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M Labuda

Publications and source records attributed to M Labuda.

At least 55 records · Page 3Linked to original sources
PubMed1994

Salivary gland extracts of partially fed Dermacentor reticulatus ticks decrease natural killer cell activity in vitro.

The salivary glands and saliva of ticks (Arachnida, Acari, Ixodida) play a vital role in blood feeding, including manipulation of the host's immune response to tick infestation. Furthermore, a diverse number of tick-borne pathogens are transmitted to vertebrate hosts via tick saliva. A factor synthesized in the salivary glands of feeding ticks potentiates the transmission of certain tick-borne viruses. We show that salivary gland extracts (SGE) derived from Dermacentor reticulatus female ticks fed for 6 days on laboratory mice (SGED6) induced a decrease in the natural killer (NK) activity of effector cells obtained from 16 healthy blood donors. The decreased activity ranged from 14 to 69% of NK activity observed with the respective untreated effector cells. Such a decrease was not observed after treatment of effector cells with SGE from unfed ticks. Ten-fold dilution of SGED6 significantly reduced the capacity to decrease NK activity and a further 10-fold dilution almost eliminated the effect. After addition of IFN-alpha 2, the SGED6-induced decrease in NK activity was restored to activity levels approaching those of untreated cells. The apparent reversibility of the inhibition indicates that the effect of SGED6 on NK activity was not due to cytotoxicity. The results demonstrate the presence of a factor(s) in the salivary gland products of feeding D. reticulatus female ticks that influences human NK activity in vitro. These data suggest a possible mechanism by which tick SGE potentiates the transmission of some tick-borne viruses through suppression of NK activity.

Animals↗
PubMed1993

Non-viraemic transmission of tick-borne encephalitis virus: a mechanism for arbovirus survival in nature.

The vectors of arthropod-borne viruses (arboviruses) become infected by feeding on the viraemic blood of an infected animal. This theory is based on transmission studies involving artificial infection of vertebrate hosts by syringe inoculation. To reproduce natural conditions of virus transmission, infected and uninfected vectors (ticks) of tick-borne encephalitis virus, the most important arbovirus in Europe, were allowed to feed together on uninfected wild vertebrate hosts. The greatest numbers of infected ticks were obtained from susceptible host species that had undetectable or very low levels of viraemia. The results suggest that 'nonviremic transmission' is an important mechanism for the survival of certain arboviruses in nature.

Animals↗
PubMed1993

Human 25-hydroxyvitamin D 24-hydroxylase cytochrome P450 subunit maps to a different chromosomal location than that of pseudovitamin D-deficient rickets.

We have cloned part of the human 25-OHD 24-hydroxylase cytochrome P450 (P450cc24) cDNA. The characterized sequence consists of 776 bp of the coding and 720 bp of the 3'-untranslated region interrupted by an intron. In the coding region we found 79.8% similarity in DNA and 87.5% in deduced amino acid sequences between human and rat, with no similarity in the 3'-untranslated region. By Southern blot hybridization of DNA from human-hamster somatic cell hybrids and by in situ immunofluorescence hybridization, we mapped P450cc24 to human chromosome 20q13.1. This location of P450cc24 is different from that of pseudovitamin D-deficient rickets (PDDR), previously assigned to chromosome 12q14 by linkage analysis, thus excluding it as a target of the PDDR mutation. Since it is likely that PDDR is caused by a mutation in the 25-OHD 1 alpha-hydroxylase P450 subunit (P450cc1 alpha) our results do not support the hypothesis that the two cytochromes are encoded by a single gene.

Amino Acid Sequence↗
PubMed1993

Efficient transmission of tick-borne encephalitis virus between cofeeding ticks.

Most of the data on oral infections of ticks with tick-borne encephalitis virus have been derived from experiments using animals infected by syringe inoculation. To mimic the natural conditions of virus transmission, tick-borne encephalitis virus-infected Ixodes ricinus (Linnaeus) or Rhipicephalus appendiculatus Neumann adults (donors) were cofed with uninfected nymphs (recipients) of either tick species on uninfected guinea pigs. Two tick-retaining cells were attached to each guinea pig: cell 1 contained uninfected nymphs and virus-infected adults, and cell 2 contained uninfected nymphs. Following engorgement, 55% of I. ricinus nymphs and 65% of R. appendiculatus nymphs were shown to have acquired the virus while cofeeding with I. ricinus donor ticks. Similarly, 66% of R. appendiculatus recipient nymphs that cofed with R. appendiculatus virus-infected adults were infected. Some of the guinea pigs on which the ticks cofed were apparently nonviremic. The results indicate that efficient transmission of tick-borne encephalitis virus can occur between cofeeding ticks even when the host on which they feed does not develop a detectable viremia.

