Tetrahymena pyriformis infection in the tiger barb, Puntius tetrazona: Parasite characterization and pathology of infected fish

Aquaculture ◽  
2021 ◽  
pp. 737725
Author(s):  
Xuming Pan ◽  
Wenyu Li ◽  
Alan Warren ◽  
Zhongdian Dong
Keyword(s):  
Tetrahymena Pyriformis ◽  
Infected Fish

scholarly journals Isolation of Tetrahymena pyriformis From Several Infected Pet Fish Species And a Regime For Its Treatment

2005 ◽  
Vol 29 (1) ◽  
pp. 190-195
Author(s):  
Omar Bassim Ahmed Al- Tayyar
Keyword(s):  
Methylene Blue ◽  
Water Temperature ◽  
Carassius Auratus ◽  
Poecilia Reticulata ◽  
Tetrahymena Pyriformis ◽  
Infected Fish ◽  
Mucus Hypersecretion ◽  
Goldfish Carassius Auratus ◽  
Poecilia Sphenops ◽  
Pterophyllum Scalare

Tetrahymena pyriformis has been firstly isolated from brood Goldfish(Carassius auratus) Common, Fantail, Ryukin, Veiltail and Moor, Black molly(Poecilia sphenops), Gourami (Trichogaster trichopterus), red Swordtail(Xiphophorus helleri), Guppy (Poecilia reticulata), deep Angelfish(Pterophyllum scalare) and brood Algae eater (Hypostomus plecostomus) inIraq. The infected fish suffered from mucus hypersecretion large hyperemicareas on the skin, and slight shedding of the scales. The incidence percentage ofinfection was 100 %. Rising water temperature was up to 29 – 30cْ for one timeand methylene blue was at a concentration of 5 ppm for 24 hours. Sodiumchloride at a concentration of 2 % for one minute and two minutes has noobvious effect on Tetrahymena pyriformis. Treatment with NaCl at theconcentration of 1% for 20 minutes for three consecutive days achieved the bestresults.

Albumin-Induced Endocytic Vacuoles in Tetrahymena Pyrijormis

1975 ◽  
Vol 33 ◽  
pp. 694-695
Author(s):  
L. J. Brenner ◽  
D. G. Osborne ◽  
B. L. Schumaker
Keyword(s):  
Electron Microscopy ◽  
Bovine Serum Albumin ◽  
Bovine Serum ◽  
Protein Concentration ◽  
Tetrahymena Pyriformis ◽  
Sequence Of Events ◽  
Cytoplasmic Bodies ◽  
Food Vacuoles ◽  
Mouse Ascites ◽  
Normal Human

Exposure of the ciliate, Tetrahymena pyriformis, strain WH6, to normal human or rabbit sera or mouse ascites fluids induces the formation of large cytoplasmic bodies. By electron microscopy these (LB) are observed to be membrane-bounded structures, generally spherical and varying in size (Fig. 1), which do not resemble the food vacuoles of cells grown in proteinaceous broth. The possibility exists that the large bodies represent endocytic vacuoles containing material concentrated from the highly nutritive proteins and lipoproteins of the sera or ascites fluids. Tetrahymena mixed with bovine serum albumin or ovalbumin solutions having about the same protein concentration (7g/100 ml) as serum form endocytic vacuoles which bear little resemblance to the serum-induced LB. The albumin-induced structures (Fig. 2) are irregular in shape, rarely spherical, and have contents which vary in density and consistency. In this paper an attempt is made to formulate the sequence of events which might occur in the formation of the albumin-induced vacuoles.

Разработка интегративного критерия безопасности продуктов питания

2015 ◽  
pp. 14-21
Author(s):  
Валерий Васильевич Воробьев
Keyword(s):  
Tetrahymena Pyriformis ◽  
Stylonychia Mytilus

В статье рассматриваются ускоренные методы определения токсичности пищевого сырья и продуктов питания на основе использования инфузорий Tetrahymena pyriformis и Stylonychia mytilus. Показано, что применение экспресс-метода с использованием стилонихий по определению общей токсичности лососевой икры, пресервов из соленой кеты, горбуши и сельди с различными консервантами, по сравнению с методикой определения уровня токсичности с помощью тетрахимены, позволяет сократить продолжительность констатации в 5 – 16 раз.

