美国南卡罗莱纳牡蛎中奈氏单孢子虫的发生。

W. Dougherty, T. Cheng, V. Burrell
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It, along with Perkinsus marinus, another protistan parasite, are undoubtedly the major causes of the decline of the oyster industry in both the Delaware and Chesapeake Bays. Although H. nelsoni has been known by a few investigators to parasitize C. virginica in South Carolina, its occurrence in this state has never been recorded (Burrell, 1986). MATERIALS AND METHODS During November and December 1991 and January 1992, we examined 35 young oysters, 5-6 cm long, collected intertidally in Charleston Harbor (salinity 15-17%oo at Fort Johnson. The soft tissues of these bivalves appeared watery, with recessed mantles, and in each one of the six clusters studied, at least one or two were dead. These were native, wild oysters, the ancestors of which had inhabited Charleston Harbor for at least 100 years. No drought had occurred for at least three years prior to the time of collection. Moreover, no mass mortalities of oysters had been reported at the time. 1 This research was supported by a grant (NA16FL0408-01) from the National Marine Fisheries Service, U.S. Department of Commerce. TRANS. AM. MICROSC. Soc., 112(1): 75-77. 1993. ? Copyright, 1993, by the American Microscopical Society, Inc. This content downloaded from 157.55.39.224 on Wed, 14 Dec 2016 05:02:50 UTC All use subject to http://about.jstor.org/terms TRANS. AM. MICROSC. SOC. All of the living oysters were removed from their shells and processed for histopathologic examination. All were fixed in 10% seawater formalin, embedded in paraffin, sectioned at 7 ,im, and stained with hematoxylin and eosin for light microscopy. RESULTS AND DISCUSSION Intercellular plasmodia of Haplosporidium nelsoni were found in each oyster. All of the observed plasmodia were in relatively early stages of karyokinesis in that none was observed to include more than 10 nuclei. A few dividing nuclei, with conspicuous spindle fibers, also were observed (Farley, 1967). The plasmodia observed measured 6-10 ,um in greatest diameter. Although the majority of the plasmodia occurred between Leydig cells (i.e., vesicular connective tissue cells) situated between acini of the digestive diverticula and in the matrices of gill filaments, some also were found in various hemolymph sinuses and vessels as well as suprabranchial chambers, thus indicating systematic infections (Kanaley & Ford, 1990). In addition to plasmodia, spores, each measuring 6-8 Aim in length, were observed. These were located between Leydig cells in the hosts' digestive diverticula. H. nelsoni spores are seen rarely and to date have been reported only by Couch et al. (1966) and Barrow & Taylor (1966). The fact that we observed spores in the oysters examined during November through January in South Carolina is of interest because in the Chesapeake and Delaware Bays, sporulation of H. nelsoni usually occurs in June and July (Couch et al., 1966). Our finding