Mutagenicity and genotoxicity in juvenile African catfish, Clarias gariepinus exposed to formulations of glyphosate and paraquat.

The aquatic ecosystem is under increasing pressure from environmental contaminants due to anthropogenic activities. This study investigated the potential of glyphosate and paraquat to induce DNA damage and other cell abnormalities in juvenile African Catfish, Clarias gariepinus. Juvenile fish were exposed for 96 h to 0.36, 0.48, 0.60, 0.72 and 0.84 mg/L glyphosate; and 0.018, 0.037, 0.055, 0.110 and 0.221 mg/L paraquat. Following the exposure, the fish liver and blood were analysed for DNA damage and micronucleus respectively. DNA damage was analysed using comet assay while the micronucleus test was used for assessing nuclear abnormalities. Both herbicides induced DNA damage in fish, with paraquat exhibiting higher toxicity. The severity in liver DNA damage was observed to be dependent on concentration. The herbicides triggered formation of micronuclei, bean-shaped cells, lobed nuclei, and apoptosis in blood cells of fish. Both herbicides also increased the frequency of occurrence of these cell abnormalities in erythrocytes and showed mutagenic potential in fish. Glyphosate and Paraquat both have mutagenic potentials in fish and this is a reflection of the threat these contaminants pose to fish and other forms of aquatic life in our natural water bodies. Low concentrations of these herbicides should be encouraged when usage is inevitable.

Testicular pathology, gonadal and epididymal sperm reserves of Yankasa rams infected with experimental Trypanosoma brucei brucei and Trypanosoma evansi.

AIM: The study was conducted to evaluate the pathological effects of trypanosomosis on the testes, gonadal, and epididymal sperm reserves of Yankasa rams for 98 days. MATERIALS AND METHODS: A total of 16 Yankasa rams, aged between 24 and 30 months and weighed between 22 and 25 kg, were acclimatized for a period of 2-months in a clean fly proof house and were adequately fed and given water ad-libitum. Of the 16 rams, 12 that were clinically fit for the experiment at the end of the acclimatization period were randomly divided into four groups: Groups I, II, III, and IV, each having 3 rams. Groups I and II were each challenged singly with experimental Trypanosoma brucei brucei (Federer strain) and Trypanosoma evansi (Sokoto strain), respectively, while Group III was challenged with mixed T. brucei brucei and T. evansi parasites (50% of each species in the infective inoculum) and Group IV was left as an uninfected control. Each infected ram received 2 mL of the infected blood containing 2×10(6) trypomastigotes via the jugular vein, while the control group received 2 mL each, normal saline. RESULTS: All the infected rams developed clinical signs typical of trypanosomosis at varying pre-patent periods. The gross lesions observed in the infected rams in Group II were moderate and more severe in those of Groups I and III. Histological sections of the testes of infected rams (Groups I, II, and III) showed moderate (T. evansi-infected group) to severe (mixed and T. brucei brucei-infected groups) testicular degenerations with reduction in number of spermatogenic cell layers, degenerated seminiferous tubules, congested interlobular spaces, loss of tissue architecture with significant (p<0.01) depletion, and loss of gonadal and epididymal sperm reserves in Groups I and III in comparison to Group II and the control Group IV. No observable clinical signs and histopathological lesions were found in those rams of the control Group IV. CONCLUSION: The study concluded that trypanosomosis due to experimental T. brucei brucei or T. evansi or mixed infections (of both parasites) caused testicular damage, decreased epididymal and gonadal sperm reserves and an important cause of infertility in Yankasa rams.

Studies on mosquitoes breeding in rock pools on inselbergs around Zaria, northern Nigeria.

BACKGROUND & OBJECTIVES: Rainwater often collects in depressions on rocks to form pools that are ideal breeding sites of mosquito vectors of diseases. Knowledge on the existence of disease vectors in these remote and relatively inaccessible locations could improve epidemiologic understanding and control capabilities. This study identifies mosquito species, their relative abundance and physicochemical characteristics of breeding microhabitats in rock pools on four inselbergs in northern Nigeria. METHODS: Soup ladle dipper was used to obtain representative samples of larval mosquitoes breeding in 141 rock pools on four inselbergs. Physicochemical parameters (depth, electrical conductivity, pH, surface area, temperature and total dissolved solids) of the pools were determined. Larvae were preserved in 70% alcohol and identified microscopically to species using taxonomic keys. Statistical correlation analysis and ANOVA were used to test the associations between physicochemical parameters and mosquito abundance, and for differences amongst inselbergs. RESULTS: Of 2991 larvae, five species of mosquito distributed in three genera (Anopheles, Aedes and Culex) including Ae. vittatus (92.88%), An. ardensis (0.13%), An. distinctus (1.67%), An. wilsoni (0.13%) and Cx. ingrami (5.18%) bred in the rock pools, Up to five species occurred per pool in various conspecific and heterogeneric combinations. Except for Ae. vittatus, the physicochemical parameters of the pools correlate significantly with species abundance. CONCLUSION: Ae. vittatus, a potential vector of yellow fever in Nigeria breeds profusely in rock pools on inselbergs around Zaria. For comprehensive vector implication and control, rock pools should be amongst the habitats of focus in yellow fever epidemiology.