https://articles.mercola.com/sites/articles/archive/2019/08/10/new-tick-species.aspx

This tick bites, clones itself and lays 2,000 eggs

Analysis by Dr. Joseph MercolaFact Checked
new tick species

STORY AT-A-GLANCE

  • The Asian longhorned tick, first found in the U.S. in 2010, is now established in 11 states along the East Coast. The female is capable of laying 2,000 eggs without mating and an infestation may kill livestock from the blood loss
  • While ticks are known vectors of disease, thus far this species has not transmitted disease in the U.S. It is known to carry thrombocytopenia syndrome virus triggering human hemorrhagic fever, responsible for killing 15% of those the tick bites in Asia
  • The number of ticks and range in which they live have been expanding dramatically. Tickborne illnesses include Lyme disease, infecting 300,000 each year in the U.S., Rocky Mountain spotted fever, babesiosis, Powassan virus and Bourbon virus
  • As Lyme disease rates skyrocket, it’s important to do a quick check each time you come back inside after being in a grassy area or near trees and bushes; Lyme disease may be successfully treated when caught early. Your risk of infection is lower if you effectively remove the tick as soon as possible

While you might have thought a tick is an insect, it really belongs to the arachnid family, along with spiders, scorpions and mites.1 A tick survives by feeding on the blood of a host, growing from the size of an apple seed before food and swelling to more than double their size after feeding.2

Ticks are more active during the summer months, between March and November in the northern hemisphere. Most enjoy living in warm moist places, such as bushes, tall grasses and shrubs. Animals and humans get ticks while walking through these areas.3

Of the 899 species of ticks found throughout the world, only 90 reside in the U.S.,4 and just a select few are known to bite humans.5 After a tick gets on you, it doesn’t usually bite right away but will crawl around to find an acceptable place to latch on and feed. They look for soft, moist areas, including near your ears, hair, underarms and groin. They also like to settle under the waistband of your pants.6

After piercing your skin with its mouth, the tick inserts a tube to feed on your blood until it’s full. This may take up to two weeks.7 Tick bites are often painless so it may be difficult to tell if you’ve been bitten.

First new tick species in US in 50 years

In the past decade the U.S. has become home to a new species, the Asian longhorn. Dr. Gregory Poland from the Mayo Clinic says this tick represents the first time in 50 years a new species has made its way to the U.S.8 Because it is an emerging threat in the U.S. the CDC recommends that surveillance should include testing for pathogens.9

Ticks are associated with diseases in humans and animals. The Asian longhorn tick is known to carry human hemorrhagic fever caused by thrombocytopenia syndrome virus10 in Asia.11 This species has been found in 11 states, including:12

Arkansas Connecticut Kentucky
Maryland North Carolina New Jersey
New York Pennsylvania Tennessee
Virginia West Virginia

However, while it appears to be spreading across the eastern U.S., the CDC has reported there is currently no evidence these ticks have transmitted disease to humans or animals.13 Asian longhorned ticks in Asia carry a virus responsible for killing 15% of those they bite.14

In recent years, this population has spread to several Pacific Islands, Australia and New Zealand. Although some experts warn against extrapolating information to the Asian longhorn tick carrying serious viruses in the U.S.,15 this species also represents additional dangers to livestock and other animals.16

North Carolina State veterinarian Dr. Doug Meckes sent out information17 reminding farmers and pet owners to be vigilant with preventive measures to avoid ticks in their animals. Five cows in Surry County, North Carolina, recently died due to acute anemia triggered by a tick infestation.18


Asian tick sounds like something from a horror film

Samples from the cows confirmed the ticks were Asian longhorn. According to Meckes, this was the fourth confirmed case since 2018 and the first in 2019.19 One young bull presented to the diagnostic lab for necropsy had 1,000 ticks. As described in this short video, the ticks are aggressive biters, feeding on both animals and humans.

