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1.
吕惠序  杨九强 《养猪》2011,(3):73-75
猪渗出性皮炎又称葡萄球菌性皮炎、皮脂溢性皮炎,俗称"猪油皮病",是由能产生表皮脱落毒素的猪葡萄球菌引起的哺乳仔猪和刚断奶仔猪的一种急性和超急性接触传染性皮肤病,一般呈散发性,对个别猪群可造成很大损失。  相似文献   

2.
猪渗出性皮炎   总被引:4,自引:0,他引:4  
猪渗出性皮炎是由猪葡萄球菌引起猪的出现全身油脂样渗出、形成皮痂并脱落,甚至导致脱水和死亡等临床症状的一种急性传染病。论文综述了近年来有关猪渗出性皮炎的病原学、流行病学和致病机理方面的研究结果,并就猪渗出性皮炎的诊断和防治进行了简要介绍。  相似文献   

3.
<正>引起猪皮肤疾病的原因有很多,细菌、病毒和寄生虫感染及蚊虫叮咬、过敏反应等都会在猪的皮肤上出现病变。现将常见的以皮肤病变为主要特征的猪皮肤疾病及其防治措施介绍如下,供大家参考。1渗出性皮炎引起猪渗出性皮炎的病原是猪葡萄球菌,这种菌可以产生热敏感性表皮脱落毒素,同时猪圆环病毒2型的感染会促使渗出性皮炎的发生。渗出性皮炎主要发生于1~4周龄的哺乳仔  相似文献   

4.
<正>仔猪渗出性皮炎的临床症状主要表现为仔猪急性或超急性感染,患猪全身性皮炎,可引起脱水和死亡。渗出性皮炎是一种扩散性的真皮炎,波及全身体表,急性型常侵害哺乳仔猪,慢性则多见于断奶仔猪。仔猪渗出性皮炎由葡萄球菌引起,该菌可产生热敏感性表皮脱落毒素,营养、卫生、免疫、皮肤破损、疥螨感染等因素均可影响该病的严重程度和病程。据研究表明,猪圆环病毒2型和猪细小病毒在渗出性皮炎的爆发中扮演着重要角色。随着年龄的  相似文献   

5.
正猪油皮病也称猪渗出性皮炎,此病是由葡萄球菌侵入破损的皮肤引起。葡萄球菌产生的毒素吸收入体内,可损害肝脏和肾脏。渗出性皮炎在哺乳仔猪通常只致个体发病,但对后备猪群与断奶仔猪则可能导致严重的问题。有研究表明:在母猪分娩前数天内,细菌已在母猪阴道中大量增殖。仔猪通常在出生时或产后不久被感染。轻微的渗出性皮炎可因仔猪在争夺乳头或奶水时,锋利的犬齿损伤脸颊,或吸奶时膝  相似文献   

6.
仔猪渗出性皮炎(Exudative Epidermitis,EE),也叫猪油皮病,是一种以表皮脱落、皮肤油脂样渗出以及体表结痂为特征的体表接触性传染病.该病多发于寒冷潮湿的冬春季节,哺乳仔猪及刚断奶保育猪多发,通常散发或小范围群发于猪群中,虽然发病率不高,但治愈率低,耐过猪生长速度受到严重影响.仔猪渗出性皮炎的病原主要为葡萄球菌,包括猪葡萄球菌、松鼠葡萄球菌[1].主要的致病因素是病原菌侵入血液循环造成的败血症及细菌繁殖产生的表皮脱落毒素.本文主要报道在临床见到1例仔猪渗出性皮炎,通过临床症状观察及流行病学调查初步判断为仔猪渗出性皮炎,实验室检验分离到1株细菌,经生化试验,PCR分子鉴定,基因序列分析,确定为猪葡萄球菌.我们通过药敏试验筛选敏感药物,清洁环境,结合其他有效的综合防控措施,控制了该病的蔓延.  相似文献   

7.
<正>仔猪渗出性皮炎是葡萄球菌引起的急性接触性传染病,病猪以出现渗出性皮炎为特征。猪渗出性皮炎又称猪葡萄球菌性皮炎或油皮病,是一种人畜共患病。大肠杆菌病、疥螨病可诱发仔猪渗出性皮炎。1流行特点葡萄球菌在自然界中广泛存在,尘埃、污水及土壤中都有葡萄球菌存在,它也是动物体表  相似文献   

8.
仔猪渗出性皮炎又称仔猪油皮病,因患病猪全身油脂样渗出而得名。是葡萄球菌引起的一种传染病。患病仔猪全身油脂样渗出,形成皮痂并脱落,严重的脱水死亡。本病一年四季均可发生,在猪群种一般呈散发性,  相似文献   

