MOLECULAR DETECTION AND CHARACTERIZATION OF HEMOPLASMAS IN CATTLE FROM THE LOWER SHABELLE REGION, SOMALIA – PRELIMINARY DATA
Larissa D.R. Ferrari, Ahmed A. Hassan-Kadle, Flavia C.M. Collere, Nathalia A. Soares, Abdalla M. Ibrahim, Aamir M. Osman, Mohamed A. Shair, Marcos R. André, Thállitha S.W.J. Vieira, Rosangela Z. Machado, Rafael F.C. Vieira
Presenter: Larissa Dantas Roeder Ferrari
UNIVERSIDADE FEDERAL DO PARANÁ
Vector-Borne Diseases Laboratory
BRAZIL
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HEMOPLASMAS
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Somalia
28.7 million goats 13.6 million sheep 7.1 million camels 3.9 million cattle
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Lower Shabelle
Middle Shabelle
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OBJECTIVE
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MATERIALS AND METHODS
DNA extraction
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Real-time (qPCR)
Mycoplasma spp.
16S rRNA gene
Positive samples
Mycoplasma wenyonii (16S rRNA gene)
‘Candidatus Mycoplasma haematobovis’ (16S rRNA gene)
Conventional PCR
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RESULTS
74/131
(56.48%)
Positive for Mycoplasma spp
qPCR
Mycoplasma wenyonii 31/74 (41.89%)
‘Candidatus Mycoplasma haematobovis’ 3/74 (4.05%)
Co-infection 34/74 (45.94%)
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RESULTS (Cont.)
6/74 (8.1%) negative species-specific conventional PCR
positive semi-nested PCR (16S rRNA gene)
Improving detection rate
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PHYLOGENETIC ANALYSIS
Phylogenetic analysis of hemotropic Mycoplasma sp. 16S rRNA genes from species-specific PCR assays confirmed that animals were infected with M. wenyonii and ‘Ca. M. haematobovis’
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Sequencing of the 16S, 23S rRNA, and RNAse P gene fragments of the hemoplasma-positive samples by the semi-nested PCR assay will later confirm the hemoplasma species infecting animals.
NEXT STEPS
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First study on the detection and molecular characterization of hemoplasmas in cattle from Somalia
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22 - 24 March -2022
Thank you!
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