The first identified case, in 2010, involved a white-tailed deer from West Virginia.20 In other reports the tick was found in New Jersey in 201721 when a woman discovered them on her sheep.22

The first recorded human bite was reported by a 66-year-old man from Yonkers, New York, in June 2018. He removed the tick from his leg and subsequently took it to the Lyme Disease Diagnostic Center in Westchester County for testing.23 After confirmation that it was the Asian longhorned tick, sampling was done near his home and nearby park, finding 90 ticks.24

A unique characteristic of this species is its ability to reproduce quickly and prolifically without mating.25 The female does not need a male to lay as many as 2,000 eggs at a time.26 The threat to livestock may be significant. A dairy cow may experience a 25% drop in milk production after becoming a host.27

As the species continues to multiply and spread, it is conceivable millions of animals could be exposed.28 A study published in the Journal of Medical Entomology29 developed a model demonstrating the wide area of North America where favorable conditions for the Asian longhorned tick may exist.30

Study author Ilia Rochlin, Ph.D., is a professor at Rutgers University. She believes the adaptability of this species means it has the potential to spread across the U.S. and southern Canada.31 The ability of the tick to reproduce without mating may make it extremely hard to control. Rochlin said,32 “In practice, it’s impossible to eradicate this species.”

Tick population rising, along with the diseases they carry

The number of all ticks and the range in which they live have both increased. According to the CDC,33the lone star tick has expanded from the southeastern U.S. into the northern and Midwestern states. The range of the black-legged tick, responsible for many cases of Lyme disease, has more than doubled in the past 20 years. Between 1993 and 2012, the number of counties in the U.S. at high risk for Lyme disease rose by more than 300%.34

Although the Asian longhorned does not yet carry disease, many other ticks do. The CDC announced it will begin monitoring the population and diseases ticks carry as the number of people diagnosed with diseases carried by ticks has more than doubled. Anna Perea, from the CDC’s Division of Vector-Borne Diseases, commented on the new monitoring:35

“For the first time this year, the CDC is funding states to conduct widespread surveillance of ticks and the pathogens they can transmit, in addition to funding human disease surveillance and education and prevention. Taken together, the data can help define areas where ticks are spreading, the infectious pathogens that they carry, and where risk of tick-borne disease is increasing.”

Tick-borne diseases may include Lyme disease, suspected to affect nearly 300,000 people each year.36 Rocky Mountain spotted fever, anaplasmosis, ehrlichiosis and babesiosis are also spread by ticks. New infections have also been detected, including the Bourbon virus, Heartland virus37 and Powassan virus.38 Ticks spread disease by virtue of the way they find nutrients.

In order to transition through life stages, ticks must have a blood meal to survive.39 Through the process of hatching from the egg, going through the larvae, nymph and adult stage, they may live up to three years. If unable to find a suitable host, they die.40 As they ingest blood, they also suck up any pathogens from the host and spread it to their next host.

Lyme disease rates skyrocketing

The rising number of ticks and their spreading habitat has meant an increase in the number diagnosed with tick-borne diseases. Lyme disease is the most prevalent of those conditions. CDC41data show that in 1997, there were 12,801 confirmed cases which more than doubled to 29,513 confirmed and 13,230 probable cases in 2017.

Data also show more males than females are affected, with the age group of 5 to 9 years having the greatest number affected. The disease is most frequently diagnosed in the months of June and July.42One study from researchers at Carnegie Mellon University43 called the rising epidemic of Lyme disease a “Ticking Bomb.”

These researchers found a relationship between rising temperatures and the incidence of Lyme disease, predicting the number of people diagnosed may rise by more than 20% by midcentury.44 In addition to temperature playing a role in the rising number of tickborne illnesses, researchers find smaller patches of forest may also increase the number of Lyme carrying ticks.

White-footed mice, also known to carry Lyme disease,45 are often the first blood meal for the larval tick.46 In smaller forest fragments measuring less than 5 acres, the mice are abundant because smaller areas of forest support fewer predators.47

Felicia Keesing from Bard College, New York, and other researchers have found an average of three times the number of ticks in a three-acre forest fragment than in larger areas. As many as 80% of the arachnids in the smallest patches were infected.48

Challenges of diagnosis and treatment for Lyme disease

Although the disease has been around for thousands of years, the medical community only began describing it in the 1970s. An autopsy of a 5,300-year-old mummy found the presence of the bacteria and a German physician first wrote about symptoms more than 130 years ago.49

Lyme disease is caused by a bacterium, which when left untreated may spread to the joints, heart and nervous system. The bacterium, Borrelia burgdorferi, may be treated successfully when found early.50 However, while commonly acknowledged now, Lyme disease has historically been a challenge to diagnose.

