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Drug-resistant bacterial infections kill 1m people annually – WHO

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The World Health Organisation (WHO) says drug-resistant bacterial infections kill about one million people globally every year, calling for coordinated action across human, animal, food and environmental sectors to curb the growing threat.

Jean-Pierre Nyemazi, Acting Director of the AMR Department at WHO Headquarters, said this at a virtual media conference marking an exhibition at the European Parliament on AMR and its human impact.

The virtual conference preceded the exhibition, “AMR: The Human Stories Behind a Silent Pandemic,” being held at the European Parliament from 28 September to 2 October and featuring stories of people affected by AMR across Europe.

“AMR is taking many lives. One million people die every year due to drug-resistant bacteria alone – that is, two people every minute die of bacterial AMR,” Mr Nyemazi said.

He said the scale of deaths meant that AMR should no longer be treated as a “silent pandemic”, stressing that “we know what works” to prevent and control the threat.

“Preventing infections is the number one priority. This can be done through better vaccination, infection prevention and control, Water, Sanitation and Hygiene (WASH), and improved animal husbandry,” he said.

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“All of these work and can prevent AMR.”

Mr Nyemazi said strengthening surveillance, responsible use of antimicrobials, access to quality medicines and diagnostics, and reduction of environmental contamination could also make a difference.

“The tools exist, and the evidence is there, but the cost of inaction is rising. The longer we delay action, the higher the cost becomes,” he said.

He said the One Health approach, which recognises the links between human, animal, plant and environmental health, was essential because drug-resistant pathogens could move across sectors and borders.

According to him, parliamentarians have a critical role in ensuring that national AMR commitments are supported by legislation, financing and accountability.

“The media also plays an indispensable role. Journalists help bring AMR out of scientific circles and into public debate,” he said.

“They raise awareness, combat misinformation, and ensure that AMR remains visible to decision-makers and the public alike.”

He said WHO Member States approved an updated Global Action Plan on AMR at the World Health Assembly in May, providing a framework for combating AMR over the next 10 years through a One Health approach.

Mr Nyemazi said the updated plan placed stronger emphasis on prevention, governance, behavioural change and measurable targets, and that the four Quadripartite organisations developed it jointly.

He said the organisations comprised the Food and Agriculture Organisation (FAO), United Nations Environment Programme (UNEP), WHO and World Organisation for Animal Health (WOAH).

“What is new about the updated Global Action Plan on AMR for the next 10 years is that it is truly multi-sectoral – a genuine One Health plan.

“The previous plan was heavily focused on human health; this time the four Quadripartite organisations worked together and engaged all sectors,” he said.

Mr Nyemazi said a 10 per cent reduction in AMR was achievable through infection prevention and control, vaccination and improved access to quality antimicrobials, with better coordination, education and surveillance capable of delivering further gains.

He also called for investment in new antibiotics, antifungals, phage therapy and other technologies, while stressing the need to preserve existing medicines.

He said there was also a major access problem, with many regions unable to obtain even existing antibiotics.

A member of the European Parliament, Martin Häusling, said excessive antibiotic use in food-producing animals was contributing to the problem, particularly through mass treatment.

“When it comes to food-producing animals, we still use far too many last-resort antibiotics, and we must get away from that,” Mr Häusling said.

He said AMR was a global issue that could affect anyone, adding that it could destroy families and livelihoods.

To tackle it, the parliamentarian said it was important to create public awareness so that parliaments could address the issue properly, adding that the issue was still not taken as seriously as a future challenge should be.

Rob Purdie, an AMR survivor and member of the WHO Task Force of AMR Survivors, said his experience demonstrated the consequences of delayed diagnosis and treatment.

Mr Purdie said an infection that began with a headache eventually progressed to fungal meningitis after he received antibiotics for a condition that had not been properly diagnosed.

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He said he eventually spent about $250,000 on hospital costs and had been unable to work for about five years.

“My ability to earn a living was eliminated for about five years in a single-income household where I provided for my wife and two children,” he said.

Mr Purdie said his experience underscored the need to keep AMR visible in public discussions.

“That is why it is so important for those of us who have survived and can speak, to remove the word ‘silent’ from the ‘silent pandemic’,” he said.

(NAN)


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Health

France reports first human case of Shamonda virus as patient dies

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France has reported the world’s first documented human infection with Shamonda virus (Shav) in a patient with a severely weakened immune system who died in early October.

According to a BBC report, French health authorities said it was an “exceptional case in a severely immunocompromised patient” and there was currently no risk to the public.

Shav is a disease that primarily affects cattle and can be spread by infected midges. Cases have also occurred in sheep, goats, alpacas and horses, but infections in people were previously unheard of.

The World Health Organisation (WHO) and European Centre for Disease Prevention and Control (ECDC) said they were monitoring the situation, with French officials still investigating how the virus had spread to a human.

In a post on his official X account, WHO Director-General, Tedros Ghebreyesus, said the agency was working with French authorities to establish the source of the infection, possible routes of transmission and any potential public health risks.

Mr Ghebreyesus said the French patient was in an area where the Shamonda virus was circulating in animals and where Culicoides midges were also present.

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“WHO is in contact with French authorities who are collecting information to better understand the source of infection in the first human patient, possible routes of transmission and any potential risk to public health,” he said.

