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[Osteomyelitis and papillary renal adenoma in a red panda (Ailurus fulgens fulgens)]. [小熊猫(Ailurus fulgens fulgens)的骨髓炎和肾乳头状腺瘤]
M Kummerfeld, A Knieriem, P Wohlsein

A 13 year-old female Red Panda (Ailurus fulgens fulgens) kept in a zoological garden was euthanatized due to poor general condition. Pathological examination revealed a chronic bacterial ulcerative to necrotizing dermatitis and osteomyelitis at the lower jaw with subsequent pyogranulomatous pneumonia and diffuse hydropic degeneration of the liver. Additionally, in the kidney a papillary renal adenoma was found. Immunohistochemistry revealed an expression of cytokeratins 8 and/or 19 indicating an origin from the renal tubular epithelium.

动物园饲养的一只13岁雌性小熊猫(Ailurus fulgens fulgens)因身体状况不佳而被安乐死。病理检查显示慢性细菌性溃疡到坏死性皮炎和下颚骨髓炎,随后脓肉芽肿性肺炎和肝脏弥漫性水肿变性。另外,在肾脏中发现一乳头状肾腺瘤。免疫组化显示细胞角蛋白8和/或19的表达,表明其起源于肾小管上皮。
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引用次数: 0
Clostridium perfringens toxin types from freshwater fishes in one water reservoir of Shandong Province of China, determined by PCR. 山东省某水库淡水鱼产气荚膜梭菌毒素类型的PCR测定。
Y Cai, J Gao, X Wang, T Chai, X Zhang, H Duan, S Jiang, B A Zucker, G Schlenker

Four hundred and twenty intestinal content samples (not including intestinal tissues) of freshwater fishes (60 silver carps, 100 carps, 100 crucian carps, 60 catfishes and 100 zaieuws) caught from one water reservoir were examined bacteriologically for the occurrence of C. perfringens. Isolates were examined by polymerase chain reaction (PCR) for genes encoding the four lethal toxins (alpha, beta, epsilon and iota) for classification into toxin types and for genes encoding enterotoxin and the novel beta2 toxin for further subclassification. C. perfringens could be isolated in 75 intestinal contents samples (17.9%) from freshwater fish including: 13 silver carps, 2 carps, 12 crucian carps, 40 zaieuws, and 8 catfishes. In 75 isolates, 58 strains (77.3%) were C. perfringens toxin type C (alpha and beta toxin positive), 13 strains (17.3%) were toxin type A (alpha toxin positive) and 4 strains (5.3%) were toxin type B (alpha, beta and epsilon toxin positive). In addition, the gene encoding for beta2 toxin was found in 47 strains (62.7%) of all the isolates, seven from type A, two from type B, and 38 from type C. The gene encoding for enterotoxin was not found in any isolate. These amplified toxin gene fragment were cloned and sequenced and compared with reference strains, the identity varied from 98.15% to 99.29%. This is the first report of C. perfringens alpha, beta, epsilon, beta2 toxins in freshwater fish and of beta, epsilon toxins in fish in general, and is the first discovery that the beta2 toxin could be detected in strains of type B. The origin of this bacterium and its importance to human food poisoning in freshwater fish is discussed.

对某水库捕获的淡水鱼(鲢鱼60条、鲫鱼100条、鲫鱼100条、鲶鱼60条、鲤鱼100条)共420份肠道内容物(不含肠道组织)进行了产气荚膜荚膜杆菌的细菌学检测。采用聚合酶链反应(PCR)对分离物进行编码4种致死毒素(α、β、epsilon和iota)的基因分类,并对编码肠毒素和新型β 2毒素的基因进行进一步的亚分类。在淡水鱼肠道内容物中检出产气荚膜荚膜菌75份(17.9%),其中银鲤13条、鲫鱼2条、鲫鱼12条、鲤鱼40条、鲶鱼8条。75株分离株中,产气荚膜菌毒素C型58株(77.3%)、A型13株(17.3%)、B型4株(5.3%)(α、β、epsilon毒素阳性)。其中,A型菌株7株、B型菌株2株、c型菌株38株(占62.7%)检出β 2毒素编码基因,未检出肠毒素编码基因。对扩增的毒素基因片段进行克隆和测序,与对照菌株的同源性在98.15% ~ 99.29%之间。本文首次报道了淡水鱼中产气荚膜芽孢杆菌α, β, epsilon, β 2毒素和一般鱼类中β, epsilon毒素,并首次发现β 2毒素可在b型菌株中检测到。本文讨论了该细菌的来源及其在淡水鱼中人类食物中毒中的重要性。
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引用次数: 0
[Problems with oral administration of antimicrobially effective substances in animals--the situation with poultry]. [动物口服抗菌有效物质的问题——家禽的情况]。
U Löhren

