Neisseria gonorrhoeae is treated with a combination of drugs because the organism is resistant to many, including penicillin and fluoroquinolones.
Gonorrhoeae is a contender to produce an incurable illness due to the development or acquisition of resistance mechanisms for sulfonamides, penicillins, tetracyclines, ciprofloxacin, and more recently azithromycin and ceftriaxone during the past 80 years.
The Neisseria gonorrhoeae bacteria is the source of the sexually transmitted illness (STD) known as gonorrhea. The urethra in both men and women as well as the cervix, uterus, and fallopian tubes in women are all affected by N. gonorrhoeae infection.
Penicillin is the first drug that has been shown to be effective against syphilis and gonorrhea. However, compared to the dosage required to treat syphilis, which is often approximately 1,000,000 units, the drug used to treat gonorrhea is frequently administered in doses of just around 100,000 units.
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Answer:
The water-soluble vitamins comprises all the 8 B vitamins and vitamin C. When one consumes these vitamins, they get dissolved in water and then get mediated to various parts of the body via bloodstream. The body utilizes the vitamins it requires, and then the extra vitamin if got consumed is eliminated from the body via urine.
As the water-soluble vitamins are excreted time to time, one requires to meet the needs for water-soluble vitamins each day. The fat-soluble vitamins are vitamins A, E, D and K. When one consumes fat-soluble vitamins, they get dissolved in fat prior to getting mediated via the bloodstream.
The body utilizes the required fat-soluble vitamins and then accumulates any extra vitamins in the liver. However, if one consumes huge concentrations of fat-soluble vitamins spontaneously, then one may develop a condition known as vitamin toxicity or hypervitaminosis. The condition can be chronic or acute.
Answer:
Examples include light, heat, radio waves, and X-rays.
X-rays are a form of electromagnetic radiation that can be used for
and therapeutic purposes.
Explanation:
Answer:
Excess cholesterol and a lack of ATP inhibit the activity of HMG-CoA reductase in the liver to decrease cholesterol synthesis