of spores during the stated collection period may reflect the warmer temperatures that prevail during autumn and winter in South Carolina coastal waters. Haplosporidium nelsoni has been reported along the Atlantic coast of the United States from Massachusetts, Connecticut, New York, New Jersey, Delaware, Maryland, Virginia, North Carolina, and the Atlantic Coast of Florida (Haskin & Andrews, 1988). Recently, H. nelsoni was reported in C. virginica from coastal Georgia (Lewis et al., 1992). 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SOC. All of the living oysters were removed from their shells and processed for histopathologic examination. All were fixed in 10% seawater formalin, embedded in paraffin, sectioned at 7 ,im, and stained with hematoxylin and eosin for light microscopy. RESULTS AND DISCUSSION Intercellular plasmodia of Haplosporidium nelsoni were found in each oyster. All of the observed plasmodia were in relatively early stages of karyokinesis in that none was observed to include more than 10 nuclei. A few dividing nuclei, with conspicuous spindle fibers, also were observed (Farley, 1967). The plasmodia observed measured 6-10 ,um in greatest diameter. 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引用次数: 5

摘要

在美国南卡罗莱纳的美洲牡蛎中首次发现了致病性单孢子虫(Haplosporidium nelsoni),最初在1957年被认为是导致特拉华湾美洲牡蛎(Crassostrea virginica)大量死亡的病原体,由于其与其他生物的系统关系尚不清楚,因此将其命名为MSX(多核球体X)。随后,Haskin et al.(1966)将其命名为Minchinia nelsoni。再后来,Sprague(1979)将该种转移到单孢子虫属(Balanosporida: Haplosporidiidae)。nelsoni对C. virginica的破坏性影响是众所周知的(见Lauckner, 1983;Sindermann, 1990;火花,1985)。毫无疑问,它和另一种原生寄生虫——海生螺(Perkinsus marinus)是导致特拉华湾和切萨皮克湾牡蛎产业衰退的主要原因。虽然一些研究人员已经知道H. nelsoni寄生在南卡罗来纳州的C. virginica上,但该州从未记录过它的发生(Burrell, 1986)。材料与方法1991年11、12月和1992年1月,我们在查尔斯顿港潮间带采集了35只幼牡蛎,体长5 ~ 6cm(盐度15 ~ 17%)。这些双壳类动物的软组织是水汪汪的,有凹陷的外壳,在我们所研究的六群双壳类动物中,每一群至少有一两个是死的。这些是当地的野生牡蛎,它们的祖先在查尔斯顿港生活了至少100年。在采集时间之前至少三年没有发生过干旱。此外,当时并无蚝大量死亡的报告。本研究由美国商务部国家海洋渔业局拨款(NA16FL0408-01)支持。反式。点。MICROSC。Soc。生物医学工程学报,12(1):75-77。1993. ? 版权所有,1993年,美国显微学会,Inc。此内容于2016年12月14日星期三05:02:50 UTC下载于157.55.39.224所有内容以http://about.jstor.org/terms TRANS为准。点。MICROSC。SOC。所有活牡蛎都从壳中取出,进行组织病理学检查。所有细胞均固定在10%海水福尔马林中,石蜡包埋,在7,im处切片,苏木精和伊红染色,光镜下观察。结果与讨论在每只牡蛎中均发现奈氏单孢子虫胞间疟原虫。所有观察到的疟原虫都处于核分裂的相对早期阶段,没有观察到超过10个细胞核。也观察到一些分裂的核,有明显的纺锤状纤维(Farley, 1967)。所观察到的疟原虫最大直径为6-10微米。虽然大多数疟原虫发生在消化憩室腺泡之间的间质细胞(即水疱结缔组织细胞)和鳃丝基质之间,但也有一些在各种血淋巴窦和血管以及鳃上腔中发现,从而表明系统性感染(Kanaley & Ford, 1990)。除疟原虫外,还观察到孢子,每个孢子长6-8 Aim。它们位于宿主消化憩室的间质细胞之间。nelsoni孢子很少见到,迄今为止只有Couch等人(1966)和Barrow & Taylor(1966)报道过。我们在11月至1月期间在南卡罗来纳州的牡蛎中观察到孢子,这一事实令人感兴趣,因为在切萨皮克湾和特拉华湾,H. nelsoni的孢子通常发生在6月和7月(Couch et al., 1966)。我们在规定的收集期间发现的孢子可能反映了南卡罗来纳沿海水域秋冬季节普遍存在的较温暖的温度。据报道,在美国的大西洋沿岸,从马萨诸塞州、康涅狄格州、纽约州、新泽西州、特拉华州、马里兰州、弗吉尼亚州、北卡罗来纳州和佛罗里达州的大西洋沿岸都有nelsoni单孢子虫(Haskin & Andrews, 1988)。最近,在乔治亚州沿海的C. virginica中发现了H. nelsoni (Lewis et al., 1992)。我们的观察记录了南卡罗莱纳尼氏蜱出现的第一个记录。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Occurrence of the pathogen Haplosporidium nelsoni in oysters, Crassostrea virginica, in South Carolina, USA.