Animals↗
PubMed1993

Enhancement of tick-borne encephalitis virus transmission by tick salivary gland extracts.

To investigate the role of ticks in TBE virus transmission, salivary gland extract (SGE) was derived from partially fed female Ixodes ricinus, Dermacentor reticulatus and Rhipicephalus appendiculatus ticks. Guinea-pigs were infested with uninfected R. appendiculatus nymphs and inoculated with a mixture of TBE virus and SGE or with virus alone. The number of ticks which on average acquired virus from feeding on animals inoculated with TBE virus and SGE from partially fed ticks was 4-fold greater than the number that became infected by feeding on animals inoculated with virus alone or virus plus SGE from unfed I. ricinus. Viraemia was detected in 67% of guinea-pigs inoculated with virus plus SGE compared to 30% of guinea-pigs inoculated with virus alone. Virus titres in the blood were similar for both groups of animals [range 2.0-2.8 log10 plaque-forming units (PFU)/ml of blood]; however, the number of ticks that became infected was significantly higher on animals inoculated with virus plus SGE from partially fed ticks. No significant difference was observed with respect to the tick species used to derive SGE. The results indicate that TBE virus transmission is enhanced by factor(s) associated with the salivary glands of feeding ticks, and that these factor(s) may facilitate efficient transmission of TBE virus between infected and uninfected ticks even when they feed on hosts that have no detectable viraemia.

Animals↗
PubMed1993

Amplification of tick-borne encephalitis virus infection during co-feeding of ticks.

Following engorgement of Rhipicephalus appendiculatus larvae on guinea-pigs infected with tick-borne encephalitis (TBE) virus, none of the engorged larvae or emergent nymphs contained detectable infectious virus. However, one of twelve pools, each containing three of the unfed nymphs, was positive when screened by polymerase chain reaction (PCR), indicating a low prevalence of TBE virus infection in the unfed nymphs. After engorgement of the nymphs on four uninfected guinea-pigs, 19/24 (79%) fed nymphs from one guinea-pig and 4/25 (16%) fed nymphs from a second guinea-pig were infected; all the ticks examined from the other two guinea-pigs were uninfected. The results suggest that TBE virus was transmitted from a low proportion of infected nymphs (infected as larvae) to uninfected nymphs as they fed together on an uninfected guinea-pig. Such amplification of the initial infection, at the population level, could play an important role in maintaining TBE virus infections in nature, particularly if there is a low level of vertical transmission from one tick generation to the next.

Animals↗
PubMed1993

Further isolation of murine herpesviruses from small mammals in southwestern Slovakia.

A total of 69 small mammals of 6 species were collected in localities Marcelová and Kopác (southwestern Slovakia) and investigated. Two strains of murine herpesvirus (MHV) have been isolated and reisolated from Apodemus flavicollis. Both virus strains killed suckling mice after i.c. and i.p. inoculation. Adult mice were killed 4-7 days after i.c. inoculation. Cross antigenic reactions among 14C aminoacid hydrolysate labelled MHV-72 infected Vero cells and mouse immune sera against the two new isolates and rabbit immune sera raised against purified MHV strains No. 72 and No. 76 were done. Profiles of immunoprecipitated proteins are almost identical. All used immune sera crossreacted with major proteins of MHV-72 strain. We conclude that the two virus isolates from Apodemus flavicollis are new strains of MHV.

Animals↗
PubMed1992

Linkage mapping by simultaneous screening of multiple polymorphic loci using Alu oligonucleotide-directed PCR.

We present the use of our recently described multiple-loci polymorphic DNA markers ("alumorphs") for linkage mapping of the human genome. By using the polymerase chain reaction (PCR) with an Alu-specific primer we could reveal, in a single experiment, up to 20 genomic polymorphisms seen as the presence or absence of amplified DNA fragments originating from genomic segments flanked by Alu repeats. Using this approach we examined genomic DNA samples from two families with a history of pseudovitamin D-deficiency rickets (PDDR), an autosomal recessive disorder. An indication of linkage with the PDDR phenotype was found for one of the polymorphic bands, denoted 30A. A significant linkage [logarithm-of-odds (lod) score greater than 3.0] was obtained between this polymorphism and a number of chromosome 12q markers tightly linked to PDDR. The 30A band specifically hybridized to DNA digests from hybrid cell lines carrying a human chromosome 12, thus independently assigning the 30A marker to this chromosome. Since Alu elements are ubiquitous in human DNA, the use of alternative Alu-specific primers, which reveal different sets of Alu-flanked loci, should provide an efficient and rapid approach to human genetic mapping.

