动物营养学报
動物營養學報
동물영양학보
ACTA ZOONUTRIMENTA SINICA
2014年
6期
1521-1526
,共6页
曾东%颜宗凯%曾燕%倪学勤%王印%李涛
曾東%顏宗凱%曾燕%倪學勤%王印%李濤
증동%안종개%증연%예학근%왕인%리도
猪%唾液%细菌%PCR-DGGE%聚类分析%主成分分析
豬%唾液%細菌%PCR-DGGE%聚類分析%主成分分析
저%타액%세균%PCR-DGGE%취류분석%주성분분석
pig%saliva%bacteria%PCR-DGGE%cluster analysis%principal component analysis
本试验旨在研究健康猪唾液细菌结构及多样性。试验采用聚合酶链式反应-变性梯度凝胶电泳(PCR-DGGE)技术结合 PCR-DGGE 图谱及特异性条带的克隆和测序,同时采用主成分分析和聚类分析方法分析试验结果。结果表明:PCR-DGGE 图谱中仔猪唾液细菌平均条带数为23条,而育肥猪为28条;育肥猪唾液细菌种群的多样性指数、均匀度和丰富度均较高,分别为3.34、0.877和28.40,而仔猪分别为3.17、0.834和23.20;聚类分析显示,虽然不同生长阶段猪唾液细菌群落具有一定差异性,但所有样品间相似性系数均高于0.66。PCR-DGGE 图谱中共性条带属于发酵乳杆菌( Lactobacillus fermentum)、大肠杆菌( Escherichia coli)、Mycobacterium arosiense、厚壁菌(Firmicutes)和猪链球菌( Streptococcus suis),它们是猪口腔中的优势菌群;仔猪的特异性条带属于 Neisseria dentiae 和 Neisseria shayeganii,而育肥猪的特异性条带主要是葡萄球菌亚种(Staphylococcus sp.)。结果提示,健康仔猪和育肥猪唾液细菌结构存在明显差异,随着猪的生长发育,唾液细菌多样性增加且趋于稳定。
本試驗旨在研究健康豬唾液細菌結構及多樣性。試驗採用聚閤酶鏈式反應-變性梯度凝膠電泳(PCR-DGGE)技術結閤 PCR-DGGE 圖譜及特異性條帶的剋隆和測序,同時採用主成分分析和聚類分析方法分析試驗結果。結果錶明:PCR-DGGE 圖譜中仔豬唾液細菌平均條帶數為23條,而育肥豬為28條;育肥豬唾液細菌種群的多樣性指數、均勻度和豐富度均較高,分彆為3.34、0.877和28.40,而仔豬分彆為3.17、0.834和23.20;聚類分析顯示,雖然不同生長階段豬唾液細菌群落具有一定差異性,但所有樣品間相似性繫數均高于0.66。PCR-DGGE 圖譜中共性條帶屬于髮酵乳桿菌( Lactobacillus fermentum)、大腸桿菌( Escherichia coli)、Mycobacterium arosiense、厚壁菌(Firmicutes)和豬鏈毬菌( Streptococcus suis),它們是豬口腔中的優勢菌群;仔豬的特異性條帶屬于 Neisseria dentiae 和 Neisseria shayeganii,而育肥豬的特異性條帶主要是葡萄毬菌亞種(Staphylococcus sp.)。結果提示,健康仔豬和育肥豬唾液細菌結構存在明顯差異,隨著豬的生長髮育,唾液細菌多樣性增加且趨于穩定。
본시험지재연구건강저타액세균결구급다양성。시험채용취합매련식반응-변성제도응효전영(PCR-DGGE)기술결합 PCR-DGGE 도보급특이성조대적극륭화측서,동시채용주성분분석화취류분석방법분석시험결과。결과표명:PCR-DGGE 도보중자저타액세균평균조대수위23조,이육비저위28조;육비저타액세균충군적다양성지수、균균도화봉부도균교고,분별위3.34、0.877화28.40,이자저분별위3.17、0.834화23.20;취류분석현시,수연불동생장계단저타액세균군락구유일정차이성,단소유양품간상사성계수균고우0.66。PCR-DGGE 도보중공성조대속우발효유간균( Lactobacillus fermentum)、대장간균( Escherichia coli)、Mycobacterium arosiense、후벽균(Firmicutes)화저련구균( Streptococcus suis),타문시저구강중적우세균군;자저적특이성조대속우 Neisseria dentiae 화 Neisseria shayeganii,이육비저적특이성조대주요시포도구균아충(Staphylococcus sp.)。결과제시,건강자저화육비저타액세균결구존재명현차이,수착저적생장발육,타액세균다양성증가차추우은정。
This experiment was conducted to study the structure and diversity of salivary bacteria of healthy pigs. The bacterial diversity was studied using polymerase chain reaction-denaturing gradient gel electrophoresis ( PCR-DGGE),cluster analysis and principal component analysis. Some common and special bands were iden-tified by clone and sequencing at the same time. The results showed that in PCR-DGGE profile,the average band number of piglets was 23 and the average band number of finishing pigs was 28;the diversity index, richness and evenness of finishing pigs were higher,and they were 3.34,0.877 and 28.40,respectively,while the diversity index,richness and evenness of piglets were 3.17,0.834 and 23.20,respectively;the cluster a-nalysis suggested that there were some differences in salivary bacterial population during different growth stages of pigs,but the similarity coefficient in all the samples was higher than 0.66. In PCR-DGGE profile,Lactoba-cillus fermentum,Escherichia coli,Mycobacterium arosiense,Firmicutes and Streptococcus suis were predom-inant in mouth cavity of pigs;the special bacteria in saliva of piglets were Neisseria dentiae and Neisseria shayeganii,and the special bacteria in saliva of finishing pigs was Staphylococcus sp.. There is a significant difference in the diversity of salivary bacteria between piglets and finishing pigs. The diversity of salivary bacte-ria is increasing and gradually stabilized with the growth of pigs.