CNN reported51 on a U.S. Air Force enlisted man, Ruben Lee Sims, who was voted the “top enlisted management analyst of the year” in 1977. Only seven years later he was discharged and labeled a hypochondriac when the military was unable to diagnose Lyme disease. Misdiagnosed for more than three decades, he now shares his story to help others.

Early symptoms resemble the flu and the bullseye rash is not always recognized.52 Within 30 days of being bitten, you may experience fever, chills, fatigue and muscle and joint aches. Up to 80% of those infected will have a rash resembling a bull’s-eye target at the site of the tick bite, which gradually reaches 12 inches or more across.53

Later on, signs of infection may include severe headache and neck stiffness, a spreading rash on other areas of your body, severe arthritis pain and swelling, facial palsy, heart palpitations and possibly an irregular heartbeat.54 If left untreated, you may develop inflammation of the brain and spinal cord. This can lead to pain, numbness and tingling in the hands and feet as well as problems with short-term memory.55

Some people have seen multiple physicians and undergone a plethora of tests before being given a correct diagnosis.56 Early tests may not detect antibodies to the bacteria as it may take several weeks to rise to detectable levels.

Since early treatment is most effective57 some physicians begin treatment before offering a definitive diagnosis.58 The Lyme antibody test looks for exposure to the bacteria, but it may take your immune system several weeks to produce measurable levels. This can result in a false negative test with early testing.59

You’ve found a tick — now what?

Anytime you’re out in grassy areas or around trees and bushes do a quick skin check when you get back inside. Look for small brown to black spots or crawling, eight-legged arachnids. If the tick is unattached to your skin and has not fed, slip a sheet of paper under it and seal it in a container with alcohol.

However, if it’s become attached to your skin, it’s important to remove it to lower your risk of infection. While there are several tools on the market you may want to consider, a set of fine-tipped tweezers will also do the job. According to the CDC you should:60

  • Grasp the tick close to the skin’s surface.
  • Using steady and even pressure, pull the tick upward. Twisting or jerking may cause the mouth parts to remain in the skin. If the mouth parts are left behind, try to remove them with clean tweezers. If you are unable to remove them easily, allow the skin to heal.
  • Clean the area and your hands thoroughly with rubbing alcohol or soap and water.
  • Do not crush the tick as this forces blood and pathogens into your body.61

Avoid using techniques such as painting the tick with nail polish or covering it with petroleum jelly. This will not suffocate it. Likewise, poking it or using heat to make it detach are not recommended.62

Once a tick has been safely removed drop it in a sealed container with alcohol and take it to your health department or Lyme disease center for identification. Keep an eye on the area for the next several weeks. If you develop a rash or flu-like symptoms, see a doctor who’s experienced in treating Lyme disease.

_________________

**Comment**

A few points for consideration:

