World Toilet Day 2024: Unclean Toilets Can Lead To UTI

Updated Nov 19, 2024 | 04:47 PM IST

SummaryThe UN also states that 3.5 billion people live without proper sanitation and many children also lose their lives due to poor sanitation and unsafe water. This is why World Toilet Day is observed to raise awareness on this issue.
World Toilet Day

Every year, World Toilet Day is observed to raise awareness about the global sanitation crisis and encourage action to solve it. The goal set by the United Nation is to achieve safe toilets for all by 2023, as a part of their Sustainable Development Goals.

The UN also states that 3.5 billion people live without proper sanitation and many children also lose their lives due to poor sanitation and unsafe water. This is why World Toilet Day is observed to raise awareness on this issue.

Theme

This year, the theme for World Toilet Day 2024 is "Toilets - A Place for Peace'. This focuses on the growing threat to sanitation that is caused by conflict, climate change, disaster and neglect. When there is a threat to using toilets, it can lead to many health risks.

Not using toilets for too long may lead to Urinary Tract Infection or UTI. For many who do not have access to clean toilets do not drink enough liquid or hold pee for too long. Doctors suggest that holding in pee for too long can cause bacteria to multiply and lead to UTI. By not drinking enough water, your bladder fails to tell the body to pee often, and can cause the bacteria to spread through the urinary tract, which can lead to infection.

Symptoms of UTI:

  • Burning or stinging feeling while urinating
  • Pain in pelvis or lower abdomen
  • Constant urge to empty the bladder
  • Strong or foul smelling urine
  • Consistently dark urine
  • Blood in urine

Holding in pee for too long can also cause your bladder to stretch, making it difficult or even impossible for the bladder to contract and release pee normally. It can also damage your pelvic floor muscles or could lead to kidney stones.

World Toilet Day History And Significance

To prevent such conditions, it is important that everyone has access to clean and safe toilets. In terms of history, the day was established in 2001, by the World Toilet Organization (WTO), which was founded by Jack Sim. However, it was officially recognised by the UN in 2013. The Government of Singapore worked with WTO to create the first UN resolution called Sanitation for All.

India too promotes safe and hygiene toilet through its Swachh Bharat Yojna.

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Severe COVID-19 Can Reactivate Dormant Viruses, May Fuel Long COVID Symptoms: Study

Updated Aug 6, 2026 | 01:00 PM IST

Summary The Nature study found that viral reactivation frequently occurred in people who were healthy before developing COVID-19. It led to an increase inflammation, worsened tissue injury, and prolonged recovery.
Severe COVID-19 Can Reactivate Dormant Viruses, May Fuel Long COVID Symptoms: Study

Credit: iStock

A severe COVID-19 infection may awaken dormant viruses that remain hidden in the body for life, even in people with otherwise healthy immune systems, according to a study published in Nature.

The study, which analyzed more than 1,100 hospitalized COVID-19 patients, found that viral reactivation was common and may contribute to long COVID symptoms. Researchers said the findings suggest COVID-19 can disrupt the body's internal ecosystem of dormant viruses, creating a state they describe as "dysvirosis."

"This finding suggests that COVID-19 may not always act as a single viral infection and may disrupt the body's internal ecosystem of dormant viruses, creating a state of 'dysvirosis'," said lead author Cole Maguire from Dell Medical School at The University of Texas at Austin.

Which Dormant Viruses Were Reactivated?

Nearly half of the hospitalized patients had at least one dormant virus reactivate during their COVID-19 illness. The viruses identified included:

  • Epstein-Barr virus (EBV), which causes mononucleosis
  • Herpes family viruses
  • Enteroviruses
  • Cytomegalovirus (CMV)
  • Herpes simplex virus-1 (HSV-1)
  • Human herpesvirus-6 and -7 (HHV-6/7)
  • Anelloviridae, a lesser-known family of chronic viruses

Also read: Lab Leak 'More Likely' Origin of COVID-19, Says Former Biden Adviser Dr. Ashish Jha

How Viral Reactivation Affects The Body

The researchers found that viral reactivation was more common in patients with severe COVID-19 and those who had longer hospital stays, and caused:

  • Increase inflammation
  • Worsened tissue injury
  • Prolonged recovery

The study also noted that these viruses have previously been linked to autoimmune conditions such as multiple sclerosis and lupus.

