Blood parasite infections in a wild population of ravens (Corvus corax) in Bulgaria

Shurulinkov P, Spasov L, Stoyanov G, Chakarov N (2018)
Malaria journal 17(33): 33.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
Download
OA 1.48 MB
Autor*in
Shurulinkov, Peter; Spasov, Lachezar; Stoyanov, Georgi; Chakarov, NaydenUniBi
Abstract / Bemerkung
Background: Blood parasites have been studied intensely in many families of avian hosts, but corvids, a particularly cosmopolitan family, remain underexplored. Haemosporidian parasites of the common raven (Corvus corax) have not been studied, although it is the largest, most adaptable, and widespread corvid. Genetic sequence data from parasites of ravens can enhance the understanding of speciation patterns and specificity of haemosporidian parasites in corvids, and shed light how these hosts cope with parasite pressure. Methods: A baited cage trap was used to catch 86 ravens and a nested PCR protocol was used to amplify a 479 bp fragment of the haemosporidian cytochrome b gene from the samples. The obtained sequences were compared with the MalAvi database of all published haemosporidian lineages and a phylogenetic tree including all detected raven parasites was constructed. An examination of blood smears was performed for assessment of infection intensity. Results: Twenty blood parasite lineages were recovered from ravens caught in a wild population in Bulgaria. The prevalence of generalist Plasmodium lineages was 49%, and the prevalence of Leucocytozoon lineages was 31%. Out of 13 detected Leucocytozoon lineages six were known from different corvids, while seven others seem to be specific to ravens. A phylogenetic reconstruction suggests that Leucocytozoon lineages of ravens and other corvids are not monophyletic, with some groups appearing closely related to parasites of other host families. Conclusions: Several different, morphologically cryptic groups of Leucocytozoon parasites appear to infect corvids. Ravens harbour both generalist corvid Leucocytozoon as well as apparently species-specific lineages. The extraordinary breeding ecology and scavenging lifestyle possibly allow ravens to evade vectors and have relatively low blood parasite prevalence compared to other corvids.
Stichworte
Avian malaria; Leucocytozoon; Host specificity; Corvids; Passerines; Prevalence; Tolerance; Resistance
Erscheinungsjahr
2018
Zeitschriftentitel
Malaria journal
Band
17
Ausgabe
33
Art.-Nr.
33
ISSN
1475-2875
Page URI
https://pub.uni-bielefeld.de/record/2917040

Zitieren

Shurulinkov P, Spasov L, Stoyanov G, Chakarov N. Blood parasite infections in a wild population of ravens (Corvus corax) in Bulgaria. Malaria journal. 2018;17(33): 33.
Shurulinkov, P., Spasov, L., Stoyanov, G., & Chakarov, N. (2018). Blood parasite infections in a wild population of ravens (Corvus corax) in Bulgaria. Malaria journal, 17(33), 33. doi:10.1186/s12936-018-2179-7
Shurulinkov, Peter, Spasov, Lachezar, Stoyanov, Georgi, and Chakarov, Nayden. 2018. “Blood parasite infections in a wild population of ravens (Corvus corax) in Bulgaria”. Malaria journal 17 (33): 33.
Shurulinkov, P., Spasov, L., Stoyanov, G., and Chakarov, N. (2018). Blood parasite infections in a wild population of ravens (Corvus corax) in Bulgaria. Malaria journal 17:33.
Shurulinkov, P., et al., 2018. Blood parasite infections in a wild population of ravens (Corvus corax) in Bulgaria. Malaria journal, 17(33): 33.
P. Shurulinkov, et al., “Blood parasite infections in a wild population of ravens (Corvus corax) in Bulgaria”, Malaria journal, vol. 17, 2018, : 33.
Shurulinkov, P., Spasov, L., Stoyanov, G., Chakarov, N.: Blood parasite infections in a wild population of ravens (Corvus corax) in Bulgaria. Malaria journal. 17, : 33 (2018).
Shurulinkov, Peter, Spasov, Lachezar, Stoyanov, Georgi, and Chakarov, Nayden. “Blood parasite infections in a wild population of ravens (Corvus corax) in Bulgaria”. Malaria journal 17.33 (2018): 33.
Alle Dateien verfügbar unter der/den folgenden Lizenz(en):
Copyright Statement:
Dieses Objekt ist durch das Urheberrecht und/oder verwandte Schutzrechte geschützt. [...]
Volltext(e)
Access Level
OA Open Access
Zuletzt Hochgeladen
2019-09-06T09:18:56Z
MD5 Prüfsumme
84a0f27180e044d1c4a3992eb34d6e0b


1 Zitation in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Avian haemosporidians in the cattle egret (Bubulcus ibis) from central-western and southern Africa: High diversity and prevalence.
Villar Couto CM, Cumming GS, Lacorte GA, Congrains C, Izbicki R, Braga EM, Rocha CD, Moralez-Silva E, Henry DAW, Manu SA, Abalaka J, Regalla A, da Silva AS, Diop MS, Del Lama SN., PLoS One 14(2), 2019
PMID: 30794584

50 References

Daten bereitgestellt von Europe PubMed Central.


