Ultrastructural and molecular characterization of Haplosporidium montforti n. sp., parasite of the European abalone Haliotis tuberculata

被引:33
作者
Azevedo, Carlos
Balseiro, Pablo
Casal, Graca
Gestal, Camino
Aranguren, Raquel
Stokes, Nancy A.
Carnegie, Ryan B.
Novoa, Beatriz
Burreson, Eugene M.
Figueras, Antonio
机构
[1] Univ Porto, Dept Cell Biol, Inst Biomed Sci, ICBAS, P-4099003 Oporto, Portugal
[2] Univ Porto, Lab Protoparasitol, CIIMAR, P-4099003 Oporto, Portugal
[3] CSIC, Inst Invest Marinas, Vigo 36208, Pontevedra, Spain
[4] High Inst Hlth Sci, Dept Sci, P-4585116 Gandra, Portugal
[5] Coll William & Mary, Virginia Inst Marine Sci, Gloucester Point, VA 23062 USA
关键词
Haplosporidia; Haliotis tuberculata; Haplosporidium montforti ii. sp; abalone; SEM; TEM; SSU rRNA gene; ultrastructure; parasite; aquaculture;
D O I
10.1016/j.jip.2006.02.002
中图分类号
Q95 [动物学];
学科分类号
071002 ;
摘要
A new member of the parasitic phylum Haplosporidia, which was found infecting the connective tissue, gill, digestive gland, and foot A muscle of Haliotis tuberculata imported from Ireland and experimentally grown in Galicia (NW Spain), is described. Scanning electron A microscopy, transmission electron microscopy, and molecular characterization of the small subunit ribosomal RNA (SSU rRNA) gene were carried out to confirm the description of this species. The ultrastructural morphology of the spores and their surrounding ornaments attached to the spore wall was described from light, scanning, and transmission electron microscopy observations. Systemic infection with uninucleated and multinucleated plasmodia containing spherical nuclei was observed among several sporocysts containing the different spore maturation stages. The spores were spherical to slightly ellipsoidal (2.42 +/- 0.5 x 2.31 +/- 0.6 mu m). The apical zone of the spore wall was modified into a complex opercular system covering a circular orifice that measured about 0.5 mu m in diameter. The operculum was connected to the spore wall by a hinge. The spore wall was about 110 run thick, with 4 filaments (20-28 mu m long). The filaments were composed of the same material that formed the wall. The cross-sections through the base of these filaments showed T-like and X-like sections. internally, the uninucleated endosporoplasm contained typical haplosporidian structures, such as, haplosporosomes, a spherulosome, and mitochondria with vesicular cristae. The SSU rRNA gene sequence was different from previously reported haplosporidian SSU rRNA gene sequences, corroborating morphological data that this was all undescribed species. Based on differences from previously described haplosporidians in ultrastructural characteristics of the spore and SSU rRNA gene sequence.. we describe the abalone haplosporidian as Haplosporidium montforti n. sp. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:23 / 32
页数:10
相关论文
共 50 条
[31]  
Lauckner G, 1983, DIS MARINE ANIMALS
[32]   ULTRASTRUCTURE OF MINCHINIA-CADOMENSIS SP-N (HAPLOSPORIDA), PARASITE OF RHITHROPANOPEUS-HARRISII-TRIDENTATUS (DECAPODA) MAITLAND IN CANAL FROM CAEN TO SEA (CALVADOS, FRANCE) [J].
MARCHAND, J ;
SPRAGUE, V .
JOURNAL OF PROTOZOOLOGY, 1979, 26 (02) :179-185
[33]   ULTRASTRUCTURE OF MINCHINIA SP SPORES FROM SHIPWORMS (TEREDO SPP) IN THE WESTERN NORTH-ATLANTIC, WITH A DISCUSSION OF TAXONOMY OF THE HAPLOSPORIDIIDAE [J].
MCGOVERN, ER ;
BURRESON, EM .
JOURNAL OF PROTOZOOLOGY, 1990, 37 (03) :212-218
[34]   THE CHARACTERIZATION OF ENZYMATICALLY AMPLIFIED EUKARYOTIC 16S-LIKE RRNA-CODING REGIONS [J].
MEDLIN, L ;
ELWOOD, HJ ;
STICKEL, S ;
SOGIN, ML .
GENE, 1988, 71 (02) :491-499
[35]   Molecular detection of a haplosporidian parasite in carpet shell clam Ruditapes decussatus from Spain [J].
Novoa, B ;
Balseiro, P ;
Figueras, A .
DISEASES OF AQUATIC ORGANISMS, 2004, 61 (1-2) :89-93
[36]  
ORMIERES R, 1968, CR ACAD SCI D NAT, V266, P1134
[37]  
ORMIERES R, 1980, PROTISTOLOGICA, V16, P467
[38]   Development of a multiplex PCR for the detection of Haplosporidium nelsoni, Haplosporidium costale and Perkinsus marinus in the eastern oyster (Crassostrea virginica, Gmelin, 1971) [J].
Penna, MS ;
Khan, M ;
French, RA .
MOLECULAR AND CELLULAR PROBES, 2001, 15 (06) :385-390
[39]  
Perkins F.O., 1991, P261
[40]  
Perkins Frank O., 2002, P1328