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1.
J Equine Vet Sci ; 132: 104980, 2024 Jan.
Article in English | MEDLINE | ID: mdl-38070586

ABSTRACT

Horse traits under selection are largely quantitative and affected by multiple genes. Horse face shape is an example of a continuous trait, which due to the reliance on observational assessments, is classified into; "dished", "straight", and "roman-nosed". This categorization is often inadequate to convey the full spectrum of the face shape variation especially for genetic studies. The first objective of the current study was to use geometric morphometric methods to quantitatively phenotype face shapes and examine its variation across horse breeds. The second objective was to analyze the face shape variation within Arabian horses since face shape is (1) favored, valued, and genetically selected in certain lineages (e.g. Egyptian), (2) is evaluated by registries and scored in shows, and (3) in its extreme forms pose health concerns. We digitized landmarks on lateral profile photos, particularly on the dorsal curvature of the rostrum, and subjected these landmarks to Generalized Procrustes Analysis to generate independent shape and size variables which were statistically compared across breeds and within Arabians. Horse breeds varied in nasal curvature, ranging from extremely concave to extremely convex, with over 70 % of horse breeds exhibiting intermediate concavity (i.e., straight profile). Interestingly, Arabian horses possessed the highest diversity in face profile and individuals clustered into three distinct shape sub-groups (one dished and two straight profile clusters). Our quantitative phenotyping method can be the basis of future genetic studies of facial profile within Arabian lineages as a favored traits and potentially manage its extreme forms as a likely genetic disease.


Subject(s)
Horses , Animals , Horses/genetics
2.
Intervirology ; 31(1): 14-22, 1990.
Article in English | MEDLINE | ID: mdl-2159955

ABSTRACT

The addition of tegument or matrix proteins and the outermost membrane to human cytomegalovirus (strain AD 169) replicating in human cells appeared to occur differently in the nucleus than in the cytoplasm. In the nucleus cytomegalovirus was completed structurally within intranuclear sacs, as envelopment at the end of tubular structures, containing an electron-dense material, included tegument and outer membrane simultaneously. In the cytoplasm structural completion occurred in separate steps. Tegument could be added by association with dense bodies; then, interaction with the membranes of vacuoles or vesicles provided the outermost covering. Tubes originating in intranuclear sacs have been described previously only in guinea pig cells infected with guinea pig cytomegalovirus.


Subject(s)
Cell Nucleus/microbiology , Cytomegalovirus/growth & development , Cytoplasm/microbiology , Antibodies, Monoclonal , Cell Nucleus/ultrastructure , Cells, Cultured , Cytomegalovirus/ultrastructure , Cytoplasm/ultrastructure , Fibroblasts , Humans , Intracellular Membranes , Nuclear Envelope
3.
J Virol ; 56(3): 839-45, 1985 Dec.
Article in English | MEDLINE | ID: mdl-2999439

ABSTRACT

Cytomegalovirus (CMV) strain AD-169 replicated in smooth muscle cell (SMC) cultures derived from human umbilical arteries, producing enveloped infectious virions. However, unlike the effects of CMV on fully permissive human lung fibroblasts, the effects of strain AD-169 on SMC cultures were delayed and prolonged, resulting in extended survival of a fraction of the starting population. This period of survival did not exceed the life-span of the control SMC cultures. Infectious CMV continued to be isolated from the surviving SMC cultures after extinction of the original inoculum by dilution and after treatment of the cultures with CMV neutralizing antibody. The implications of these findings for the pathogenesis of atherosclerosis are discussed.


Subject(s)
Cytomegalovirus/growth & development , Muscle, Smooth, Vascular/microbiology , Virus Replication , Cells, Cultured , Fibroblasts/immunology , Fluorescent Antibody Technique , Humans , Microscopy, Electron
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