The presence of the pathogenic protozoan Haplosporidium nelsoni is documented for the first time in the American oyster, Crassostrea virginica, from South Carolina, U.S.A. Initially incriminated in 1957 as the causative agent of mass mortalities in the American oyster, Crassostrea virginica, in Delaware Bay, Haplosporidium nelsoni was given the acronym MSX (multinucleated sphere X) because its systematic relationship to other organisms was unknown. Subsequently, it was designated as Minchinia nelsoni by Haskin et al. (1966). Still later, Sprague (1979) transferred the species to the genus Haplosporidium (Balanosporida: Haplosporidiidae). The devastating effects of H. nelsoni on C. virginica are well known (see reviews by Lauckner, 1983; Sindermann, 1990; Sparks, 1985). It, along with Perkinsus marinus, another protistan parasite, are undoubtedly the major causes of the decline of the oyster industry in both the Delaware and Chesapeake Bays. Although H. nelsoni has been known by a few investigators to parasitize C. virginica in South Carolina, its occurrence in this state has never been recorded (Burrell, 1986). MATERIALS AND METHODS During November and December 1991 and January 1992, we examined 35 young oysters, 5-6 cm long, collected intertidally in Charleston Harbor (salinity 15-17%oo at Fort Johnson. The soft tissues of these bivalves appeared watery, with recessed mantles, and in each one of the six clusters studied, at least one or two were dead. These were native, wild oysters, the ancestors of which had inhabited Charleston Harbor for at least 100 years. No drought had occurred for at least three years prior to the time of collection. Moreover, no mass mortalities of oysters had been reported at the time. 1 This research was supported by a grant (NA16FL0408-01) from the National Marine Fisheries Service, U.S. Department of Commerce. TRANS. AM. MICROSC. Soc., 112(1): 75-77. 1993. ? Copyright, 1993, by the American Microscopical Society, Inc. This content downloaded from 157.55.39.224 on Wed, 14 Dec 2016 05:02:50 UTC All use subject to http://about.jstor.org/terms TRANS. AM. MICROSC. SOC. All of the living oysters were removed from their shells and processed for histopathologic examination. All were fixed in 10% seawater formalin, embedded in paraffin, sectioned at 7 ,im, and stained with hematoxylin and eosin for light microscopy. RESULTS AND DISCUSSION Intercellular plasmodia of Haplosporidium nelsoni were found in each oyster. All of the observed plasmodia were in relatively early stages of karyokinesis in that none was observed to include more than 10 nuclei. A few dividing nuclei, with conspicuous spindle fibers, also were observed (Farley, 1967). The plasmodia observed measured 6-10 ,um in greatest diameter. Although the majority of the plasmodia occurred between Leydig cells (i.e., vesicular connective tissue cells) situated between acini of the digestive diverticula and in the matrices of gill filaments, some also were found in various hemolymph sinuses and vessels as well as suprabranchial chambers, thus indicating systematic infections (Kanaley & Ford, 1990). In addition to plasmodia, spores, each measuring 6-8 Aim in length, were observed. These were located between Leydig cells in the hosts' digestive diverticula. H. nelsoni spores are seen rarely and to date have been reported only by Couch et al. (1966) and Barrow & Taylor (1966). The fact that we observed spores in the oysters examined during November through January in South Carolina is of interest because in the Chesapeake and Delaware Bays, sporulation of H. nelsoni usually occurs in June and July (Couch et al., 1966). Our finding of spores during the stated collection period may reflect the warmer temperatures that prevail during autumn and winter in South Carolina coastal waters. Haplosporidium nelsoni has been reported along the Atlantic coast of the United States from Massachusetts, Connecticut, New York, New Jersey, Delaware, Maryland, Virginia, North Carolina, and the Atlantic Coast of Florida (Haskin & Andrews, 1988). Recently, H. nelsoni was reported in C. virginica from coastal Georgia (Lewis et al., 1992). Our observations document the first record of the occurrence of H. nelsoni in South Carolina.
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