Maciej Skoracki
Adam Mickiewicz University in Poznań
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Publication
Featured researches published by Maciej Skoracki.
Journal of Medical Entomology | 2003
Jerzy Michalik; Teresa Hofman; Alicja Buczek; Maciej Skoracki; Bozena Sikora
Abstract During 1998–1999, Ixodes ricinus (L.) populations were investigated in three different biotopes (deciduous, mixed, coniferous forest) situated in popular recreational areas in Poznań, Poland. In total, 1,123 questing ticks (1,002 nymphs, 69 males, 52 females) were collected by flagging vegetation. Additionally, in 1998 between May and September small rodents were trapped and inspected for feeding ticks. Altogether, 213 rodents of three species: Apodemus agrarius Pall., A. flavicollis Melchior, Clethrionomys glareolus Schreber were captured. Of 323 engorged ticks, 304 were larvae and 19 nymphs. All ticks collected from vegetation, as well as from rodents were examined for the presence of Borrelia burgdorferi Johnson, Schmid, Hyde, Steigenwalt & Brenner s.l. spirochetes by indirect immunofluorescence assay (IFA) using PAB 1B29. The seasonal pattern of activity of questing I. ricinus was always bimodal (May/June and August/September). The most abundant tick population occurred in the deciduous forest. The total infection rate in questing ticks was 16.2%. Differences in mean infection prevalence of host-seeking ticks between three biotopes each year were not significant. On average more larvae parasitized on the genus of Apodemus than on C. glareolus. 17.8% of larvae and 31.6% of nymphs fed on rodents harbored spirochetes. The three rodent species contributed to a different degree in to transmission of the pathogen to subadult stages. ≈27% of larvae infested on A. agrarius, 22% on C. glareolus, and only 4.2% on A. flavicollis contained spirochetes. The results suggest that the prevalence of A. agrarius and C. glareolus in disturbed urban forests used for leisure activities seems to be crucial for the maintenance of B. burgdorferi s.l. in I. ricinus populations.
Journal of Medical Entomology | 2005
Jerzy Michalik; Bogumiła Skotarczak; Maciej Skoracki; Beata Wodecka; Bozena Sikora; Teresa Hofman; Anna Rymaszewska; Marek Sawczuk
Abstract Wild rodents and the subadult Ixodes ricinus (L.) ticks infesting them were examined for the presence of Borrelia burgdorferi Johnson, Schmid, Hyde, Steigerwalt & Brenner s.l. in a sylvatic habitat in west central Poland during May–September 2002. In total, 818 feeding ticks were recovered from 73 infested yellow-necked mice, Apodemus flavicollis Melchior; in addition, bank voles, Clethrionomys glareolus Schreber, were rarely captured and proved to be weakly parasitized. Only 2.7% of A. flavicollis and 2.2% of 320 engorging larvae were polymerase chain reaction (PCR) positive for the bacterium. All spirochete-PCR-positive samples yielded exclusively B. burgdorferi s.s. This genospecies was also the most prevalent in questing nymphs and accounted for 87.5% of the total number of Borrelia infections in nymphal ticks collected during May and June 2 yr later. The presence of the same genospecies both in naturally engorged larvae and blood-positive animals as well as the high predominance of B. burgdorferi s.s. in questing nymphs strongly differs from most study sites investigated in Europe. This unique pattern of Borrelia-diversity in both rodents and ticks seems to be determined by highly site-specific host vertebrate cenosis, and yellow-necked mice are involved in the maintenance of B. burgdorferi s.s. in the forest habitat. However, the transmission efficiency of this spirochete from the mice to the I. ricinus vector seems to be very low. The research provides additional information on the complexity of B. burgdorferi s.l. ecology in Europe, pointing to the importance of the local host community.
