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Dive into the research topics where Eva R. Kallio is active.

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Featured researches published by Eva R. Kallio.


Emerging Infectious Diseases | 2003

Cowpox with severe generalized eruption, Finland.

Paula Pelkonen; Kyllikki Tarvainen; Arja Hynninen; Eva R. Kallio; Heikki Henttonen; Airi Palva; Antti Vaheri; Olli Vapalahti

Cowpox with a severe, generalized eruption was diagnosed in an atopic 4-year-old girl by electron microscopy, virus isolation, polymerase chain reaction, and immunoglobulin (Ig) M and low-avidity IgG antibodies. The hemagglutinin gene of the isolate clustered with a Russian cowpox virus strain, and more distantly, with other cowpox and vaccinia virus strains. The patient’s dog had orthopoxvirus-specific antibodies, indicating a possible transmission route.


Ecology | 2007

ENDEMIC HANTAVIRUS INFECTION IMPAIRS THE WINTER SURVIVAL OF ITS RODENT HOST

Eva R. Kallio; Liina Voutilainen; Olli Vapalahti; Antti Vaheri; Heikki Henttonen; Esa Koskela; Tapio Mappes

The influence of pathogens on host fitness is one of the key questions in infection ecology. Hantaviruses have coevolved with their hosts and are generally thought to have little or no effect on host survival or reproduction. We examined the effect of Puumala virus (PUUV) infection on the winter survival of bank voles (Myodes glareolus), the host of this virus. The data were collected by monitoring 22 islands over three consecutive winters (a total of 55 island populations) in an endemic area of central Finland. We show that PUUV infected bank voles had a significantly lower overwinter survival probability than antibody negative bank voles. Antibody negative female bank voles from low-density populations living on large islands had the highest survival. The results were similar at the population level as the spring population size and density were negatively correlated with PUUV prevalence in the autumn. Our results provide the first evidence for a significant effect of PUUV on host survival suggesting that hantaviruses, and endemic pathogens in general, deserve even more attention in studies of host population dynamics.


Proceedings of the National Academy of Sciences of the United States of America | 2009

Host–pathogen time series data in wildlife support a transmission function between density and frequency dependence

Matthew J. Smith; Sandra Telfer; Eva R. Kallio; Sarah Burthe; Alex R. Cook; Xavier Lambin; Michael Begon

A key aim in epidemiology is to understand how pathogens spread within their host populations. Central to this is an elucidation of a pathogens transmission dynamics. Mathematical models have generally assumed that either contact rate between hosts is linearly related to host density (density-dependent) or that contact rate is independent of density (frequency-dependent), but attempts to confirm either these or alternative transmission functions have been rare. Here, we fit infection equations to 6 years of data on cowpox virus infection (a zoonotic pathogen) for 4 natural populations to investigate which of these transmission functions is best supported by the data. We utilize a simple reformulation of the traditional transmission equations that greatly aids the estimation of the relationship between density and host contact rate. Our results provide support for an infection rate that is a saturating function of host density. Moreover, we find strong support for seasonality in both the transmission coefficient and the relationship between host contact rate and host density, probably reflecting seasonal variations in social behavior and/or host susceptibility to infection. We find, too, that the identification of an appropriate loss term is a key component in inferring the transmission mechanism. Our study illustrates how time series data of the host–pathogen dynamics, especially of the number of susceptible individuals, can greatly facilitate the fitting of mechanistic disease models.


Proceedings of the Royal Society of London B: Biological Sciences | 2006

Maternal antibodies postpone hantavirus infection and enhance individual breeding success

Eva R. Kallio; Antti Poikonen; Antti Vaheri; Olli Vapalahti; Heikki Henttonen; Esa Koskela; Tapio Mappes

The transfer of maternal antibodies from mother to progeny is a well-known phenomenon in avian and mammalian species. Optimally, they protect the newborn against the pathogens in the environment. The effect of maternal antibodies on microparasite transmission dynamics may have important consequences for both the fitness of the host and the epizootic processes of the pathogens. However, there is a scarcity of studies examining these effects in free-living wild species. We studied the influence of maternal antibodies against the zoonotic Puumala hantavirus (PUUV) on the fitness of bank voles (Clethrionomys glareolus) and on PUUV transmission by exposing young maternal antibody-positive (MatAb+) and negative (MatAb−) bank voles (n=160) to PUUV in experimental populations. PUUV-specific maternal antibodies delayed the timing of infection. Females were more susceptible to PUUV infection than males. Interestingly, both the females and the males with maternal antibodies matured earlier than the other individuals in the population. Our results highlight the significance of maternal antibodies in the transmission of a pathogen and in the breeding success of the carriers.