Further, the study found that dormant viruses do not reactivate simultaneously after SARS-CoV-2 infection.

  • Epstein-Barr virus and anelloviruses tended to reactivate early, shortly after hospital admission.
  • Cytomegalovirus and herpes simplex viruses generally emerged around three weeks later, primarily in the respiratory system.

Not Limited to People With Weak Immune Systems

Earlier research had mainly observed viral reactivation in people with weakened immune systems. However, this study found that reactivation frequently occurred in people who were healthy before developing COVID-19.

According to the researchers, this suggests viral reactivation may be more common than previously believed and could contribute to worse outcomes even in otherwise healthy individuals.

How Are the Dormant Viruses Linked to Long COVID?

Read More: Can Long COVID Be Prevented Before It Starts? Study Suggests Early Paxlovid May Help

While the study does not prove that viral reactivation causes long COVID, it provides strong evidence that dormant viruses may contribute to the condition.

Researchers found that Anelloviridae appeared more frequently in patients with long COVID who experienced persistent fatigue and reduced physical function.

"Our findings have important implications for patient care. Tests already exist for several of the chronic viruses studied, and some viruses in the herpes family can be treated with existing antiviral drugs," said study principal investigator Melamed, assistant professor of neurology at Dell Medical School.

"The next step is determining whether identifying and treating reactivated viruses can improve outcomes for patients with acute COVID-19 and long COVID."

The study may also influence future treatment strategies. Researchers noted that, instead of targeting only SARS-CoV-2, clinicians may eventually be able to use existing antiviral drugs against reactivated viruses, particularly herpesviruses.

A Phase II clinical trial is already underway to evaluate antiviral therapies targeting herpesviruses in people with long COVID.

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FDA Approves Moderna's First mRNA Flu Vaccine, Marking A Milestone In Influenza Prevention

Updated Aug 6, 2026 | 12:00 PM IST

SummaryThe US Food and Drug Administration (FDA) has approved the first mRNA-based seasonal influenza vaccine manufactured by pharma giant Moderna.
FDA Approves Moderna's First mRNA Flu Vaccine, Marking A Milestone In Influenza Prevention

Credit: AI

In a landmark decision, the US Food and Drug Administration (FDA) has approved Moderna's first mRNA-based seasonal influenza vaccine.

This makes it the first flu shot developed on messenger RNA (mRNA) technology to receive clearance in the United States.

The vaccine, branded mFlusiva, has been approved for adults over the age of 50 and older, paving the way for a new generation of influenza vaccines beyond the traditional egg-based approach.

Who Is Eligible To Receive The Vaccine?

The approval has given Moderna commercial drug built on the mRNA platform that powered its COVID-19 vaccine. The development is expected to strengthen the company's efforts to grow its respiratory vaccine portfolio.

According to the FDA, the following groups of people are eligible to receive mFlusiva:

  • Traditional approval for adults aged 50 to 64 years.
  • Accelerated approval for adults aged 65 years and older, requiring Moderna to conduct additional studies to confirm the vaccine's benefit in this age group.

Also read: Ebola Outbreak: Moderna Begins First Human Trial Of Bundibugyo Vaccine As Cases Rise to 3,748

What Did The Trial Show?

The approval was based on a late-stage clinical trial involving more than 40,000 adults aged 50 years and above. According to trial results, mFlusiva was:

  • 26.6% more effective than a licensed standard-dose flu vaccine in preventing influenza.
  • It also produced stronger immune responses than Sanofi's high-dose flu vaccine in adults aged 65 years and older, although Moderna will now need to verify whether this translates into better real-world protection for seniors.

Commenting on the approval, Moderna said, "Flu remains a significant public health challenge, and mFlusiva provides an important new option for America's seniors."

Earlier this year, Moderna CEO Stéphane Bancel had expressed confidence that the vaccine could become available ahead of the 2026-27 flu season if approved by regulators.

Also read: Protective Antibodies Fade After COVID-19 Vaccination- Should You Get A Booster Shot?

Why mRNA Could Revolutionise Flu Vaccination?

Unlike traditional flu vaccines, which are developed using viruses grown in chicken eggs, mRNA vaccines work by transmitting genetic instructions that alert the body's cells to produce harmless influenza proteins for an immune response.