What is Shamonda virus?

Shamonda virus primarily affects animals, particularly cattle, and spreads between animals through the bites of infected Culicoides midges, small biting insects. It has also been detected in sheep, goats and horses.

The virus was first identified in Nigeria in the 1960s and has circulated in parts of Africa and Asia for decades without any previously documented human infection.

French authorities believe the patient may have contracted the virus through a midge bite in eastern France, where infections had been detected in animals during the spring and summer.

The patient was receiving treatment for a ‘serious’ illness at a hospital in Lyon when he/she developed neurological complications that preliminary findings suggested were very likely linked to the virus.

Investigations are continuing to determine how the infection occurred and whether the virus contributed to the patient’s death.

Emerging disease concerns

The development comes amid international attention to other infectious disease threats this year, including hantavirus and Ebola.

Hantavirus is a group of viruses primarily transmitted to humans through contact with infected rodents or their urine, droppings and saliva. Depending on the strain, infection can cause severe respiratory illness or affect the kidneys.

In May, a cluster of hantavirus infections linked to a cruise ship prompted an international response after three people died among 13 reported cases. The outbreak was declared over in July.

Ebola, meanwhile, causes a severe illness that can include fever, vomiting, diarrhoea and, in some cases, internal or external bleeding. The disease spreads through direct contact with the blood or other bodily fluids of infected people and contaminated materials.

Nigeria confirmed an imported case of Ebola caused by the Bundibugyo virus in the Federal Capital Territory on 20 October, following an outbreak that began in the Democratic Republic of the Congo (DRC) and spread to other countries.

The WHO has said the Shamonda virus case appears isolated based on current evidence, although investigations into how the patient became infected and the potential public health implications are continuing.


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Africa CDC blames global neglect for lack of Bundibugyo Ebola vaccine

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The Africa Centres for Disease Control and Prevention (Africa CDC) has criticised the lack of investment in developing a vaccine against the Bundibugyo strain of Ebola, nearly two decades after the virus was first identified in Uganda.

The agency’s Director-General, Jean Kaseya, said the absence of an approved vaccine reflected the international community’s failure to prioritise diseases largely affecting African countries.

Speaking on Channels Television’s The Morning Brief on Thursday, Mr Kaseya argued that the situation would have been different if outbreaks of the disease had occurred in Western countries.

“If this outbreak was in Western countries, vaccines will already be available,” he said.

Mr Kaseya said the Bundibugyo virus was first identified 19 years ago and had caused three outbreaks, yet no vaccine had been approved specifically to prevent the disease.

He said the situation highlighted the need for African countries to invest in vaccine research, clinical trials and local manufacturing rather than depend almost entirely on international partners.

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Africa pushes for vaccine development

Mr Kaseya said Africa CDC was working with partners to advance research into vaccines against the Bundibugyo virus, including efforts involving an African manufacturer in Egypt.

He said the agency was also collaborating with the Democratic Republic of the Congo (DRC) and Uganda to explore possible research and emergency-use options involving existing Ebola vaccines.

One of the vaccines under consideration, Ervebo, is approved for preventing disease caused by the Ebola virus, formerly known as the Zaire strain. However, it is not approved for preventing disease caused by the Bundibugyo virus.

Mr Kaseya said the ongoing efforts were intended to strengthen Africa’s ability to respond to disease outbreaks without relying heavily on external support for vaccines and other essential medical products.

“We don’t want to see Africa left behind,” he said.

He maintained that Africa had the scientific expertise, skilled personnel and manufacturing potential needed to develop and produce vaccines, medicines and diagnostic tools.

Nigeria’s Ebola case

Mr Kaseya’s remarks come as Nigeria responds to its first confirmed case of Ebola virus disease, following an outbreak that began in the DRC in May.

As PREMIUM TIMES reported on Thursday, the confirmed patient is the wife of a diplomat who had travelled to Kampala, Uganda, before returning to Abuja. She developed symptoms shortly after her return and initially sought treatment for what was believed to be malaria before her infection was confirmed.

The Nigerian government said the patient is receiving medical care in isolation, while health authorities have identified 44 contacts for monitoring.

The case makes Nigeria the latest country affected by the cross-border spread of the disease.

The ongoing outbreak has also affected the DRC and Kenya, while Uganda previously recorded cases before declaring its outbreak over.

Greater control of vaccine production

Mr Kaseya said the response to the current outbreak should mark a turning point in how Africa prepares for and manages infectious disease emergencies.

He identified three priorities: expanding vaccine manufacturing on the continent, improving coordination among international partners and increasing domestic funding for public health responses.

According to him, 28 African countries had contributed funding to support the response, which he described as a significant demonstration of growing continental ownership of health emergencies.

He said African countries must continue to mobilise resources rather than depend almost entirely on international assistance when outbreaks occur.

Mr Kaseya also stressed that the organisation had a responsibility to protect the continent’s estimated 1.5 billion people across 55 countries, adding that its response to the Nigerian case was being coordinated with the country’s health authorities and international partners.

He said that the current outbreak should accelerate efforts to build a more self-reliant African health system, with stronger domestic financing and greater capacity to develop and produce essential medical supplies.

“After Ebola, Bundibugyo will not be like before Bundibugyo,” he said, expressing confidence that the continent’s approach to vaccine development and outbreak response would change.


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