Valkiūnas G., 2005
Are chronic avian haemosporidian infections costly in wild birds?
Asghar M, Hasselquist D, Bensch S., 2011
Chronic infection. Hidden costs of infection: chronic malaria accelerates telomere degradation and senescence in wild birds.
Asghar M, Hasselquist D, Hansson B, Zehtindjiev P, Westerdahl H, Bensch S., Science 347(6220), 2015
PMID: 25613889
Prevalence and differential host-specificity of two avian blood parasite genera in the Australo-Papuan region.
Beadell JS, Gering E, Austin J, Dumbacher JP, Peirce MA, Pratt TK, Atkinson CT, Fleischer RC., Mol. Ecol. 13(12), 2004
PMID: 15548295

Bishop MA, Bennett GF., 1992
Low prevalence of infection by haemoparasites in Cetti’s Warblers (Cettia cetti) from central Spain
Merino S, Seoane J, De J, Bermejo A., 2000
Plasmodium and Leucocytozoon (Sporozoa: Haemosporida) of wild birds in Bulgaria
Shurulinkov P, Golemansky V., 2003
The ecology of host immune responses to chronic avian haemosporidian infection.
Ellis VA, Kunkel MR, Ricklefs RE., Oecologia 176(3), 2014
PMID: 25179282
Immune responses link parasite genetic diversity, prevalence and plumage morphs in common buzzards
Chakarov N, Pauli M, Krüger O., 2017
Host escape behavior and blood parasite infections in birds
Garcia-Longoria L, Garamszegi LZ, Moller AP., 2014
Correction: Parasite Prevalence Corresponds to Host Life History in a Diverse Assemblage of Afrotropical Birds and Haemosporidian Parasites.
Lutz HL, Hochachka WM, Engel JI, Bell JA, Tkach VV, Bates JM, Hackett SJ, Weckstein JD., PLoS ONE 10(5), 2015
PMID: 25984782
Leucocytozoids of 7 Old World passeriform families
Bennett GF, Peirce MA., 1992
Prevalence of new and known species of haemoparasites in feral pigeons in northwest Italy.
Scaglione FE, Pregel P, Cannizzo FT, Perez-Rodriguez AD, Ferroglio E, Bollo E., Malar. J. 14(), 2015
PMID: 25888761
Carrion crows (Corvus corone) of southwest Germany: important hosts for haemosporidian parasites.
Schmid S, Fachet K, Dinkel A, Mackenstedt U, Woog F., Malar. J. 16(1), 2017
PMID: 28899382
Genetic sequence data reveals widespread sharing of Leucocytozoon lineages in corvids.
Freund D, Wheeler SS, Townsend AK, Boyce WM, Ernest HB, Cicero C, Sehgal RN., Parasitol. Res. 115(9), 2016
PMID: 27189064

