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1.
为了探究公鸡弱精症的发病机理,本研究对前期应用数字基因表达谱技术(Digital gene expression,DGE)及生物信息学分析得到的与公鸡弱精症相关的6个候选基因(COX7B、PTGDS、hPGDS、SPAG6、WNT2、CCNF)进行表达分析。选取300只42周龄的北京油鸡公鸡,进行为期4周的精液品质检测,从中筛出弱精及正常个体各15只。采用RT-qPCR对这6个候选基因在两组个体的睾丸组织的表达量进行相对定量检测。结果发现,COX7B、PTGDS在弱精组个体睾丸的表达量显著高于正常个体(P0.01),WNT2、hPGDS、CCNF在弱精组个体的表达量显著低于正常个体(P0.05),SPAG6在两组睾丸中的表达量没有显著差异,该结果与DGE的结果相吻合。通过DGE筛选出与弱精症相关的6个候选基因的表达模式在本研究的群体中得到进一步验证,可作为公鸡弱精症的重要候选基因,进一步进行功能分析与验证,为揭示公鸡弱精症的发病机理提供依据。  相似文献   

2.
试验旨在探究公猪精液冷冻保存对其精子功能的影响。取长白猪的鲜精和优质冻精,用精子分析仪检测精子的运动能力,台盼蓝染色检测精子活率,体外受精(IVF)试验检测卵裂率与囊胚率,采用不同功能检测试剂盒检测冻精和鲜精的顶体完整率、线粒体膜通道孔(MPTP)活性、线粒体膜电位(MMP)、线粒体活性、线粒体氧化应激活性氧(ROS)以及精子DNA完整性,实时荧光定量PCR检测弱精子症相关蛋白基因SMCPTEKT3、DNAH1、TCTE3的表达。结果表明,与猪鲜精相比,猪冻精的活率及活力均显著降低(P<0.05),冻精的顶体完整率也明显下降(P<0.05);冻精的卵裂率和囊胚率显著低于鲜精(P<0.05);精子线粒体功能分析结果显示,冻精的MPTP相对荧光单位值(RFU)、线粒体膜电位荧光比率以及线粒体活性光密度(OD)值均显著低于鲜精(P<0.05);精子线粒体ROS检测发现,冻精的RFU值显著高于鲜精(P<0.05);精子DNA完整性检测结果显示,冻精拖尾率显著高于鲜精(P<0.05);而弱精子症相关蛋白基因的表达与鲜精相比,差异不显著(P>0.05)。综上所述,冷冻导致猪精子活率、活力、线粒体功能、DNA完整性下降,最终使得冷冻精液精子的受精能力降低。  相似文献   

3.
本研究对课题组前期在京星黄鸡转录组研究中筛选到的与肌内脂肪(IMF)差异沉积相关的14个候选基因进行验证,检测其在中外两个鸡种群体中与胸肌IMF沉积的关联性。以98日龄慢速型地方鸡京星黄鸡和42日龄快速型白羽科宝肉鸡胸肌组织为素材,通过胸肌甘油三酯(TG)含量区分高低表型组,并检测候选基因在组间的基因表达差异。结果表明,在京星黄鸡胸肌TG高、低组间ATP结合盒亚家族B成员8(ABCB8)、脂联素(ADIPOQ)、第6号染色体开放阅读框65(BEND6)、CD74分子(CD74)、核糖基5-磷酸转移酶(FKTN)、组蛋白乙酰转移酶1(HAT1)、硫酸乙酰肝素-氨基葡萄糖3-磺基转移酶5(HS3ST5)、介体复合物亚基4(MED4)、肿瘤坏死因子超家族成员8(TNFSF8)和TNFAIP3相互作用蛋白1(TNIP1)共10个基因表达差异显著(P<0.05);在科宝肉鸡TG高、低组间ADIPOQ、BEND6、FKTN、HAT1、HS3ST5、MED4和TNIP1共7个基因表达差异显著(P<0.05);ADIPOQ、FKTN、HAT1、HS3ST5、MED4和TNIP1共6个基因在两个品种中差异表达趋势一致(P<0.05)。本研究提供了鸡IMF沉积相关新候选基因,为IMF分子调控机理研究和相关分子标记筛选研究奠定了良好的基础。  相似文献   