The most prevalent method of application of drugs under veterinary prescription including antimicrobials is the oral administration. This paper describes the three possible and legal ways of applying veterinary drugs to animals: --as feed medication in a specialized feed mill which must be registered according to Section 13 of our national medicinal act; --as powder for oral application and medication with the feed on the premises of the farm; --dissolved in the drinking water for the relevant flock. Drinking water application is by far the most relevant method of applying antimicrobials to poultry flocks, if medication is needed. The most prevalent systems for drinking water application in poultry flocks are technically described: header tanks or dose pumps. As far as dose pumps are concerned both systems: proportional dose pumps as well as electronic dose pumps are in use. With poultry the use of antimicrobials is based on clinical judgement of the flock, laboratory diagnosis, including bacterial isolation and sensitivity testing (wherever possible), medical knowledge and experience of the involved veterinarian, economic considerations, epidemiological background and information at the flock level. Responsible use of antimicrobials is a major topic which discriminates German poultry meat producers (e.g. Wiesenhof) from third world meat producers. One reason for the uncritical use of Antimicrobials can be the so called "vet hopping" which is practised with some other meat delivering animals. This is ruled out by the guidelines of the major German Poultry Meat producers. These companies organise regular meetings with their caretaking vets to find out if there is still use of antimicrobials with some of their contractors as alternative to good Hygiene and Biosecurity. Some Poultry Integrations have additional restrictions on the use of some critical antimicrobials like Fluorquinolones and Tetracyclines.

兽医处方下最普遍的药物应用方法包括抗菌剂是口服给药。本文介绍了兽药在动物身上应用的三种可能和合法的方式:一是在专门的饲料厂作为饲料用药,必须根据我国国家医药法第13条进行注册;——作为口服药的粉剂和在猪场的饲料中使用的药物;——溶解在相关畜群的饮用水中。如果需要药物治疗,到目前为止,饮用水应用是对家禽群施用抗菌剂的最相关方法。在技术上描述了家禽群中最普遍的饮用水应用系统:集水罐或剂量泵。就剂量泵而言,两种系统:比例剂量泵和电子剂量泵都在使用。对于家禽,使用抗菌剂是基于对禽群的临床判断、实验室诊断,包括细菌分离和敏感性测试(尽可能)、相关兽医的医学知识和经验、经济考虑、流行病学背景和禽群一级的信息。负责任地使用抗菌剂是区分德国禽肉生产商(如Wiesenhof)与第三世界肉类生产商的一个主要话题。不加批判地使用抗菌素的一个原因可能是所谓的“兽医跳跃”,这是对其他一些肉类输送动物的做法。德国主要禽肉生产商的指导方针排除了这种情况。这些公司与负责护理的兽医定期召开会议,以查明是否仍在与一些承包商一起使用抗菌药物,以替代良好的卫生和生物安全。一些家禽整合对氟喹诺酮类药物和四环素类药物等一些关键抗菌素的使用有额外限制。
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引用次数: 0
[Veterinary drug legal situation for oral medication in animal facilities in Germany]. 【德国动物机构口服兽药的法律情况】。
U Buettner-Peter

