A total of 345 faecal samples were collected from domestic, captive and wild birds in rural areas, urban areas and a Zoo in Algeria. Samples were screened for the presence of parasites belonging to the genus Cryptosporidium Tyzzer, 1910 by microscopy and PCR analysis of the small-subunit rRNA (SSU), actin and 60-kDa glycoprotein (gp60) genes. Cryptosporidium spp. were detected in 31 samples. Sequence analysis of SSU and actin genes revealed the presence of C. baileyi Current, Upton et Haynes, 1986 in domestic chicken broilers (n = 12), captive ostriches (n = 4) and a wild mallard (n = 1), and C. meleagridis Slavin, 1955 in a graylag goose (n = 1), chickens (n = 11) and turkeys (n = 2). Twenty-three chicken and two turkey broilers from five farms were positive for cryptosporidia, with an overall prevalence of 2% and 6%, respectively. Both C. meleagridis and C. baileyi were detected in farmed chicken broilers, with a prevalence ranging from 9% to 69%. Farmed turkeys broilers were positive only for C. meleagridis, with a 13% prevalence at the animal level. Subtyping of C. meleagridis isolates at the gp60 locus showed the presence of subtype IIIgA22G3R1 in graylag goose and chicken broilers and IIIgA23G2R1 in chicken and turkey broilers. Infection with cryptosporidia was not associated with any clinical diseases. The results of the present study, which provides the first data on the prevalence of Cryptosporidium spp. in wild birds in Africa, demonstrate the presence of human pathogenic C. meleagridis in both domestic and wild birds in Algeria., Abd Elkarim Laatamna, Nikola Holubová, Bohumil Sak, Martin Kváč., and Obsahuje bibliografii
a1_Understanding of the diversity of species of Cryptosporidium Tyzzer, 1910 in tortoises remains incomplete due to the limited number of studies on these hosts. The aim of the present study was to characterise the genetic diversity and biology of cryptosporidia in tortoises of the family Testudinidae Batsch. Faecal samples were individually collected immediately after defecation and were screened for presence of cryptosporidia by microscopy using aniline-carbol-methyl violet staining, and by PCR amplification and sequence analysis targeting the small subunit rRNA (SSU), Cryptosporidium oocyst wall protein (COWP) and actin genes. Out of 387 faecal samples from 16 tortoise species belonging to 11 genera, 10 and 46 were positive for cryptosporidia by microscopy and PCR, respectively. All samples positive by microscopy were also PCR positive. Sequence analysis of amplified genes revealed the presence of the Cryptosporidium tortoise genotype I (n = 22), C. ducismarci Traversa, 2010 (n = 23) and tortoise genotype III (n = 1). Phylogenetic analyses of SSU, COWP and actin gene sequences revealed that Cryptosporidium tortoise genotype I and C. ducismarci are genetically distinct from previously described species of Cryptosporidium. Oocysts of Cryptosporidium tortoise genotype I, measuring 5.8-6.9 µm × 5.3-6.5 µm, are morphologically distinguishable from C. ducismarci, measuring 4.4-5.4 µm × 4.3-5.3 µm. Oocysts of Cryptosporidium tortoise genotype I and C. ducismarci obtained from naturally infected Russian tortoises (Testudo horsfieldii Gray) were infectious for the same tortoise but not for Reeve's turtles (Mauremys reevesii [Gray]), common garter snake (Thamnophis sirtalis [Linnaeus]), zebra finches (Taeniopygia guttata [Vieillot]) and SCID mice (Mus musculus Linnaeus)., a2_The prepatent period was 11 and 6 days post infection (DPI) for Cryptosporidium tortoise genotype I and C. ducismarci, respectively; the patent period was longer than 200 days for both cryptosporidia. Naturally or experimentally infected tortoises showed no clinical signs of disease. Our morphological, genetic, and biological data support the establishment of Cryptosporidium tortoise genotype I as a new species, Cryptosporidium testudinis sp. n., and confirm the validity of C. ducismarci as a separate species of the genus Cryptosporidium., Jana Ježková, Michaela Horčičková, Lenka Hlásková, Bohumil Sak, Dana Květoňová, Jan Novák, Lada Hofmannová, John McEvoy, Martin Kváč., and Obsahuje bibliografii
Studies of insect population under field conditions to establish survival rates, longevity and dispersal rates are rare in the literature. These types of studies are important and can be used to inform studies of the effects of landscape composition and configuration on levels of biodiversity. Here the Cantharidae beetle, Rhagonycha fulva is studied under field conditions to derive estimates of daily survival rates for both males and females as well as local dispersal rates. Survival was studied at two sites, one in Wales and another in England, whilst dispersal was examined only at the Welsh site. Beetles were marked using different coloured enamel paints at the mid-point of a 200 m linear transect. The beetles were almost exclusively found (and marked) on common hogweed, Heracleum sphondylium. No difference in survival was found between males and females at both of the sites. The survival rates found at the two sites also did not differ. The overall daily survival rate was 0.771 equating with a median longevity of 4.37 days. Casual observations yielded a small number of marked individuals in excess of 400 m away from the point of marking. Movement of males along the transect differed from females. Marked females were never found far from the point of marking whilst males moved further away with time. This difference in behaviour is discussed in terms of hypothesized insect dispersal behaviour following emergence as mobile adults., Laura E. Rodwell, Jennifer J. Day, Christopher W. Foster, Graham J. Holloway., and Obsahuje bibliografii