Base Sequence↗
PubMed1992

Two hereditary defects related to vitamin D metabolism map to the same region of human chromosome 12q13-14.

We have localized the locus for the vitamin D receptor (VDR) responsible for hypocalcemic vitamin D-resistant rickets (HVDRR), close to the pseudovitamin D-deficient rickets (PDDR) locus, another disorder related to impaired vitamin D metabolism. PDDR (formerly vitamin D dependency type I, VDD1) was recently mapped to human chromosome 12q14 by linkage analysis. Here we report on the assignment of VDR to 12q13-14 by in situ hybridization and by linkage analysis. Linkage analysis between VDR, PDDR, and several RFLP markers show close linkage, with no recombination (theta = 0) between VDR and PDDR (Z = 1.94), a COL2A1 haplotype (Z = 4.03), ELA1 (Z = 0.98), and D12S15 (Z = 4.17). The analysis of extended haplotypes in one of the PDDR families provides evidence for recombination between VDR and PDDR and localizes VDR together with COL2A1 proximal to PDDR. Complete allelic association detected between VDR and COL2A1 loci on PDDR chromosomes and lower association between VDR and PDDR suggests a VDR location very close to COL2A1 and one more distant to PDDR. We propose the following order of loci: (VDR, COL2A1), (PDDR, ELA1, D12S15), D12S4, (D12S14, D12S17), D12S6. Thus, two clearly distinct loci involved in the control of vitamin D activity map close to each other in the region 12q13-14.

Chromosomes, Human, Pair 12↗
PubMed1991

Arthropod vectors in the evolution of bunyaviruses.

Viruses from each genus of Bunyaviridae have preferential relationships to the arthropods of only one or two families, i.e. Bunyavirus to mosquitoes (Culicidae), Phlebovirus to sand flies (Psychodidae) and mosquitoes, Uukuvirus and Nairovirus to ticks (Ixodidae and Argasidae). An exception is genus Hantavirus not proven to be transmitted by vectors. Within the Bunyavirus genus 16 serogroups have been recognized on the basis of their antigenic relationship. Based on isolations from the nature each serogroup is preferentially linked with arthropod species (mostly mosquitoes) of one, or two genera. For 8 out of 16 serogroups Culex mosquitoes are the main insect vectors. Two serogroups are linked with Aedes mosquitoes, three with Anopheles mosquitoes. Aedeomyia mosquitoes, Culicoides bitting miges and Hyalomma ticks are vectors of one serogroup each. Evolutionary trends within the genus Bunyavirus and within the family Bunyaviridae can be recognized based on relationships of bunyaviruses to their arthropod vectors.

Animals↗
PubMed1991

Vertical and venereal transmission of California group viruses by Aedes triseriatus and Culiseta inornata mosquitoes.

Aedes triseriatus and Culiseta inornata mosquitoes were compared in their ability to transmit vertically La Crosse (LAC) and snowshoe hare (SSH) viruses. LAC virus was transovarially transmitted by 53% of Ae. triseriatus, the natural vector, and by 22% of Cs. inornata mosquitoes. SSH virus was transovarially transmitted by 89% of Cs. inornata, a proposed natural vector, and by 29% of Ae. triseriatus. A genetic approach, using LAC, SSH, and LAC/SSH reassortant viruses was then used to elucidate viral genetic determinants of transovarial transmission of bunyaviruses by Ae. triseriatus mosquitoes. Viruses containing the LAC medium sized (M) RNA segment were most efficiently transovarially transmitted by Ae. triseriatus mosquitoes. LAC, SSH, and Tahyna (TAH) viruses were compared in their ability to be venerally transmitted. All three viruses replicated in the reproductive tract of male Aedes triseriatus and were venereally transmitted to female mosquitoes. LAC and TAH viruses infected previously blood fed (BF) but not non-blood fed (NBF) Aedes triseriatus female mosquitoes.

Aedes↗
PubMed1991

Interference between the viruses of tick-borne encephalitis complex in the Ixodes ricinus ticks.

The interference of two closely related viruses of the tick-borne encephalitis complex (TBE) in Ixodes ricinus ticks has been observed. 42.9 to 65.0% of dually infested ticks developed virus neutralization antibodies in mice without signs of illness, which contrasts with the control ticks infected with 198 strain only. Other explanations of this interference could include alteration of viral receptors on host cells or induction of antiviral activity in the infected ticks and/or other vectors such as mosquitoes.

Animals↗
PubMed1990

Mapping autosomal recessive vitamin D dependency type I to chromosome 12q14 by linkage analysis.

