Going Viral: Gossip vs. Ebola

In the sci-fi movie I Am Number Four one of the characters states that "gossip spreads like Ebola." The point being made is that gossip spreads quickly and widely. Although this type of spread is definitely applicable to gossip, it's really a false analogy because Ebola, thankfully, doesn't spread like gossip. 

Ebola outbreaks, which can be explosive, do not sustain themselves. The highly lethal virus appears to spillover from its animal reservoir (probably bats) to apes, monkeys, antelopes, and humans for an unknown reason. Once in a human population, it often exploits lax care practices that expose caretakers--including healthcare personnel--to bodily fluids. In fact, once minimal infection control procedures are instituted, new infections cease.

Additionally, diseases which kill fast with severe symptoms can strictly delimit the ability of the virus to find new individuals to infect. The fact that one is basically confined to a bed with Ebola coupled to the fact that Ebola transmission is via bodily fluids, provides little opportunity to spread the virus beyond close contacts.

Understanding the cycle of why Ebola outbreaks is the subject of some fascinating research (see Spillover) but, barring some mutations, gossip is more viral than the Ebola virus.

Is that Justinian's Plague Caught in-between Your Teeth?

Justinian's Plague, long thought to be the result of infection with Yersinia pestis, was responsible for killing approximately 50 million individuals in 541. Justinian's plague represented the 1st pandemic of plague and was followed about 800 years later by the more famous 2nd plague pandemic, The Black Death. 

In 576, about 35 years following this outbreak, the Roman Empire fell and some historians credit the plague's decimation of the population with weakening the already ailing Empire to the point where it was unable to fend off barbarian attacks (see Justinian's Flea). 

Using a remnant of a tooth found in a burial pit in Germany that dates from the time of Justinian, a research team was able to extract the DNA of the plague bacillus from dental pulp confirming that Y.pestis indeed was the culprit organism. 

It's interesting to imagine what the fate of the world would have been had this plague not occurred. I tend to think that the Roman Empire was already on a death spiral and the plague may only have served to hasten its fall.

Epidemics and their impact on history are a fascinating topic and one of the reasons the subject provides endless enjoyment for me. 

 

How's Your Microbiome?

Increasingly, awareness of a person's microbiome--the total population of bacteria that live within an individual, and their genetic material--has shaped how disease is approached. Not only are treatments that disrupt the microbiome beginning to be viewed as harmful, but also the idea that one's microbiome can be associated with specific conditions.

In the January issue of the Mayo Clinic Proceedings, an excellent review article provides a concise summary of the role of the microbiome in clinical diseases including:

  • Clostridium difficile: probably the most paradigmatic example of microbiome alteration
  • Irritable Bowel Syndrome
  • Inflammatory Bowel Disease
  • Obesity: a really fascinating phenomenon that will definitely be the focus of more research
  • Allergic Disease
  • Neuropsychiatric Diseases

The fact that in a human body the number of bacterial cells outnumber human cells (by a factor of 10) is impressive and will condition the current and future treatment of infectious diseases (as well as other illnesses).

Measles Made the Dark Ages Darker

Today, at the ASM Biodefense and Emerging Diseases Research Meeting I am attending, a speaker mentioned that measles first jumped into the human species about 1100 years ago, derived from the recently eradicated animal disease rinderpest.

While these facts weren't new to me, it prompted me to think about measles in the context of human history.

When measles made its zoonotic jump into the human species, life was harsh in the Western World.  The Roman Empire had fallen 400 years earlier and the Dark Ages followed. Roman Emperor Charlemagne's brief attempt at reunification of Europe had just failed with the partition of Europe into 3 distinct domains for each of his grandsons plunging Europe back into the dark for several hundred years more.

In this era, measles must have killed at a harrowing pace. 

It was only in the 1960s that the brilliant and legendary Nobel Prize winner John Enders developed the measles vaccine.

Today, thanks to Dr. Enders, life is lived generally free of the threat of measles. In fact, measles is one of the candidate diseases for eradication. However, Dr. Enders' heroic work may be for naught if suboptimal vaccination rates, linked to unwarranted fear of vaccines, allow this killer to again roam wild as it first did in the Dark Ages. 

Post-Lyme Syndrome: The Result of Altered Immunity, not Chronic Infection

One of the controversies in infectious diseases surrounds Lyme Disease. There is a large group of patients who, once adequately treated for the infection, continue to experience symptoms such as chronic pains, malaise, and related complaints. 

Although patients--and some clinicians--attribute this to ongoing replication of Borrelia burgdorferi, there is no evidence that a chronic form of infection amenable to antimicrobial therapy exists. A recent paper has shown that some Borrelia antigens may persist in a mouse model, but that does not mean long term antimicrobial therapy is warranted or beneficial in humans. The IDSA guidelines, which unfortunately continue to spark controversy, reflect this position.

Many infectious disease physicians believe that post-Lyme symptoms are the result of the specific immune constitution of individuals and, as such, prolonged antimicrobial therapy offers no benefit as clinical trials have shown.

A recent study, published in Clinical Infectious Diseases, attempted to assess if there are  immune differences in those that experience chronic Lyme symptoms. One of the fascinating results of this study was that, even prior to treatment, those that develop chronic Lyme symptoms have an altered polarity of their immune system when compared to those who suffer no chronic symptoms. Specifically, elevations of IL-23, a molecule which promotes the proliferation of Th 17 T cells, a specific class of immune cell linked to the development of autoimmune phenomena, were found to be associated with the development of chronic Lyme symptoms. One caveat: the study was conducted in Europe where B.afzelii is the culprit bacteria, which may limit its generalizability to the US setting.

The importance of this study is that it will, hopefully, dissuade those who demand chronic antimicrobial therapy from such requests while, at the same time, point the way towards fruitful areas of research that may yield effective treatment.