Archive for the ‘research’ Category

What Makes Ticks Tick: Researcher Studies Their Every Move

https://www.lymedisease.org/what-makes-ticks-tick/

What makes ticks tick: researcher studies their every move

Systemic Bartonellosis Manifesting With Endocarditis and Membranoproliferative Glomerulonephritis

https://pubmed.ncbi.nlm.nih.gov/33155512/

Systemic Bartonellosis Manifesting With Endocarditis and Membranoproliferative Glomerulonephritis

Free PMC article

Abstract

Cat scratch disease caused by Bartonella species is mostly benign and self-limiting condition. Systemic infection is uncommon in immunocompetent host. We describe the case of a 66-year-old male who presented with sudden painless left eye blindness and brown-colored urine. Laboratory findings revealed progressively rising serum creatinine in association with nephrotic-range proteinuria at 7 g/day and glomerular hematuria on urinalysis. An echocardiogram demonstrated mitral and tricuspid valve vegetations despite multiple negative blood cultures. The left eye blindness was attributed to retinal artery occlusion from septic valvular embolus. Kidney biopsy showed membranoproliferative glomerulonephritis pattern of injury with “full house” pattern on immunofluorescent staining with subendothelial deposits on electron microscopy. Markedly elevated IgG (immunoglobulin G) titers for B henselae and B quintana were discovered. The patient had several cats at home. Kidney failure rapidly progressed to require hemodialysis. Once the diagnosis of systemic bartonellosis was confirmed, doxycycline (for 4 months) with rifampicin (for 3 months) were initiated. Repeat echocardiogram in 4 months demonstrated a resolution of valvular vegetations; however, the left eye blindness was permanent. In the present case the correct diagnosis of systemic bartonellosis allowed institution of appropriate antibiotic therapy and to also achieve a partial recovery of renal function and to discontinue hemodialysis.

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**Comment**

I must object to Bartonella being “mostly benign and self-limiting.”  Anyone who has ever had this beast will agree.  It’s not fun and it’s very tenacious.  I could rattle off over 20 cases of systemic infection with Bartonella in immunocompetent patients – some quite severe.

Researchers need to cease and desist from stating prevalence when testing for all tick-borne infections is abysmal – missing thousands of infected patients.  Since these patients are not being diagnosed, they aren’t counted – which means nobody has a clue on how many are infected.  Researchers can state there are limited recorded cases in the literature, but that is a far cry from reality.  They need to refrain from diminishing this any longer.  It’s almost becoming humorous – if it wasn’t so devastating.

For more:  

Monitoring Roadkill for Borrelia Genospecies

https://pubmed.ncbi.nlm.nih.gov/33266311/

Hedgehogs, Squirrels, and Blackbirds as Sentinel Hosts for Active Surveillance of Borrelia miyamotoi and Borrelia burgdorferi Complex in Urban and Rural Environments

Affiliations expand

PMID: 33266311DOI: 10.3390/microorganisms8121908

Free article

Abstract

Lyme borreliosis (LB), caused by spirochetes of the Borrelia burgdorferi sensu lato (s.l.) complex, is one of the most common vector-borne zoonotic diseases in Europe. Knowledge about the enzootic circulation of Borrelia pathogens between ticks and their vertebrate hosts is epidemiologically important and enables assessment of the health risk for the human population. In our project, we focused on the following vertebrate species:

  • European hedgehog (Erinaceus europaeus)
  • Northern white-breasted hedgehog (E. roumanicus)
  • Eurasian red squirrel (Sciurus vulgaris)
  • Common blackbird (Turdus merula).

The cadavers of accidentally killed animals used in this study constitute an available source of biological material, and we have confirmed its potential for wide monitoring of B. burgdorferi s.l. presence and genospecies diversity in the urban environment.

High infection rates were observed in all four target host species; mixed infections by several genospecies were detected on the level of individuals, as well as in particular tissue samples.
  • 90% for E. erinaceus
  • 73% for E. roumanicus
  • 91% for S. vulgaris
  • 68% for T. merula

These findings show the usefulness of multiple tissue sampling as tool for revealing the occurrence of several genospecies within one animal and the risk of missing particular B. burgdorferi s.l. genospecies when looking in one organ alone.

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**Comment**

You have to admire their tenacity!

And this needs to be done on human autopsies!  The high infection rates aren’t surprising because they are looking in multiple tissues.  This should be shared widely as a reason why human patients are not getting the attention they deserve.