4.
试验旨在了解在鸡睾丸中高表达的1个长链非编码RNA (long non-coding RNA,lncRNA)及其预测靶基因的时空表达规律,研究二者在鸡弱精子症中的调控作用。根据弱精子症和正常北京油鸡公鸡睾丸转录组测序筛选到的1个高表达的lncRNA (MSTRG.15568.9),采用顺式(cis)作用模式预测其潜在靶基因SPAG4(sperm-associated antigen 4),进一步采用实时荧光定量PCR方法进行表达量分析。分别选择3只0、5、20、30、45、60周龄正常北京油鸡公鸡,检测MSTRG.15568.9与SPAG4基因在不同周龄公鸡睾丸中的表达量差异;选择30周龄3只正常公鸡,采集睾丸、肝脏和脾脏等8个部位组织样品,检测MSTRG.15568.9与SPAG4基因在不同组织间的表达规律;选择45周龄弱精子症公鸡和正常公鸡各3只,对比MSTRG.15568.9与SPAG4基因在睾丸的表达量差异。结果显示,MSTRG.15568.9与SPAG4存在明显的时空表达差异,且二者表达趋势基本一致。在不同周龄的鸡睾丸组织中,MSTRG.15568.9和SPAG4的表达趋势相近,MSTRG.15568.9在20周龄的表达量显著高于0、5、30、45、60周龄(P<0.05),0和5周龄表达量显著低于20、30、45和60周龄(P<0.05);SPAG4在45周龄表达量最高,其次是20周龄(P<0.05)。MSTRG.15568.9和SPAG4在睾丸和肝脏中的表达量均显著高于脾脏、肾脏等组织(P<0.05);在正常睾丸组织中的表达量均显著高于弱精子症睾丸组织(P<0.05)。综上所述,MSTRG.15568.9与SPAG4基因具有较明显的组织表达特异性,且MSTRG.15568.9可能调控SPAG4基因的表达,参与精子发生与精子活力调控;但其具体作用机制需要进一步探索。本研究可为鉴定与鸡弱精子症调节机制相关的功能基因提供参考。  相似文献   

5.
实验旨在探究羊精浆生化指标与精子质量常规参数之间的相关性,选择2~3岁、健康状况良好的13只山羊和10只绵羊,分别检测精子数、浓度、活力、曲线速率、直线速率、平均速率、线性指数、直线指数和振动指数等精子质量常规参数;检测相应精浆的14项生化指标,并与精子质量常规参数进行关联分析。结果表明:绵羊的鲜精活力达78%以上,精子密度达2 167.78×106/mL,精浆中含有蛋白质、酶、胆固醇、甘油三酯等多种生化成分;山羊鲜精活力达88%,精子密度达1 205.02×106/mL,精浆中含丰富的蛋白质以及多种生化酶成分。山羊精浆中总蛋白(TP)、球蛋白(GLB)、白蛋白(ALB)、果糖胺(FUN)、肌酸激酶(CK)、肌酐(CREA-S)高于绵羊(P<0.01),总胆固醇(TC)也高于绵羊(P<0.05);绵羊精浆中乳酸脱氢酶(LDH)、甘油三酯(TG)、钙(Ca)、磷(P)、丙氨酸氨基转移酶(ALT)高于山羊精浆同组分(P<0.01)。绵羊和山羊精浆TP与精子数量呈正相关(P>0.05),天门冬氨酸氨基转移酶(AST)、TC、FUN、ALT、GLB、LDH与精子活力呈正...  相似文献   

