scholarly journals Selection of suitable reference genes for normalization of quantitative RT-PCR in peripheral blood samples of bottlenose dolphins (Tursiops truncatus)

2015 ◽  
Vol 5 (1) ◽  
Author(s):  
I-Hua Chen ◽  
Lien-Siang Chou ◽  
Shih-Jen Chou ◽  
Jiann-Hsiung Wang ◽  
Jeffrey Stott ◽  
...  
PLoS ONE ◽  
2018 ◽  
Vol 13 (3) ◽  
pp. e0191558 ◽  
Author(s):  
Ramneek Kaur ◽  
Monika Sodhi ◽  
Ankita Sharma ◽  
Vijay Lakshmi Sharma ◽  
Preeti Verma ◽  
...  

2019 ◽  
Vol 46 (4) ◽  
pp. 4545-4553 ◽  
Author(s):  
Teng Cheng ◽  
Fenglin Zhu ◽  
Jiajing Sheng ◽  
Lingling Zhao ◽  
Fasong Zhou ◽  
...  

2020 ◽  
Vol 1 (1) ◽  
pp. 61-75 ◽  
Author(s):  
Abby M. McClain ◽  
Risa Daniels ◽  
Forrest M. Gomez ◽  
Sam H. Ridgway ◽  
Ryan Takeshita ◽  
...  

Bottlenose dolphins (Tursiops truncatus) have a worldwide distribution in temperate and tropical waters and often inhabit estuarine environments, indicating their ability to maintain homeostasis in low salinity for limited periods of time. Epidermal and biochemical changes associated with low salinity exposure have been documented in stranded bottlenose dolphins; however, these animals are often found severely debilitated or deceased and in poor condition. Dolphins in the U.S. Navy Marine Mammal Program travel globally, navigating varied environments comparable to those in which free-ranging dolphins are observed. A retrospective analysis was performed of medical records from 46 Navy dolphins and blood samples from 43 Navy dolphins exposed to a variety of salinity levels for different durations over 43 years (from 1967–2010). Blood values from samples collected during low salinity environmental exposure (salinity ranging from 0–30 parts per thousand (ppt) were compared to samples collected while those same animals were in a seawater environment (31–35 ppt). Epidermal changes associated with low salinity exposure were also assessed. Significant decreases in serum sodium, chloride, and calculated serum osmolality and significant increases in blood urea nitrogen and aldosterone were observed in blood samples collected during low salinity exposure. Epidermal changes were observed in 35% of the animals that spent time in low salinity waters. The prevalence of epidermal changes was inversely proportional to the level of salinity to which the animals were exposed. Future work is necessary to fully comprehend the impacts of low salinity exposure in bottlenose dolphins, but the physiological changes observed in this study will help improve our understanding of the upper limit of duration and the lower limit of salinity in which a bottlenose dolphin can maintain homeostasis.


2015 ◽  
Vol 123 (1) ◽  
pp. 35-42 ◽  
Author(s):  
Susanne Grube ◽  
Tatjana Göttig ◽  
Diana Freitag ◽  
Christian Ewald ◽  
Rolf Kalff ◽  
...  

2003 ◽  
Vol 21 (5) ◽  
pp. 767-773 ◽  
Author(s):  
Giuseppe Palmieri ◽  
Paolo A. Ascierto ◽  
Francesco Perrone ◽  
Sabrina M.R. Satriano ◽  
Alessandro Ottaiano ◽  
...  

Purpose: Factors that are predictive of prognosis in patients who are diagnosed with malignant melanoma (MM) are widely awaited. Detection of circulating melanoma cells (CMCs) by reverse transcriptase-polymerase chain reaction (RT-PCR) has recently been postulated as a possible negative prognostic factor. Two main questions were addressed: first, whether the presence of CMCs, defined as the patient being positive for any of the three markers, had a prognostic role; and second, what the predictive value of each individual marker was. Patients and Methods: A consecutive series of 200 melanoma patients observed between January 1997 and December 1997, with stage of disease ranging from I to IV, was analyzed by semiquantitative RT-PCR. Tyrosinase, p97, and MelanA/MART1 were used as markers to CMCs on baseline peripheral blood samples. Progression-free survival (PFS) was used as a unique end point and was described by the product limit method. Multivariable analysis was applied to verify whether the auspicated prognostic value of these markers was independent of the stage of disease, and a subgroup analysis was performed that excluded patients with stage IV disease. Results: Overall, 32% (64 of 200) of patients progressed, and a median PFS of 52 months in the whole series was observed. The presence of CMCs and the markers individually or combined was predictive of prognosis in the univariate analysis but did not provide additional prognostic information to the stage of disease in multivariable models. In the subgroup analysis of stage (ie, I–III subgroup), similar results were observed. Conclusion: Detection of CMCs in peripheral blood samples at the time of MM diagnosis by semiquantitative RT-PCR does not add any significant predictive value to the stage of disease. Thus, this approach should not be used in clinical practice, and further studies are required to determine its usefulness.


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