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海水贝类养殖作为各国水产养殖业中的重要组成部分,经常遭受严重的病害影响。贝类弧菌病作为影响最严重的细菌性疾病,制约着贝类养殖业的发展。本文综述了国内外海水养殖贝类弧菌病病原种类及其流行暴发,分析了副溶血弧菌(Vibrio parahaemolyticus)、溶藻弧菌(Vibrio alginolyticus)和创伤弧菌(Vibrio vulnificus)等主要病原弧菌的耐药性状况,并着重介绍了与弧菌病发生相关的关键环境因子及其影响,同时对贝类弧菌病的研究方向进行探讨和展望,以期为今后贝类养殖业的发展提供参考。 相似文献
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类立克次体的感染可以引起海洋贝类病害的发生,并且有时会导致贝类的大规模死亡,成为在世界范围内影响海洋贝类养殖业发展的重要制约因素.本文首先从海洋贝类类立克次体的分类地位、宿主种类及地理分布、海洋贝类类立克次体及其包涵体的生物学特征、致病性、传播途径、检测与防治方法等方面进行了系统的阐述.文章提出对海洋贝类类立克次体进行研究的必要性,分析了研究的重点及难点,展望了此研究领域的发展趋势. 相似文献
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为了掌握广东大鹏澳海域产麻痹性贝毒(paralytic shellfish poisoning,PSP)藻类的分布状况和贝类染毒情况,于2013年8月至2014年10月在广东大鹏澳海域的牡蛎养殖区、牡蛎养殖外区及湾口海域逐月采集水样以及牡蛎样品进行分析。调查结果显示,大鹏澳海域的牡蛎养殖外区和湾口存在塔玛亚历山大藻(Alexandrium tamarensis),链状亚历山大藻(A. catenella)和链状裸甲藻(Gymnodinium catenatum)三种PSP产毒藻,但密度较低,时间分布不连续,牡蛎养殖区未发现产PSP毒素藻类。在季节分布上,产毒藻呈现冬季检出率低,春秋季高的特点。在大鹏澳牡蛎样品中共检测出8种PSP成分,分别是GTX1、GTX4、GTX5、dcGTX2、dcGTX3、NEO、C1和C2,贝类中PSP的检出率冬季最高,达66.7%,秋季、夏季次之,春季最低。PSP产毒藻和贝类染毒在时间上不完全同步,贝类染毒率最高的时间晚于PSP产毒藻最高密度出现时间。 相似文献
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南海海域重要养殖水域牡蛎体中的腹泻性贝类毒素 总被引:1,自引:0,他引:1
对2006年和2007年南海海域23个重要养殖水域牡蛎体中腹泻性贝类毒素(DSP)进行了调查,结果表明:甲子港、唐家湾、镇海湾、安埔港、防城港、八所港和榆林港等7个水域牡蛎体DSP毒性呈阳性结果,占调查水域的30.4%,其DSP值均为0.05MU/g.2006年牡蛎体DSP检出率为8.7%(n=23),2007年为21.7%(n=23).调查期间,牡蛎体DSP检出值0.05MU/g已达到了FDA(美国食品药物管理局)、日本、加拿大、澳大利亚、新西兰、朝鲜等6个国家食用贝类标准警戒限量水平,和超出了我国<无公害食品水产品中有毒有害物质的限量>规定贝类DSP不得检出标准,表明了近期南海海域某些养殖水域的牡蛎已经受到了DSP毒化的威胁. 相似文献
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近年我国海域有害赤潮频发,赤潮优势种的变化显著,最近7a记录了51种引发赤潮的优势赤潮生物,其中由有毒微藻引发的赤潮增加。有毒微藻在我国海域广泛分布,至少3个株产麻痹性贝毒的亚历山大藻,5种能产生腹泻性贝毒软海绵酸毒素和鳍藻毒素、以及扇贝毒素的鳍藻在我国沿海都有分布;产生虾夷扇贝毒素的三种甲藻在北黄海常年存在。我国多种贝类中已发现麻痹性贝毒、软海绵酸毒素和鳍藻毒素、扇贝毒素、虾夷扇贝毒素和环亚胺毒素等多种微藻毒素。本文较系统的归纳综述了我国有害赤潮、优势种的变化趋势和分布特点,产生的藻毒素结构;我国双壳贝类等海洋生物中存在的微藻毒素的种类结构;首次利用风险商值法研究评估了我国贝类的健康风险。结果表明,只有春季来自福建的2个样品具有食用风险;但大连海区的贝类样品、评估值全都接近安全限值,可能表明具有某种区域性风险;在春末夏初,大窑湾的贻贝风险最大,其次是扇贝,牡蛎的风险最小;不同的贝器官,富集藻毒素的能力差别大,消化腺中的藻毒素含量远高于其它器官,不同的食用方式可能会导致不同的中毒风险。总体上,我国沿海常见种双壳贝类的麻痹性贝毒和虾夷扇贝毒素食用风险低。 相似文献
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Li-ping Ma Feng Zhao Lin Yao Xin-guang Li De-qing Zhou Rui-ling Zhang 《Food and environmental virology》2013,5(2):81-86
Noroviruses (NoVs) are commonly occurring pathogens that cause gastroenteritis. Outbreaks of viral diseases have often been ascribed to the consumption of contaminated shellfish. Our objective was to evaluate the presence and contamination levels of NoV in shellfish sold at seafood markets in China. We tested 840 shellfish samples (Crassostrea gigas, Mytilus edulis, Azumapecten farreri, SinoNoVacula constricta, Scapharca subcrenata, Ruditapes philippinarum) that were collected from seven cities around the Yellow and Bohai Seas in China between December 2009 and November 2011. We used real-time RT-PCR to detect NoV in purified concentrates from the stomach and digestive diverticula of these shellfish. NoV was detected in 19.35 % (N = 155), 16.67 % (N = 114), 5.70 % (N = 158), 8.82 % (N = 136), 13.74 % (N = 131), and 16.44 % (N = 146) of oyster, mussel, scallop, razor clam, ark shell, and clam samples, respectively. The average detection rate was 13.33 % (112/840). Nucleotide sequencing of the NoV RT-PCR products demonstrated that all strains belonged to NoV genotype GII.12, except two that belonged to GI.3. More than 102 copies of the NoV genome were detected in 69 of 112 positive shellfish samples. Our results suggest that ~13 % of shellfish harbor NoV, and GII.12 NoV is the primary strain in shellfish purchased at markets in seven coastal cities in China. 相似文献