We studied a population of the regionally endangered marsh fritillary butterfly Euphydryas aurinia inhabiting a system of loosely connected dry calcareous grasslands in sub-Mediterranean Slovenia. Our goal was to set the basis for a long-term monitoring of this butterfly in four meadows using mark-release-recapture (MRR). We determined its demographic parameters, dispersal, behaviour and utilization of nectar plants in different quality patches. Total population size was estimated to be approximately 347 males (95% confidence interval: 262-432) and 326 females (95% confidence interval: 250-402), with an unbiased sex ratio. The average lifespans were 6.3 and 8.6 days, respectively. Daily population sizes followed a parabola with marked protandry. Both sexes were relatively highly mobile with both occasionally moving over half a kilometre. The spatial distribution of animals seemed to be associated with patch size, host plant densities and nectar sources, resulting in much higher population densities in the largest patch. Adult behaviour differed between the sexes, with females resting more and flying less than males. Behaviour also changed during daytime and with the progression of the season. Adults were confirmed to be opportunistic feeders, since as many as ten nectar sources were detected. We conclude that demographic parameters differ greatly among regions and habitats, thus conservation aims should be planned accordingly. Although the population studied is apparently in good condition, there are threats that may hamper the long-term persistence of the species in this area: succession, intensification of mowing and overgrazing., Jure Jugovic, Costanza Uboni, Sara Zupan, Martina Lužnik., and Obsahuje bibliografii
Estimating the spatial dispersion of pest arthropods is crucial for the development of reliable sampling programs and one of the main components of integrated pest management. The natural spatial distribution of a population of a species may be random, uniform, or aggregated and can be so classified based on calculation of variance to mean relations and related dispersion indices. In this work some classical density-invariant dispersion indices and related regression models are used for the first time to quantify the spatial dispersion of an important peach pest Anarsia lineatella Zeller (Lepidoptera: Gelechiidae) and construct fixed precision sequential sampling schemes. Taylor's power law, Iwao's patchiness regression and Nachman's model were used to analyse the damage to peaches caused by A. lineatella. All three regression models fit the data well, although the results indicate that Iwao's patchiness model provides a better description of the relationship between variance and mean density. Taylor's b and Iwao's b regression indices were both significantly smaller than 1, indicating that the distribution of individuals was uniform rather than random or aggregated. According to Green's and Kuno's models, the minimum sample size at the precision level of 0.2 varies from 3 samples, when total population density is more than 3 larvae/sample, to 10 samples, when population density is between 1 and 2 larvae/sample. Kuno's fixed sampling plan indicates that a small number of samples (i.e., 3-10 branches with fruit) is sufficient to estimate the mean population density of A. lineatella larvae with a precision of 0.2. The Resampling for validation of sampling plans (RVSP) method confirmed that the average level of precision of the fixed sequential plans matched the desired precision in most cases. The sampling plan presented here provides a level understanding of A. lineatella spatial ecology suitable for pest manage, Petros Damos., and Obsahuje bibliografii
The lung-dwelling nematode Rhabdias engelbrechti sp. n. was found in five of eight examined banded rubber frogs in Limpopo Province, South Africa. The species is differentiated from species of Rhabdias Stiles et Hassall, 1905 occurring in the Afrotropical Realm based on the presence of a globular cuticular inflation at the anterior end, the buccal capsule walls being distinctly divided into anterior and posterior parts, the buccal capsule size (6-9 μm × 16-18 μm), and the body length (3.8-6.1 mm). Rhabdias engelbrechti is the tenth species of the genus found in Afrotropical anurans. Our molecular phylogenetic analysis based on the complete sequences of the ITS region and partial sequences of large subunit (28S) gene of the nuclear ribosomal RNA demonstrates that the new species is more closely related to the Eurasian species Rhabdias bufonis (Schrank, 1788) than to two other species from sub-Saharan Africa represented in the tree. In addition, partial sequences of the mitochondrial protein coding cox1 and ribosomal 12S genes of the new species have shown significant differences from all previously published sequences of these genes from African species of Rhabdias., Yuriy Kuzmin, Ali Halajian, Sareh Tavakol, Wilmien J. Luus-Powell, Vasyl V. Tkach., and Obsahuje bibliografii