  1. While human infection from the Asian Long-horned tick has not been documented in the U.S., it may still be happening. Remember, in Asia, it causes illness that KILLS 15% of those whom contract it. Don’t take this lightly.
  2. These “new” diseases aren’t new and there are plenty more out there that aren’t even named yet. While authorities are collecting climate data, which is erroneous to this issue, patients continue to suffer and yes, DIE, due to lack of good science and flat-out neglect:  https://madisonarealymesupportgroup.com/2018/11/07/ticks-on-the-move-due-to-migrating-birds-and-photoperiod-not-climate-change/
  3. The white-footed mouse is not the sole perp, in fact according to independent Canadian tick researcher John Scott, established tick populations exist in areas devoid of the mouse:  https://madisonarealymesupportgroup.com/2018/08/13/study-shows-lyme-not-propelled-by-climate-change/. Many mammals transport ticks – particularly birds, and reptiles play a role, especially down South:  https://madisonarealymesupportgroup.com/2019/01/25/bb-in-s-italian-ectoparasites-reptiles/  Please read comment after article as well.  https://madisonarealymesupportgroup.com/2019/01/14/python-covered-with-more-than-500-ticks-rescued-in-australia/
  4. “Rising temperatures” have nothing to do with this. In fact, research has shown warmer winters are actually lethal to black legged ticks. They also survive in 3 degrees for 24 hours:  https://madisonarealymesupportgroup.com/2016/01/20/polar-vorticks/
  5. Unfortunately, Ruben Lee Sims’ story is all too common:   https://madisonarealymesupportgroup.com/2017/09/21/its-all-in-your-head-untilfinally-a-lyme-diagnosis/, https://madisonarealymesupportgroup.com/2019/04/22/its-just-crazy-why-is-lyme-disease-treatment-so-difficult-to-find-in-mississippi/, https://madisonarealymesupportgroup.com/2016/09/24/arkansas-kids-denied-lyme-treatment/….I could literally go on and on with such examples.
  6. Regarding what to do when you find an attached tick – again – insanity is doing the same thing over and over and expecting different results. Since everyone admits catching this early makes all the difference, why are people still telling people to “wait and see?”  No, do NOT wait and see! By that point it will be TOO LATE!  Treat this as seriously as a heart attack and treat it prophylactically if you are bitten by a tick. It’s not worth the risk, trust me.  A month’s worth of cheap antibiotics are worth it. Take probiotics, avoid sugar, and live to see another day, or take your chances, spend $15K a year for potentially ever, and hope you can keep working to keep the lights on, as well as keep your family intact. People STILL are not “getting” the seriousness of this. Here’s better advice on what to do if you are bitten:  https://madisonarealymesupportgroup.com/2019/05/25/help-ive-been-bitten-by-a-tick-now-what/ and go here for better info on prevention:  https://madisonarealymesupportgroup.com/2019/04/12/tick-prevention-2019/

 

https://www.lymedisease.org/idsa-extends-lyme-deadline/

TOUCHED BY LYME: IDSA extends comment period and allows downloads

By Dorothy Kupcha Leland

Aug. 10, 2019

https://natcaplyme.org/psla/in-no-way-does-natcaplyme-endorse-the-adoption-of-the-idsas-updated-lyme-disease-guidelines/?

In no way does NatCapLyme endorse the adoption of the IDSA’s updated Lyme disease guidelines!

NatCapLyme Submitted Its Response to the IDSA Regarding Their Updated Lyme Disease Guidelines During the Public Comment Period

August 7, 2019

The National Capital Lyme Disease Association (NatCapLyme) is submitting this letter as the organization’s official response to the Infectious Diseases Society of America’s (IDSA) public comment period regarding its draft of their updated Lyme disease guidelines.

Before addressing the guidelines, we would like to comment on the format in which the IDSA provided access to the draft guidelines for review. Specifically, while the document was posted online, the IDSA restricted the ability to download or print the document, thereby requiring the reviewer to read the entire publication online. To expect a reader to fully analyze such a comprehensive and complex document ONLY online was an obvious ploy by the IDSA to make the review of this material as difficult as possible. The Lyme community sees through this disingenuous behavior, as did Forbes Magazine,which published an article on the proposed draft guidelines. After the IDSA denied a request from Forbes and the article’s author to receive a PDF version of the draft guidelines, the author wrote, “Their refusal makes me feel they really don’t want people to comment on their 81-page draft and 203 page supplement.”Engaging in such underhanded behavior distracts from their transparency and greatly harms the relationship with the Lyme community and reinforces the belief that the IDSA is not in touch with or cares about the growing number of patients suffering from Lyme and other tick-borne diseases.