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Noroviruses are the most common cause of acute gastroenteritis associated with bivalve shellfish consumption. This study aimed to detect and characterize noroviruses in three bivalve shellfish species: oysters (Saccostrea forskali), cockles (Anadara nodifera), and mussels (Perna viridis). The virus concentration procedure (adsorption-twice elution-extraction) and a molecular method were employed to identify noroviruses in shellfish. RT-nested PCR was able to detect known norovirus GII.4 of 8.8 × 10?2 genome copies/g of digestive tissues from oyster and cockle concentrates, whereas in mussel concentrates, the positive result was seen at 8.8 × 102 copies/g of digestive tissues. From August 2011 to July 2012, a total of 300 shellfish samples, including each of 100 samples from oysters, cockles, and mussels were collected and tested for noroviruses. Norovirus RNA was detected in 12.3 % of shellfish samples. Of the noroviruses, 7.7 % were of the genogroup (G) I, 2.6 % GII, and 2.0 % were mixed GI and GII. The detection rate of norovirus GI was 2.1 times higher than GII. With regards to the different shellfish species, 17 % of the oyster samples were positive, while 14.0 and 6.0 % were positive for noroviruses found in mussels and cockles, respectively. Norovirus contamination in the shellfish occurred throughout the year with the highest peak in September. Seventeen norovirus-positive PCR products were characterized upon a partial sequence analysis of the capsid gene. Based on phylogenetic analysis, five different genotypes of norovirus GI (GI.2, GI.3, GI.4, GI.5, and GI.9) and four different genotypes of GII (GII.1, GII.2, GII.3, and GII.4) were identified. These findings indicate the prevalence and distribution of noroviruses in three shellfish species. The high prevalence of noroviruses in oysters contributes to the optimization of monitoring plans to improve the preventive strategies of acute gastroenteritis. 相似文献
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Laila Benabbes Joanna Ollivier Julien Schaeffer Sylvain Parnaudeau Houria Rhaissi Jalal Nourlil Françoise S. Le Guyader 《Food and environmental virology》2013,5(1):35-40
The aim of this study was to evaluate the presence of human enteric viruses in shellfish collected along the Mediterranean Sea and Atlantic Coast of Morocco. A total of 77 samples were collected from areas potentially contaminated by human sewage. Noroviruses were detected in 30 % of samples, with an equal representation of GI and GII strains, but were much more frequently found in cockles or clams than in oysters. The method used, including extraction efficiency controls, allowed the quantification of virus concentration. As in previous reports, results showed levels of contamination between 100 and 1,000 copies/g of digestive tissues. Sapoviruses were detected in 13 % of samples mainly in oyster and clam samples. Hepatitis A virus was detected in two samples, with concentrations around 100 RNA copies/g of digestive tissues. Only two samples were contaminated with enterovirus and none with norovirus GIV or Aichi virus. This study highlights the interest of studying shellfish samples from different countries and different production areas. A better knowledge of shellfish contamination helps us to understand virus levels in shellfish and to improve shellfish safety, thus protecting consumers. 相似文献