Antibiotic-loving bacteria don't just resist drugs, they get a kick out of them
Developing antibiotic resistance has been found to give the disease-causing bacterium E. coli an additional boost, making it grow faster and become fitter after repeated exposure the antibiotic doxycycline.
The mutations that give E. Coli resistance to doxycycline also made them reproduce faster and grow colonies three times larger than ordinary, non-resistant E. Coli. The research is published in the journal Nature Ecology and Evolution.
The researchers exposed E. Coli to eight rounds of antibiotics over four days. In that period, the bacteria gained a number of mutations. One of the mutations was linked to antibiotic resistance, giving the bacteria more pumps to remove the drug from the cell.
The second mutation was to delete a large section of its genome that is normally involved in helping the bacteria coat a surface by forming a 'biofilm'. This section of DNA is actually the remnants of a virus, which causes the cell to split and spill its contents, helping other cells to grow nearby to form a film.
The E. Coli in the study were grown in a liquid culture, in a similar environment to the human bloodstream. Here, without the need to form a biofilm, the E. Coli cut out this section of DNA – which makes up 4% of its genome – when exposed to doxycycline, allowing it to devote its energy to growing faster and forming larger colonies instead. Even when the exposure to doxycycline was stopped, the bacteria did not lose this newly-gained trait.
"We didn't anticipate the viral change at all," study author Robert Beardmore of the University of Exeter told IBTimes UK. "That was much stronger than the pump mutation in evolutionary terms. We saw more strength with selection and a faster change on quite a large chunk of the genome."
This property was not unique to doxycycline, and similar features were found in two different classes of antibiotics, Beardmore said. However, only certain strains of E. Coli gained these mutations when exposed to the antibiotic.
"It's not every antibiotic and it's not every E. Coli, and certainly not every bacterium. But it is pretty strange that that feature is there," Beardmore said. "There's something special about the way doxycycline is inhibiting the cell that causes these features."
Doxycycline is a broad-spectrum antibiotic used for a number of infections, such as chlamydia, Lyme disease, pneumonia and acne. It's also used as a preventative treatment for malaria, and can be taken for months for a trip to a country where the disease is prevalent. This widespread use means the antibiotic can be found in the environment, such as in rivers and soil.
If E. Coli is exposed to doxycycline in the environment, it could quickly develop the mutations to grow larger colonies as well as becoming resistant to the antibiotic, Beardmore said. However, he said that doxycycline should not be dropped as a treatment for various kinds of infection.
"Doxycycline may be a perfectly good drug to treat a range of bacteria with. But when E. Coli comes into contact with it in a river or field, if it's got the right kind of genome then you'll see these effects and doxycycline will boost the growth."
Source: http://www.ibtimes.co.uk/antibiotic-loving-bacteria-dont-just-resist-drugs-they-get-kick-out-them-1603881
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Friday, May 15, 2026
When Calcium Channel Blockers Like Diltiazem Are Used for Blood Pressure and Heart Rate
Calcium channel blockers form one of the primary drug classes in cardiovascular medicine, treating a range of conditions from hypertension to angina and certain heart rhythm disorders. Among them, diltiazem occupies a distinctive position because of its dual action on both vascular smooth muscle and cardiac conduction tissue, making it relevant in situations where blood pressure control and heart rate management are needed simultaneously. Calcium ions flowing into smooth muscle cells trigger vascular contraction. In cardiac conduction tissue, calcium movement drives the electrical activity that controls heart rate and rhythm. Calcium channel blockers interfere with calcium entry through specific channel types. Diltiazem is a non-dihydropyridine calcium channel blocker, a subclass that affects both vascular and cardiac tissue, unlike dihydropyridine agents like amlodipine that act primarily on blood vessels. In hypertension, diltiazem reduces blood pressure by relaxing arterial walls and decreasing peripheral vascular resistance. Blood flows more easily through relaxed vessels, requiring less cardiac force and resulting in lower pressure measurements. For patients with both elevated blood pressure and elevated resting heart rate or specific cardiac arrhythmias, diltiazem addresses both concerns simultaneously. Angina, the chest pain resulting from reduced oxygen delivery to heart muscle, is another key indication. Diltiazem relieves angina by two mechanisms. Arterial dilation reduces the workload the heart must perform to pump blood forward. Additionally, slowing the heart rate allows more time between beats for coronary blood flow to occur during the relaxation phase of the cardiac cycle. Certain arrhythmias, particularly atrial fibrillation and atrial flutter with rapid ventricular response, respond to diltiazem through its action on the atrioventricular node. By slowing conduction through the AV node, diltiazem reduces how many atrial electrical impulses reach the ventricles, bringing ventricular rate into a safer physiological range. Patient selection for diltiazem considers co-existing conditions carefully. Patients with significant systolic heart failure require caution because reducing heart rate and contractility in an already weakened heart can worsen cardiac output. Beta-blockers should not be combined with diltiazem without specialist guidance because both drugs slow AV nodal conduction, creating risk of excessive heart rate reduction. For patients whose provider recommends this medication, learning more about diltiazem for blood pressure management helps clarify what specific cardiovascular conditions it addresses and what distinguishes it from other antihypertensive options. Regular follow-up is important for patients on diltiazem to confirm blood pressure and heart rate targets are being met without excessive reduction. Symptom reporting, including any dizziness, unusual fatigue, or palpitations, provides important clinical information between appointments. For comprehensive guidance on calcium channel blocker therapy and blood pressure management approaches, reviewing blood pressure treatment and medication options supports informed medical conversations with the prescribing provider.
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