Antibody response of carp, Cyprinus carpio to the cestode, Bothriocephalus acheilognathi

Parasitology ◽  
1999 ◽  
Vol 118 (6) ◽  
pp. 635-639 ◽  
Author(s):  
P. NIE ◽  
D. HOOLE
Keyword(s):  
Antibody Response ◽  
Cyprinus Carpio ◽  
Serum Antibody ◽  
Infected Fish ◽  
Immune Protection ◽  
Carp Cyprinus Carpio ◽  
Bothriocephalus Acheilognathi ◽  
Protection Against Infection ◽  
Antibody Levels ◽  
Antibody Secreting Cells

The humoral antibody response and the number of pronephric antibody-secreting cells were examined in naturally Bothriocephalus acheilognathi-infected carp. Cyprinus carpio, and in those injected intraperitoneally with an extract of the cestode. In the extract-injected fish, specific antibody was detected 3 weeks after a second injection given 2 weeks after the primary injection, and antibody levels persisted for more than 200 days. A third injection also enhanced the antibody level in the extract-injected carp. The numbers of antibody-secreting cells were significantly higher in carp injected 3 times with the extract than in the control. In naturally-infected fish, the serum antibody levels and the number of pronephric antibody-secreting cells were higher in infected fish than in uninfected individuals although this difference was not statistically significant. The relevance of these results to immune protection against infection is discussed.

Biology of Crassicutis cichlasomae, a parasite of cichlid fishes in Mexico and Central America

1995 ◽  
Vol 69 (1) ◽  
pp. 69-75 ◽  
Author(s):  
T. Scholz ◽  
M.C.F. Pech-Ek ◽  
R. Rodriguez-Canul
Keyword(s):  
Central America ◽  
Developmental Stages ◽  
Infected Fish ◽  
Constant Darkness ◽  
Intermediate Hosts ◽  
Cichlid Fishes ◽  
Feeding Experiments ◽  
Light Darkness ◽  
Higher Temperature ◽  
Cichlasoma Urophthalmus

AbstractField study on the biology of Crassicutis cichlasomae Manter, 1936 (Digenea: Homalometridae) was carried out in a small swamp in a limestone factory near Mérida, Yucatán, Mexico. Aquatic snails, Littorina (Littoridinopsis) angulifera, harbouring C. cichlasomae rediae, cercariae and metacercariae, served both as the first and second intermediate hosts. Feeding experiments confirmed the conspecificity of metacercariae from naturally infected snails with adults from naturally infected fish. Gravid C. cichlasomae worms were obtained from experimentally infected fish 19 days post exposure at 22–24°C. Examination of fish from the swamp in Mitza and other localities in the Yucatan Peninsula showed that the cichlids Cichlasoma urophthalmus and C. meeki were definitive hosts of C. cichlasomae. There was no pronounced preference of C. cichlasomae adults for the site of their location in the intestine of the definitive host; a slightly higher proportion (41%) of worms was only found in the anterior third of the gut. The time of miracidium development varied from 18.5 to 27.5 days; different temperature (20.1–35.7°C) or light/darkness regimes influenced only slightly the rate of embryonic development, with shorter development times at higher temperature (34.8–35.7°C) and constant darkness and/or light. With the exception of the sporocyst, all developmental stages are described and figured.

scholarly journals Effect of temperature, CO2 and O2 on motility and mobility of Anisakidae larvae

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Aiyan Guan ◽  
Inge Van Damme ◽  
Frank Devlieghere ◽  
Sarah Gabriël
Keyword(s):  
Enzymatic Digestion ◽  
Infected Fish ◽  
Effect Of Temperature ◽  
Video Recordings ◽  
Different Temperatures ◽  
Semi Solid ◽  
Zoonotic Parasites ◽  
The Impact ◽  
Phosphate Buffered Saline

AbstractAnisakidae, marine nematodes, are underrecognized fish-borne zoonotic parasites. Studies on factors that could trigger parasites to actively migrate out of the fish are very limited. The objective of this study was to assess the impact of different environmental conditions (temperature, CO2 and O2) on larval motility (in situ movement) and mobility (migration) in vitro. Larvae were collected by candling or enzymatic digestion from infected fish, identified morphologically and confirmed molecularly. Individual larvae were transferred to a semi-solid Phosphate Buffered Saline agar, and subjected to different temperatures (6 ℃, 12 ℃, 22 ℃, 37 ℃) at air conditions. Moreover, different combinations of CO2 and O2 with N2 as filler were tested, at both 6 °C and 12 °C. Video recordings of larvae were translated into scores for larval motility and mobility. Results showed that temperature had significant influence on larval movements, with the highest motility and mobility observed at 22 ℃ for Anisakis spp. larvae and 37 ℃ for Pseudoterranova spp. larvae. During the first 10 min, the median migration of Anisakis spp. larvae was 10 cm at 22 ℃, and the median migration of Pseudoterranova spp. larvae was 3 cm at 37 ℃. Larval mobility was not significantly different under the different CO2 or O2 conditions at 6 °C and 12 ℃. It was concluded that temperature significantly facilitated larval movement with the optimum temperature being different for Anisakis spp. and Pseudoterranova spp., while CO2 and O2 did not on the short term. This should be further validated in parasite-infected/spiked fish fillets.

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