6.
为探索水牛高低活力精子的差异表达蛋白质(Differentially Expressed Proteins,DEPs)变化,并揭示水牛精子活力相关蛋白质的分子调控机制,本研究通过液相色谱-串联质谱(LC-MS/MS)技术,对成年摩拉水牛精浆、精子、精浆外泌体蛋白质种类及表达量进行比较分析。按照精子活力分为高活力组(0.67±0.02)和低活力组(0.34±0.04),分别提取其精浆外泌体蛋白质进行差异表达分析,鉴定到DEPs共160个。通过GO分析和KEGG通路分析发现,DEPs显著富集到精子部位的顶体素结合蛋白(ACRBP)、精子发育相关的生物调节过程以及“FcγR介导的吞噬作用”、“PPAR信号通路”等多个信号通路。通过构建精浆外泌体DEPs互作网络进一步分析发现,ACRBP、IZUMO1、SPACA1、ADAM2等蛋白质在精子发育调控通路发挥重要作用。  相似文献   

7.
为了研究宁都黄鸡公鸡体尺和屠宰性状之间的相关性,试验对16周龄健康的495只宁都黄鸡公鸡的活体重、体尺和屠宰性状的15个指标进行测定,并对各性状指标之间进行相关性分析、主成分分析及回归分析。结果表明:体尺性状的变异系数相较于屠宰性状的变异系数偏小,宁都黄鸡公鸡的产肉性能良好;宁都黄鸡公鸡的体斜长、胸围、龙骨长与活体重和屠宰性状之间存在强相关关系(相关系数≥0.60,P0.01),可通过体斜长、胸围、龙骨长等体尺性状对活重和屠宰性状进行预测和筛选;运用逐步回归分析法建立了通过体尺性状预测屠宰性状的回归方程,均达到极显著水平(P≤0.01),主成分分析将15项指标综合成3个主成分,累计贡献率为69.62%。说明宁都黄鸡公鸡选育可以以体重为主,兼顾胸宽、髋骨宽和胫宽。  相似文献   

8.
试验旨在克隆蛋鸡CYP19A1基因,对其遗传结构进行生物信息学分析并探究其在太行鸡不同组织中及不同产蛋量个体中的表达情况。以河北省太行鸡为研究对象,通过设计引物对CYP19A1基因CDS区进行克隆测序,运用生物信息学软件对其功能结构进行预测。结果显示,CYP19A1基因含有一个1 509 bp的开放阅读框(ORF),编码502个氨基酸。同源性比对和系统发生树分析结果表明,太行鸡CYP19A1基因与鸭的同源性较高(90.7%),并且在不同物种间高度保守。对CYP19A1蛋白理化性质进行预测分析发现,该蛋白为亲水蛋白,蛋白分子式为C2602H4103N675O719S36,分子质量为57.51 ku,理论等电点为5.99,其中含量最高的是亮氨酸(为14.0%)。蛋白质二级结构由α-螺旋、延伸链、β-折叠及无规则卷曲4种结构组成,所占比例分别为58.95%、2.18%、3.93%和34.93%。组织表达谱分析发现,CYP19A1基因在不同组织中均有表达,但其在卵巢中表达量最高。实时荧光定量PCR结果显示,CYP19A1基因在太行鸡高产组卵巢中的表达量显著高于低产组(P<0.05)。上述结果为研究太行鸡CYP19A1基因提供了重要的研究数据,为进一步挖掘太行鸡高产基因提供了参考。  相似文献   

9.
本研究旨在通过对意大利水牛精液品质分析、睾丸周径测量、精浆中的氧化应激水平检测和精子活力相关基因表达情况来探究影响精液质量的相关因素。试验检测了6头意大利水牛精液的活力、畸形率、采精量,并在测量其阴囊周径后进行相关性分析;检测了意大利水牛精浆中氧化应激水平指标(丙二醛(MDA)、总超氧化物歧化酶(T-SOD)、谷胱甘肽过氧化物酶(GSH-Px))并进行了相关性分析;分析了意大利水牛精子β-微管蛋白-2c(TUBB2C)、外周致密纤维2(ODF2)、筑丝蛋白2(TEKT2)、筑丝蛋白4(TEKT4)基因的表达定量及相关性。结果显示,意大利水牛阴囊周径与精液产量、活力、畸形率之间相关系数分别为0.423(P>0.05)、0.750(P<0.01)、-0.827(P<0.01),即阴囊周径与精子活力呈显著正相关关系、与畸形率呈显著负相关关系;意大利水牛精子活力与MDA、T-SOD、GSH-Px指标之间相关系数分别为-0.522(P<0.05)、0.333(P>0.05)、0.474(P<0.05),即精子活力与MDA含量之间存在显著负相关关系,与GSH-Px活性之间存在显著正相关关系,与T-SOD活性相关性不显著;意大利水牛精子活力与TUBB2CODF2、TEKT2、TEKT4基因指标之间相关系数分别为0.930(P<0.01)、0.726(P<0.01)、0.924(P<0.01)、0.839(P<0.01),即精子活力与以上基因表达量存在显著正相关关系。本研究结果为了解影响意大利水牛精液质量的因素提供参考,也为意大利种公水牛的筛选提供理论依据。  相似文献   

