FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W4221002967> ?p ?o ?g. }

• W4221002967 endingPage "738166" @default.
• W4221002967 startingPage "738166" @default.
• W4221002967 abstract "Cryptocaryon irritans are the main pathogens of “white spot disease” on the body surface of marine teleosts, but the seawater environment affects pathogen development and virulence. This study investigated C. irritans tomont formation, cell division, hatching, and infectivity to Larimichthys crocea under eight salinity gradients (S 0 , S 5 , S 10 , S 20 , S 30 , S 40 , S 45 , and S 50 ) to understand how C. irritans grows, develops and harms host fish in a variable natural environment. The results showed that the protomont hatching rate in S 5 , S 10 , S 20 and S 30 significantly increased over time, but the highest and lowest values appeared in S 20 and S 30 , respectively; and the hatching rate in S 20 is significantly higher than S 30 .The rate of tomont formation increased over treatment time, and the highest and lowest rates were observed in S 20 and S 0 groups, respectively. Seawater at extreme salinity (S 0, S 40 , S 45 , and S 50 ) significantly reduced the encystment duration to <5 min. In addition, the tomont division rate at S 5 , S 10 , S 20 , S 30 , S 40 and S 45 significantly increased over time, and the highest and the lowest values were recorded in S 20 and S 45 , respectively; and the division rate at S 20 is significantly higher than S 45 . The hatching rate in S 5 , S 10 , S 20 , S 30 , and S 40 also significantly increased over time, but the highest and lowest values appeared in S 20 and S 5 , respectively; and the hatching rate in S 20 is significantly higher than S 5 . The tomonts treated with seawater of 5–45‰ salinity divided evidently, but most tomonts under 0 and 50‰ salinity dissolved. TEM observation showed the pellicular alveoli of tomonts in S 40 and S 45 were wider than S 20 , the chromatin was loose, and the cyst wall was separately compressed into thin-layered layers. Finally, the aspect ratios of the theronts hatched at S 5 , S 10 , S 20 , S 30 , and S 40 significantly increased than those at S 20 , and the theronts became long and thin. The infectivity of the theronts hatched from tomonts under S 5 and S 40 salinity treatments were significantly lower than the control (S 20 ) because of the changes of theront number and morphology. In conclusion, salinity changes regulate the formation and development of C. irritans tomonts. Low (S 5 ) or high (S 40 ) salinity inhibits the infectivity of incubated theronts. • The Cryptocaryon irritans protomonts rapidly encysted at high salinity. • Salinity changes resulted in a close arrangement of cyst wall layers, widening pellicular alveoli, and chromatin dispersions. • Salinity levels of 5and 40‰ significantly reduced the infectivity of the hatched theronts." @default.
• W4221002967 created "2022-04-03" @default.
• W4221002967 creator A5002461253 @default.
• W4221002967 creator A5003938756 @default.
• W4221002967 creator A5007084033 @default.
• W4221002967 creator A5035404593 @default.
• W4221002967 creator A5045265859 @default.
• W4221002967 creator A5045498522 @default.
• W4221002967 creator A5053422724 @default.
• W4221002967 creator A5055841844 @default.
• W4221002967 date "2022-05-01" @default.
• W4221002967 modified "2023-09-30" @default.
• W4221002967 title "Salinity regulates the formation and hatching of Cryptocaryon irritans tomonts, affecting infectivity to Larimichthys crocea" @default.
• W4221002967 cites W1881752730 @default.
• W4221002967 cites W1967913937 @default.
• W4221002967 cites W1975878124 @default.
• W4221002967 cites W1976776466 @default.
• W4221002967 cites W1978480720 @default.
• W4221002967 cites W1981748895 @default.
• W4221002967 cites W1983564432 @default.
• W4221002967 cites W2002915025 @default.
• W4221002967 cites W2004638792 @default.
• W4221002967 cites W2010137543 @default.
• W4221002967 cites W2018468715 @default.
• W4221002967 cites W2032190660 @default.
• W4221002967 cites W2040875106 @default.
• W4221002967 cites W2054176860 @default.
• W4221002967 cites W2055116497 @default.