This doctor shows how Lyme is in tissues and doesn’t hang out long in the blood:  https://madisonarealymesupportgroup.com/2020/12/15/lyme-disease-is-a-small-vessel-disease-dr-klemann/  This is why serology testing and short-term treatments don’t work.

The Desperate Need for an Accurate Lyme Disease Test

https://www.linkedin.com/pulse/desperate-need-accurate-lyme-disease-test-rosie-milsom/

The desperate need for an accurate Lyme disease test

1607078449009Stephen Bullough before and after Lyme disease

Rosie Milsom

Fundraising & Comms Manager | Helping charities to diversify and increase their income, engage with their supporters, and make a difference

Yesterday, as part of our Big Give Christmas Challenge, we got a very strong reaction and boost to the campaign when we shared the story of Stephen Bullough. I’d like to share that with you now, and the best way is within an article because it’s too long to fit into a LinkedIn post.

His story helps demonstrate the importance of having an accurate test available on the NHS – and a better understanding of the disease from the medical profession.

An 8th Dan in karate and World, European and British champion, Stephen fell ill 2016 after recalling rash in 2015. He had neurological symptoms including seizures, and later vision problems.

He saw several consultants, but no one joined up the dots between the symptoms, and he was diagnosed with Functional Neurological Disorder (FND).

Feeling failed by the NHS, Stephen’s wife Angela began doing her own research and sent his bloods to a lab in Europe, which showed positive for Lyme. Tests done on the NHS had returned as negative.

The positive test was dismissed by Stephen’s neurologist, who said not wanting to believe he had FND was another symptom of the illness.

In 2018, Stephen suffered a series of seizures that resulted in him losing his sight and use of his legs. Still, he got no treatment.

He was certified as blind by a top local ophthalmologist, but again his neurology consultants didn’t accept this as true.

On Father’s Day this year, Stephen was blue lighted to hospital with a Glasgow Coma Scale 3 after series of back to back seizures. He was referred to ICU, but once in ward a doctor refused to treat him, saying that his medical notes suggested the seizures were fake. Luckily, a nurse’s son had epilepsy. She recognised the seizures and subsequently reported the doctor.

Stephen now has severe issues with his heart and nervous system, and is unlikely to ever walk again. He needs round the clock care.

After a recent stay in hospital, a community response doctor was sent to visit Stephen at his home. He happened to be a member of Global Lyme Alliance and listened to Angela’s story in shock.

He consequently carried out a thorough examination, confirming that Stephen has late stage Lyme with secondary and extensive damage to the central nervous system.

He is now on extensive medication and vitamins to help manage his condition.

Angela says:

“To say we’ve been living through four years of hell is an understatement.  If there was a more accurate test on the NHS, we could have gotten Stephen diagnosed and treated more quickly. Now, our lives have been devastated by this illness, and the stress has impacted my health too.”

At the time of writing this, we’re just £138 away from our Big Give Christmas Challenge target. Funds raised are going towards our Innovation Fund for Lyme disease, which will see us give grants to research projects which aim to find a truly accurate test and effective treatments for Lyme disease.

The campaign is accepting donations until Tuesday 8th December at 12pm, but will only be doubled up to £6,000. If you’re moved to support us, please donate via the link below, or get in touch with me if you’d like to talk about other opportunities for support after this time.

Thank you

https://donate.thebiggive.org.uk/campaign/a051r00001fHSDfAAO

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**Comment**

While COVID testing is purposely designed to show mostly ALL positives, Lyme/MSIDS testing is designed to show nearly ALL negatives:

How Many “Negative” Lyme Tests Are Due to B. Miyamotoi?

https://www.lymedisease.org/lyme-sci-miyamotoi-or-lyme/

LYME SCI: How many “negative” Lyme tests are due to B. miyamotoi?

By Lonnie Marcum

July 20, 2020

 
 
Since Borrelia miyamotoi is not a reportable illness to the CDC, no one has any clue about prevalence but reports are coming in continually that it’s highly likely to be a much bigger problem than ‘authorities’ believe.
 
It was recently discovered that:

Also, Borrelia miyamotoi has been in California ticks for a long time:

https://madisonarealymesupportgroup.com/2018/02/15/b-miyamotoi-in-ca-ticks-for-a-long-time/

The following case shows how you can become infected while traveling:  https://madisonarealymesupportgroup.com/2020/10/24/a-case-of-borrelia-miyamotoi/

For more:  https://madisonarealymesupportgroup.com/2020/11/18/what-you-need-to-know-about-borrelia-miyamotoi/

https://madisonarealymesupportgroup.com/2020/06/17/borrelia-miyamotoi-infection-in-a-highly-endemic-area-of-lyme-disease/