10.
QDPR基因克隆及其在乌蒙凤鸡不同生长阶段组织表达研究   总被引:1,自引:0,他引:1  
旨在克隆乌蒙凤鸡醌型二氢生物喋呤还原酶(quinoid dihydropteridine reductase,QDPR)基因,并检测其在不同性别乌蒙凤鸡不同生长阶段各组织中的表达差异,以研究QDPR基因在乌蒙凤鸡生长发育过程中的调控作用。本试验对乌蒙凤鸡QDPR基因CDS区进行PCR扩增和克隆,并对得到的序列进行生物信息学分析,通过实时荧光定量PCR检测QDPR基因在4、12、20和28周龄乌蒙凤鸡公鸡及母鸡的心、肝、脾、肺、肾、胸肌和腿肌组织中的相对表达量。结果表明,QDPR基因开放阅读框长度为417 bp,共编码139个氨基酸,编码蛋白为酸性不稳定蛋白,乌蒙凤鸡的QDPR基因序列与原鸡、日本鹌鹑和珠鸡的QDPR基因同源性较高;QDPR基因在不同性别乌蒙凤鸡不同生长阶段各组织中均有表达,其中,公鸡4、12和20周龄肺组织中QDPR基因表达量最高,极显著高于同一周龄其他组织(P<0.01),母鸡4周龄肝、脾、肺中QDPR基因相对表达量为所有时期最高,极显著高于12、20周龄(P<0.01),公鸡大多数组织中QDPR基因表达量随时间增长总体呈现出先升后降的趋势,母鸡为先降后升。结果显示,QDPR基因在乌蒙凤鸡内脏组织中的表达均高于肌肉组织,且公母鸡不同时期表达情况有所差异,试验结果可为进一步研究QDPR基因在鸡生长发育中的调控作用提供参考。  相似文献   

11.
The present study aimed at characterization of fertility-associated proteins in PR and RIR x Local roosters and was conducted on two generations of birds. Roosters were divided into high- (>50%) and low-fertility groups (<50%) based on sperm function tests and fertility rate in both the generations. Polyclonal antibodies were raised in rabbits against sperm proteins of first generation highly fertile roosters and tested for characterization of fertility-associated sperm proteins in the second generation of same roosters. IgG fraction against proteins (anti-SP IgG) was reacted with sperm proteins of both high and low fertile roosters of second generation on immunoblots. SDS-PAGE of sperm extracts of PR and RIR x Local cross breeds resulted in resolution of 12 and 23 proteins on 12% acrylamide gels and anti-SP IgG reacted only with 8 and 9 sperm proteins of PR and RIR x Local cross roosters on immunoblots. The SDS-PAGE and immunoblotting analysis also indicated a variation in sperm proteins among two breeds and high/low fertile roosters. It can be concluded that the selection of roosters on the based on proteins of 65/ 25; 70/ 46/ 30 kDa may be specifically associated with high fertility of PR and RIR x Local cross, respectively. The proteins 62 kDa (PR) and 40kDa (RIR x Local cross) may be specifically responsible for low fertility.  相似文献   

