scholarly journals Sequence and Phylogenetic Analysis of the Thrombospondin-Related Adhesive Protein (TRAP) Gene of Babesia gibsoni Isolates from Dogs in Taiwan

2010 ◽  
Vol 72 (10) ◽  
pp. 1329-1335 ◽  
Author(s):  
Chung-Chan LEE ◽  
Yu-Chen HSIEH ◽  
Chia-Chia HUANG ◽  
Chau-Loong TSANG ◽  
Yang-Tsung CHUNG
2022 ◽  
Vol 86 ◽  
pp. 102477
Author(s):  
Christophe Angeline Felicia Bora ◽  
Anju Varghese ◽  
Chundayil Kalarickal Deepa ◽  
Ashwathappa Nandini ◽  
Lanchalung Malangmei ◽  
...  

2021 ◽  
Vol 20 (1) ◽  
Author(s):  
Li-Yun Lin ◽  
Hui-Ying Huang ◽  
Xue-Yan Liang ◽  
Dong-De Xie ◽  
Jiang-Tao Chen ◽  
...  

Abstract Background Thrombospondin-related adhesive protein (TRAP) is a transmembrane protein that plays a crucial role during the invasion of Plasmodium falciparum into liver cells. As a potential malaria vaccine candidate, the genetic diversity and natural selection of PfTRAP was assessed and the global PfTRAP polymorphism pattern was described. Methods 153 blood spot samples from Bioko malaria patients were collected during 2016–2018 and the target TRAP gene was amplified. Together with the sequences from database, nucleotide diversity and natural selection analysis, and the structural prediction were preformed using bioinformatical tools. Results A total of 119 Bioko PfTRAP sequences were amplified successfully. On Bioko Island, PfTRAP shows its high degree of genetic diversity and heterogeneity, with π value for 0.01046 and Hd for 0.99. The value of dN–dS (6.2231, p < 0.05) hinted at natural selection of PfTRAP on Bioko Island. Globally, the African PfTRAPs showed more diverse than the Asian ones, and significant genetic differentiation was discovered by the fixation index between African and Asian countries (Fst > 0.15, p < 0.05). 667 Asian isolates clustered in 136 haplotypes and 739 African isolates clustered in 528 haplotypes by network analysis. The mutations I116T, L221I, Y128F, G228V and P299S were predicted as probably damaging by PolyPhen online service, while mutations L49V, R285G, R285S, P299S and K421N would lead to a significant increase of free energy difference (ΔΔG > 1) indicated a destabilization of protein structure. Conclusions Evidences in the present investigation supported that PfTRAP gene from Bioko Island and other malaria endemic countries is highly polymorphic (especially at T cell epitopes), which provided the genetic information background for developing an PfTRAP-based universal effective vaccine. Moreover, some mutations have been shown to be detrimental to the protein structure or function and deserve further study and continuous monitoring.


PLoS ONE ◽  
2014 ◽  
Vol 9 (2) ◽  
pp. e90522 ◽  
Author(s):  
Jun Ohashi ◽  
Yuji Suzuki ◽  
Izumi Naka ◽  
Hathairad Hananantachai ◽  
Jintana Patarapotikul

2006 ◽  
Vol 148 (2) ◽  
pp. 190-198 ◽  
Author(s):  
Jinlin Zhou ◽  
Shinya Fukumoto ◽  
Honglin Jia ◽  
Naoaki Yokoyama ◽  
Guohong Zhang ◽  
...  

2016 ◽  
Vol 78 (8) ◽  
pp. 1355-1360 ◽  
Author(s):  
Masahiro YAMASAKI ◽  
Yoshihiro TSUBOI ◽  
Yusuke TANIYAMA ◽  
Naohiro UCHIDA ◽  
Reeko SATO ◽  
...  

2002 ◽  
Vol 110 (1-2) ◽  
pp. 123-129 ◽  
Author(s):  
M Yamasaki ◽  
M Tajima ◽  
K.W Lee ◽  
J.R Jeong ◽  
O Yamato ◽  
...  

2013 ◽  
Vol 10 (2) ◽  
pp. 249-254 ◽  
Author(s):  
MH Talukder ◽  
A Matsuu ◽  
A Iguchi ◽  
BC Roy ◽  
N Nishii ◽  
...  

To identify tick-borne pathogens in blood samples from 68 dogs were examined for Babesia, Anaplasma/Ehrichia, Mycoplasma, and Hepatozoon spp. by using a molecular tool. The detection of DNA was performed using specific primers for partial 16S rRNA or 18S rRNA sequence, and amplicon sequences were analyzed. Our investigation detected Babesia gibsoni (26 dogs) and Anaplasma sp. AnHl446 (2 dogs), Mycoplasma haemocanis (27 dogs), and an unknown Mycoplasma spp were detected (2 dogs), which was most closely related to Candidatus Mycoplasma turicensis, on the basis of phylogenetic analysis. Hepatozoon DNA could not be detected in this study.DOI: http://dx.doi.org/10.3329/jbau.v10i2.14915 J. Bangladesh Agril. Univ. 10(2): 249-253, 2012


Sign in / Sign up

Export Citation Format

Share Document