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Crayfish plague Aphanomyces astaci detected in redclaw crayfish, Cherax quadricarinatus in Taiwan
被引:25
|作者:
Hsieh, Chia-Yu
[1
,2
]
Huang, Chen-Wei
[3
]
Pan, Yi-Cheng
[3
]
机构:
[1] Natl Pingtung Univ Sci & Technol, Anim Hosp, 1 Shuehful Rd, Pingtung 91201, Taiwan
[2] Natl Pingtung Univ Sci & Technol, Southern Taiwan Aquat Anim Hlth Ctr, Pingtung 91201, Taiwan
[3] Miaoli Cty Anim Protect & Hlth Inspect Off, Miaoli City, Miaoli County, Taiwan
关键词:
Aphanomyces astaci;
Freshwater redclaw crayfish;
In situ hybridization;
PCR;
GENETIC DIVERSITY;
PATHOGEN;
WATER;
ADAPTATION;
DIAGNOSIS;
GENOTYPES;
D O I:
10.1016/j.jip.2016.03.015
中图分类号:
Q95 [动物学];
学科分类号:
071002 ;
摘要:
Between December 2013 and January 2014, five outbreaks of an unknown disease with moderate to high cumulative mortality were observed among the freshwater redclaw crayfish (Cherax quadricarinatus) populations at four crayfish farms in Miaoli and Changhua counties (northern Taiwan) and at one crayfish farm in Pingtung County (southern Taiwan). Polymerase chain reaction (PCR) analysis allowed the detection of Aphanomyces astaci DNA in dead crayfish. Histopathological examination revealed an infection of host tissue by fungal hyphae that presented as typical non-septate hyphae within the soft abdominal cuticle from the first to second segment and in the tail fan. In PCR assays completed for the detection of crayfish plague, an expected 568-bp product, specific for the A. astaci ITS gene, was obtained from all sub-adults and adults examined. In a comparison of our strains with the known strains of A. astaci in Europe, nucleotide sequence identities were very similar, with 99.8-100% sequence similarity in that gene region. Positive reactions to in situ hybridization, using a digoxigenin (DIG)-labelled DNA probe, further confirmed A. astaci as the causative agent. This is the first report concerning natural infection of A. astaci in freshwater redclaw crayfish in Asia. (C) 2016 Elsevier Inc. All rights reserved.
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页码:117 / 123
页数:7
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