12.
Birds obtained by embryo engineering are used to study embryo development and to produce transgenic birds. As this method of producing birds still generate strong emotions of the public opinion head ornaments, testes and semen characteristics of sex chimera roosters were examined to check whether they differ from chickens obtained by non‐manipulated methods. Measurements of head ornaments, testes and semen were correlated with each other. Semen quality factor (SQF) was calculated, as well as the level of fluctuating asymmetry (FA) of bilateral traits (wattles and testes). Positive correlation was found for comb width and wattle length and comb thickness and sperm concentration. Semen characteristics and FA did not exceed the level encounter in other chicken lines. Results obtained indicate that germline chimeras are similar in appearance of secondary sexual traits, and semen and testes characteristics to chickens produced in non‐manipulated way.  相似文献   

13.
旨在对绵羊附睾头、体和尾部的精子进行蛋白质组学分析,获得差异表达蛋白,对数据进行功能富集分析,挖掘精子发生/成熟关键蛋白质。本研究选择12月龄左右健康的3只雄性湖羊为试验动物,分离附睾并按区域收集精子,3组样本(附睾头部组、附睾体部组和附睾尾部组),每组3个生物学重复,共计9例绵羊精子细胞样本。基于TMT标定定量蛋白质组学分析和R语言等工具,在获取的差异表达蛋白中进行GO和KEGG富集分析,并利用蛋白质免疫印迹(Western bolt)、免疫荧光(immunofluorescence)和流式细胞术(flow cytometry)试验验证结果的可靠性。从22 841个唯一性肽中鉴定到差异蛋白质616种,其中,尾vs头组鉴定出309个差异表达蛋白(上调213个,下调96个);尾vs.体组鉴定出167个差异表达蛋白(上调107个,下调60个);体vs头组鉴定出140个差异表达蛋白(上调88个,下调52个)。根据差异倍数与蛋白质功能,筛选出可能与精子成熟、核质物质转运相关的关键蛋白-KPNA4。本研究揭示了绵羊附睾不同部位精子的特点与差异,这些数据为研究雄性绵羊的生殖机制和精子成熟提供了丰富的资源。  相似文献   

14.
旨在分析静原鸡白羽、麻羽、黑羽保种群之间的遗传变异,挖掘调控特征性状的关键候选基因。本研究利用RAD-seq技术对180日龄特征明显、发育正常且健康的白羽、麻羽、黑羽静原鸡(每个羽色选取60个个体,40只母鸡,20只公鸡)进行测序,基于SNP标记计算观察杂合度(Ho)、群体内核酸多态性(Pi)、群体的平均近交系数(Fis)等指标,分析静原鸡3个类群的遗传多样性和群体结构,并通过选择性清除分析和全基因组关联分析(GWAS)筛选出候选基因,利用KOBAS对候选基因进行KEGG (Kyoto Encyclopedia of Genes and Genomes)通路富集,最终筛选出调控静原鸡羽色的候选基因。测序结果表明,静原鸡180个样品共产生198.83 Gb Clean Data,Q30达到93%以上。遗传多样性分析表明,白羽、麻羽、黑羽静原鸡分别鉴定出238 533、233 562和240 820个SNPs标记,HoPiFis分别在0.273 2~0.278 2、0.304 9~0.309 6和0.096 1~0.109 8之间。群体结构分析表明,静原鸡根据不同羽色分为不同类群。通过选择性清除分析和全基因组关联分析共筛选出11个(FZD4、WNT16、EDNRBTYRKRASCTNNB1、DDCMC1R、CAMK2A、PRKCBPRKCA)与静原鸡羽色相关的候选基因,富集结果显示这些基因主要与黑色素生成、酪氨酸代谢和Wnt信号传导等通路相关。综上所述,本研究利用SNPs标记信息可以全面地评价静原鸡的保种现状,为静原鸡的遗传资源保护奠定理论基础。同时,筛选出了与静原鸡羽色性状相关的候选基因,为静原鸡不同羽色的品系化培育提供新的遗传标记和基因靶点。  相似文献   