9.
仔猪渗出性皮炎的实验室诊断   总被引:5,自引:1,他引:5  
睢艳平  徐镔蕊  王勇  屈哲  李伟  任艳丽 《中国畜牧兽医》2006,33(10):I0013-I0016
猪葡萄球菌是引起猪渗出性皮炎的致病因素,能引起猪以油脂溢出、表皮脱落以及水泡形成为特征的全身性皮肤感染。某养殖户所养仔猪大批发病,临床症状和病理变化具有仔猪渗出性皮炎的特征,通过临床特征性症状和典型病理变化以及实验室分离,证实为致病性猪葡萄球菌,确诊该养殖户仔猪发生渗出性皮炎。  相似文献   

10.
猪渗出性皮炎主要发生于1月龄以内仔猪的传染性皮炎。病猪全身皮肤有脂性黄褐色渗出物胶着,被毛像汗浸湿样,混有尘埃和脱落的表皮等皮垢,被毛呈特有的黑褐色,似煤烟覆盖。重症猪因皮肤呼吸困难、衰弱,伴有脱水症状,呈败血症死亡。本病俗称脂溢性皮炎或煤烟病,是由皮炎葡萄球菌皮炎亚种感染引起的疾病。  相似文献   

11.
Staphylococcus chromogenes is closely related to Staphylococcus hyicus, which is recognised as the causative agent of exudative epidermitis (EE) in pigs. S. chromogenes is part of the normal skin flora of pigs, cattle and poultry and has so far been considered non-pathogenic to pigs. A strain of S. chromogenes producing exfoliative toxin type B, ExhB, was identified by the use of a multiplex PCR specific for the exfoliative toxins from S. hyicus. The exfoliative toxin from S. chromogenes reacted in immunoblot analysis with polyclonal and monoclonal antibodies specific to ExhB from S. hyicus and had an apparent molecular weight of 30 kDa. Sequencing the gene encoding the exfoliative toxin from S. chromogenes revealed that the molecular weight of the toxin with the signal peptide and the mature toxin was 30,553 and 26,694 Da, respectively. Comparison of the exhB genes from S. chromogenes strain VA654 and S. hyicus strain 1289D-88 showed differences in seven base pairs of the DNA sequences and in two amino acid residues in the deduced amino acid sequences. Pigs were experimentally inoculated with S. chromogenes strain VA654. By clinical observations and histopathological evaluation of the skin alterations, all pigs revealed development of generalized exudative epidermitis. No toxin producing S. hyicus was isolated from the pigs and all ExhB-positive bacterial isolates were identified as S. chromogenes. This confirmed that the disease-causing agent was the inoculated S. chromogenes strain VA654. The results of this study show that S. chromogenes may cause exudative epidermitis in pigs.  相似文献   

12.
Exudative epidermitis (EE) is an acute, often fatal skin disease of piglets caused by Staphylococcus hyicus. Clinical and histopathological manifestations of EE are similar to those of staphylococcal scalded skin syndrome (SSSS), a human blistering skin disease, in which exfoliative toxins produced by Staphylococcus aureus digest the extracellular domains of desmoglein (Dsg) 1 and cause loss of epidermal cell-cell adhesion. The aims of this study were to isolate and characterize cDNA for full length of swine Dsg1, and to determine whether the extracellular domains of swine Dsg1 produced by baculovirus (sDsg1-His) could be digested by four isoforms of exfoliative toxin produced by S. hyicus (ExhA, ExhB, ExhC and ExhD). Nucleotide sequencing revealed that swine Dsg1 cDNA consisted of an open reading frame of 3138 bp, encoding a precursor protein of 1045 amino acids. Deduced amino acid sequence of the swine Dsg1 precursor were highly homologous to corresponding bovine, canine, human and murine sequences. Immunoadsorption assay with a secreted form of sDsg1-His revealed that sDsg1-His specifically absorbs the immunoreactivity of 10 human pemphigus foliaceus sera against swine keratinocyte cell surfaces, suggesting its proper conformation. When sDsg1-His was incubated in vitro with Exhs, all four isoforms of Exh directly digested sDsg1-His into smaller peptides, whereas removal of calcium from sDsg1-His completely inhibited its proteolysis by these four Exhs. Recognition and digestion of calcium-stabilized structure on the extracellular domains of swine Dsg1 by Exhs indicated that EE shares similar molecular pathophysiological mechanisms of intra-epidermal splitting with SSSS in humans.  相似文献   

