The Establishment of the North American Bullfrog, Rana catesbeiana (Amphibia, Anura, Ranidae) in Jamaica

1977 ◽  
Vol 11 (2) ◽  
pp. 197 ◽  
Author(s):  
Robin Mahon ◽  
Karl Aiken
2011 ◽  
Vol 42 (4) ◽  
pp. 680-685 ◽  
Author(s):  
Larry J. Minter ◽  
Elsburgh O. Clarke ◽  
Jenessa L. Gjeltema ◽  
Kate E. Archibald ◽  
Lysa P. Posner ◽  
...  

2017 ◽  
Author(s):  
S. Austin Hammond ◽  
René L. Warren ◽  
Benjamin P. Vandervalk ◽  
Erdi Kucuk ◽  
Hamza Khan ◽  
...  

AbstractFrogs play important ecological roles as sentinels, insect control and food sources. Several species are important model organisms for scientific research to study embryogenesis, development, immune function, and endocrine signaling. The globally-distributed Ranidae (true frogs) are the largest frog family, and have substantial evolutionary distance from the model laboratory Xenopus frog species. Consequently, the extensive Xenopus genomic resources are of limited utility for Ranids and related frog species. More widely applicable amphibian genomic data is urgently needed as more than two-thirds of known species are currently threatened or are undergoing population declines.Herein, we report on the first genome sequence of a Ranid species, an adult male North American bullfrog (Rana [Lithobates] catesbeiana). We assembled high-depth Illumina reads (66-fold coverage), into a 5.8 Gbp (NG50 = 57.7 kbp) draft genome using ABySS v1.9.0. The assembly was scaffolded with LINKS and RAILS using pseudo-long-reads from targeted denovo assembler Kollector and Illumina Synthetic Long-Reads, as well as reads from long fragment (MPET) libraries. We predicted over 22,000 protein-coding genes using the MAKER2 pipeline and identified the genomic loci of 6,227 candidate long noncoding RNAs (IncRNAs) from a composite reference bullfrog transcriptome. Mitochondrial sequence analysis supported Lithobates as a subgenus of Rana. RNA-Seq experiments identified ~6,000 thyroid hormone– responsive transcripts in the back skin of premetamorphic tadpoles; the majority of which regulate DNA/RNA processing. Moreover, 1/6th of differentially-expressed transcripts were putative lncRNAs. Our draft bullfrog genome will serve as a useful resource for the amphibian research community.


2014 ◽  
Vol 48 (17) ◽  
pp. 10439-10447 ◽  
Author(s):  
Nik Veldhoen ◽  
Rachel C. Skirrow ◽  
Lorraine L. Y. Brown ◽  
Graham van Aggelen ◽  
Caren C. Helbing

2006 ◽  
Vol 2 (3) ◽  
pp. 455-459 ◽  
Author(s):  
Trenton W.J Garner ◽  
Matthew W Perkins ◽  
Purnima Govindarajulu ◽  
Daniele Seglie ◽  
Susan Walker ◽  
...  

Batrachochytrium dendrobatidis is the chytridiomycete fungus which has been implicated in global amphibian declines and numerous species extinctions. Here, we show that introduced North American bullfrogs ( Rana catesbeiana ) consistently carry this emerging pathogenic fungus. We detected infections by this fungus on introduced bullfrogs from seven of eight countries using both PCR and microscopic techniques. Only native bullfrogs from eastern Canada and introduced bullfrogs from Japan showed no sign of infection. The bullfrog is the most commonly farmed amphibian, and escapes and subsequent establishment of feral populations regularly occur. These factors taken together with our study suggest that the global threat of B. dendrobatidis disease transmission posed by bullfrogs is significant.


2010 ◽  
Vol 13 ◽  
pp. 53-61 ◽  
Author(s):  
L. M. Schloegel ◽  
C. M. Ferreira ◽  
T. Y. James ◽  
M. Hipolito ◽  
J. E. Longcore ◽  
...  

1988 ◽  
Vol 66 (7) ◽  
pp. 724-734 ◽  
Author(s):  
Z. C. Dhanarajan ◽  
Peter A. Merrifield ◽  
Burr G. Atkinson

Myosin heavy chain (MHC) and tropomyosin (Tm) have been isolated from limb muscles of the North American bullfrog, Rana catesbeiana, and injected into rabbits to raise monospecific antibodies. These antibodies were used to study the localization and synthesis of myosin heavy chain and tropomyosin in the limb buds of premetamorphic (stage VI–VII) tadpoles treated with triiodothyronine (T3) to induce metamorphosis. Indirect immunofluorescence localization detects the accumulation of both MHC and Tm in the developing thigh region within 24 h of T3 treatment. During the subsequent 48 h, the accumulation of these proteins is enhanced in the thigh and progresses from the thigh to the distal regions of the limb. Quantitative immunochemical determinations indicate that within 24 h of T3 treatment, synthesis of Tm and MHC are increased 23-fold and 6-fold, respectively. Following 5 days of T3 treatment, the synthetic rates of Tm and MHC are 266 and 70 times the control values, respectively. Both methods suggest that Tm is synthesized and accumulated at a greater rate than myosin heavy chain. These observations suggest that T3 promotes the differentiation of muscle in the limb buds of premetamorphic tadpoles and that limb development promoted by T3 in tadpoles is similar to that described during the embryonic development of higher vertebrates.


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