Clinical Microbiology and Infection | 2009
Joanna Stańczak; Maria Racewicz; Jerzy Michalik; Stella Cieniuch; Bozena Sikora; Maciej Skoracki
In Poland, Ixodes ricinus plays an important role as the vector of the TBE virus, Borrelia burgdorferi s.l., Anaplasma phagocytophilum and Babesia spp. Moreover, recent studies have shown that it can also serve as a vector for Rickettsia helvetica, the newly recognised human pathogen of the spotted fever group rickettsiae (SFG), which is widely distributed in questing ticks, with the prevalence ranging from 1.3% to 11.4% [1]. However, reports are still lacking on its occurrence in naturally infected wild animals and ticks feeding on them. So, this study was designed to detect rickettsial organisms in blood samples of various tick hosts that may serve as reservoirs of infection, as well as in I. ricinus parasitising them.
Insect Systematics & Evolution | 2004
Andre V. Bochkov; Georges Wauthy; Maciej Skoracki
The genus Picobia Haller (Acari: Syringophilidae) is revised. The species of this genus are permanent parasites living in quills of bird body feathers. In total 19 species are recognized. Four new species are described from passerine birds (Passeriformes): Picobia locustella sp. n. from Locustella naevia (Sylviidae), P. biarmicus sp. n. from Panurus biarmicus (Panuridae), P. sturni sp. n. from Sturnus vulgaris (Sturnidae) and P. cissa sp. n. from Cissa chinensis (Corvidae). Two species are redescribed: P. dryobatis (Fritsch) and P. zumpti (Lawrence). A neotype for P. dryobatis is designated. A new diagnosis for the genus Picobia and a key to females are provided. Parsimony analysis of the genus is conducted. Host-parasite relationships are briefly discussed.
Journal of Medical Entomology | 2010
Maciej Skoracki; Sarah A. Hendricks; Greg S. Spicer
ABSTRACT Five new species of the genus Picobia are described and illustrated: 1) P. leucophaeus sp. nov. from the Laughing Gull Leucophaeus atricilla L. (Charadriiformes: Laridae) from Texas; 2) P. troglodytes sp. nov. from the House Wren Troglodytes aedon Vieillot (Passeriformes: Troglodytidae) from California; 3) P. cardinalis sp. nov. from the Northern Cardinal Cardinalis cardinalis (L.) (Passeriformes: Cardinalidae) from Texas; 4) P. carpodacus sp. nov. from the Purple Finch Carpodacus purpureus (Gmelin) (Passeriformes: Fringillidae) from California; and 5) P. psaltriparus sp. nov. from the Bushtit Psaltriparus minimus (Townsend) (Passeriformes: Aegithalidae) from Texas. Two avian species from the family Picidae (Piciformes) are recorded as new hosts for P. dryobatis (Fritsch, 1958): the Downy Woodpecker Picoides pubescens (L.) from Texas and the Ladder-backed Woodpecker Picoides scalaris (Wagler) from California. Additionally, all named species of the genus Picobia with their host associations and distributions are summarized in tabular form.
Zootaxa | 2016
Maciej Skoracki; Bozena Sikora; Greg S. Spicer
The fauna of quill mites of the subfamily Picobiinae Johnston and Kethley, 1973 (Acariformes: Cheyletoidea: Syringophilidae) is comprehensively revised. All of 78 known species, which are grouped into 11 genera, are examined and diagnosed or redescribed. Data on picobiine hosts and distribution are summarized, including new host and locality records. The following new species are described: Charadriineopicobia apricaria sp. nov. ex Pluvialis apricaria (Linnaeus) (Charadriiformes: Charadriidae) from France, Neopicobia pari sp. nov. ex Periparus venustulus Swinhoe (type host) (Passeriformes: Paridae) from China, Parus major Linnaeus (Paridae) from Macedonia and Finland, and Poecile varius Temminck and Schlegel (Paridae) from Japan, Picobia magellani sp. nov. ex Scytalopus magellanicus (Gmelin) (Passeriformes: Rhinocryptidae) from Colombia, Picobia lonchura sp. nov. ex Lonchura leucogastra (Blyth) (Passeriformes: Estrildidae) from Indonesia, Picobia makoli sp. nov. ex Xiphocolaptes promeropirhynchus (Lesson) (Passeriformes: Furnariidae) from Colombia. The species Picobia polonica Skoracki, Magowski and Dabert, 2001 syn. nov. is a junior synonym of C. khulkhaskhani Kivganov and Sharafat, 1995. The following new combinations are proposed: Neopicobia ictericus (Skoracki and Glowska, 2010) comb. nov., Rafapicobia brotogeris (Fain, Bochkov and Mironov, 2000) comb. nov., and Rafapicobia ramphastos (Fain, Bochkov and Mironov, 2000) comb. nov. Keys to the all picobiine genera and species are presented, along with a check-list of picobiine species and their hosts.