Vector-borne and Zoonotic Diseases | 2011

Orthopox virus infections in Eurasian wild rodents.

Paula M. Kinnunen; Heikki Henttonen; Bernd Hoffmann; Eva R. Kallio; Christian Korthase; Juha Laakkonen; Jukka Niemimaa; Airi Palva; Mathias Schlegel; Hanan Sheikh Ali; Paula Suominen; Rainer G. Ulrich; Antti Vaheri; Olli Vapalahti

The genus Orthopoxvirus includes variola (smallpox) virus and zoonotic cowpox virus (CPXV). All orthopoxviruses (OPV) are serologically cross-reactive and cross-protective, and after the cessation of smallpox vaccination, CPXV and other OPV infections represent an emerging threat to human health. In this respect CPXV, with its reservoir in asymptomatically infected wild rodents, is of special importance. In Europe, clinical cowpox has been diagnosed in both humans and animals. The main objective of this study was to elucidate the prevalence of OPV infections in wild rodents in different parts of Eurasia and to compare the performance of three real-time polymerase chain reaction (PCR) methods in detecting OPV DNA in wildlife samples. We investigated 962 wild rodents from Northern Europe (Finland), Central Europe (Germany), and Northern Asia (Siberia, Russia) for the presence of OPV antibodies. According to a CPXV antigen-based immunofluorescence assay, animals from 13 of the 17 locations (76%) showed antibodies. Mean seroprevalence was 33% in Finland (variation between locations 0%-69%), 32% in Germany (0%-43%), and 3.2% (0%-15%) in Siberia. We further screened tissue samples from 513 of the rodents for OPV DNA using up to three real-time PCRs. Three rodents from two German and one Finnish location were OPV DNA positive. The amplicons were 96% to 100% identical to available CPXV sequences. Further, we demonstrated OPV infections as far east as the Baikal region and occurring in hamster and two other rodent species, ones previously unnoticed as possible reservoir hosts. Based on serological and PCR findings, Eurasian wild rodents are frequently but nonpersistently infected with OPVs. Results from three real-time PCR methods were highly concordant. This study extends the geographic range and wildlife species diversity in which OPV (or CPXV) viruses are naturally circulating.


PLOS ONE | 2012

Environmental change and disease dynamics: effects of intensive forest management on Puumala hantavirus infection in boreal bank vole populations.

Liina Voutilainen; Sakeri Savola; Eva R. Kallio; Juha Laakkonen; Antti Vaheri; Olli Vapalahti; Heikki Henttonen

Intensive management of Fennoscandian forests has led to a mosaic of woodlands in different stages of maturity. The main rodent host of the zoonotic Puumala hantavirus (PUUV) is the bank vole (Myodes glareolus), a species that can be found in all woodlands and especially mature forests. We investigated the influence of forest age structure on PUUV infection dynamics in bank voles. Over four years, we trapped small mammals twice a year in a forest network of different succession stages in Northern Finland. Our study sites represented four forest age classes from young (4 to 30 years) to mature (over 100 years) forests. We show that PUUV-infected bank voles occurred commonly in all forest age classes, but peaked in mature forests. The probability of an individual bank vole to be PUUV infected was positively related to concurrent host population density. However, when population density was controlled for, a relatively higher infection rate was observed in voles trapped in younger forests. Furthermore, we found evidence of a “dilution effect” in that the infection probability was negatively associated with the simultaneous density of other small mammals during the breeding season. Our results suggest that younger forests created by intensive management can reduce hantaviral load in the environment, but PUUV is common in woodlands of all ages. As such, the Fennoscandian forest landscape represents a significant reservoir and source of hantaviral infection in humans.


Vector-borne and Zoonotic Diseases | 2014

First report of Anaplasma phagocytophilum and Babesia microti in rodents in Finland.

