Vibrio diseases of marine fish populations

SeveralVibrio spp. cause disease in marine fish populations, both wild and cultured. The most common disease, vibriosis, is caused byV. anguillarum. However, increase in the intensity of mariculture, combined with continuing improvements in bacterial systematics, expands the list ofVibrio spp. that cause fish disease. The bacterial pathogens, species of fish affected, virulence mechanisms, and disease treatment and prevention are included as topics of emphasis in this review.     

THE BREEDING OF HEUGLIN'S MASKED WEAVER AND ITS NESTING ASSOCIATION WITH THE RED WEAVER ANT

Grimes, L. G. 1973. The breeding of Heuglin's Masked Weaver and its nesting association with the Red Weaver Ant. Ostrich 44: 170–175.

The breeding season of Heuglin “s Masked Weaver Ploceus heuglini at Legon began in the latter half of the major dry season in January and February; continued through the main wet season and ceased in late August and for the rest of the year. The Accra colony had a similar breeding activity but in addition was active for a short period in November which had ended by mid-December. Although the majority of males formed colonies in which the number of males ranged from two to twenty, solitary breeding occurred equally frequently. Most males within the Legon colony, and possibly this is true for all colonies, were polygynous while most solitary males were monogamous. More nests were built by each male than the number of females involved in the polygyny.

A close nesting association with the Red Weaver Ant Oecophylla longinoda existed and the data suggested that the weaver sought the ant. Two cases were found of nesting association with the wasp Belanogaster grisens.     

Gamma-irradiated peripheral blood mononuclear cells can express LAK activity

Peripheral blood mononuclear cells (PBMC) irradiated with high dose gamma-radiation (1000-5000 rad) are commonly used as feeder cells during the cloning of T lymphocytes, natural killer (NK) and lymphokine activated killer (LAK) cells. We report here that such gamma-irradiated PBMC can be stimulated with interleukin 2 (IL-2) to express the ability to lyse a variety of tumor cell targets. The non-major histocompatibility complex (MHC) restricted cytotoxicity demonstrated by irradiated PBMC is, however, lower than that expressed by their non-irradiated counterparts. The numbers of viable, gamma-irradiated LAK cells are significantly increased by the addition of the mitogen, phytohemagglutinin (PHA). Purification of the gamma-irradiated cells expressing cytotoxic activity by flow cytometry determined that the effector cells were predominantly CD3- cells, although some CD3+ cells also expressed moderate LAK activity. The ability of gamma-irradiated cells to proliferate in the presence of PHA alone, or with IL-2 + PHA, was maximal at day 4-5; but proliferation, as detected by 3H-thymidine uptake, was not detectable beyond 12-15 days of in vitro culture. Because many of the LAK, T cell and NK cell cloning procedures require the presence of feeder layers, growth factors (usually IL-2) and mitogens, the presence of residual feeder cells expressing cytotoxic activity may affect the specificity of such clones. Thus, efforts should be made to ensure that such gamma-radiation-resistant cells capable of expressing cytotoxic activity are completely eliminated before the cloned cells are used for further experiments.