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Detection of Chromosomal and Plasmid-Mediated Quinolone Resistance Amo | IDR – Dove Medical Press

Noura E Esmaeel, 1 Marian A Gerges, 1 Thoraya A Hosny, 2 Ahmed R Ali, 3 Manar G Gebriel 1

1Medical Microbiology and Immunology Department, Faculty of Medicine, Zagazig University, Zagazig, Egypt; 2Clinical Pathology Department, Faculty of Medicine, Zagazig University, Zagazig, Egypt; 3Urology Department, Faculty of Medicine, Zagazig University, Zagazig, Egypt

Correspondence: Marian A GergesMedical Microbiology and Immunology Department, Faculty of Medicine, Zagazig University, 44519, EgyptTel +20 1003819530Email maromicro2006@yahoo.com

Introduction: Resistance to fluoroquinolones (FQ) in uropathogenic Escherichia coli (UPEC) has emerged as a growing problem. Chromosomal mutations and plasmid-mediated quinolone resistance (PMQR) determinants have been implicated. Data concerning the prevalence of these determinants in UPEC in our hospital are quite limited.Purpose: To investigate the occurrence and genetic determinants of FQ resistance in UPEC isolated from urinary tract infection (UTI) cases in Zagazig University Hospitals.Patients and Methods: Following their isolation, the identification and susceptibility of UPEC isolates were performed by matrix-assisted laser desorption/ionization-time-of-flight mass spectrometer (MALDI-TOF MS). FQ resistance was detected by the disc diffusion method. Ciprofloxacin minimal inhibitory concentration (MIC) was determined using E-test. Chromosomal mutations in the gyrA gene were detected using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP), and for detection of PMQR, a couple of multiplex PCR reactions were used.Results: Among a total of 192 UPEC isolates, 46.9% (n=90) were FQ resistant. More than half of the isolates (57.8%) exhibited high-level ciprofloxacin resistance (MIC > 32 g/mL). Mutations in gyrA were detected in 76.7% of isolates, with 34.4% having mutations at more than one site. PMQR determinants were detected in 80.1% of UPEC isolates, with aac(6)-Ib-cr gene being the most frequent found in 61.1% of isolates.Conclusion: There is a high prevalence of both gyrA mutations and PMQR determinants among UPEC isolates in our hospital which contribute to high-level ciprofloxacin resistance, a finding that may require the revision of the antibiotics used for empirical treatment of UTI.

Keywords: gyrA mutations, qnr determinants, uropathogenic E. coli, ciprofloxacin resistance

This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution - Non Commercial (unported, v3.0) License.By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms.

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Detection of Chromosomal and Plasmid-Mediated Quinolone Resistance Amo | IDR - Dove Medical Press

Assistant/Associate, Department of Medical Microbiology and Immunology job with UNITED ARAB EMIRATES UNIVERSITY | 195856 – Times Higher Education…

Job Description

The Department of Medical Microbiology & Immunology, College of Medicine and Health Sciences (CMHS), UAE University, seeks candidates for a faculty position at the rank of Assistant/Associate Professor in Microbiology. We are particularly looking for an innovative investigator who has an established, or a clear potential to establish an independent research program in host-parasite interactions at the cellular and molecular level. Preference will be given to candidates with a strong background in computational and systems biology, genomics or bioinformatics. The College of Medicine operates an internationally recognized, integrated, problem/team-based learning curriculum and provides excellent research facilities. English is the language of instruction. Current research in the department focuses on cancer immunology, autoimmune diseases, antibiotic resistance, host-pathogen interactions, retroviral RNA packaging, dimerization and gene expression, EBV and its role in the pathogenesis of human diseases, and public health.

Minimum Qualification

The successful candidate must have a PhD or MD/PhD from an accredited institution.

Preferred Qualification

As above

Expected Skills/Rank/Experience

It is expected that the successful candidate will also have experience in teaching medical students, and postgraduate students. Importantly, candidates must demonstrate the potential to establish an independent and sustained research program in their area of expertise and be able to obtain peer-reviewed internal and external funding. International collaboration is encouraged.

Special Instructions to Applicant

Attach CV and publication list, names & contact information of 3 referees, and a cover letter describing research and teaching experience.

Division College of Medicine&Health Sciences

Department Microbiology - (CMHS)

Job Close Date open until filled

Job Category Academic - Faculty

Salary 28000-35000 UAE Dirhams per month, based on experience

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Assistant/Associate, Department of Medical Microbiology and Immunology job with UNITED ARAB EMIRATES UNIVERSITY | 195856 - Times Higher Education...

