Near-complete genome of SARS-CoV-2 Delta variant of concern identified in a symptomatic dog (Canis lupus familiaris) in Botswana.

We sought to investigate whether SARS-CoV-2 was present, and to perform full-length genomic sequencing, in a 5-year-old male crossbreed dog from Gaborone, Botswana that presented overt clinical signs (flu-like symptoms, dry hacking cough and mild dyspnoea). It was only sampled a posteriori, because three adult owners were diagnosed with SARS-CoV-2 infection. Next-generation sequencing based on Oxford Nanopore Technology (ONT) was performed on amplicons that were generated using a reverse transcriptase real-time polymerase chain reaction (RT-qPCR) of confirmed positive SARS-CoV-2 nasopharyngeal and buccal swabs, as well as a bronchoalveolar lavage with mean real cycle threshold (qCt) value of 36 based on the Nucleocapsid (N) gene.

Selenium-vitamin E responsive myopathy in farmed ostriches (Struthio camelus) in Botswana.

Four adult ostriches developed sudden onset paresis and were unable to stand up when disturbed. After treatment with selenium and vitamin E, one of the birds could stand and move normally. The others died and post mortem examination revealed pale patches in the thigh muscles.

Diseases of indigenous chickens in Bokaa village, Kgatleng district, Botswana.

This study examined flock size and management, level of internal and external parasite burden and seroprevalence of antibodies to poultry pathogens in indigenous chickens in Bokaa village, Kgatleng district, Botswana. The mean flock size was 22.6 +/- 6.

Yolk sac utilization in ostrich (Struthio camelus) chicks.

The mass of residual yolk sac expressed as a percentage of initial mass of the egg from which the chick hatched decreased sharply in the first 2 days post-hatching. A gradual reduction occurred between 3 and 10 days after which a sharp decline was noted between 11 and 13 days post-hatching. The highest number of chicks with unabsorbed yolk sac was noted on day 5 post-hatching followed by days 6 and 7.

Seasonal fluctuation of parasitic infestation in donkeys (Equus asinus) in Oodi village, Kgatleng District, Botswana.

During the period March to September 2000, a study was conducted in Oodi village, Kgatleng District, Botswana, to investigate the seasonal fluctuation of internal, external and blood parasites of donkeys. Twelve adult donkeys were randomly selected from a farmer with a herd of 15 donkeys. Monthly visits were made to the farmer when the donkeys were examined for parasites.

A note on endoparasites of wild ostriches (Struthio camelus) in the Mokolodi Nature Reserve, Gaborone, Botswana.

A study was undertaken to investigate the prevalence of endoparasites of wild ostriches at Mokolodi Nature Reserve, Gaborone, over a 7-month period. Large numbers of strongyle eggs were recovered from faecal material in April and September and a decline in the strongyle egg counts was evident during June and July. Noteworthy was the absence of helminth eggs in faecal samples collected from chicks and coccidia oocysts from any of the ostriches.

Biochemical composition of urine from farmed ostriches (Struthio camelus) in Botswana.

Biochemical and qualitative evaluation of the supernatant of urine from hydrated farmed ostriches (Struthio camelus) indicated that the urine was comparable to that described by other workers. The disparities obtained between the biochemical constituents in the present and previous studies were partly attributed to the state of hydration influenced by climatic factors. Results of the cytological examination of the supernatant and the sediment concurred with the observations of other workers.

Antibodies to Newcastle disease virus in the sera of indigenous chickens in Oodi, Kgatleng, Botswana.

A serological survey was conducted to determine the prevalence of antibodies to Newcastle disease virus in apparently healthy and unvaccinated adult indigenous chickens. Haemagglutination inhibiting antibodies to Newcastle disease virus were found in the sera of 51 out of 89 (57.3%) chickens sampled.

Helminth parasites of indigenous chickens in Oodi, Kgatleng District, Botswana.