Regarding the proposed updated guidelines, there appear to be only minor changes from the IDSA’s previously published and decades old guidelines.  The new draft is still based on outdated and, in some cases, discredited studies. Patient groups have clearly demonstrated that thousands who suffer from Lyme and associated tick-borne diseases are losing their battle for health and the pursuit of happiness due to the failure of our national and professional institutions to address this growing epidemic in any meaningful way. To paraphrase the great physician, philosopher and scientist Moses Maimonides: there is no point to science without progress.

Meanwhile, the Centers for Disease Control and Prevention (CDC) and National Institutes of Health (NIH) continue to divert their focus to the highly dubious goal of creating a vaccine before developing a reliable test for Lyme or classifying all the strains of the disease. Without these prerequisite measures, the production of an effective vaccine is significantly compromised. Of course, NatCapLyme would like to see a “safe and effective” vaccine brought to market. However, the current effort narrowly focuses on a few strains of Borrelia in a rush to certify a vaccine. This offers only a limited public-health benefit and harbors a serious potential health risk by suggesting to those vaccinated that they are protected from all strains of Lyme and co-infections.

NatCapLyme is a nationally recognized Lyme advocacy organization that continues to hold face-to-face support group meetings. We also have a telephone hotline to take calls from those seeking help regarding Lyme and tick-borne diseases, and each day we are on the phone for hours providing information, references and support.

While the IDSA continues to stand behind outdated and biased research, we see and hear what is really happening across America.

Standing on the front lines of this growing health epidemic, we are told the same story time and time again. At staggering rates, patients report being misdiagnosed, inadequately treated, or worst of all, dismissed by the medical community as “hypochondriacs.” In reality many of these individuals have real bacterial, viral, or parasitic infections ravaging their bodies resulting from a tick bite. Children, who are most at risk, are losing their childhoods and may spend their entire lives chronically ill, never to appreciate one day of good health or happiness. Once healthy adults are losing their livelihoods, because they are now too sick to continue working. Families are bankrupted by escalating medical costs as they try to find an answer to their multi-systemic symptoms and illness.

A 2015 research study published by the Johns Hopkins Bloomberg School of Public Health found that Lyme disease costs the U.S. health care system between $712 million to $1.3 billion to treat each year.

Again, we are only talking about Lyme disease, not other co-infections. Add to that the indirect costs, such as lost wages and taxes, and the total cost of Lyme disease is in the billions each year.

NatCapLyme sees that the updated Lyme disease guidelines proposed by the IDSA are just status quo and woefully inadequate to address the true extent of the tick-borne disease epidemic reeking havoc across the U.S. With an estimated 427,000 new cases of Lyme disease contracted each year, as published by the CDC, and with little progress in the identification, diagnosis and treatment of tick-borne illnesses, NatCapLyme believes that an increasing number of people will become infected and may subsequently remain sick perhaps indefinitely. In reality, thousands of U.S. citizens are being stricken with a potentially life-long debilitating medical condition that is not, or is barely, recognized by the IDSA. Based on the proposed draft guidelines, we believe that the status quo will be perpetuated for years to come.

Tick-borne illness, especially in the chronic form, will continue to be discounted by the vast majority of physicians, government policy makers and researchers as the IDSA clings to the belief that Lyme disease is hard to catch and easy to treat.

Unfortunately, the Lyme community’s past experience with the IDSA demonstrates the serious challenge of achieving significant change. Little progress is made when a professional medical society that promulgates guidelines to diagnosis and treat tick-borne diseases only recognizes and supports the same old cast of researchers who repeatedly test the same old ideas. In an article published by the Washington Post titled https://www.washingtonpost.com/outlook/why-we-shouldnt-take-peer-review-as-the-gold-standard/2019/08/01/fd90749a-b229-11e9-8949-5f36ff92706e_story.html?noredirect=onWord did not find any entries for your table of contents. It states that,

“peer review can act as a shield to protect the status quo and suppress research viewed as radical or contrary to the established perspectives of referees.”  Moreover, “groundbreaking studies by Sir Frank MacFarlane Burnet, Rosalind Yalow, Baruch Blumberg and others were rejected by peer reviewers, yet later led to Nobel Prizes.”

