Literature DB >> 9504346

Light and electron microscopic studies on the chronological development of Myxobolus cerebralis to the actinosporean stage in Tubifex tubifex.

M El-Matbouli1, R W Hoffmann.   

Abstract

Whirling disease caused by Myxobolus cerebralis has become the most widely known disease of salmonids in the 1990s. In the last 5 years we have studied many aspects regarding the host-pathogen relationship of this parasite. The parasite's histozoic development causes significant damage to cartilage and induces CNS symptoms by pressure on the brain and spinal cord. Myxobolus cerebralis has a two-host life-cycle involving a salmonid fish and a tubificid oligochaete. Two different stages of sporogony occur, one in each host. Early developmental stages in the fish can be found multiplying in the epidermis and peripheral and central nervous systems. The presporogenic stages then migrate to vertebral and cranial cartilages, where the first sporogonic phase occurs. Mature M. cerebralis spores found in fish cartilage are infectious for T. tubifex when ingested by the oligochaete after destruction of the infected fish. In the gut lumen of the tubificid, the spores extrude their polar capsules and attach to the gut epithelium by polar filaments. The shell valves then open along the suture line and the sporoplasm penetrates between the gut epithelial cells. The binucleate sporoplasm multiplies by schizogony, producing many one-cell stages which begin gamogonic development. As a result of the multiplication process, the intercellular space of the epithelial cells in more than 10 neighbouring worm segments may become infected. At this time (60-90 days p.i.), pansporocysts with eight zygotes start the sporogonic phase. The final stage of this development is a pansporocyst containing eight folded triactinomyxon spores. Shortly afterwards, the spores are liberated into the gut lumen. The spores reach the water either by egestion or following the death of the infected tubificids. Infected tubificids can release triactinomyxons for at least 1 year. The ultrastructure of all four phases, schizogony, gametogony, gametogamy and sporogony, is demonstrated and discussed.

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Year:  1998        PMID: 9504346     DOI: 10.1016/s0020-7519(97)00176-8

Source DB:  PubMed          Journal:  Int J Parasitol        ISSN: 0020-7519            Impact factor:   3.981


  17 in total

1.  Cell formation by myxozoan species is not explained by dogma.

Authors:  David J Morris
Journal:  Proc Biol Sci       Date:  2010-04-14       Impact factor: 5.349

2.  Morphological and genetic differences among actinosporean stages of fish-parasitic myxosporeans (Myxozoa): difficulties of species identification.

Authors:  Edit Eszterbauer; Szilvia Marton; Orsolya Z Rácz; Márta Letenyei; Kálmán Molnár
Journal:  Syst Parasitol       Date:  2006-05-05       Impact factor: 1.431

3.  Involvement of aurantiactinomyxon in the life cycle of Thelohanellus testudineus (Cnidaria: Myxosporea) from allogynogenetic gibel carp Carassius auratus gibelio, with morphological, ultrastructural, and molecular analysis.

Authors:  Dan Dan Zhao; Yan Hua Zhai; Yang Liu; Si Jia Wang; Ze Mao Gu
Journal:  Parasitol Res       Date:  2017-07-13       Impact factor: 2.289

4.  Characterisation of carbohydrate-binding sites in developmental stages of Myxobolus cerebralis.

Authors:  Martin Knaus; Mansour El-Matbouli
Journal:  Parasitol Res       Date:  2005-10-07       Impact factor: 2.289

5.  Occurrence of actinosporean stages (Myxozoa) in the Nera River system (Umbria, central Italy).

Authors:  Caterina Marcucci; Monica Caffara; Enzo Goretti
Journal:  Parasitol Res       Date:  2009-08-19       Impact factor: 2.289

6.  Molecular methods clarify morphometric variation in triactinomyxon spores (Myxozoa) released from different oligochaete hosts.

Authors:  Sascha L Hallett; Stephen D Atkinson; Christer Erséus; Mansour El-Matbouli
Journal:  Syst Parasitol       Date:  2004-01       Impact factor: 1.431

7.  Arrested development of the myxozoan parasite, Myxobolus cerebralis, in certain populations of mitochondrial 16S lineage III Tubifex tubifex.

Authors:  D V Baxa; G O Kelley; K S Mukkatira; K A Beauchamp; C Rasmussen; R P Hedrick
Journal:  Parasitol Res       Date:  2007-09-22       Impact factor: 2.289

8.  Survivability of Kudoa septempunctata in human intestinal conditions.

Authors:  Takahiro Ohnishi; Marina Fujiwara; Akiko Tomaru; Tomoya Yoshinari; Yoshiko Sugita-Konishi
Journal:  Parasitol Res       Date:  2016-04-02       Impact factor: 2.289

9.  Relative quantification of immune-regulatory genes in two rainbow trout strains, Oncorhynchus mykiss, after exposure to Myxobolus cerebralis, the causative agent of whirling disease.

Authors:  Vanessa I C Severin; Mansour El-Matbouli
Journal:  Parasitol Res       Date:  2007-05-27       Impact factor: 2.289

10.  Evaluation of quantitative real-time PCR for rapid assessments of the exposure of sentinel fish to Myxobolus cerebralis.

Authors:  Garry O Kelley; Mark A Adkison; Francisco J Zagmutt-Vergara; Christian M Leutenegger; Jeffery W Bethel; Karin A Myklebust; Terry S McDowell; Ronald P Hedrick
Journal:  Parasitol Res       Date:  2006-03-23       Impact factor: 2.289

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