• W4221002967 cites W2059041807 @default.
• W4221002967 cites W2065214114 @default.
• W4221002967 cites W2068407871 @default.
• W4221002967 cites W2104713062 @default.
• W4221002967 cites W2134797886 @default.
• W4221002967 cites W2144736829 @default.
• W4221002967 cites W2157517268 @default.
• W4221002967 cites W2161335214 @default.
• W4221002967 cites W2161573102 @default.
• W4221002967 cites W2167055482 @default.
• W4221002967 cites W2169685731 @default.
• W4221002967 cites W2174507759 @default.
• W4221002967 cites W2313099951 @default.
• W4221002967 cites W2361950470 @default.
• W4221002967 cites W2412072147 @default.
• W4221002967 cites W2562343682 @default.
• W4221002967 cites W2581854647 @default.
• W4221002967 cites W2626882960 @default.
• W4221002967 cites W2770102996 @default.
• W4221002967 cites W2900499696 @default.
• W4221002967 cites W2998871673 @default.
• W4221002967 cites W3012894110 @default.
• W4221002967 cites W3038938210 @default.
• W4221002967 cites W3096453940 @default.
• W4221002967 cites W4244727552 @default.
• W4221002967 doi "https://doi.org/10.1016/j.aquaculture.2022.738166" @default.
• W4221002967 hasPublicationYear "2022" @default.
• W4221002967 type Work @default.
• W4221002967 citedByCount "3" @default.
• W4221002967 countsByYear W42210029672023 @default.
• W4221002967 crossrefType "journal-article" @default.
• W4221002967 hasAuthorship W4221002967A5002461253 @default.
• W4221002967 hasAuthorship W4221002967A5003938756 @default.
• W4221002967 hasAuthorship W4221002967A5007084033 @default.
• W4221002967 hasAuthorship W4221002967A5035404593 @default.
• W4221002967 hasAuthorship W4221002967A5045265859 @default.
• W4221002967 hasAuthorship W4221002967A5045498522 @default.
• W4221002967 hasAuthorship W4221002967A5053422724 @default.
• W4221002967 hasAuthorship W4221002967A5055841844 @default.
• W4221002967 hasConcept C104317684 @default.
• W4221002967 hasConcept C106358424 @default.
• W4221002967 hasConcept C129513315 @default.
• W4221002967 hasConcept C140793950 @default.
• W4221002967 hasConcept C159047783 @default.
• W4221002967 hasConcept C18903297 @default.
• W4221002967 hasConcept C197248824 @default.
• W4221002967 hasConcept C2522874641 @default.
• W4221002967 hasConcept C2776460866 @default.
• W4221002967 hasConcept C2777744765 @default.
• W4221002967 hasConcept C55493867 @default.
• W4221002967 hasConcept C60987743 @default.
• W4221002967 hasConcept C86803240 @default.
• W4221002967 hasConcept C89423630 @default.
• W4221002967 hasConceptScore W4221002967C104317684 @default.
• W4221002967 hasConceptScore W4221002967C106358424 @default.
• W4221002967 hasConceptScore W4221002967C129513315 @default.
• W4221002967 hasConceptScore W4221002967C140793950 @default.
• W4221002967 hasConceptScore W4221002967C159047783 @default.
• W4221002967 hasConceptScore W4221002967C18903297 @default.
• W4221002967 hasConceptScore W4221002967C197248824 @default.
• W4221002967 hasConceptScore W4221002967C2522874641 @default.
• W4221002967 hasConceptScore W4221002967C2776460866 @default.
• W4221002967 hasConceptScore W4221002967C2777744765 @default.
• W4221002967 hasConceptScore W4221002967C55493867 @default.
• W4221002967 hasConceptScore W4221002967C60987743 @default.
• W4221002967 hasConceptScore W4221002967C86803240 @default.
• W4221002967 hasConceptScore W4221002967C89423630 @default.
• W4221002967 hasLocation W42210029671 @default.
• W4221002967 hasOpenAccess W4221002967 @default.
• W4221002967 hasPrimaryLocation W42210029671 @default.

• next