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Bleeding Eye’ Virus Sparks Travel Warning and Worldwide Concern – What Is the Incurable Disease?

A mysterious and deadly virus has captured global attention, leaving health officials scrambling to contain its spread. Known as the Marburg virus, this rare yet devastating pathogen has been making headlines for its alarming symptoms and high fatality rates. Dubbed the “Bleeding Eyes Virus” due to its striking physical effects, it’s a disease that commands both fear and intrigue.
What makes this virus so dangerous? Where did it come from, and how does it spread? As outbreaks emerge in various corners of the world, understanding the threat becomes more urgent than ever.
The History and Origins of the Marburg Virus
The Marburg virus, a member of the Filoviridae family, was first identified in 1967 during simultaneous outbreaks in Marburg and Frankfurt, Germany, and Belgrade, Serbia. These outbreaks were linked to laboratory work involving African green monkeys (Cercopithecus aethiops) imported from Uganda.
The initial outbreak resulted in 31 infections and seven deaths, marking a significant medical event. The virus was named after the city of Marburg, where the first cases were identified.
Subsequent research identified fruit bats, particularly the Egyptian fruit bat (Rousettus aegyptiacus), as natural hosts of the Marburg virus. Transmission to humans can occur through prolonged exposure to environments inhabited by these bats, such as caves or mines.
Since its discovery, Marburg virus disease has caused several outbreaks with varying fatality rates, ranging from 24% to 88%, depending on virus strain and case management. Notable outbreaks have occurred in Angola, the Democratic Republic of the Congo, Kenya, South Africa, and Uganda.
The World Health Organization has identified Marburg virus disease as having pandemic potential, underscoring the importance of ongoing research and surveillance to prevent future outbreaks.
How the Marburg Virus Spreads

The Marburg virus, a member of the Filoviridae family, is notorious for its rapid transmission and high fatality rates. Understanding its transmission dynamics is crucial for effective prevention and control.
Primary Transmission: Animal to Human
Marburg virus is zoonotic, meaning it originates in animals and can be transmitted to humans. The primary reservoirs are fruit bats, particularly the Egyptian fruit bat (Rousettus aegyptiacus). Humans can contract the virus through prolonged exposure to environments inhabited by these bats, such as caves or mines. Additionally, contact with non-human primates, like African green monkeys, has been associated with transmission events.
Secondary Transmission: Human to Human
Once the virus infects a human, it can spread to others through direct contact with bodily fluids, including blood, saliva, sweat, urine, and vomit. Even minute amounts of these fluids can facilitate transmission.
Biology Insights Transmission can also occur via contact with surfaces and materials (e.g., bedding, clothing) contaminated with these fluids.
Additional Considerations
Healthcare workers are particularly vulnerable during outbreaks due to their close contact with patients and potential exposure to infectious materials. Proper use of personal protective equipment (PPE) is essential to mitigate this risk.
Notably, Marburg virus transmission via infected semen has been documented up to seven weeks after clinical recovery, indicating that sexual transmission is possible even after apparent recovery.
The virus can persist on surfaces contaminated with infectious fluids, leading to indirect transmission. Therefore, strict hygiene practices and disinfection protocols are vital in preventing the spread.
Global Impact and Recent Outbreaks
SSince its discovery in 1967, the Marburg virus has been responsible for multiple outbreaks, primarily in sub-Saharan Africa, with varying fatality rates. Its high mortality rate and potential for rapid spread have established it as a significant global health concern. Among the most notable outbreaks was the Angola epidemic of 2004-2005, which claimed 227 lives out of 252 cases, resulting in a staggering fatality rate of approximately 90%. Similarly, the Democratic Republic of the Congo experienced a severe outbreak between 1998 and 2000, with 154 cases and 128 deaths, equating to an 83% fatality rate. In Uganda, a 2012 outbreak was less severe, involving 15 cases and four deaths, with a fatality rate of 27%.
Recent years have seen the emergence of Marburg virus in new regions, underscoring its growing geographic spread. West Africa’s first outbreak occurred in Guinea in 2021, involving a single confirmed case that resulted in death but was swiftly contained. In July 2022, Ghana reported its first outbreak, with all three confirmed cases proving fatal. Tanzania experienced its first outbreak in March 2023, resulting in nine cases and six deaths before it was declared over in June 2023. More recently, Rwanda faced its first outbreak in September 2024, with 66 cases and 15 deaths. Thanks to swift containment measures, the outbreak was controlled by November 2024.
The rising frequency and spread of Marburg virus outbreaks have prompted a stronger global response. The World Health Organization (WHO) has classified Marburg virus disease as a priority pathogen, emphasizing its epidemic potential and the urgent need for specific treatments and vaccines. Efforts to develop vaccines and antiviral therapies are ongoing, as the international community works to strengthen surveillance, enhance preparedness, and mitigate the impact of future outbreaks.

