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Low Genetic Polymorphism in the Immunogenic Sequences of Rhipicephalus microplus Clade C.
Zeb, Ismail; Almutairi, Mashal M; Alouffi, Abdulaziz; Islam, Nabila; Parizi, Luís Fernando; Safi, Sher Zaman; Tanaka, Tetsuya; da Silva Vaz, Itabajara; Ali, Abid.
Afiliação
  • Zeb I; Department of Zoology, Abdul Wali Khan University Mardan, Mardan 23200, Pakistan.
  • Almutairi MM; Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.
  • Alouffi A; King Abdulaziz City for Science and Technology, Riyadh 12354, Saudi Arabia.
  • Islam N; Department of Chemistry, Abdul Wali Khan University Mardan, Mardan 23200, Pakistan.
  • Parizi LF; Centro de Biotecnologia and Faculdade de Veterinária, Universidade Federal do Rio Grande do Sul, Campus do Vale, Porto Alegre 91501-970, RS, Brazil.
  • Safi SZ; Faculty of Medicine, Bioscience and Nursing, MAHSA University, Jenjarom 42610, Malaysia.
  • Tanaka T; Laboratory of Infectious Diseases, Joint Faculty of Veterinary Medicine, Kagoshima University, 1-21-24 Korimoto, Kagoshima 890-0065, Japan.
  • da Silva Vaz I; Centro de Biotecnologia and Faculdade de Veterinária, Universidade Federal do Rio Grande do Sul, Campus do Vale, Porto Alegre 91501-970, RS, Brazil.
  • Ali A; Department of Zoology, Abdul Wali Khan University Mardan, Mardan 23200, Pakistan.
Vaccines (Basel) ; 10(11)2022 Nov 11.
Article em En | MEDLINE | ID: mdl-36423005
ABSTRACT
Rhipicephalus microplus tick highly affects the veterinary sector throughout the world. Different tick control methods have been adopted, and the identification of tick-derived highly immunogenic sequences for the development of an anti-tick vaccine has emerged as a successful alternate. This study aimed to characterize immunogenic sequences from R. microplus ticks prevalent in Pakistan. Ticks collected in the field were morphologically identified and subjected to DNA and RNA extraction. Ticks were molecularly identified based on the partial mitochondrial cytochrome C oxidase subunit (cox) sequence and screened for piroplasms (Theileria/Babesia spp.), Rickettsia spp., and Anaplasma spp. PCR-based pathogens-free R. microplus-derived cDNA was used for the amplification of full-length cysteine protease inhibitor (cystatin 2b), cathepsin L-like cysteine proteinase (cathepsin-L), glutathione S-transferase (GST), ferritin 1, 60S acidic ribosomal protein (P0), aquaporin 2, ATAQ, and R. microplus 05 antigen (Rm05Uy) coding sequences. The cox sequence revealed 100% identity with the nucleotide sequences of Pakistan's formerly reported R. microplus, and full-length immunogenic sequences revealed maximum identities to the most similar sequences reported from India, China, Cuba, USA, Brazil, Egypt, Mexico, Israel, and Uruguay. Low nonsynonymous polymorphisms were observed in ATAQ (1.5%), cathepsin-L (0.6%), and aquaporin 2 (0.4%) sequences compared to the homologous sequences from Mexico, India, and the USA, respectively. Based on the cox sequence, R. microplus was phylogenetically assembled in clade C, which includes R. microplus from Pakistan, Myanmar, Malaysia, Thailand, Bangladesh, and India. In the phylogenetic trees, the cystatin 2b, cathepsin-L, ferritin 1, and aquaporin 2 sequences were clustered with the most similar available sequences of R. microplus, P0 with R. microplus, R. sanguineus and R. haemaphysaloides, and GST, ATAQ, and Rm05Uy with R. microplus and R. annulatus. This is the first report on the molecular characterization of clade C R. microplus-derived immunogenic sequences.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Vaccines (Basel) Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Vaccines (Basel) Ano de publicação: 2022 Tipo de documento: Article