Oral medication of animal stocks can be administered via oral ready-to-use veterinary medicinal products or by using medicated feedingstuffs. The regulations contained in the German Drug Act (Arzneimittelgesetz - AMG) and the ordinances derived from the AMG are applicable to both types of medicinal product. The legal requirements relating to the manufacture, authorisation, marketing, dispensing and proper use of these medicinal products in respect of oral medication are dealt with in detail. Pursuant to Section 13 AMG, companies that manufacture medicated feedingstuffs require a manufacturing licence. To take into account the special features of these medicinal products, specific stipulations have been laid down regarding the manufacture and dispensing of medicated feedingstuffs by these companies. The use of medicated feedingstuffs is for various reasons in steep decline, while oral ready-to-use medicinal products are, according to reports on practice in the relevant sector, increasingly being used to treat animal stocks as well. When dispensing veterinary medicinal products, the veterinarian must comply with the state of the art and make sure that the animal keeper is able to use the drugs properly. In order to react to doubts regarding compliance with these legal requirements, recommendations for use of oral medication should be developed which provide veterinarians with an aid to assist them in deciding which type of drugs are most suited for the respective case, and what is to be complied with in their use. The recommendations for use are intended to facilitate the correct application of oral medication in respect of both types of veterinary medicinal product.

牲畜的口服药物可以通过口服即食兽药产品或使用药物饲料进行管理。《德国药品法》(Arzneimittelgesetz - AMG)所载的条例和源自该法的条例适用于这两种类型的药品。与这些药品的生产、批准、销售、配药和正确使用有关的法律要求在口服药物方面进行了详细的处理。根据AMG第13条,生产药用饲料的公司需要生产许可证。考虑到这些药品的特点,对这些公司生产和分配药用饲料制定了具体规定。由于各种原因,药用饲料的使用正在急剧下降,而根据有关部门的实践报告,口服即食药品也越来越多地用于治疗牲畜。在配发兽药时,兽医必须符合最新技术,并确保动物饲养员能够正确使用药物。为了对是否遵守这些法律要求的疑问作出反应,应制定使用口服药物的建议,为兽医提供帮助,帮助他们决定哪种药物最适合各自的情况,以及在使用时应遵守哪些规定。使用建议旨在促进两种兽药产品口服药物的正确应用。
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引用次数: 0
[The problem of oral administration of antimicrobially effective substances. Experiences from Switzerland]. 口服抗菌有效物质的问题。来自瑞士的经验]。
X Sidler

The oral medication of sick animals is very common and a very preserve therapy. This method of therapy demands a high level of know-how for the veterinarians and also for meet-producers relating to food safety and bacterial resistance. In the new ordinance on veterinary medicine in 2004 many aspects of production and application of medicated feed are regulated in the legislation. This ordinance pretends to control all technical equipments used for production, transport and application of medicated feed by a qualified person (QP) on farms. Important criteria are defined in the ordinance on veterinary medicines.

患病动物的口服药物治疗非常普遍,也是一种非常有效的治疗方法。这种治疗方法要求兽医和奶制品生产商在食品安全和细菌耐药性方面具有高水平的专业知识。在2004年的新兽药条例中,对含药饲料的生产和应用的许多方面进行了立法规定。本条例假装控制由合格人员(QP)在农场生产、运输和施用含药饲料的所有技术设备。《兽药条例》界定了重要的准则。
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引用次数: 0
[Bluetongue virus serotype 8 (BTV-8)-associated brain malformations in two calves]. [蓝舌病毒血清型8 (BTV-8)相关的两只小牛脑畸形]。
M Peters, S Mösenfechtel, B Jacobsen, A Beineke, P Wohlsein

Congenital brain malformations such as hydranencephaly as well as internal and external hydrocephalus combined with porencephaly were diagnosed in two calves which were born in spring 2008. In both calves bluetongue virus was detected by real-time PCR. Teratogenic pestiviruses were not found by serological, molecular or immunohistological methods. A causal relationship between the malformations and the bluetongue serotype 8 epidemic in 2007 has to be considered.