Traditional flu vaccines must be designed and manufactured months before the flu season begins, requiring scientists to predict which influenza strains will circulate. If the circulating viruses keep evolving differently, the effectiveness of the vaccine can decline.

mRNA technology has a major advantage because it can potentially be updated and manufactured much faster, allowing vaccines to better match the strains that are spreading during a particular season.

In February 2026, the FDA initially declined to review Moderna's application, citing concerns that the company had compared its vaccine against a standard-dose flu shot rather than the high-dose vaccine commonly recommended for older adults.

After discussions with regulators, Moderna revised its submission, and the FDA agreed to proceed with the review under a condition that included additional studies for older patients.

Experts say the FDA's decision represents more than the approval of a single vaccine. It marks the first regulatory endorsement of mRNA technology for seasonal influenza, a milestone that could accelerate the development of next-generation vaccines against various infectious diseases.

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Salmonella Outbreak in US Linked to Jalapeños; Cases Climb to Nearly 350: How to Stay Safe

Updated Aug 6, 2026 | 10:57 AM IST

SummaryThe US Centers for Disease Control and Prevention (CDC) has urged businesses to check their inventory for recalled jalapeño peppers and stop selling or serving them.
Salmonella Outbreak in US Linked to Jalapeños; Cases Climb to Nearly 350: How to Stay Safe

Credit: iStock

Even as the US battles a Cyclospora outbreak that has caused two deaths and thousands of illnesses, the country is now grappling with a multistate Salmonella outbreak linked to Mexican jalapeño peppers.

The outbreak has sickened 345 people across 27 states and hospitalized 36, prompting recalls and renewed concerns over food safety. The US Centers for Disease Control and Prevention (CDC) has urged businesses to check their inventory for recalled jalapeño peppers and stop selling or serving them.

Outbreak Linked to Jalapeños from Mexico

The US Food and Drug Administration (FDA) and CDC, along with state and local partners, are investigating a multistate outbreak of Salmonella Javiana infections linked to jalapeño peppers grown in Sinaloa, Mexico, and distributed by Coast Citrus Distributors to distributors, restaurants, and food service companies, including Mexican-style restaurants across the US.

According to the CDC, illnesses began between June 19 and July 20. Of the 191 people interviewed, 177 (93%) reported eating at a Mexican-style restaurant before becoming ill, including Chipotle Mexican Grill and QDOBA, with meal dates ranging from June 14 to July 14.

Source Identified, Restaurants Take Action

The CDC said epidemiological and traceback investigations identified jalapeño peppers from Sinaloa, Mexico, distributed by Coast Citrus Distributors, as the source of the outbreak.

After being notified, Chipotle Mexican Grill and QDOBA stopped serving the affected jalapeño peppers. The CDC and FDA said there is no ongoing risk to consumers at these establishments, as the products have been removed.

Coast Citrus Distributors has also agreed to recall the affected jalapeño peppers.

The CDC estimates Salmonella cause about 1.35 million infections in the United States every year. Contaminated food is the source for most of these illnesses.

Recalled Product

  • Jalapeño peppers
  • Distributed by Coast Citrus Distributors
  • Grown in Sinaloa, Mexico

What Consumers Should Do

The recalled jalapeño peppers were primarily distributed to restaurants and wholesalers. Consumers should check with the place where they purchased or consumed jalapeños to confirm their source.

The FDA is investigating whether the affected peppers were also sold in grocery stores. If additional retail recalls are identified, the agency will announce them on its recalls page.

If you have recalled jalapeño peppers at home, do not eat them.

Symptoms of Salmonella Infection

Salmonella illness usually develops 12 to 72 hours after consuming contaminated food and typically lasts four to seven days.

Common symptoms include:

Diarrhea

Fever

Abdominal cramps

Children under 5 years, older adults, and people with weakened immune systems are at greater risk of developing severe illness.

When to Seek Medical Care

Contact a healthcare provider if you experience:

Diarrhea with a fever higher than 102°F

Diarrhea lasting more than three days without improvement

Bloody diarrhea

Vomiting that prevents you from keeping liquids down

Signs of dehydration, including:

Urinating less than usual

Dry mouth and throat

Dizziness when standing

Advice for Businesses

  • The health officials also advised businesses to:
  • Stop selling or serving recalled jalapeño peppers.
  • Wash and sanitize all items and surfaces that may have come into contact with the recalled product.
  • Follow the FDA's advisory for additional guidance.

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