Cramp S, Simmons KEL., 1980

Glutz U, Bauer K, Bezzel E., 1971
Territory quality affects the relative importance of habitat heterogeneity and interference competition in a long-lived territorial songbird
Grünkorn T, Potiek A, Looft V, Jonker RM, Chakarov N, Krüger O., 2014
Population regulation by habitat heterogeneity or individual adjustment?
Kruger O, Chakarov N, Nielsen JT, Looft V, Grunkorn T, Struwe-Juhl B, Moller AP., J Anim Ecol 81(2), 2011
PMID: 21950339
Effect of weather conditions on the communal roosting behaviour of common ravens Corvus corax with unlimited food resources
Janicke T, Chakarov N., 2007
Do individual branches of immune defence correlate? A comparative case study of scavenging and non-scavenging birds
Blount JD, Houston DC, Møller AP, Wright J., 2003
Immunity, resistance and tolerance in bird-parasite interactions.
Sorci G., Parasite Immunol. 35(11), 2013
PMID: 23800152
Decomposing health: tolerance and resistance to parasites in animals.
Raberg L, Graham AL, Read AF., Philos. Trans. R. Soc. Lond., B, Biol. Sci. 364(1513), 2009
PMID: 18926971
Absence of blood parasites in Griffon vultures from Spain.
Blanco G, Gajon A, Doval G, Martinez F., J. Wildl. Dis. 34(3), 1998
PMID: 9706578
Phylogenetic comparison of avian haemosporidian parasites from resident and migratory birds in northern Japan.
Yoshimura A, Koketsu M, Bando H, Saiki E, Suzuki M, Watanabe Y, Kanuka H, Fukumoto S., J. Wildl. Dis. 50(2), 2014
PMID: 24484482
MrBayes 3: Bayesian phylogenetic inference under mixed models.
Ronquist F, Huelsenbeck JP., Bioinformatics 19(12), 2003
PMID: 12912839
Prevalence of blood parasites in Japanese wild birds.
Murata K., J. Vet. Med. Sci. 64(9), 2002
PMID: 12399602
Blood parasites in hooded crows (Corvus corone cornix) in Northwest Italy.
Scaglione FE, Cannizzo FT, Pregel P, Perez Rodriguez AD, Bollo E., Vet. Ital. 52(2), 2016
PMID: 27188825
Malaria immunity in man and mosquito: insights into unsolved mysteries of a deadly infectious disease.
Crompton PD, Moebius J, Portugal S, Waisberg M, Hart G, Garver LS, Miller LH, Barillas-Mury C, Pierce SK., Annu. Rev. Immunol. 32(), 2014
PMID: 24655294
Fitness in common buzzards at the cross-point of opposite melanin–parasite interactions
Chakarov N, Boerner M, Krüger O., 2008
Apparent vector-mediated parent-to-offspring transmission in an avian malaria-like parasite.
Chakarov N, Linke B, Boerner M, Goesmann A, Kruger O, Hoffman JI., Mol. Ecol. 24(6), 2015
PMID: 25688585
Age-specific haemosporidian infection dynamics and survival in Seychelles warblers.
Hammers M, Komdeur J, Kingma SA, Hutchings K, Fairfield EA, Gilroy DL, Richardson DS., Sci Rep 6(), 2016
PMID: 27431430
Does the niche breadth or trade-off hypothesis explain the abundance-occupancy relationship in avian Haemosporidia?
Drovetski SV, Aghayan SA, Mata VA, Lopes RJ, Mode NA, Harvey JA, Voelker G., Mol. Ecol. 23(13), 2014
PMID: 24689968
Dynamics of parasitemia of malaria parasites in a naturally and experimentally infected migratory songbird, the great reed warbler Acrocephalus arundinaceus.
Zehtindjiev P, Ilieva M, Westerdahl H, Hansson B, Valkiunas G, Bensch S., Exp. Parasitol. 119(1), 2008
PMID: 18280472
Occurrence of haemosporidian parasites in the paddyfield warbler, Acrocephalus agricola (Passeriformes, Sylviidae)
Zehtindjiev P, Ilieva M, Krizanauskiene A, Oparina O, Oparin M, Bensch S., 2009
Genetic diversity of avian blood parasites in SE Europe: cytochrome b lineages of the genera Plasmodium and Haemoproteus (Haemosporida) from Bulgaria
Dimitrov D, Zehtindjiev P, Bensch S., 2010
Evolution of seasonal transmission patterns in avian blood-borne parasites.
Perez-Rodriguez A, de la Hera I, Bensch S, Perez-Tris J., Int. J. Parasitol. 45(9-10), 2015
PMID: 25957160
Detecting shifts of transmission areas in avian blood parasites: a phylogenetic approach.
Hellgren O, Waldenstrom J, Perez-Tris J, Szoll E, Si O, Hasselquist D, Krizanauskiene A, Ottosson U, Bensch S., Mol. Ecol. 16(6), 2007
PMID: 17391413
Prevalence of blood parasites in European passeriform birds.
Scheuerlein A, Ricklefs RE., Proc. Biol. Sci. 271(1546), 2004
PMID: 15306334
Avian haemosporidians in haematophagous insects in the Czech Republic.
Synek P, Munclinger P, Albrecht T, Votypka J., Parasitol. Res. 112(2), 2012
PMID: 23224608
Host shift and cospeciation rate estimation from co-phylogenies.
Alcala N, Jenkins T, Christe P, Vuilleumier S., Ecol. Lett. 20(8), 2017
PMID: 28662544
Export

Markieren/ Markierung löschen
Markierte Publikationen

Open Data PUB

Web of Science

Dieser Datensatz im Web of Science®
Quellen

PMID: 29338711
PubMed | Europe PMC

Suchen in

Google Scholar