15.
试验通过开展快慢羽群体的鉴定,并对比其在羽毛发育、生长和繁殖性能方面的差异,旨在为北京油鸡种鸡选育和科学养殖提供数据支持。选用北京油鸡纯系公鸡,出雏时,按照主翼羽与覆主翼羽的羽长差值将其分为快慢羽亚群,其中快羽包括K1(主翼羽长于覆主翼羽>5 mm)和K2(主翼羽长于覆主翼羽2~5 mm),慢羽包括M1(主翼羽与覆主翼羽等长或主翼羽长于覆主翼羽<2 mm)和M2(主翼羽短于覆主翼羽)和M3(主翼羽未长出)。1~7日龄每隔1 d测量1次主翼羽与覆主翼羽羽长,7~42日龄每隔1周测量1次;1~8周龄每周测量体重,9~18周龄每隔1周测定体重;10周龄时,观测公鸡全身羽毛发育情况;47周龄时,测定公鸡常规精液品质性状、精子动力学参数、受精率及孵化率。结果显示,快羽公鸡占北京油鸡公鸡总数的11.60%,慢羽占88.40%,慢羽又以M2型为主,有少量M1型和M3型。育雏育成期(1~18周)北京油鸡快慢羽公鸡各周龄体重均无显著差异(P>0.05)。在育雏育成期,慢羽公鸡主翼羽和覆主翼羽生长均慢于快羽公鸡。其10周龄时,背部和腿部羽毛生长完全的鸡的比例仅为44%,且不同类型的慢羽公鸡的比例也不一,其中等长型或微长型慢羽最高,超过90%,未长出型慢羽最低,仅为17%左右。47周龄时快羽鸡和慢羽鸡的常规精液品质无差异,但是快羽公鸡精子直线性显著高于慢羽鸡(P<0.05),直线速率高于慢羽公鸡(P=0.06),快羽北京油鸡公鸡受精率显著高于慢羽公鸡(P<0.05),且入孵蛋孵化率和受精蛋孵化率有高于慢羽公鸡的趋势,但差异不显著(P>0.05)。本研究结果表明,快慢羽北京油鸡公鸡的羽毛生长和繁殖性能有一定差异,需要加强慢羽公鸡羽毛发育缓慢原因和鉴定方法的研究,也需加强慢羽公鸡精液品质选育。  相似文献   

16.
The objective of this study was to detect the reasons of rooster's fertility decrease at 50 weeks of age. Therefore, the reproductive system of broiler breeder roosters was laparoscopic, macroscopic and histopathology evaluated, and a comparison of the anatomical aspect with the sperm analysis and birds’ age was realized. Cobb roosters (n = 59) were distributed into two groups (30 and 50 weeks). Evaluations were performed with laparoscopy, macroscopy and histopathology, and seminal quality, blood serum testosterone concentration and weight were also determined. The old roosters presented smaller testicle size, higher intensity epididymal lithiasis and lower testicle sperm production, compared to the young roosters. The use of the endoscope could easily distinguish a normal‐sized testicle than an atrophic one. Four old roosters with severe testicular atrophy did not show spermatogenesis, although three still had sperm in the ejaculate. This would falsely indicate a wrong diagnosis of normal fertility before the testicular atrophy took place. In conclusion, in addition to the weight increase with age, the testicular atrophy and impairment of sperm production seemed to be the main reason to the decrease in the rooster's fertility at 50 weeks of age. Therefore, the use of the laparoscopy as a way to detect the roosters with testicular atrophy before 50 weeks of age and their removal from them flock could be useful as a diagnostic tool to prevent the birds’ fertility loss.  相似文献   