在2008年春季出生的两只小牛中诊断出先天性脑畸形,如无脑畸形以及内外部脑积水合并颅孔畸形。实时荧光定量PCR检测两只小牛蓝舌病毒。血清学、分子学和免疫组织学均未发现致畸鼠疫病毒。必须考虑畸形与2007年蓝舌病血清8型流行之间的因果关系。
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引用次数: 0
[Genetics of recurrent airway obstruction (RAO)]. [复发性气道阻塞(RAO)的遗传学]。
V Gerber, J E Swinburne, S C Blott, P Nussbaumer, A Ramseyer, J Klukowska-Rötzler, G Dolf, E Marti, D Burger, T Leeb

Recurrent airway obstruction (RAO) is a multifactorial and polygenic disease. Affected horses are typically 7 years of age or older and show exercise intolerance, increased breathing effort, coughing, airway neutrophilia, mucus accumulation and hyperreactivity as well as cholinergic bronchospasm. The environmental factors responsible are predominantly allergens and irritants in haydust, but the immunological mechanisms underlying RAO are still unclear. Several studies have demonstrated a familiar predisposition for RAO and it is now proven that the disease has a genetic basis. In offspring, the risk of developing RAO is 3-fold increased when one parent is affected and increases to almost 5-fold when both parents have RAO. Segregation analysis in two high-prevalence families demonstrated a high heritability and a complex inheritance with several major genes. A whole genomescan showed chromosome-wide significant linkage of seven chromosomal regions with RAO. Of the microsatellites, which were located near atopy candidate genes, those in a region of chromosome 13 harboring the IL4R gene were strongly associated with the RAO phenotype in the offspring of one RAO-affected stallion. Furthermore, IgE-levels are influenced by hereditary factors in the horse, and we have evidence that RAO-affected offspring of the same stallion have increased levels of specific IgE against moldspore allergens. The identification of genetic markers and ultimately of the responsible genes will not only allow for an improved prophylaxis, i.e. early identification of susceptible individuals and avoidance of high-risk matings, but also improve our ability to find new therapeutic targets and to optimize existing treatments.

复发性气道阻塞(RAO)是一种多因素、多基因的疾病。受影响的马通常为7岁或以上,表现为运动不耐受,呼吸困难,咳嗽,气道中性粒细胞增多,粘液积聚和高反应性以及胆碱能支气管痉挛。环境因素主要是干草粉尘中的过敏原和刺激物,但RAO的免疫学机制尚不清楚。一些研究已经证明了RAO的易感性,现在已经证明该疾病具有遗传基础。在后代中,当父母一方受到影响时,患RAO的风险增加3倍,当父母双方都患有RAO时,患RAO的风险增加近5倍。对两个高流行家族的分离分析表明,遗传力高,具有多主基因的复杂遗传。整个基因组可以显示出7个染色体区域与RAO的全染色体显著连锁。在位于特应性候选基因附近的微卫星中,位于13号染色体含有IL4R基因区域的微卫星与一只受RAO影响的种马后代的RAO表型密切相关。此外,马的IgE水平受遗传因素的影响,我们有证据表明,同一种马的rao影响的后代对霉菌过敏原的特异性IgE水平增加。遗传标记的鉴定和最终的责任基因不仅可以改善预防,即早期识别易感个体和避免高风险交配,而且还可以提高我们寻找新的治疗靶点和优化现有治疗方法的能力。
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引用次数: 0
[Functional genome analysis investigating resistance to respiratory tract disease in a porcine Actinobacillus pleuropneumoniae infection model]. [研究猪胸膜肺炎放线杆菌感染模型呼吸道疾病耐药性的功能基因组分析]。
T Rehm, L Benga, E Danilowicz, M Drungowski, D Hoeltig, D Kahlisch, W Oehlmann, I Probst, G F Gerlach

Here we present the work of the multidisciplinary consortium IRAS (Development of Genetic Markers for Immune Defence and Resistance in the Porcine Respiratory Tract) which includes different commercial and research institutions and was formed as a response to the call "Functional Genome Analysis in the Animal Organism (FUGATO)" by the German Ministry of Education and Research. IRAS started work in the fall of 2005 and--using the experimental infection of pigs with Actinobacillus pleuropneumoniae as model pathogen--aims at i) characterizing the course of infection by clinical as well as advanced laboratory tools (phenotypic-genetic approach) and ii) defining the diversity and distribution of allels known to be associated with immune defence in mouse and man (homolog-genetic approach). The intention is to identify genetic markers for increased resistance to infection thereby providing additional tools for the estimation of breeding values to the pig industry.

