Myxobolus species infecting the cartilaginous rays of the gill filaments in cyprinid fishes

2008 ◽  
Vol 53 (4) ◽  
Author(s):  
Kálmán Molnár ◽  
Gábor Cech ◽  
Csaba Székely

AbstractDuring a survey on myxosporean parasites of cyprinid fishes in Hungary, Myxobolus infections were found in the cartilaginous rays of the gill filaments in roach (Rutilus rutilus) and bleak (Alburnus alburnus). Myxobolus spp. causing the infections were studied by morphological, histological and molecular methods. Small plasmodia surrounded by chondrocytes contained relatively few spores which differed from each other and from the known Myxobolus spp. both in their morphology and 18S rDNA sequences. Both species, described as M. feisti sp. nov. and M. susanlimae sp. nov., are characterised by a specific cartilaginous histotropism.

2018 ◽  
Vol 66 (2) ◽  
pp. 250-257 ◽  
Author(s):  
Réka Borzák ◽  
Kálmán Molnár ◽  
Gábor Cech ◽  
Csaba Székely

Infection of the cornea in fishes by Myxobolus plasmodia is a common but still little known site preference of myxosporeans. A sporadic but striking infection in the cornea of the roach (Rutilus rutilus) was observed in Lake Balaton, Hungary. Relatively small, round plasmodia 250 to 500 μm in diameter developed in the dense connective tissue of the cornea. Morphological and molecular biological examination of spores collected from cysts in the cornea demonstrated that this infection is caused by Myxobolus fundamentalis, a species hitherto reported only from the cartilaginous gill arch of the roach. The 18S rDNA sequences of spores from the cornea showed 99.9% identity to the sequences of spores from the gill arch, and they also shared 99.9% identity with the sequences of triactinomyxon actinospores obtained from the oligochaete Isochaetides michaelseni.


1969 ◽  
Vol 26 (11) ◽  
pp. 2795-2805 ◽  
Author(s):  
I. Mackay ◽  
K. H. Mann

Egg production by two cyprinids in the River Thames at Reading, England, was studied quantitatively from January to June 1966. Roach (Rutilus rutilus) had a short spawning period, shedding all their eggs in one batch, whereas bleak (Alburnus alburnus) had a protracted spawning period and produced two or three batches of eggs. The relationship between egg numbers (Y) and age (X) for roach was given by log Y = 0.0840X + 3.2085; the estimated fecundity of a 6-year-old fish was 5157 with 95% confidence limits at 4725 and 5631. For bleak the relationship was log Y = 0.0564X + 3.5221, and the estimated fecundity of a 5-year-old fish was 6356 with 95% confidence limits at 5987 and 6776. Combining previously obtained data on population density with new data on sex ratio and percentage breeding in each age class, the population fecundity for roach was about 600 eggs/m2 and for bleak about 3000 eggs/m2.The roach population had lower fecundity than roach populations in other studies and there was some evidence that a proportion of females ceased egg production during the period of the study. The possibility that low fecundity was a response to food shortage is discussed.


2012 ◽  
Vol 57 (4) ◽  
Author(s):  
Gábor Cech ◽  
Kálmán Molnár ◽  
Csaba Székely

AbstractWhile studying Myxobolus gill infections of cyprinid fishes, the authors found large, segmented plasmodia in three species: ide (Leuciscus idus), asp (Aspius aspius) and white bream (Blicca bjoerkna). As regards their size and morphology, the spores from these plasmodia corresponded to those of M. dujardini described from chub (Leuciscus cephalus). However, the 18S rDNA sequences of spores from the three cyprinids differed from those of M. dujardini. Based on molecular differences, this paper describes two new species: M. alvarezae sp. nov. from ide and asp, and M. sitjae sp. nov. from white bream. The two new species and M. dujardini had a similar tissue tropism, and infected the multilayered epithelium of the gill filaments. Histological examination of the infected filaments demonstrated that the large plasmodia with multiple buddings were formed from amalgamating small plasmodia. Besides carrying infection in the filamental epithelium, the three above fish species were infected by small intralamellar plasmodia as well. These plasmodia were filled by spores that resembled the roach parasite M. intimus both in morphology and seasonal development. The 18S rDNA sequences of ‘intimus-like’ spores from ide and asp differed only in some base pairs from spores found in the type host roach, and were identified as belonging to M. intimus. The spores found in white bream, however, showed 3.6-5.0% difference in DNA sequence from those of M. intimus; therefore, they have been described as M. eirasianus sp. nov. The aim of this paper was to demonstrate the importance of using molecular methods for separating and identifying morphologically corresponding or closely similar Myxobolus spp.


2012 ◽  
Vol 60 (1) ◽  
pp. 69-82
Author(s):  
Kálmán Molnár ◽  
Gábor Cech ◽  
Csaba Székely

During a survey on the Myxobolus infection of two cyprinid fishes, the ide (Leuciscus idus) and the roach (Rutilus rutilus), myxosporean developmental stages were found around the arteries of the gill filaments and in the gill lamellae. An analysis of the 18S rDNA sequences of these stages revealed that plasmodia developing in the ide belonged to Myxobolus elegans, those developing in the gill lamellae of the roach corresponded to M. intimus, while plasmodia developing in close contact with the cartilaginous gill rays proved to be developmental stages of M. feisti. A strict seasonal cycle with a very long intrapiscine development was recorded for M. elegans and M. intimus. Developing plasmodia of the latter Myxobolus spp. occurred from early summer to next spring, and spore formation took place only in April. No seasonality associated with M. feisti infections was found. Developing plasmodia and mature spores of this species occurred simultaneously in different seasons of the year. Myxobolus feisti spore formation always occurred in close contact with the cartilaginous tissue of the gill filaments but spores were rarely encapsulated in the cartilaginous gill rays.