We believe that the key to any progress lies in advancing research in all aspects of the diseases, especially in the development of better diagnostic tools for the detection of all tick-borne diseases. Clearly these guidelines do not do that. We appeal to the IDSA and the research community to expand its focus on emerging and promising research that comes from fresh and new perspectives. It should bring together the best minds and best theories of ALL parties, and require that ALL theories be examined and considered. NatCapLyme believes that true solutions to the dilemma of Lyme and tick-borne infections may be found only when all parties are willing to consider the view that each party holds. Perhaps if we all work together we can forever end this terrible pandemic.

In conclusion, NatCapLyme in no way endorses the adoption of the IDSA’s updated Lyme disease guidelines. The patient community is extremely angry about the lack of scientific and medical progress with respect to Lyme and our masses are growing by the tens-of-thousands each year. This problem is not going away until all parties are invested in creating real solutions that benefit all patients, and society as well. Despite being sick, in pain, exhausted, frustrated and financially drained, we are committed to this cause and will not stop until we regain our health, halt this epidemic, and ensure that these terrible tick-borne diseases do not burden future generations.

https://natcaplyme.org

_______________

For more:  

https://madisonarealymesupportgroup.com/2019/06/27/idsa-aan-acr-2109-draft-lyme-guidelines-public-comments-allowed-until-aug-10-2019/

https://madisonarealymesupportgroup.com/2019/07/09/idsa-lyme-disease-treatment-management-business-as-usual-leaves-those-with-persisting-symptoms-to-suffer-die/

https://madisonarealymesupportgroup.com/2019/07/22/idsas-insincere-request-for-guidelines-feedback/

https://www.ncbi.nlm.nih.gov/pubmed/31348120

2019 Jul 16. doi: 10.1097/ICB.0000000000000893. [Epub ahead of print]

MULTIMODAL IMAGING OF TWO UNCONVENTIONAL CASES OF BARTONELLA NEURORETINITIS.

Abstract

PURPOSE:

To report two cases of cat-scratch fever with atypical posterior segment manifestations.

METHODS:

Two cases were retrospectively reviewed.

RESULTS:

  • A 27-year-old woman presented with painless blurring of central vision in her left eye. Clinical examination revealed a small focal area of retinitis within the macula associated with a subtle macular star. Spectral-domain optical coherence tomography showed a hyper-reflective inner retinal lesion in addition to subretinal and intraretinal fluid as well as hyperreflective foci within the outer plexiform layer. Serology was positive for anti-B. henselae IgM (titer 1:32).
  • A 34-year-old woman presented with painless loss of vision in both eyes associated with headaches and pain with extraocular movement. Spectral-domain optical coherence tomography depicted subretinal fluid, intraretinal fluid, and hyperreflective deposits within the outer plexiform layer. A focal collection of vitreous cell was observed overlying the optic nerve in the left eye. Bilateral disk leakage was identified on fluorescein angiography. Serology revealed high-titer anti-B. henselae antibodies (IgM titers 1:32, IgG titers 1:256).

CONCLUSION:

Our cases highlight the necessity of recognizing more unusual posterior segment presentations of ocular bartonellosis. Multimodal retinal imaging including spectral-domain optical coherence tomography may help better characterize lesions.

_______________

For more:  https://madisonarealymesupportgroup.com/2019/07/28/treatment-strategies-for-neuroretinitis-due-to-bartonella-current-options-emerging-therapies/

https://madisonarealymesupportgroup.com/2018/07/10/bartonella-henselae-neuroretinitis-in-patients-without-cat-scratch/

https://madisonarealymesupportgroup.com/2017/07/21/bartonella-and-neuroretinitis/

https://madisonarealymesupportgroup.com/2018/05/10/bartonella-neuroretinitis-not-atypical/

https://madisonarealymesupportgroup.com/2019/04/08/case-series-bartonella-ocular-manifestations/

https://madisonarealymesupportgroup.com/2019/02/27/advanced-imaging-found-bartonella-around-pic-line/  Bartonella, like Lyme, can be persistent causing chronic infection.

 

https://www.galaxydx.com/bartonella-and-the-brain/

Bartonella and the Brain