17.
Boltz DA  Nakai M  Bahra JM 《Avian diseases》2004,48(4):909-915
The formation of epididymal stones in the rooster epididymis is a widespread problem that has detrimental effects on sperm production and fertility. The cause of epididymal stones is unknown, but an infectious agent, the avian infectious bronchitis virus (AIBV), has been implicated. The goal of this study was to determine if administering the live attenuated AIBV vaccine to male chicks increases the incidence of stones in the epididymal region of the adult rooster. Specific pathogen free (SPF) Leghorn roosters were divided into two groups: a vaccine-free group (n = 7) and a group vaccinated with AIBV (n = 12). The vaccine was administered orally at 2, 4, 10, and 14 wk of age. Blood was drawn weekly to monitor antibodies to AIBV. At 26 wk of age, blood was obtained to determine testosterone concentrations, and reproductive tracts were removed to analyze daily sperm production and to detect epididymal stones. Nine of 12 vaccinated roosters developed stones, whereas those not given the vaccine did not develop stones. Serum testosterone concentrations were significantly (P < 0.05) reduced in vaccinated roosters with epididymal stones (3.6 +/- 0.30 ng/ml) when compared with nonvaccinated roosters that did not have epididymal stones (7.0 +/- 1.63 ng/ml). Testis weight was significantly (P < 0.05) reduced in vaccinated roosters with epididymal stones (12.1 +/- 0.76 g), as compared with nonvaccinated roosters without epididymal stones (15.2 +/- 0.81 g). Daily sperm production was significantly (P < 0.05) decreased in vaccinated roosters with epididymal stones (5.03 +/- 0.31 x 10(8) sperm/testis/day) when compared with nonvaccinated roosters without epididymal stones (7.43 +/- 0.52 x 10(8) sperm/testis/day). Comparing daily sperm production on a per gram basis, vaccinated roosters with epididymal stones had 4.38 +/- 0.14 x 10(7) sperm/g of testis, which was significantly (P < 0.05) smaller than nonvaccinated roosters without epididymal stones, which had 5.17 +/- 0.17 x 10(7) sperm/g of testis. We conclude that the use of a live attenuated AIBV vaccine increases the incidence of epididymal stones in roosters, resulting in decreased sperm production and decreased serum testosterone concentrations.  相似文献   

18.
The objective of this study was to evaluate the effect of dietary supplementation of whole flaxseed on sperm traits and sperm fatty acid profile in aged broiler breeder roosters. Twelve Ross 308 broiler breeder roosters (age: 52 weeks; weight: 4,900 ± 210 g) haphazardly allotted to three dietary treatments (each treatment contained four replicates and one bird in each replicate) for six weeks. Treatments were different levels of flaxseed (0% flaxseed [GFL0], 2% flaxseed [GFL2] and 4% flaxseed [GFL4]). The feed intake quadratically decreased (p < .05) with increasing whole flaxseed levels for the period (58 to 60 weeks). Sperm traits (semen volume and sperm concentration, sperm total and forward motility, sperm viability and morphology, sperm plasma membrane functionality) were evaluated every two weeks (four times), and sperm fatty acid profile was assessed at the end of the experiment. Semen volume, sperm concentration and sperm morphology were not affected by treatments. On week 60, GFL2 group showed a significantly lower percentage of total and progressive sperm motility and sperm membrane functionality in comparison with the control and GFL4 groups. Also, sperm viability was lower in GFL2 group compared with other groups on week 58 (p < .05). In terms of sperm fatty acid profile, GFL2 group significantly reduced the percentage of linoleic acid (C18:2 [n-6]) in comparison with other groups. However, any of the other fatty acids were not affected by dietary flaxseed. In conclusion, dietary supplementation of whole flaxseed could not improve the quality of aged broiler breeder roosters' sperm in this study, nor it could alter the sperm fatty acid profile; thus, it seems necessary to use some antioxidants such as vitamin E in the diet of aged broiler breeder roosters, when supplementing the diets with oils or oilseeds such as flaxseed.  相似文献   

19.
采用全天观察法,对京海黄鸡公鸡的性行为进行记录,获得京海黄鸡公鸡性行为的过程,总结京海黄鸡公鸡性行为规律,分析京海黄鸡公鸡个体间性行为的差异,并通过检测精液品质,研究京海黄鸡公鸡性行为与精液质量的关系;通过观察晴天与阴天时的性行为,分析不同的天气对京海黄鸡公鸡性行为的影响,结果显示:京海黄鸡性行为个体间差异不大,受天气的影响较为明显。本文通过对京海黄鸡公鸡性行为的观察研究,为进一步提高京海黄鸡公鸡自然交配的授精率和繁殖性能提供一定的科学依据。  相似文献   

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