Acta Parasitologica | 2014
Maciej Skoracki; Markus Unsoeld; Katarzyna Kavetska; Katarzyna Kaszewska
The paper contains a review of quill mites of the subfamily Picobiinae (Acari: Prostigmata: Syringophilidae) associated with woodpeckers (Aves: Piciformes: Picidae). Three new species are described: Picobia mentalis Skoracki et Unsoeld sp. nov. from Picus mentalis Temminck, Neopicobia ea Skoracki et Unsoeld sp. nov. from Celeus flavus (St. Mueller) (type host), C. elegans (St. Mueller), C. torquatus (Boddaert), and Neopicobia freya Skoracki et Unsoeld sp. nov. from Dryocopus galeatus (Temminck) (type host) and Piculus rubiginosus (Swainson). Additionally, six new host species for Picobia heeri Haller, 1878 and 12 new host species for Picobia dryobatis (Fritsch, 1956) are reported. A complete list of the picobiines parasitising birds of the family Picidae is presented in the tabular form.
Systematic Parasitology | 2013
Maciej Skoracki; Markus Unsoeld; Michał Ozminski
A new monotypic genus Colisyringophilus n. g. is established for C.tanzanicus n. sp., quill mites parasitising two mouse bird species from Tanzania, Colius striatus Gmelin and Urocolius macrourus (Linnaeus). This new genus is closely related to Neoaulobia Fain, Bochkov & Mironov, 2000, but differs from it by the following features: the stylophore is rounded posteriorly, the propodonotal shield is reduced to triangular sclerite bearing bases of setae vi and ve, the hysteronotal shield is absent, legs I are longer than legs II, and apodemes I are distinctly elongated. This is the first record of syringophilid mites from hosts of the order Coliiformes.
Zootaxa | 2016
Maciej Skoracki; Greg S. Spicer; Barry M. OConnor
Quill mites belonging to the subfamily Syringophilinae Lavoipierre, 1953 associated with the Nearctic passeriform birds are revised. All of the 49 known species, which are grouped in seven genera, are recorded. Among them, four new species are described: Syringophiloidus audubioni sp. nov. from Spizella breweri (Cassini) (Emberizidae), Syringophilopsis catesbyi sp. nov. from Vireo olivaceus (Linnaeus) (Vireonidae), S. wilsoni sp. nov. from Pheucticus melanocephalus (Swainson) (Cardinalidae), and S. bartrami sp. nov. from Spizella passerina (Bechstein) (Emberizidae). The species Syringophilopsis hylocichlae Clark, 1964 syn. nov. is synonymized with Syringophilopsis turdus (Fritsch, 1958), and Syringophiloidus zonotrichia syn. nov. is synonymized with Betasyringophiloidus seiuri (Clark, 1964) comb. nov. Six species are recorded from the Nearctic region for the first time: Syringophiloidus delichonum Bochkov, 2001, S. glandarii (Fritsch, 1958), S. weiszii Skoracki et al., 2001, S. bombycillae Skoracki, 2002, Syringophilopsis mimidus Sikora et al., 2011, and Torotrogla merulae Skoracki et al., 2000. Data on Nearctic syringophiline species, their hosts and distribution are summarized and the keys to all species are constructed.
Systematic Parasitology | 2012
Maciej Skoracki; Bozena Sikora; Michał Ozminski
Tinamiphilopsis ariconte n. sp., a syringophilid mite, is described from three tinamou species (Tinamidae), Rhynchotus rufescens (Temminck) and Nothuraboraquira (Spix) in Paraguay and N.minor (Spix) in Brazil. These data indirectly support the hypothesis that the cheyletoid-like predatory ancestor of the Syringophilidae switched to parasitism before the divergence of the avian hosts into the two major clades Palaeognathae and Neognathae.