在这里,我们介绍了多学科联盟IRAS(猪呼吸道免疫防御和抗性遗传标记开发)的工作,该联盟包括不同的商业和研究机构,是为了响应德国教育和研究部的“动物有机体功能基因组分析(FUGATO)”的号召而成立的。IRAS于2005年秋季开始工作,利用猪胸膜肺炎放线杆菌的实验感染作为模型病原体,旨在i)通过临床和先进的实验室工具(表型遗传方法)描述感染过程,ii)确定已知与小鼠和人类免疫防御相关的等位基因的多样性和分布(同源遗传方法)。目的是确定增加感染抗性的遗传标记,从而为估计养猪业的育种价值提供额外的工具。
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引用次数: 0
[Genetics of recurrent airway obstruction (RAO)]. [复发性气道阻塞(RAO)的遗传学]。
Pub Date : 2008-07-01 DOI: 10.2376/0341-6593-115-271
V. Gerber, J. Swinburne, S. Blott, P. Nussbaumer, A. Ramseyer, J. Klukowska-Rötzler, G. Dolf, E. Marti, D. Burger, T. Leeb
Recurrent airway obstruction (RAO) is a multifactorial and polygenic disease. Affected horses are typically 7 years of age or older and show exercise intolerance, increased breathing effort, coughing, airway neutrophilia, mucus accumulation and hyperreactivity as well as cholinergic bronchospasm. The environmental factors responsible are predominantly allergens and irritants in haydust, but the immunological mechanisms underlying RAO are still unclear. Several studies have demonstrated a familiar predisposition for RAO and it is now proven that the disease has a genetic basis. In offspring, the risk of developing RAO is 3-fold increased when one parent is affected and increases to almost 5-fold when both parents have RAO. Segregation analysis in two high-prevalence families demonstrated a high heritability and a complex inheritance with several major genes. A whole genomescan showed chromosome-wide significant linkage of seven chromosomal regions with RAO. Of the microsatellites, which were located near atopy candidate genes, those in a region of chromosome 13 harboring the IL4R gene were strongly associated with the RAO phenotype in the offspring of one RAO-affected stallion. Furthermore, IgE-levels are influenced by hereditary factors in the horse, and we have evidence that RAO-affected offspring of the same stallion have increased levels of specific IgE against moldspore allergens. The identification of genetic markers and ultimately of the responsible genes will not only allow for an improved prophylaxis, i.e. early identification of susceptible individuals and avoidance of high-risk matings, but also improve our ability to find new therapeutic targets and to optimize existing treatments.
复发性气道阻塞(RAO)是一种多因素、多基因的疾病。受影响的马通常为7岁或以上,表现为运动不耐受,呼吸困难,咳嗽,气道中性粒细胞增多,粘液积聚和高反应性以及胆碱能支气管痉挛。环境因素主要是干草粉尘中的过敏原和刺激物,但RAO的免疫学机制尚不清楚。一些研究已经证明了RAO的易感性,现在已经证明该疾病具有遗传基础。在后代中,当父母一方受到影响时,患RAO的风险增加3倍,当父母双方都患有RAO时,患RAO的风险增加近5倍。对两个高流行家族的分离分析表明,遗传力高,具有多主基因的复杂遗传。整个基因组可以显示出7个染色体区域与RAO的全染色体显著连锁。在位于特应性候选基因附近的微卫星中,位于13号染色体含有IL4R基因区域的微卫星与一只受RAO影响的种马后代的RAO表型密切相关。此外,马的IgE水平受遗传因素的影响,我们有证据表明,同一种马的rao影响的后代对霉菌过敏原的特异性IgE水平增加。遗传标记的鉴定和最终的责任基因不仅可以改善预防,即早期识别易感个体和避免高风险交配,而且还可以提高我们寻找新的治疗靶点和优化现有治疗方法的能力。
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引用次数: 14
Association studies of lung function in mice. 小鼠肺功能的关联研究。
K Ganguly, H Schulz

