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1.
J Anat ; 236(3): 398-424, 2020 03.
Artículo en Inglés | MEDLINE | ID: mdl-31777085

RESUMEN

A retractable larynx and adaptations of the vocal folds in the males of several polygynous ruminants serve for the production of rutting calls that acoustically announce larger than actual body size to both rival males and potential female mates. Here, such features of the vocal tract and of the sound source are documented in another species. We investigated the vocal anatomy and laryngeal mobility including its acoustical effects during the rutting vocal display of free-ranging male impala (Aepyceros melampus melampus) in Namibia. Male impala produced bouts of rutting calls (consisting of oral roars and interspersed explosive nasal snorts) in a low-stretch posture while guarding a rutting territory or harem. For the duration of the roars, male impala retracted the larynx from its high resting position to a low mid-neck position involving an extensible pharynx and a resilient connection between the hyoid apparatus and the larynx. Maximal larynx retraction was 108 mm based on estimates in video single frames. This was in good concordance with 91-mm vocal tract elongation calculated on the basis of differences in formant dispersion between roar portions produced with the larynx still ascended and those produced with maximally retracted larynx. Judged by their morphological traits, the larynx-retracting muscles of male impala are homologous to those of other larynx-retracting ruminants. In contrast, the large and massive vocal keels are evolutionary novelties arising by fusion and linear arrangement of the arytenoid cartilage and the canonical vocal fold. These bulky and histologically complex vocal keels produced a low fundamental frequency of 50 Hz. Impala is another ruminant species in which the males are capable of larynx retraction. In addition, male impala vocal folds are spectacularly specialized compared with domestic bovids, allowing the production of impressive, low-frequency roaring vocalizations as a significant part of their rutting behaviour. Our study expands knowledge on the evolutionary variation of vocal fold morphology in mammals, suggesting that the structure of the mammalian sound source is not always human-like and should be considered in acoustic analysis and modelling.


Asunto(s)
Antílopes/anatomía & histología , Músculos Laríngeos/anatomía & histología , Laringe/anatomía & histología , Vocalización Animal/fisiología , Acústica , Animales , Antílopes/fisiología , Músculos Laríngeos/fisiología , Laringe/fisiología , Masculino , Pliegues Vocales/anatomía & histología , Pliegues Vocales/fisiología
2.
J Gen Virol ; 95(Pt 11): 2480-2485, 2014 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-25063552

RESUMEN

The order Nidovirales contains large, enveloped viruses with a non-segmented positive-stranded RNA genome. Nidoviruses have been detected in man and various animal species, but, to date, there have been no reports of nidovirus in reptiles. In the present study, we describe the detection, characterization, phylogenetic analyses and disease association of a novel divergent nidovirus in the lung of an Indian python (Python molurus) with necrotizing pneumonia. Characterization of the partial genome (>33 000 nt) of this virus revealed several genetic features that are distinct from other nidoviruses, including a very large polyprotein 1a, a putative ribosomal frameshift signal that was identical to the frameshift signal of astroviruses and retroviruses and an accessory ORF that showed some similarity with the haemagglutinin-neuraminidase of paramyxoviruses. Analysis of genome organization and phylogenetic analysis of polyprotein 1ab suggests that this virus belongs to the subfamily Torovirinae. Results of this study provide novel insights into the genetic diversity within the order Nidovirales.


Asunto(s)
Boidae/virología , Infecciones por Nidovirales/veterinaria , Nidovirales/genética , Nidovirales/aislamiento & purificación , Neumonía Viral/veterinaria , Animales , Secuencia de Bases , Variación Genética , Genoma Viral , Pulmón/patología , Pulmón/virología , Datos de Secuencia Molecular , Nidovirales/clasificación , Infecciones por Nidovirales/patología , Infecciones por Nidovirales/virología , Filogenia , Neumonía Viral/patología , Neumonía Viral/virología , ARN Viral/genética , Homología de Secuencia de Ácido Nucleico , Proteínas Virales/genética
3.
Vet Immunol Immunopathol ; 168(3-4): 140-6, 2015 Dec 15.
Artículo en Inglés | MEDLINE | ID: mdl-26672912

RESUMEN

The raccoon (Procyon lotor) is a highly adaptable carnivore that has rapidly conquered Europe over the last decades and represents a potential candidate as pathogen reservoir, bearing the risk for transmission of infectious agents, as zoonosis or spill-over, to other wild life and domestic animals and man. Comprehensive investigations of infectious diseases in raccoons require a detailed knowledge of the participating immune cell populations. To close this gap of knowledge, various antibodies were tested for cross-reactivity with leukocytes in lymphoid organs and peripheral blood of raccoons using immunohistochemistry and flow cytometry, respectively. Eight out of 16 antibodies, directed against CD3, CD79α, Pax-5, IgG, CD44, MHC class II, myeloid/histiocyte antigen (MAC387), and Iba-1 exhibited a specific immunoreaction with cells in distinct anatomical compartments in formalin-fixed paraffin-embedded lymphoid tissues. Flow cytometric analysis revealed that 7 out of 18 antibodies directed against CD11c, CD14, CD21, CD44, CD79α, MHC class I and II cross-reacted with peripheral blood-derived raccoon leukocytes. Summarized, the usefulness of several cross-reacting antibodies was determined for the characterization of raccoon immune cells in immunohistochemistry and flow cytometry, offering the opportunity to study the raccoon immune system under normal and diseased conditions.


Asunto(s)
Antígenos CD/metabolismo , Inmunofenotipificación/veterinaria , Leucocitos/fisiología , Tejido Linfoide/citología , Mapaches/inmunología , Animales , Antígenos , Clonación Molecular , Citometría de Flujo , Leucocitos/inmunología
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