Symptoms and Progression of the Disease
The disease progresses through distinct stages, with an incubation period ranging from 2 to 21 days. Symptoms begin abruptly with a sudden high fever, severe headache, profound malaise, and muscle aches. By the third day, gastrointestinal symptoms such as severe watery diarrhea, abdominal pain, cramping, nausea, and vomiting typically emerge, contributing to dehydration and weakness.
Between days 2 and 7, a non-itchy rash may appear, aiding clinical diagnosis. Around the fifth day, hemorrhagic symptoms often develop, marked by fresh blood in vomitus and feces, bleeding from the nose, gums, and vagina, and uncontrolled bleeding at venepuncture sites.
In advanced stages, patients may experience jaundice, pancreatitis, delirium, shock, and multi-organ dysfunction, with death often occurring between 8 and 9 days after symptom onset due to severe blood loss and shock. Early recognition and prompt medical intervention are critical for improving survival rates.
Preventive Measures and Risk Mitigation
Preventing the spread of Marburg virus disease (MVD) requires a comprehensive approach that integrates public health measures, personal protective actions, and community involvement.
- Avoid Contact with Fruit Bats and Other Wild Animals: Fruit bats, particularly the Egyptian fruit bat (Rousettus aegyptiacus), are natural reservoirs of the Marburg virus. Limiting exposure to these bats by avoiding caves and mines they inhabit can reduce transmission risks. Additionally, minimize contact with non-human primates and other wild animals that may carry the virus, and use protective equipment when handling animals.
- Practice Good Hygiene: Regular handwashing with soap and water or using alcohol-based hand sanitizers is essential, especially after contact with potentially contaminated surfaces. Avoid touching the eyes, nose, and mouth to prevent introducing the virus into the body.
- Use Protective Gear: Healthcare workers caring for patients with suspected or confirmed MVD should wear gloves, masks, gowns, and eye protection, adhering to strict infection control measures. Laboratory personnel handling MVD samples must work in biosafety level 4 facilities to ensure safety.
- Implement Safe Burial Practices: Traditional burial rites involving direct contact with deceased individuals can spread the virus. Promoting safe and culturally sensitive burial practices through community engagement can mitigate this risk.
- Ensure Safe Sexual Practices: Survivors of MVD should practice safer sex for at least 12 months from the onset of symptoms or until their semen tests negative for the virus twice, as the virus can persist in bodily fluids.
- Community Engagement and Education: Raising public awareness about MVD transmission, symptoms, and preventive measures is crucial. Educating healthcare workers on infection prevention and control protocols further reduces transmission risks.
- Surveillance and Contact Tracing: Effective surveillance systems help promptly detect new cases, while contact tracing identifies and monitors individuals exposed to infected persons to prevent further spread.
- Travel Advisories: Following travel advisories from health authorities and participating in health screenings at borders and airports are essential for controlling outbreaks in affected regions.

Current Challenges in Treatment and Research
Marburg virus disease (MVD) remains a formidable challenge in the realms of treatment and research, primarily due to its high fatality rate and the lack of approved vaccines or specific antiviral therapies. The World Health Organization underscores the reality that, so far, only supportive care is available to manage this deadly illness. Current treatments focus on symptom management and preventing complications. Maintaining hydration and electrolyte balance is critical for patients suffering from severe diarrhea and vomiting. Monitoring blood pressure and oxygen levels is essential to reduce the risk of shock and organ failure, while antibiotics or antifungal agents help prevent secondary infections in those with compromised immune systems.
Experimental therapies are also under investigation, though none have yet been approved. Antiviral agents such as Galidesivir and Favipiravir have shown potential in preclinical studies by targeting the viral RNA polymerase, thereby disrupting replication. Monoclonal antibodies, which mimic the immune system’s pathogen-fighting capabilities, have demonstrated promise when combined with drugs like remdesivir, effectively neutralizing the virus and halting its progression in advanced cases. RNA interference therapies, which use small RNA molecules to degrade viral RNA and inhibit protein synthesis, have also shown encouraging results in animal models.
Efforts to develop a vaccine are ongoing, with researchers exploring several approaches. Nucleic acid vaccines, including DNA and mRNA platforms encoding Marburg virus glycoproteins, have elicited immune responses in preclinical studies. Vector-based vaccines, which use viral vectors to deliver Marburg antigens, are also being tested for safety and effectiveness. However, these initiatives face significant hurdles. The sporadic nature of Marburg outbreaks limits the availability of clinical data, making it difficult to understand the disease’s progression or evaluate treatment efficacy fully. Ethical and logistical challenges also arise when conducting trials during outbreaks, particularly in ensuring informed consent and maintaining the integrity of studies in high-pressure settings. Additionally, the regions most affected by Marburg virus often lack the necessary healthcare infrastructure, complicating the implementation of advanced research and therapeutic interventions.
Recent efforts in Rwanda highlight the global commitment to tackling MVD. Following a recent outbreak, a vaccine trial was launched using 700 doses provided by the Sabin Vaccine Institute, prioritizing health workers, emergency responders, and individuals exposed to confirmed cases. Rwanda has also implemented strict isolation measures and is testing treatments like remdesivir and the monoclonal antibody MBP091 in clinical trials to control the outbreak. These measures underscore the importance of combining public health strategies with innovative research to mitigate the impact of this devastating disease.and contribute to the global understanding of MVD management.
A Collective Call to Action Against a Deadly Threat
The Marburg virus remains one of the most lethal and enigmatic pathogens in the world, with its recent outbreaks highlighting the critical importance of vigilance and preparedness. Understanding its history, symptoms, transmission, and the measures needed to mitigate its spread is not only a public health priority but also a shared global responsibility.
While significant strides are being made in research and experimental treatments, the lack of approved vaccines and antiviral therapies underscores the need for continued innovation and collaboration. In the face of such a formidable disease, awareness is our strongest defense.
By recognizing warning signs early and adhering to preventive measures, individuals and communities can play a vital role in curbing the impact of this deadly virus. Together, through education, research, and coordinated action, we can combat the Marburg virus and safeguard public health on a global scale.
