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1.
Transbound Emerg Dis ; 64(5): 1393-1404, 2017 Oct.
Article in English | MEDLINE | ID: mdl-27211823

ABSTRACT

African swine fever (ASF) is an important emerging transboundary animal disease (TAD), which currently has an impact on many countries in Africa, Eastern Europe, the Caucasus and the Russian Federation. The current situation in Europe shows the ability of the virus to rapidly spread, which stands to threaten the global swine industry. At present, there is no viable vaccine to minimize spread of the disease and stamping out is the main source of control. In February 2011, Ethiopia had reported its first suspected outbreaks of ASF. Genomic analyses of the collected ASF virus (ASFV) strains were undertaken using 23 tissue samples collected from domestic swine in Ethiopia from 2011 to 2014. The analysis of Ethiopian ASFVs partial p72 gene sequence showed the identification of a new genotype, genotype XXIII, that shares a common ancestor with genotypes IX and X, which comprise isolates circulating in Eastern African countries and the Republic of Congo. Analysis of the p54 gene also followed the p72 pattern and the deduced amino acid sequence of the central variable region (CVR) of the B602L gene showed novel tetramer repeats not previously characterized.


Subject(s)
African Swine Fever Virus/genetics , African Swine Fever/virology , Genetic Variation , African Swine Fever/diagnosis , African Swine Fever/epidemiology , African Swine Fever Virus/classification , African Swine Fever Virus/isolation & purification , Amino Acid Sequence , Animals , Disease Outbreaks/veterinary , Ethiopia/epidemiology , Genotype , Phylogeny , Sequence Analysis, DNA/veterinary , Swine
2.
Int J Tuberc Lung Dis ; 9(1): 25-31, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15675546

ABSTRACT

SETTING: Ntcheu District, rural Malawi. OBJECTIVES: 1) To locate smear-positive pulmonary tuberculosis patients who were identified during the first 6 months of 2000 but did not start treatment ('lost cases'); 2) to describe these patients' pathways to diagnosis, health status and socio-demographic characteristics; and 3) to explore why these patients did not start treatment. METHODS: Lost cases were traced from programme registers and interviewed using the qualitative research critical incidents narrative (CIN) interviews technique. Results were triangulated with responses from health care workers through focus group discussions. RESULTS: The laboratory registered 157 new smear-positive patients. Twenty three (15%) of these were 'lost' (did not appear in the treatment register). CIN interviews were conducted with five lost patients and 14 carers of lost patients who had died. Long pathways to diagnosis were the norm. Health system structural barriers were the main factors behind these pathways, including requirement for hospital attendance, delays in symptom recognition and receipt of sputum results, and the misconception that negative smears excluded tuberculosis. CONCLUSION: Some smear-positive cases experience very long pathways to diagnosis and are lost from this free public health system. The diagnostic process needs to become more responsive to patients' needs.


Subject(s)
Patient Dropouts , Registries/statistics & numerical data , Tuberculosis, Pulmonary/diagnosis , Tuberculosis, Pulmonary/therapy , Adult , Demography , Diagnosis, Differential , Female , Focus Groups , Follow-Up Studies , Health Status , Humans , Malawi , Male , Risk Factors , Social Class , Sputum/microbiology , Time Factors
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