Chronic obstructive pulmonary disease (COPD) is the fourth leading cause of death worldwide and an accelerating decline of lung function is the earliest and a major indicator of the onset of COPD. Therefore it has become necessary to understand the genetic basis of this complex physiological trait in order to determine the potential susceptibility factors of this disease. REINHARD et al (2005) performed the genome wide linkage analysis study with inbred mice having extremely divergent lung function (C3H/HeJ versus JF1/Msf) and identified multiple Quantitative Trait Loci (QTLs) on mouse chromosomes (mCh) 5, 15, 17, and 19 with Logarithm of odd (LOD) scores > or = 4. Significant linkages to total lung capacity (TLC) were detected on mCh 15 and 17, to dead space volume (VD) and lung compliance (C(L)) on mCh 5 and 15, to C(L) on mCh 19, and to diffusing capacity for CO (D(co)) on mCh 15 and 17. Several of the mouse chromosomal regions identified were syntenic to human chromosomal regions identified with linkage to FEV1 (forced expiratory volume-1 second), FVC (forced vital capacity), or FEV1/FVC in separate studies. Using a systematic approach of expression QTL (e-QTL) strategy and exon-wise sequencing of suggested candidate genes followed by predicted protein structure and property, GANGULY et al (2007) recently proposed four candidate genes for lung function in mice. They are superoxide dismutase 3, extracellular [SOD3; mCh 5: V(D)], trefoil factor 2 (TFF2; mCh 17: TLC and D(co)), ectonucleotide pyrophosphatase/phosphodiesterase 2 (ENPP2; mCh 15:TLC and C(L)), and relaxin 1 (RLN1; mCh 19; CL and CL/TLC). As a part of functional validation, gene-targeted Sod3-/- mice were detected with increased conducting airway volume (V(D)/TLC) compared with strain-matched control Sod3+/+ mice, consistent with the QTL on mCh 5. Findings with gene-targeted mice suggested that SOD3 is a contributing factor defining the complex trait of conducting airway volume. The human variation in these genes needs further study both in lung development and in the development of lung disease as a part of translational approach.

慢性阻塞性肺疾病(COPD)是全球第四大死亡原因,肺功能的加速下降是COPD发病的最早和主要指标。因此,有必要了解这一复杂生理性状的遗传基础,以确定该病的潜在易感因素。REINHARD等(2005)对肺功能差异极大的近交系小鼠(C3H/HeJ与JF1/Msf)进行了全基因组连锁分析研究,并在小鼠染色体(mCh) 5、15、17和19上发现了多个奇数对数(LOD)分数>或= 4的数量性状位点(qtl)。在mCh 15和17上检测到与总肺活量(TLC), mCh 5和15上的死腔体积(VD)和肺适应性(C(L)), mCh 19上的C(L)以及mCh 15和17上的CO弥散量(D(CO))有显著联系。在不同的研究中,鉴定出的几个小鼠染色体区域与鉴定出与FEV1(用力呼气量-1秒)、FVC(用力肺活量)或FEV1/FVC相关的人类染色体区域是一致的。GANGULY等人(2007)最近利用表达QTL (e-QTL)策略的系统方法,对建议的候选基因进行外显子测序,然后预测蛋白质结构和性质,提出了小鼠肺功能的四个候选基因。它们是超氧化物歧化酶3,细胞外[SOD3];mCh 5: V(D)],三叶因子2 (TFF2);mh17: TLC和D(co),外核苷酸焦磷酸酶/磷酸二酯酶2 (ENPP2);mCh 15:TLC和C(L)),松弛素1 (RLN1;妇幼保健19;CL和CL/TLC)。作为功能验证的一部分,与菌株匹配的对照Sod3+/+小鼠相比,检测到基因靶向Sod3-/-小鼠的导气管体积(V(D)/TLC)增加,与mCh 5上的QTL一致。基因靶向小鼠的研究结果表明,SOD3是决定气道容积复杂特征的一个重要因素。作为翻译方法的一部分,这些基因的人类变异需要在肺部发育和肺部疾病的发展中进一步研究。
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引用次数: 0
期刊
Dtw. Deutsche Tierärztliche Wochenschrift
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