laboratory-confirmed co-infection with another pathogen, such as HSV (antigen positive), acute Puumala virus infection (i.e., the same serum sample was positive for Puumala virus IgM), an Escherichia coli urosepsis, and impetigo contagiosa. One patient was reported to have had erythema migrans 4 weeks before sample collection, yet no antibodies against Borrelia burgdorferi were found. One patient suffered a back injury 1 week before symptom onset (Table 3).
In previous studies, the prevalence of California serogroup virus antibodies was high (30%–40%) in Nordic countries (5,8). To maintain such a high seroprevalence in Finland, >20,000 acute infections would need to occur annually during the mosquito season. Worldwide, California serogroup viruses other than INKV and CHATV have been associated with febrile illnesses and neurologic infection, but these infections have not been characterized in Finland. For that purpose, we retrospectively screened panels of serum samples that were originally collected over a period of years during the mosquito season and sent to our diagnostic laboratory for detection of antibodies to either causative agents of CNS infection (HSV1, HSV2, human herpesvirus 6, varicella zoster virus, Mycoplasma pneumoniae), Puumala virus, or INKV.
We estimated the frequency of acute human CHATV and INKV infections and characterized symptoms of these infections. The 2 patients with confirmed CHATV infection show that CHATV can cause human infection. We found symptoms that were similar to those reported for other viruses in the California serogroup. Both INKV and CHATV have remained practically unknown among physicians in Finland, and the rate of clinical suspicion has been negligible here (Table 1). The lack of awareness regarding these infections is similar to the situation with California serogroup viruses in many other countries.
A few articles from Russia have described the outcome and neurologic characteristics of INKV infection (10–12). In these studies, most patients had fever; almost 30% had neurologic symptoms (11). Studies in the Ryazan area showed that INKV infection was most frequently found in adults 21–40 years of age, and the number of cases peaked during the 2 periods of May and early August (31). In our study, 88% of the INKV cases were found during August and September or even later; only 2 cases occurred in early summer, and most patients with acute infection were <16 or 50–59 years of age. Another study from Russia included 520 selected patients; overall, 9.8% had California serogroup infection, with 2.5% and 1.2% INKV incidence in febrile and encephalitis patients, respectively (11). A more detailed study on the symptoms of the California serogroup infection included 118 patients, but INKV was confirmed in only 2 patients, 1 with multiple sclerosis and the other with meningoencephalitis (10). In that study, TAHV and undefined California serogroup infections (i.e., neutralization tests found no difference between INKV and TAHV) occurred more frequently than INKV (10). However, during 1995, the study period, CHATV had not yet been isolated but, as we now know, was already circulating in the area (14). Consequently, these infections could have been caused by CHATV.
Our study confirmed both INKV and CHATV infections in Finland. Most identified acute cases were from the Helsinki hospital district (Figure), possibly because most samples were collected in southern Finland, where the laboratory is located and where Finland’s population density is highest. The overrepresentation of samples from the southern region may have decreased the likelihood of finding acute cases because distribution of California serogroup virus seroprevalence among humans is greater in northern Finland than in southern Finland, although the seroprevalence has recently increased in southern parts of the country (5,32). Furthermore, the high seroprevalence suggests that the serogroup viruses are found abundantly in nature and that infection is fairly common, so the frequency of acute cases we observed may underestimate the actual number of cases in Finland. Most acute cases occurred in autumn, yet the population density of the INKV principal vector, O. communis, is highest in June. Further studies are needed to determine whether this time lag reflects a long incubation period, spillover to other vectors, replication cycle in amplification hosts, or a change in vector occurrence.
The high seroprevalence in Finland with the low frequency of cases requiring healthcare and low frequency of diagnostic sampling suggests that most of these infections are subclinical or manifest as mild disease. On the other hand, the patient panels used in our study were highly selected, so we could have missed INKV and CHATV cases among patients with other symptom patterns. In addition, the IgM IFA test used may not have been sensitive enough to detect IgM in all cases. The high seroprevalence in the populations in Finland may also be influenced by the newly identified California serogroup virus isolate found here, the Chatanga virus Möhkö strain (13). Results from the diagnostic test in use show cross-reactions between the serogroup viruses. Most (82%) of the acute infections in this study were INKV cases, confirmed by using PRNT, which showed >4-fold titer differences, consistent with findings that INKV is the major California serogroup agent in seroprevalence studies in Finland and Sweden (33). Although most cases seem subclinical or mild, the data in our study indicate that the clinical disease may occasionally be severe; all children with acute illness had INKV infection and were hospitalized. Although INKV infection in adults was mild, 1 adult patient with CHATV infection required hospital care.
The considerable variation in IgG and IgM titers of serum samples from patients with acute infection may suggest that the samples were taken at different stages of the acute infection, but the differences may simply reflect variation in the antibody levels in individual patients. IgM was detectable in several patients concomitantly with high titers of IgG and neutralizing antibodies, a finding suggesting that IgM may persist for several weeks. One patient had detectable IgM 17 days after symptom onset (Table 4). A follow-up sample would be needed to show seroconversion and confirm the acute infection. No patient samples were collected during the viremic stage, and all samples were RT-PCR negative. Distinct LACV strains are known to cause different symptoms (34), but neither INKV nor CHATV have been isolated from a human sample. Human isolates or sequences of these viruses would be valuable for comparing the pathogenicity of the strains and analyzing cases in patients requiring hospitalization.
Many of our cases appear to represent recent subclinical infections that were identified only because of IgM testing and were unrelated to the reason for patients’ visits to the healthcare unit. In the 2 patients with HSV cold sores, subclinical INKV infection could have triggered reactivation of HSV. Alternatively, INKV may require the presence of an underlying disease or trauma to cause a symptomatic infection (e.g., by enabling the virus to cross the blood–brain barrier). Some reports from Russia suggest that certain concomitant microbial infections may render the course of the INKV infection more severe (11).
In conclusion, we describe INKV and CHATV infections in humans and the clinical characteristics of acute disease. Symptoms of acute INKV and CHATV infections in patients in our study resembled symptoms of other California serogroup virus infections: influenza-like illness, with fever being most prominent. Most acute cases appeared to be subclinical, and a small minority of patients required hospitalization. Compared with adults, children were at higher risk for contracting more severe disease and were more often hospitalized because of INKV infection. In adults, CHATV infection appeared to be more severe than INKV infection. Further studies are required to explore in detail the clinical picture, prognosis, incubation period, and antibody kinetics of these infections. Viral isolates or RT-PCR–positive samples from patients are needed to acquire data related to INKV and CHATV strains causing the clinical cases.
Niina Putkuri is a PhD student who works at the Faculty of Medicine, University of Helsinki, where she is finalizing her thesis. Her research interests include molecular epidemiology and disease associations of California serogroup viruses in Finland.
We thank Tytti Manni and Pirjo Sarjakivi for excellent technical assistance.
This work was supported by the Finnish Cultural Foundation, the Paulo Foundation, Laboratoriolääketieteen Edistämissäätiö, Academy of Finland, and a Hospital District of Helsinki and Uusimaa Finnish State grant (TYH2014251).
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Suggested citation for this article: Putkuri N, Kantele A, Levanov L, Kivistö I, Brummer-Korvenkontio M, Vaheri A, et al. Acute human Inkoo and Chatanga virus infections, Finland. Emerg Infect Dis. 2016 May [date cited]. http://dx.doi.org/10.3201/eid2205.151015