Linkage analysis in French-Canadian families with vitamin D dependency type I (VDD1) demonstrated that the gene responsible for the disease is linked to polymorphic RFLP markers in the 12q14 region. We studied 76 subjects in 14 sibships which included 17 affected individuals and 17 obligate heterozygotes. Significant results for linkage were obtained with the D12S17 locus at the male recombination fraction (theta m) .018 (Z[theta m theta f] = 3.20) and with D126 at (theta m = .025 (Z[theta m theta f] = 3.07). Multipoint linkage analysis and studies of haplotypes and recombinants strongly suggest the localization of the VDD1 locus between the collagen type II alpha 1 (COL2A1) locus and clustered loci D12S14, D12S17, and D12S6, which segregate as a three-marker haplotype. Linkage disequilibrium between VDD1 and this three-marker haplotype supports the notion of a founder effect in the studied population. The current status of the localization of the disease allows for carrier detection in the families at risk.

Chromosome Banding↗
PubMed1990

Dual infection of Ixodes ricinus ticks with two viruses of the tick-borne encephalitis complex.

Ixodes ricinus female ticks were inoculated with Skalica (SK) virus (non-pathogenic for adult albino mice by subcutaneous route) and 14 days later they were challenged with strain 198 of Tick-borne Encephalitis (TBE) virus (highly pathogenic for adult albino mice by subcutaneous route). After additional 14 days of incubation, 42.9 to 65.0% of the adult (10-12 g) albino mice infested with these double infected ticks developed antibodies to TBE without signs of sickness (transmission of SK virus), while paralysis or death was registered in 35.0 to 57.1% of infested mice (transmission of strain 198) depending on the concentration of strain 198 used for inoculation of ticks. However, a low degree of interference to superinfection with strain 198 was observed, when the dissected tick salivary glands were examined by subcutaneous inoculation of adult albino mice (more than 90% of examined salivary glands contained strain 198 virus).

Animals↗
PubMed1990

Longitudinal study of natural foci of Central European encephalitis virus in West Slovakia.

A total of 2922 small terrestrial mammals of 12 species were collected in six localities of West Slovakia between 1981 and 1986. When examined for the prevalence of neutralizing antibodies (NA) to Central European encephalitis (CEE) virus we found that 14.6% had antibody. Nearly all (97%) of the 426 animals with antibody were Clethrionomys glareolus, the most abundant species (52.6% of mammals collected, 15.1% of those with antibody). Apodemus flavicollis (22.5% of mammals collected, 18.1% of those with antibody), Apodemus sylvaticus (14% of mammals collected, 8.5% of those with antibody), and Microtus arvalis (5.5% of mammals collected, 3.3% of those with antibody). In all locations studies the most abundant tick found on small mammals was Ixodes ricinus (larvae and nymphs). Less abundant, but present in all studied sites, were larvae and nymphs of Dermacentor reticulatus and Haemaphysalis concinna. Six strains of CEE virus were isolated from tissues of animals: four from Clethryonomys glareolus and one each from Apodemus flavicollis and Sorex araneus. Three of six isolates were from animals collected in February; none of the six had detectable neutralizing antibody to CEE virus. We discuss these observations with regard to possible mechanisms of persistence of CEE virus.

Animals↗
PubMed1989

Amplification of arbovirus transmission by mosquito intradermal probing and interrupted feeding.

Probing is the crucial phase for the successful intake of the blood by a mosquito female, saliva being ejected during the intradermal probing period. When Tahyna virus (California group, family Bunyaviridae) carrying and transmitting Aedes aegypti mosquito was allowed to feed on 3 suckling white mice for 4 hr, 66.7% of the 162 exposed mice became infected. When one infected mosquito was put in contact with 5 mice, 53.6% of the 250 exposed mice became infected. Multiple transmission of the virus to the available hosts during completion of one blood meal by a single mosquito has been demonstrated.

Aedes↗
PubMed1989

[Long-term results of surgical treatment of portal hypertension].

Large number of contradictory operative surgeries refer best to embarrasments, existed on this section of surgery. Today, from the amount of operative surgeries prevail the endoscopic sclerotization of the gastroesophageal varices. On basis of retrospective study of 48 portosystemic shunts was showed, that 28 operated patients survive average 8.1 year, till now 4 patients of them are alive, within 8-14 years. In 7 cases of azygoportal deconexion by Torres-Dengi, average time of survive was 2.5 year. There experiences led the authors to elaborate an algorithm of treatment of portal hypertension, where the postosystemic shunts are the portosystemic shunts are the effective palliative operative surgery in indicated cases.

Esophageal and Gastric Varices↗