13.
Immunoblot analysis and enzyme-linked immunosorbent assay (ELISA) confirmed previous reports that the Staphylococcus hyicus exfoliative toxins ExhA and ExhB are metalloproteins, and further indicated that ExhC is also a metalloprotein. An indirect ELISA was developed for the detection of toxigenic strains as an alternative method to the use of phage typing for selection of S. hyicus isolates to be used in autogenous vaccine against exudative epidermitis in pigs. The indirect ELISA was evaluated by investigating the presence of toxin among a total of 655 S. hyicus isolates from 69 pig skin samples, one from each of the 69 pig herds with outbreak of exudative epidermitis. Toxigenic S. hyicus were detected in 74% of the cases by ELISA. From each of the five cases, in which initially no toxigenic S. hyicus were found, a further 40 S. hyicus-like colonies were tested in ELISA. Testing of this number of colonies has a >99% probability of disclosing toxigenic S. hyicus. Toxin-producing isolates were found in only two of the five cases investigated. This may indicate the existence of one or more variants of the exfoliative toxin of S. hyicus that are not detected in the indirect ELISA or that S. hyicus may be displaced from lesions of exudative epidermitis.  相似文献   

14.
A rounding effect was demonstrated in cultured cells inoculated with the culture filtrates (CFs) of 60 strains of Staphylococcus intermedius derived from dogs affected with pyoderma. Exfoliative toxin (ET)-like toxin (ETLT) was isolated from the CF of S. intermedius strain D-52, which exhibited strong rounding activity and then was purified by gel filtration on a Sephadex G-75 column, and by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). The ETLT caused exfoliation in 1-day-old chickens, suckling Syrian hamsters, and dogs, but not in suckling mice. The ETLT was serologically different from exfoliative toxin A (ETA), exfoliative toxin B (ETB), exfoliative toxin C (ETC), S. hyicus exfoliative toxin A (SHETA), and SHETB, as shown by Western blot analysis. The molecular weight of the ETLT was estimated at 30 kDa by SDS-PAGE. In the present study, we propose the ETLT was a novel type of ET, S. intermedius exfoliative toxin (SIET).  相似文献   

15.
为分析猪葡萄球菌脱落毒素EXHC和SHETA基因结构并预测其所编码蛋白的结构和功能,本试验根据GenBank已报道的猪葡萄球菌脱落毒素EXHC和SHETA基因序列分别设计了1对特异性引物,从猪葡萄球菌GDZC株中扩增获得EXHC和SHETA基因片段,大小分别为1007和971 bp。序列分析结果表明,EXHC基因与猪葡萄球菌丹麦分离株(GenBank登录号:AF515455)及猪源松鼠葡萄球菌河北分离株(GenBank登录号:JF755400)的核苷酸序列、氨基酸序列同源性均为100.0%,而与其他葡萄球菌脱落毒素基因的核苷酸、氨基酸序列同源性分别为3.3%~53.9%和7.9%~44.2%。SHETA基因与日本分离株(GenBank登录号:AB036768)的核苷酸序列同源性为96.2%,氨基酸序列同源性为98.4%,在保守区共有31个碱基发生突变。利用DNAStar软件对EXHC和SHETA蛋白结构进行分析,结果显示EXHC基因编码的蛋白为亲水性蛋白,SHETA基因编码蛋白为疏水性蛋白,抗原性较差。本研究从猪葡萄球菌GDZC株中成功扩增获得EXHC和SHETA基因片段并对其编码的蛋白结构进行了预测,证实了中国分离的猪葡萄球菌同时携带有EXHC和SHETA 2种毒素基因,为进一步研究猪葡萄球菌的致病机理及毒素之间的相互作用提供了理论依据。  相似文献   

16.
Exfoliative toxin was isolated from the sterile cell-free filtrate of 24 h culture of Staphylococcus hyicus subsp. hyicus strain P-1. The partial purification of exfoliative toxin produced by S. hyicus (shET) was performed by precipitation with 50-80% saturated ammonium sulfate, gel filtration on a Sephadex G-75 column and column chromatography on DEAE-cellulose. Partially purified shET (pp-shET) caused exfoliation in piglets at 8 to 12 h after intradermal or subcutaneous injection. However, heat-treated pp-shET did not cause exfoliation in piglets for up to 24 h after injection. On histopathological examination of the skin at 12 h after injection of pp-shET, an intraepidermal cleavage plane was shown between the stratum corneum and stratum granulosum and at the stratum granulosum.  相似文献   