2000 ◽  
Vol 20 (2) ◽  
pp. 393-398 ◽  
Author(s):  
D. James Harris ◽  
Laura S. Maxson ◽  
Lee F. Braithwaite ◽  
Keith A. Crandall

2002 ◽  
Vol 38 (s1) ◽  
pp. 9-9
Author(s):  
M. W. Fawley ◽  
K. P. Fawley ◽  
M. L. Dean

2021 ◽  
Author(s):  
junjie hu ◽  
Jun Sun ◽  
Yanmei Guo ◽  
Hongxia Zeng ◽  
Yunzhi Zhang ◽  
...  

Abstract Background: There are limited data on Sarcocystis in insectivores. The Asian gray shrew, Crocidura attenuata, is one of the most common species of insectivores in the family Soricidae distributed in South Asia and Southeast Asia. To date, Sarcocystis has never been recorded in this host.Methods: Tissues from 42 Asian gray shrews were collected in China in 2017 and 2018. Sarcocysts were observed using light (LM) and transmission electron microscopy (TEM). To complete the parasite life cycle, muscle tissues of the host infected with sarcocysts were force-fed to two beauty rat snakes, Elaphe taeniura. Individual sarcocysts from different Asian gray shrews and oocysts/sporocysts isolated from the small intestines and feces of the experimental snakes were selected for DNA extraction, and seven genetic markers, including two nuclear loci (18S rDNA and ITS1), three mitochondrial genes (cox1, cox3 and cytb), and two apicoplastic genes (rpoB and clpC), were amplified, sequenced and analyzed.Results: Sarcocysts were found in 17 of 42 (40.5%) Asian gray shrews. Under LM, the microscopic sarcocysts were exhibited saw-tooth-like protrusions measuring 3.3–4.5 μm. Ultrastructurally, the sarcocyst wall contained numerous lancet- or leaf-like villous protrusions, similar to type 9h. The experimental beauty rat snakes shed oocysts/sporcysts measuring 11.9–16.7 × 9.2–10.6 μm with a prepatent period of 10 to 11 days. Comparing these sequences with those previously deposited in GenBank revealed that the 18S rDNA sequences and cox1 sequences shared the highest similarity with those of S. scandentiborneensis recorded in tree shrews, Tuaia minor and T. tana (i.e., 97.6–98.3% and 100% identity, respectively). Phylogenetic analysis based on 18S rDNA, ITS1 or cox1 sequences revealed that this parasite formed an independent clade with Sarcocystis spp. that utilize small animals as intermediate hosts and snakes as the known or presumed definitive host. On the basis of morphological and molecular characteristics and host specificity, the parasite was proposed as a new species, named S. attenuati.Conclusions: Sarcocysts were recorded in Asian gray shrews for the first time. The sarcocysts were characterized morphologically and molecularly. The 18S rDNA and cox1 sequences of S. attenuati, named in the present study, shared the highest identities with those of S. scandentiborneensis. However, the sarcocysts of the two species of Sarcocystis were quite different under LM and TEM. Based on experimental infection, beauty rat snakes have been proven to be a definitive host of S. attenuati. As more species of Sarcocystis from insectivores and other small mammals are properly morphologically and molecularly characterized, we may gain a better understanding of the biodiversity, host specificity and evolution of Sarcocystis in the future.


2019 ◽  
Vol 152 (3) ◽  
pp. 499-506 ◽  
Author(s):  
Oleg N. Shchepin ◽  
Martin Schnittler ◽  
Nikki H.A. Dagamac ◽  
Dmitry V. Leontyev ◽  
Yuri K. Novozhilov

Background and aims – Recent studies showed the position of two slime mould species with microscopic sporocarps, Echinosteliopsis oligospora and Echinostelium bisporum, within the class Myxomycetes. These minute species are seldom seen in studies based on detection of sporocarps and can easily be confused with protosteloid amoebozoans.Methods – We searched all published ePCR data sets that targeted myxomycete 18S rDNA for the presence of environmental sequences similar to E. oligospora and Echinosteliales in traditional circumscription, and performed phylogenetic analyses that included short environmental sequences and full-length 18S rDNA sequences representing all the major groups of myxomycetes.Key results – We report 19 unique sequences which are closely related to E. bisporum or E. oligospora based on sequence similarity (73.1–95.2% similarity) and which form well-supported monophyletic clades with these species in phylogenetic analyses. They may represent new species that are not yet described. Our phylogeny based on full-length 18S rDNA sequences further confirms the position of E. bisporum and E. oligospora within myxomycetes and the paraphyly of the order Echinosteliales in its traditional circumscription.Conclusions – Our results show that ePCR-based studies can reveal myxomycete taxa that often escape detection by traditional approaches, including potentially new species, and thus provide valuable new data on diversity and ecology of myxomycetes. As such, strategies for studying myxomycetes biodiversity should be revised, focusing also on molecular detection techniques in addition to the sporocarp-based ones.


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