Kiryu Yasunari, Blazer Vicki S, Vogelbein Wolfgang K, Kator Howard, Shields Jeffrey D
National Fish Health Research Laboratory, Biological Resources Division, U.S. Geological Survey, 11649 Leetown Road, Kearneysville, West Virginia 25430, USA.
Mycologia. 2005 May-Jun;97(3):569-75. doi: 10.3852/mycologia.97.3.569.
Oomycete infections caused by Aphanomyces invadans occur in freshwater and estuarine fishes around the world. Along the east coast of the USA, skin ulcers caused by A. invadans are prevalent in Atlantic menhaden, Brevoortia tyrannus. From laboratory observations low salinities appear crucial to transmission of the pathogen. To better understand aspects of transmission, we characterized sporulation and cyst formation of secondary zoospores of two isolates of A. invadans at different salinities and temperatures. Sporulation occurred only at low salinities. At room temperature (ca. 20-22 C), using "pond water" augmented with artificial sea salts, the endemic strain WIC and the Thailand strain PA7 of A. invadans produced free-swimming secondary zoospores at salinities of 0, 1 and 2 psu (practical salinity unit = per thousand), but not at 4 psu or higher. Secondary zoospores of another species, ATCC-62427 (Aphanomyces sp.), were observed at 1, 2, 4 and 8 psu but not at 0 and 12 psu. Secondary zoospores of all three isolates, especially WIC, were abundant and motile 1-2 d postsporulation. Sporulation was temperature dependent and occurred over a relatively narrow range. No sporulation occurred at 4, 30 or 35 C for either WIC or PA7. For both strains zoospore production within 1-3 d after the initiation of sporulation was more prolific at 25 C than at 20 and 15 C. At 15 C production of zoospores was sustained over 11 d for WIC and 5 d for PA7. At room temperature single WIC secondary zoospores remained motile 12-18 h. Salinities exceeding 4 psu or vigorous shaking caused immediate cyst formation of WIC secondary zoospores. Exposure to menhaden tissue, but not tissues of other fishes to secondary zoospores (WIC), caused rapid (2 h) cyst formation. Cysts were capable of excysting when transferred to 1 psu water within 2-3 h of cyst formation. Cysts that had remained encysted in 6.5 psu for 24 h did not excyst when transferred to 1 psu water. Salinity and temperature requirements for sporulation indicate that juvenile menhaden must acquire infections during rain or in low salinity oligohaline waters.
由入侵丝囊霉(Aphanomyces invadans)引起的卵菌感染发生在世界各地的淡水和河口鱼类中。在美国东海岸,入侵丝囊霉引起的皮肤溃疡在大西洋油鲱(Brevoortia tyrannus)中很普遍。从实验室观察来看,低盐度似乎对病原体的传播至关重要。为了更好地了解传播方面的情况,我们对入侵丝囊霉的两个分离株在不同盐度和温度下的次生游动孢子的孢子形成和孢囊形成进行了表征。孢子形成仅在低盐度下发生。在室温(约20 - 22℃)下,使用添加了人工海盐的“池塘水”,入侵丝囊霉的地方菌株WIC和泰国菌株PA7在盐度为0、1和2 psu(实用盐度单位 = 千分之一)时产生自由游动的次生游动孢子,但在4 psu或更高盐度时不产生。另一个物种ATCC - 62427(丝囊霉属(Aphanomyces sp.))的次生游动孢子在1、2、4和8 psu时被观察到,但在0和12 psu时未观察到。所有三个分离株的次生游动孢子,尤其是WIC,在孢子形成后1 - 2天数量丰富且具有运动性。孢子形成依赖于温度,且发生在相对较窄的温度范围内。WIC或PA7在4℃、30℃或35℃时均未发生孢子形成。对于这两个菌株,在孢子形成开始后的1 - 3天内,25℃时游动孢子的产生比20℃和15℃时更为丰富。在15℃时,WIC的游动孢子产生持续了11天,PA7持续了5天。在室温下,单个WIC次生游动孢子保持运动性12 - 18小时。盐度超过4 psu或剧烈摇晃会导致WIC次生游动孢子立即形成孢囊。将WIC次生游动孢子暴露于油鲱组织而非其他鱼类组织时,会导致快速(2小时)形成孢囊。孢囊在形成后2 - 3小时内转移到1 psu水中时能够脱囊。在6.5 psu中包囊24小时的孢囊转移到1 psu水中时不会脱囊。孢子形成的盐度和温度要求表明,幼年油鲱必须在降雨期间或低盐度的低盐水中感染。