ދިވެހިބަހަކީ ދިވެހިންގެ އަމިއްލަވަންތަ މާދަރީބަސް
Engineers design plants using genetically modified organisms, or GMOs, to be tougher, more nutritious, or taste better. However, people have concerns over their safety, and there is much debate about the pros and cons of using GMOs.
A manufacturer creates GMOs by introducing genetic material, or DNA, from a different organism through a process called genetic engineering.
Most currently available GMO foods are plants, such as fruit and vegetables.
All foods from genetically engineered plants on sale in the United States are regulated by the Food and Drug Administration (FDA). They must meet the same safety requirements as traditional foods.
There is some controversy over the benefits and risks of GMO foods. In this article, we discuss the pros and cons of GMO crops, taking into account their potential effects on human health and the environment.
Genetic modification can make crops more resistant to diseases as they grow.
Manufacturers use genetic modification to give foods desirable traits. For example, they have designed two new varieties of apple that turn less brown when cut or bruised.
The reasoning usually involves making crops more resistant to diseases as they grow. Manufacturers also engineer produce to be more nutritious or tolerant of herbicides.
Crop protection is the main rationale behind this type of genetic modification. Plants that are more resistant to diseases spread by insects or viruses result in higher yields for farmers and a more attractive product.
Genetically modification can also increase nutritional value or enhance flavor.
All of these factors contribute to lower costs for the consumer. They can also ensure that more people have access to quality food.
Because genetically engineering foods is a relatively new practice, little is known about the long-term effects and safety.
There are many purported downsides, but the evidence varies, and the main health issues associated with GMO foods are hotly debated. Research is ongoing.
This section discusses the evidence for a range of drawbacks that people often associate with GMO foods.
Some people believe that GMO foods have more potential to trigger allergic reactions. This is because they may contain genes from an allergen — a food that prompts an allergic reaction.
The World Health Organization (WHO) discourage genetic engineers from using DNA from allergens unless they can prove that the gene itself does not cause the problem.
It is worth noting that there have been no reports of allergic effects of any GMO foods currently on the market.
Some researchers believe that eating GMO foods can contribute to the development of cancer. They argue that because the disease is caused by mutations in DNA, it is dangerous to introduce new genes into the body.
The American Cancer Society (ACS) have said that there is no evidence for this. However, they note that no evidence of harm is not the same as proof of safety and that reaching a conclusion will require more research.
There is concern that genetic modification, which can boost a crop’s resistance to disease or make it more tolerant to herbicides, could affect the ability of people to defend against illness.
There is a small chance that the genes in food can transfer to cells the body or bacteria in the gut. Some GMO plants contain genes that make them resistant to certain antibiotics. This resistance could pass on to humans.
There is growing concern globally that people are becoming increasingly resistant to antibiotics. There is a chance that GMO foods could be contributing to this crisis.
The WHO have said that the risk of gene transfer is low. As a precaution, however, it has set guidelines for the manufacturers of GMO foods.
Outcrossing refers to the risk of genes from certain GMO plants mixing with those of conventional crops.
There have been reports of low levels of GMO crops approved as animal feed or for industrial use being found in food meant for human consumption.
Manufacturers should clearly label GMO food if it is “materially different” to its conventional counterpart.
In the U.S., no regulations mandate that foods derived from GMOs are labeled. This is because these foods must meet the same safety standards that apply to all FDA-regulated products, and there should be no need for additional regulation.
The FDA have determined that a GMO food should be labeled as such if it is “materially different” to its conventional counterpart. For example:
a GMO canola oil with more lauric acid than traditional canola oil will be labeled “laurate canola oil”
a GMO soybean oil with more oleic acid than non-GMO soybean oil must be labeled “high-oleic soybean oil”
a GMO soybean oil with a high level of stearidonic acid, which does not naturally occur in the oil, must be labeled “stearidonate soybean oil”
The new National Bioengineered Food Disclosure Standard will come into force on January 1, 2020. Under the new rules, all foods containing genetically engineered ingredients will be labeled as “derived from bioengineering” or “bioengineered.”