17.
In the present study, previously characterized Staphylococcus hyicus isolated in Russia (n=23) and Germany (n=17) were investigated for the prevalence of the exfoliative toxin encoding genes exhA, exhB, exhC and exhD by multiplex PCR resulting in the detection of exhD positive strains among the S. hyicus isolated from pigs with exudative epidermitis in Russia and the detection of exhC and exhD for one and two strains isolated from exudative epidermitis in Germany respectively. The toxin gene negative strains were generally isolated from apparently healthy pigs, from other animals and from specimens where the relation between the isolation of S. hyicus and the clinical symptoms remained unclear. Partial sequencing of the toxin genes of selected exhC and exhD positive strains and comparing the sequencing results with sequences of exhC and exhD reference strains revealed an almost complete identity. The results of the present study were in agreement with the findings of Andresen and Ahrens (J. Appl. Microbiol., 96, 2004, 1265) and Andresen (J. Vet. Rec., 157, 2005, 376) that the presented multiplex PCR could be used to investigate S. hyicus for toxinogenic potential and that there is an association between the presence of toxin genes in S. hyicus strains from exudative epidermitis. However, comparable with the S. hyicus strains isolated in Germany which were investigated previously by Andresen (J. Vet. Rec., 157, 2005, 376), exhD seems to predominate in S. hyicus strains from Russia.  相似文献   

18.
根据GenBank已发表的猪葡萄球菌的6种脱落毒素基因序列,设计合成了6对相应的特异性引物,通过特异性、敏感性和重复性试验建立了可行的多重PCR检测方法。用该方法对临床分离到的9株猪葡萄球菌进行检测,均扩增出了与预期大小相符的23SrDNA(662bp)条带;同时,其中6株分别扩增出了EXHA(316bp,2株)、EXHC(525bp,2株)和Shet-A(814bp,2株)基因特异性条带;另外3株均未扩增出任何毒素基因特异性条带,鉴定为无毒力菌株,以上结果与生化鉴定及单一PCR检测测序结果一致。结果表明,本试验所建立的多重PCR方法不仅操作快速方便、节约试验成本,而且具有高度特异性、敏感性和良好的重复性,可用于仔猪渗出性皮炎的诊断和猪葡萄球菌的快速鉴定。  相似文献   

19.
In piglets inoculated with partially purified exfoliative toxin (pp-shET) produced by Staphylococcus hyicus subsp. hyicus, exfoliation was observed at 12 h after injection. Chickens inoculated with the same dose of pp-shET also showed exfoliation within 30 min of injection. However, exfoliation was not demonstrated in mouse, rat, guinea pig, hamster, dog or cat inoculated with pp-shET until 24 h after injection. In cultured cell lines, especially L-929 and Hep-2, the rounding effect occurred after incubation with pp-shET for 1 h. The rounding effect was also seen in five other cultured cells (NCTC 2544, HeLa/S3, HmLu-1, CHO and BHK-21) 6-24 h after exposure to pp-shET. These round cells survived for 72 h after inoculation and formed a monolayer 24 h after changeover to a toxin-free medium. The rounding effect was observed in cells after the formation of the monolayer, but not before. It was suggested that the rounding effect was not caused by the increase in cyclic AMP in cells inoculated with pp-shET but by the cleavage of intracellular contacts.  相似文献   

20.
Staphylococcus hyicus strains with different phage types, plasmid profiles, and antibiotic resistance patterns were isolated from piglets with exudative epidermitis. The strains could be divided into virulent strains, producing exudative epidermitis, and avirulent strains, producing no dermal changes when injected in experimental piglets. The results showed that both virulent and avirulent strains were present simultaneously on diseased piglets. This constitutes a diagnostic problem. Concentrated culture supernatants from nine virulent strains injected in the skin of healthy piglets produced a crusting reaction in all piglets. Acanthosis was observed in the histopathological examination of the crustaceous skin. Concentrated culture supernatants from nine avirulent strains produced no macroscopic or microscopic skin changes. Protein profiles from all virulent strains and seven out of nine avirulent strains showed a high degree of protein band homology. An approximately 30 kDa protein present in all concentrated culture supernatants capable of producing skin changes, could not be detected in samples that did not produce skin changes. No other protein showed a similar association. It is concluded that crusting reaction of piglet skin is a suitable indicator of virulence in S. hyicus in relation to exudative epidermitis, and that virulent strains produce a 30 kDa protein, absent in concentrated culture supernatants from avirulent strains. This 30 kDa protein might be an exfoliative toxin.  相似文献   

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