
Agribusiness, Agriculture, Veterinary Medicine, Cassava, Garri, food security, Agritech and the Red Meat Value Chain.
Friday, April 8, 2016
CLAW LESIONS AND POOR REPRODUCTIVE PERFORMANCE IN SOW.

AGRIBUSINESS: NUTRITIONAL DIARRHEA IN PIGLETS.
AGRIBUSINESS: NUTRITIONAL DIARRHEA IN PIGLETS. Pathogenic diarrhea are quite common and are often confused with non-pathogenic secretory diarrhea. The non-pathogenic diarrhea are caused by wrong feed formulation and feed presentation.This can easily be avoided by correct feed formulation.
AGRIBUSINESS: NUTRITIONAL DIARRHEA IN PIGLETS. Pathogenic diarrhea is the most common cause of depressed performance in recently weaned piglets. The nutritional diarrhea often lead to secondary complications through pathogenic agents such as Escherichia coli and Salmonella.
These are identified by proper diagnostics, require veterinary intervention to cure symptoms and eliminate the source of offending microorganisms. Nutritional diarrhea usually follow pathogenic complications, thus a combination of nutritional and medical interventions is required.
Nutritional diarrhea originate from three main areas in the feeding program:
1) palatability of feed; feed that fail to initiate vigorous intake immediately post-weaning will cause hunger, this will be followed by over-eating when pigs finally associate dry feed with nourishment.
The short-term starvation created is capable of reducing the digestive and immune functions of the gastrointestinal system. When the pigs over-eat after a period of malnutrition, the digestion is incomplete, resulting in excess amounts of energy and protein available for proliferation of opportunistic pathogenic microorganism such as Escherichia coli or Salmonella.
2) feed quality; feed of low quality produced using second class ingredients.This will not only discourage the development of an early appetite, but their intrinsic low digestibility result in more undigested material becoming available for bacterial proliferation in the lower gastrointestinal tract. This is why a high quality diet is essential for a successful weaning.
3)feed stuff component such as soybean meal contain anti-nutritional factors that may cause gastrointestinal inflammation. This if combined with low-feed intake and excess undigested feed will result in nutritional diarrhea
.

COPPER SULPHATE AND ANTIBIOTIC- FREE PIGLET DIET.
Copper sulphate is an old additive that has received renewed interest with the ban of zinc oxide and antibiotics. Long before the advent of zinc oxide, another mineral used to dominate piglet feeds: copper sulphate. It was known to reduce or prevent piglet diarrhea and, as such, it improved animal growth rate and feed efficiency.
when the need to rotate antibiotics from batch to batch was necessary, copper sulphate remained a constant addition to even the simplest corn-soybean meal-type diets. With the introduction of zinc oxide, the effects of copper sulphate appeared to wane, but it never completely left the scene, mostly because it is very inexpensive.
Supplementing piglet diets with high dosages of zinc oxide is under pressure worldwide. The European Union which has imposed an otherwise restrictive feed legislation, it is common practice to add pharmacological doses of zinc oxide, but only under veterinary prescription.( WATTAgnet.com)
Even in the U.S., this ingredient is under scrutiny, along with growth-promoting antibiotics. Luckily, long experiences in the EU have demonstrated that we can replace both antibiotics and high dosages of zinc oxide. This is done through feed reformulation and the use of alternative additives. One of those is, naturally, copper sulphate; old technology at the rescue due to new regulations!
Using just a bit of copper sulphate to be sure is not going to harm animals, but it is not going to help them either. Going back to original research, we need 250 ppm to get the full result, and at least 150 ppm to start seeing an effect. And, if we accept the hypothesis of copper sulphate being a bactericide, then we need the highest possible dosage exactly when pathogen pressure is highest. .

NEWCASTLE DISEASE OUTBREAK

HIV RESISTS CRISPR GENE EDITING.
A recent study shows that the HIV virus can overcome new efforts to defeat it using gene-cutting CRISPR technology and that the act of editing the virus's genome could even introduce mutations that help it resist future attacks . The method to tackle HIV using CRISPR have been popular since the rise of the technique, but recent studies have found that HIV quickly continued replicating even after being treated with the gene-cutting enzyme and that mutations introduced by the cutting process rendered new HIV cells unrecognisable to the enzyme.
The research indicates that editing human genes to make HIV-resistant T cells would probably be more effective than directly editing the virus. Some researchers aim to edit genes made by the immune cells that HIV usually infects — called T helper cells — so that the virus cannot find a way in. Others take a different tack: equipping the T cells with gene-editing tools so that they can seek and destroy any HIV that infects them.
When HIV infects a T cell, its genome is inserted into the cell’s DNA and hijacks its DNA-replicating machinery to churn out more copies of the virus. But a T cell equipped with a DNA-shearing enzyme called Cas9, together with customized pieces of RNA that guide the enzyme to a particular sequence in the HIV genome, could find, cut and cripple the invader’s genome.
This seemed to work when a team led by virologist Chen Liang, at McGill University in Montreal, Canada, infected T cells that had been given the tools to incapacitate HIV. But two weeks later, Liang’s group saw that the T cells were pumping out copies of virus particles that had escaped the CRISPR attack. DNA sequencing revealed that the virus had developed mutations very near the sequence that CRISPR’s Cas9 enzyme had been programmed to cut.
The team think that the problem can be surmounted, for instance by inactivating several essential HIV genes at once, or by using CRISPR in combination with HIV-attacking drugs. Gene-editing therapies that make T cells resistant to HIV invasion (by altering human, not viral, genes) would also be harder for the virus to overcome. A clinical trial is under way to test this approach using another gene-editing tool, zinc-finger nucleases.
source;Nature news

Thursday, April 7, 2016
VETERINARY OPHTHALMOLOGY.

ANTHRAX FOUND IN A PIG IN UKRAINE.

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