Eva R. Kallio; Michael Begon; Richard J. Birtles; Esa Koskela; Tapio Mappes; Phillip C. Watts

Tick-borne diseases pose an increasingly important public health problem in Europe. Rodents are the reservoir host for many tick-transmitted pathogens, including Anaplasma phagocytophilum and Babesia microti, which can cause human granulocytic anaplasmosis and babesiosis, respectively. To estimate the presence of these pathogens in rodents in Finland, we examined blood samples from 151 bank voles (Myodes glareolus) and demonstrate, for the first time, that A. phagocytophilum and B. microti commonly infect bank voles (in 22% and 40% of animals, respectively) in Finland. Sequence analysis of a fragment of 18S rRNA showed that the B. microti strain isolated was identical to the Munich strain, which is considered to be nonzoonotic. The A. phagocytophilum strain (based on a fragment of the msp4 gene) was identical to one found earlier in rodents in the United Kingdom that is transmitted by the tick Ixodes trianguliceps, all the life stages of which feed on small mammals. The infection probability of B. microti in the bank voles was the greater the older the individual was, and males were more often infected than females. A. phagocytophilum infection probability first increased and then decreased with the age of individual without any difference between sexes. While these pathogens presumably pose a limited zoonotic risk to humans in Finland, they might have important interactions with other rodent pathogens and therefore affect infection dynamics of, for example, zoonotic pathogens.


Journal of Zoology | 2005

Survival and behaviour of captive‐born weasels (Mustela nivalis nivalis) released in nature

Paavo Hellstedt; Eva R. Kallio

The behaviour and survival of captive-born least weasels Mustela nivalis nivalis released in nature were reported in this study. Altogether 27 captive-born and six wild-caught weasels were equipped with radio transmitters and their survival was studied as a function of age and season. The daily mortality rate was generally higher in captive-born than in wild-caught weasels. The survival of captive-born weasels was highest if they were released during the summer and hence when they were young. Differences in the behavioural patterns of captive-born and wild-caught weasels were apparent. Captive-born weasels were often more visible in the field and were less timid than wild-caught weasels. Results suggest that to be successful, restocking of weasels should be done with young animals, which are preferably released during the season with abundant food resources.


Journal of General Virology | 2010

Associations between MHC genes and Puumala virus infection in Myodes glareolus are detected in wild populations, but not from experimental infection data.

Emmanuel Guivier; Maxime Galan; Pierre-Jean G. Malé; Eva R. Kallio; Liina Voutilainen; Heikki Henttonen; Gert E. Olsson; Åke Lundkvist; Katrien Tersago; Denis Augot; Jean-François Cosson; Nathalie Charbonnel

We analysed the influence of MHC class II Dqa and Drb genes on Puumala virus (PUUV) infection in bank voles (Myodes glareolus). We considered voles sampled in five European localities or derived from a previous experiment that showed variable infection success of PUUV. The genetic variation observed in the Dqa and Drb genes was assessed by using single-strand conformation polymorphism and pyrosequencing methods, respectively. Patterns were compared with those obtained from 13 microsatellites. We revealed significant genetic differentiation between PUUV-seronegative and -seropositive bank voles sampled in wild populations, at the Drb gene only. The absence of genetic differentiation observed at neutral microsatellites confirmed the important role of selective pressures in shaping these Drb patterns. Also, we found no significant associations between infection success and MHC alleles among laboratory-colonized bank voles, which is explained by a loss of genetic variability that occurred during the captivity of these voles.


Journal of General Virology | 2008

Quasispecies dynamics and fixation of a synonymous mutation in hantavirus transmission

Tarja Sironen; Eva R. Kallio; Antti Vaheri; Åke Lundkvist; Alexander Plyusnin

RNA-dependent RNA polymerases, the key enzymes in replication of RNA viruses, have a low fidelity; thus, these viruses replicate as a swarm of mutants termed viral quasispecies. Constant generation of new mutations allows RNA viruses to adapt swiftly to a novel environment through selection of both pre-existing and de novo-generated genetic variants. Here, quasispecies dynamics were studied in vivo in controlled hantavirus transmission from experimentally infected to naïve rodents through infested cage bedding. An elementary step of virus microevolution was apparent, as one synonymous mutation (A759G) repeatedly became fixed in the viral RNA quasispecies populations in the recipient animals.

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Heikki Henttonen

Finnish Forest Research Institute

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Antti Vaheri

Helsinki University Central Hospital

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Esa Koskela

University of Jyväskylä

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Tapio Mappes

University of Jyväskylä

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Jukka Niemimaa

Finnish Forest Research Institute

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Airi Palva

University of Helsinki

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