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dc.contributor.authorAneela, Aneelapt_BR
dc.contributor.authorAlmutairi, Mashal M.pt_BR
dc.contributor.authorAlouffi, Abdulazizpt_BR
dc.contributor.authorAhmed, Haroonpt_BR
dc.contributor.authorTanaka, Tetsuyapt_BR
dc.contributor.authorVaz Junior, Itabajara da Silvapt_BR
dc.contributor.authorChang, Shun-Chungpt_BR
dc.contributor.authorChen, Chien Chinpt_BR
dc.contributor.authorAli, Abidpt_BR
dc.date.accessioned2023-11-17T03:22:00Zpt_BR
dc.date.issued2023pt_BR
dc.identifier.issn2306-7381pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/267145pt_BR
dc.description.abstractTicks are hematophagous ectoparasites that transmit pathogens to animals and humans. Updated knowledge regarding the global epidemiology of tick-borne Rickettsia hoogstraalii is dispersed, and its molecular detection and genetic characterization are missing in Pakistan. The current study objectives were to molecularly detect and genetically characterize Rickettsia species, especially R. hoogstraalii, in hard ticks infesting livestock in Pakistan, and to provide updated knowledge regarding their global epidemiology. Ticks were collected from livestock, including goats, sheep, and cattle, in six districts of Khyber Pakhtunkhwa (KP) Pakistan. Overall, 183 hosts were examined, of which 134 (73.2%), including goats (number = 39/54, 72.2%), sheep (23/40, 57.5%), and cattle (71/89, 80%) were infested by 823 ticks. The most prevalent tick species was Rhipicephalus microplus (number = 283, 34.3%), followed by Hyalomma anatolicum (223, 27.0%), Rhipicephalus turanicus (122, 14.8%), Haemaphysalis sulcata (104, 12.6%), Haemaphysalis montgomeryi (66, 8.0%), and Haemaphysalis bispinosa (25, 3.03%). A subset of 210 ticks was selected and screened for Rickettsia spp. using PCRbased amplification and subsequent sequencing of rickettsial gltA and ompB fragments. The overall occurrence rate of R. hoogstraalii was 4.3% (number = 9/210). The DNA of Rickettsia was detected in Hy. anatolicum (3/35, 8.5%) and Ha. sulcata (6/49, 12.2%). However, no rickettsial DNA was detected in Rh. microplus (35), Rh. turanicus (35), Ha. montgomeryi (42), and Ha. bispinosa (14). The gltA and ompB fragments showed 99–100% identity with R. hoogstraalii and clustered phylogenetically with the corresponding species from Pakistan, Italy, Georgia, and China. R. hoogstraalii was genetically characterized for the first time in Pakistan and Hy. anatolicum globally. Further studies should be encouraged to determine the role of ticks in the maintenance and transmission of R. hoogstraalii in different hosts.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofVeterinary Sciences. Basel. Vol. 10, no. 10 (Oct. 2023), 605, 15 p.pt_BR
dc.rightsOpen Accessen
dc.subjectTicksen
dc.subjectEpidemiologiapt_BR
dc.subjectIxodidaeen
dc.subjectDoenças transmitidas por carrapatospt_BR
dc.subjectRickettsia hoogstraaliien
dc.subjectInfecções por Rickettsiapt_BR
dc.subjectFilogeniapt_BR
dc.subjectPakistanen
dc.subjectReação em cadeia da polimerasept_BR
dc.subjectCaprinospt_BR
dc.subjectOvinospt_BR
dc.subjectBovinospt_BR
dc.subjectPaquistãopt_BR
dc.titleMolecular detection of Rickettsia hoogstraalii in Hyalomma anatolicum and Haemaphysalis sulcata : updated knowledge on the epidemiology of tick-borne Rickettsia hoogstraaliipt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001185968pt_BR
dc.type.originEstrangeiropt_BR


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