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Chiari样畸形的遗传:杂交繁育能否降低脊髓空洞症的风险?

Inheritance of Chiari-Like Malformation: Can a Mixed Breeding Reduce the Risk of Syringomyelia?

作者信息

Knowler Susan P, v/d Berg Henny, McFadyen Angus, La Ragione Roberto M, Rusbridge Clare

机构信息

School of Veterinary Medicine, Faculty of Health & Medical Sciences, University of Surrey, Guildford, Surrey, United Kingdom.

Fitzpatrick Referrals, Eashing, Godalming, Surrey, United Kingdom.

出版信息

PLoS One. 2016 Mar 23;11(3):e0151280. doi: 10.1371/journal.pone.0151280. eCollection 2016.

Abstract

Canine Chiari-like malformation (CM) is a complex abnormality of the skull and craniocervical junction associated with miniaturization and brachycephaly which can result in the spinal cord disease syringomyelia (SM). This study investigated the inheritance of CM in a Griffon Bruxellois (GB) family and feasibility of crossbreeding a brachycephalic CM affected GB with a mesaticephalic normal Australian terrier and then backcrossing to produce individuals free of the malformation and regain GB breed characteristics. The study family cohort (n = 27) included five founder dogs from a previous baseline study of 155 GB which defined CM as a global malformation of the cranium and craniocervical junction with a shortened skull base and increased proximity of the cervical vertebrae to the skull. T1-weighted sagittal DICOM images of the brain and craniocervical junction were analysed for five significant traits (two angles, three lines) identified from the previous study and subsequent Qualitative Trait Loci analysis. Mean measurements for mixed breed, pure-breed and baseline study groups were compared. Results indicated that mixed breed traits posed less risk for CM and SM and were useful to distinguish the phenotype. Moreover on the MR images, the filial relationships displayed by the traits exhibited segregation and those presenting the greatest risk for CM appeared additive towards the severity of the condition. The external phenotypes revealed that by outcrossing breed types and with careful selection of appropriate conformation characteristics in the first generation, it is possible to regain the GB breed standard and reduce the degree of CM. The four GB affected with SM in the study all exhibited reduced caudal skull development compared to their relatives. The craniocervical traits may be useful for quantifying CM and assessing the possibility of SM thus assisting breeders with mate selection. However, such a system requires validation to ensure appropriateness for all breeds at risk.

摘要

犬类 Chiari 样畸形(CM)是一种与颅骨小型化和短头畸形相关的颅骨及颅颈交界处的复杂异常,可导致脊髓疾病脊髓空洞症(SM)。本研究调查了布鲁塞尔格里芬犬(GB)家族中 CM 的遗传情况,以及将患有短头畸形 CM 的 GB 与中头型正常的澳大利亚梗杂交,然后回交以培育出无该畸形且恢复 GB 品种特征个体的可行性。研究家族队列(n = 27)包括来自之前对 155 只 GB 进行的基线研究中的五只奠基犬,该研究将 CM 定义为颅骨和颅颈交界处的整体畸形,伴有缩短的颅底以及颈椎与颅骨的接近度增加。对大脑和颅颈交界处的 T1 加权矢状位 DICOM 图像进行分析,以确定从先前研究及后续数量性状位点分析中识别出的五个重要特征(两个角度、三条线)。比较了混种、纯种和基线研究组的平均测量值。结果表明,混种特征对 CM 和 SM 的风险较小,且有助于区分表型。此外,在磁共振图像上,这些特征所显示的亲子关系呈现出分离现象,而那些对 CM 风险最大的特征在病情严重程度上表现出累加性。外部表型显示,通过杂交品种类型并在第一代中仔细选择合适的形态特征,有可能恢复 GB 品种标准并降低 CM 的程度。研究中四只患有 SM 的 GB 与它们的亲属相比,均表现出颅尾发育减少。颅颈特征可能有助于量化 CM 并评估 SM 的可能性,从而协助育种者进行配偶选择。然而,这样一个系统需要进行验证,以确保对所有有风险的品种都适用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38e4/4805231/bb9bdf0bbe80/pone.0151280.g001.jpg

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