The presence of Neospora caninum Dubey, Carpenter, Speer, Topper et Uggla, 1988 in small mammals (i.e. murid rodents, Erinaceomorpha, Eulipotyphla and Scadentia) was explored for first time in South-East Asia. A total of 192 individuals from six localities across Thailand were analysed. A general prevalence of N. caninum of 22% was observed, with some variation among localities (5-36%). Four main types of habitat were included and rodents trapped in dry-land habitat (17 positive among 41 individuals) were more likely to be infected with N. caninum than those from other habitats (forest, rain-fed land and settlement). Rodent species identity and individual rodent weight had no influence on individual infection. Our results provided the first data on the presence of N. caninum in rodents in South-East Asia and first report of N. caninum in the order Scadentia., Ornampai Japa, Serge Morand, Anamika Karnchanabanthoeng, Kittipong Chaisiri, Alexis Ribas., and Obsahuje bibliografii
Fluorescence in situ hybridization (FISH) is a technique used to determine the chromosomal position of DNA and RNA probes. The present study contributes to knowledge on jumping plant-lice genomes by using FISH with 18S rDNA and telomeric (TTAGG)n probes on meiotic chromosomes of Psylla alni (2n = 24 + X), Cacopsylla mali (2n = 22 + neo-XY and 20 + neo-X1X2Y), C. sorbi (2n = 20 + neo-XY), Baeopelma foersteri (2n = 14 + X), and Rhinocola aceris (2n = 10 + X). This is the first study that has used FISH on the hemipteran superfamily Psylloidea. We found that the chromosomes of all studied species contain the insect-type telomere motif, (TTAGG)n. In C. mali and C. sorbi, the neo-sex chromosomes originating from autosome-sex chromosome fusions showed no interstitially located clusters of TTAGG repeats, suggesting their loss or inactivation. Similarly, no interstitial (TTAGG)n clusters were detected in an extremely large autosome pair of B. foersteri that most likely originated from a fusion of at least five ancestral chromosome pairs. Clusters of 18S rDNA were detected on the fused and second largest autosome pairs of B. foersteri and on one of the large autosome pairs of the remaining species. In C. mali and B. foersteri, the rDNA clusters were shown to coincide with the NORs as detected by the AgNOR method. Finally, we speculate, based on the obtained FISH markers, on the mechanisms of karyotype evolution of psylloid species differing in chromosome numbers and sex chromosome systems., Anna Maryańska-Nadachowska, Valentina G. Kuznetsova, Natalia V. Golub, Boris A. Anokhin., and Obsahuje bibliografii
Monoclonal antibody specific for an epitope of cretory-secretory antigen protein of Opisthorchis felineus (Rivolta, 1884) (Trematoda: Opisthorchiidae) with a molecular weight of 28 kDa was used in a sandwich enzyme-linked immunosorbent assay (ELISA) for immobilisation of liver fluke specific antigen to the solid phase. Examination of human sera by this ELISA compared with commercial assays demonstrated that the monoclonal antibody epitope is located within this significant parasite protein. Anti-idiotypic antibody specific for the paratope of this monoclonal antibody was obtained by a hybridoma technique. Mimicking an epitope of excretory-secretory antigen of O. felineus, it had the capacity to bind specific antibody and elicit an antibody response. The value of anti-idiotypic antibody as a substitute for the liver fluke antigen was tested by ELISA using serum samples of infected dogs. Anti-idiotypic antibody proved to be of value in both an indirect-ELISA and a competitive-ELISA for diagnosis of opisthorchiasis. Mature trematodes were isolated from all infected animals. The faecal egg counts were negative in dogs with a relatively small number of parasites, despite finding antibodies in serum by ELISA. Substitution of parasite antigen with anti-idiotype avoids the use of experimental animals and also reduces time-consuming steps of antigen preparation., Aitbay K. Bulashev, Sergey N. Borovikov, Shynar S. Serikova, Zhanbolat A. Suranshiev, Vladimir S. Kiyan, Saule Z. Eskendirova., and Obsahuje bibliografii
Dinocampus coccinellae is a parasitoid wasp usually parasitizing ladybird beetles of the tribe Coccinellini. A field survey conducted between March and November 2016 revealed three hosts of this parasitoid in the Srinagar district of the Indian state of Jammu and Kashmir: two members of the Coccinellini (Oenopia conglobata and Coccinella undecimpunctata) and one of the Chilocorini (Priscibrumus uropygialis). Proportion of the latter (atypical) host that were parasitized was 0.09 and intermediate between that recorded for C. undecimpunctata (0.06) and O. conglobata (0.14). A series of laboratory experiments revealed that while a member of Coccinellini (O. conglobata) was more often attacked by D. coccinellae than a member of Chilocorini (P. uropygialis), the proportions of each species from which parasitoids emerged did not differ significantly. There were no significant differences between D. coccinellae females bred from O. conglobata and P. uropygialis, with respect to selection of the two host species and their suitability for the development of the parasitoid. However, members of the Chilocorini other than P. uropygialis (Chilocorus infernalis and Simmondsius pakistanensis) were rarely attacked by D. coccinellae and parasitoid larvae did not emerge from any of those attacked. The results of our experiments indicate that in Kashmir Himalayas D. coccinellae is adapted to parasitize hosts belonging to both Coccinellini and Chilocorini., Amir Maqbool, Imtiaz Ahmed, Piotr Kiełtyk, Piotr Ceryngier., and Obsahuje bibliografii