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Bajer, A.

Publications and source records attributed to Bajer, A..

4 recordsLinked to original sources

Cytokine gene polymorphism and parasite susceptibility in free-living rodents: importance of non-coding variants

Associations between genetic variants and susceptibility to infections have long been studied in free-living hosts to infer contemporary evolutionary forces shaping genetic polymorphisms of the immunity genes. Despite extensive studies of receptors, such as MHC or TLR, little is known about efferent arm of the immune system. Cytokines are signalling molecules that trigger and modulate the immune response, acting as a crucial link between innate and adaptive immunity. In the present study we investigated how genetic variation in cytokines affects susceptibility to parasitic diseases in bank voles. We focused on three cytokines: tumour necrosis factor (TNF), lymphotoxin alpha (LT), and interferon beta (IFN{beta}1). Two SNPs in LT and two in IFN{beta}1 significantly affected susceptibility to nematodes, and was of them was also associated with susceptibility to microbial pathogen Bartonella. All these variants displayed signatures of selection. One of the variants was synonymous, and one was located in an intron. Our study shows that cytokines are prone to parasite-driven selection, and non-coding variants may play an important role in susceptibility to infections in wild systems.

evolutionary biology↗

Seroprevalence of Toxoplasma gondii among sylvatic rodents in Poland

Toxoplasma gondii is a significant pathogen affecting humans and animals. We conducted seromonitoring for T. gondii in four sylvatic rodent species in Poland. We report an overall seroprevalence of 5.5% (3.6% for Myodes glareolus and 20% for other vole species). Seroprevalence in bank voles varied significantly between host age and sex.

microbiology↗

Impact of Babesia microti on the initiation and course of pregnancy in murine model of vertically transmitted infection

Genus Babesia groups tick-transmitted protozoa causing babesiosis, a malaria-like disease. Vertical transmission of Babesia spp. was reported in mammals, however, the exact timing and mechanisms involved in this mode of transmission are not currently known. In this experimental study we evaluated: 1) the reproductive success, and success of vertical transmission of Babesia microti in mice mated in acute and chronic phases of the infection and in pregnant mice infected during early and advanced pregnancy; 2) possible influence of the pregnancy on the course of parasite infection (parasitaemia) in females; and 3) pathological changes in females and their embryos induced by infection. Blood smears and PCR targeting the 550 bp 18S rRNA gene fragment were used for the detection of B. microti. Histopathological examination was performed on collected tissues. Successful development of pregnancy was recorded only in females in the chronic phase of infection. The success of vertical transmission of B. microti in this group was 63% (71/112). In females mated in the acute phase of infection or on the 4th day of pregnancy, no evidence for pregnancy development were observed. In the group infected on the 12th day of pregnancy, numerous complications including pregnancy loss and stillbirth were recorded. During the acute phase of infection, parasitaemia was lower in pregnant females in comparison to infected, non-pregnant control females. Acute B. microti infection prevents pregnancy initiation and development of pregnancy at a very early stage, and causes severe complication in BALB/c mice in the second and third trimester of pregnancy. Chronic B. microti infection has no negative impact on the initiation and development of pregnancy, but resulted with congenital infections. Further study is required to determine to what extent maternal antibabesial immune responses and potential placental accumulation of parasites contribute to compromised pregnancy in the murine model of congenital Babesia infection. Author summaryThe mouse is the most common mammalian model for studying human parasitic diseases, including malaria, toxoplasmosis, Chagas disease, and babesiosis. Babesiosis is an emerging intraerythrocytic infection caused by protozoal parasites, mostly Babesia microti. Our previous work in murine model proved that vertical transmission of Babesia microti, is a third way - after tick-bite and blood/organ transfusion - to acquire babesiosis. In this study we focused on investigating how the infection influences the course of pregnancy. We were interested in how variations in infection acquisition time and infection phase influence the reproductive success of mice and vertical transmission of parasites. We expected that the infection causes severe pathological changes in the organs of infected females and their offspring. Results obtained in this study have shown that vertical transmission of B. microti was only possible in chronically infected mice, in which health status and reproductive success were not compromised by the infection. Acute infection made successful reproduction impossible, however, the infection had no significant effect on the histopathological condition of tissues. We hope that these insights into B. microti vertical transmission will lead to the better understanding of congenital babesiosis.

pathology↗

Zoonotic viruses in three species of voles (Microtus spp.) from Poland

Rodents are known to be reservoir hosts for a plethora of zoonotic viruses and therefore play a significant role in the dissemination of these pathogens. We trapped three vole species (Microtus arvalis, M. oeconomus and M. agrestis) in N.E. Poland, all of which are widely distributed species in Europe, and, using immunofluorescence assays, we assessed serum samples for the presence of antibodies to hantaviruses, arenaviruses and cowpox viruses (CPXV). We detected antibodies against CPXV and Puumala virus (PUUV), overall seroprevalence of combined viral infections of 18.2% [10.5-29.3] and mostly attributed to CPXV. Antibodies to Tula hantavirus, typical for Microtus voles, are known to cross-react strongly with the PUUV antigen used in PUUV screening, but we detected only one PUUV/TULV cross-reaction in Microtus arvalis (1.3% [0.1-7.9]). We found antibodies against CPXV in all three Microtus spp. Seroprevalence was similar in all vole species. There were no significant differences in seroprevalence between the sexes and among host age categories. Our results contribute to the increasing understanding of CPXV abundance in voles in Europe, and confirm that CPXV circulates also in Microtus spp. voles in NE Poland.

microbiology↗