Thirteen adult indigenous chickens from Oodi, Kgatleng district, Botswana, were examined for helminth parasites. Two species of nematodes, Ascaridia galli and Heterakis gallinarum, and species of the cestode genus Raillietina, were recovered. A.

Helminth parasites of domestic pigeons (Columba livia domestica) in Sebele, Gaborone, Botswana.

Twelve adult domestic pigeons from Sebele, Gaborone, Botswana, were examined for the presence of helminth parasites. The cestode genus Raillietina and two species of nematodes, Dispharynx spiralis and Ascaridia columbae were recovered. Most pigeons (75 %) were infected with Raillietina spp.

Detection of Mycoplasma gallisepticum and Mycoplasma synoviae antibodies in the sera of indigenous chickens by rapid serum agglutination test at Mmopane, Gaborone, Botswana.

The mean flock size was ten chickens per rural farmer. Antibodies to Mycoplasma gallisepticum and Mycoplasma synoviae were detected in 57.88% and 67.

Limb deformities of farmed ostrich (Struthio camelus) chicks in Botswana.

Limb deformities were detected in 135 out of 885 ostrich chicks, giving a prevalence of 15.3%. Tibiotarsal rotation affected 73% of the chicks with limb deformities, whereas rolled toes accounted for 36%.

Seroprevalence of infectious bursal disease in non-vaccinated indigenous and exotic chickens on selected farms around Gaborone, Botswana.

Sera from nine out of 30 (30.0%) apparently healthy unvaccinated indigenous (Tswana) chickens had precipitating antibodies to infectious bursal disease (IBD) virus using the agar gel precipitation test. Similarly, sera from 11 out of 49 (22.

Haemoproteus columbae in domestic pigeons in Sebele, Gaborone, Botswana.

Mature and immature stages of Haemoproteus columbae gametocytes, an avian haemosporidian protozoan parasite were found in 75% of blood smears prepared from 30 healthy domestic pigeons in Sebele location, Gaborone, Botswana. Parenteral administration of an immuno-suppressive dose of dexamethasone, lowered the level of parasitaemia, the packed cell volume and the heterophil:lymphocyte ratio in the test pigeons. However, both the dexamethasone-treated and the control pigeons remained clinically normal.

Serum biochemical values of farmed ostrich (Struthio camelus) in Botswana.

Reference biochemical values for serum analytes of 126 clinically normal farmed ostriches on one farm in Botswana were established. These included sodium, potassium, chloride, total protein, albumin, urea, creatinine, uric acid, cholesterol, total bilirubin, conjugated bilirubin, glucose, triglyceride, calcium, phosphorus, manganese, copper, zinc, alkaline phosphatase, gamma glutamyl transferase and creatinine kinase. The values obtained in this study can be used as reference values.

Coccidia oocysts in the faeces of farmed ostrich (Struthio camelus) chicks in Botswana.

Coccidia oocysts were demonstrated in the faeces of 53 (about 34%) of 156 apparently healthy ostrich chicks. Young chicks had the highest proportion of infestation while those more than 9 weeks old had no oocysts at all in their faeces. These coccidia may be considered no pathogenic since the infected chicks grew normally without any evidence of diarrhoea.

Impaction of the stomachs in farmed ostriches (Struthio camelus) in Botswana.

Impaction of the proventriculus, gizzard, and sometimes intestines due to sand was confirmed at postmortem in 25 cases involving ostriches (Struthio camelus). Although there was no age predisposition, impaction was more common in juvenile over 3 mo old. Clinical signs included sternal recumbency, outstretched neck, debility, and inability to stand.

Isolation of Theileria taurotragi and Theileria mutans from cattle in Botswana.

Two Theileria species demonstrated in peripheral Giemsa-stained blood smears of sick cattle from various parts of Botswana were subsequently identified as Theileria mutans and T. taurotragi using DNA hybridization and the polymerase chain reaction. Initial screening for Theileria species was done using microscopy, the indirect fluorescent antibody technique and the micro Elisa test.