Circulating Biomarkers of Handgrip Strength and Lung Function in Chron | COPD – Dove Medical Press

Rizwan Qaisar,1 Asima Karim,1,2 Tahir Muhammad3

1Basic Medical Sciences, College of Medicine, University of Sharjah, Sharjah, United Arab Emirates; 2University of Health Sciences, Lahore, Pakistan; 3Department of Biochemistry, Gomal Medical College, Gomal University, Dera Ismail Khan, Pakistan

Correspondence: Rizwan QaisarDepartment of Basic Medical Sciences, College of Medicine, University of Sharjah, Sharjah, United Arab EmiratesTel +971 6 505 7254Email rqaisar@sharjah.ac.ae

Purpose: COPD is a multisystem disease and there is a need for clinical serum markers that can assess the decline in lung and muscle function in COPD. The goal of this study was to evaluate the potential association of serum club-cell protein 16 (CC16), -1 acid glycoprotein (AGP) and total sialic acid (TSA) with spirometry, hand-grip strength and quality of life to assess important disease outcomes.Methods: This is a population-based cross-sectional study and data were collected from the patients at teaching hospitals of Gomal University and the University of Health Sciences in Pakistan. The study population included 1582 participants (Non-COPD; N = 788, COPD; N = 845) > 55 years of age from both sexes, with data from structural interviews, clinical examinations, laboratory investigations, spirometry and hand-grip strength measurements.Results: Serum TSA and CC16 were significant predictors of FEV1% (p < 0.05) and hand-grip strength in advanced stages of COPD (p < 0.05 each) in both sexes. Men had higher absolute and adjusted hand-grip strength than women in all groups (p < 0.05). Hand-grip strength was significantly associated with FEV1% in both genders (p < 0.05) with stronger effect in women (r2 = 0.075). Serum HDL-C was an independent predictor of hand-grip strength and FEV1% (p < 0.05) in both genders. Participants with extreme problem on EQ-5D parameters had more severe COPD and reduced hand-grip strength (all p values < 0.05).Conclusion: Taken together, these studies show that the serum expressions of TSA and CC16 have correlations with spirometry and muscle decline in COPD. Further studies should be conducted to establish their efficacy in monitoring disease progression in COPD.

Keywords: club cell protein 16, -1 acid glycoprotein, total sialic acid, EQ-5D, HDL-C

This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution - Non Commercial (unported, v3.0) License.By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms.

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Circulating Biomarkers of Handgrip Strength and Lung Function in Chron | COPD - Dove Medical Press

This Colorado College Will Start Offering A Cannabis Major In The Fall – KFSM 5Newsonline

(CNN) Students on Colorado State Universitys Pueblo campus will have the option to study cannabis beginning this fall.

State officials on Friday approved a bachelors of science degree program in Cannabis Biology and Chemistry,according to the Colorado Department of Higher Education, which said it was one of the first such programs in the country.

The new major is a pro-active response to a rapidly changing national scene regarding the cannabis plant, a proposal for the program by CSU-Pueblo officials says, citing shifting attitudes toward cannabis and its legalization for recreational use in numerous states, including Colorado.

The program will be part of CSU-Pueblos department of chemistry and consist mainly of chemistry and biology coursework with some classes in math and physics, the proposal says.

Students could choose one of two tracks either a natural products track focused on biology, or an analytical track that focuses on chemistry.

Graduates could begin careers either in the cannabis and hemp industries or in the government.But they could also be competitive in a wide variety of businesses outside of the cannabis industry, it said, such as agriculture, food science, biochemistry and environmental sciences.

Educating students who are capable of understanding cannabis science is required for the industry in all its aspects to be effective and safe for the consumer, it said.

Between 2014 and June 2019, marijuana sales in Colorado exceeded $6.56 billion, according to the states Department of Revenue. With taxes, license and fee revenue, the states revenue reached more than $1 billion.

CSU-Pueblo anticipates a strong demand for the program, its proposal said, and believe as many 60 students could be enrolled in the major after four years.

The Colorado Department of Higher Education believes it could be the first of several cannabis-focused degrees that pop up at Colorado colleges in the near future.

CSU-Pueblos program will not be the first of its kind. Its proposal cited Northern Michigan Universitys bachelor program in medicinal plant chemistry that it said was primarily tailored to those wanting to enter the cannabis field.

CNN has reached out to CSU-Pueblo for comment.

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This Colorado College Will Start Offering A Cannabis Major In The Fall - KFSM 5Newsonline

Dentists in South Africa aren’t being taught genetics. Why they should – The Conversation Africa

Genetic and genomic research has improved our understanding of the genetic origin of growth, development and disease and affects all areas of healthcare. There is also mounting evidence that many complex conditions are the result of interactions between genes. These include diabetes and hypertension.

Genomics has become increasingly important to oral health too. Dentists regularly come across obvious expressions of genetic disorders or genetic-based diseases in the oral and head and neck region. There are approximately 5,500 known inherited conditions. More than 700 of these have abnormalities which involve the oral and dental region of the face.

These insights have been gained through continued and concerted efforts to understand the genetic aspects of diseases. This understanding, in turn, has generated novel approaches to prevent, diagnose and manage them.

In the area of dentistry, teaching has unfortunately not kept up with the science, particularly in Africa. This places dentists at a disadvantage. They cant or find it difficult to contribute to the overall health of patients with genetic disorders because they dont have the necessary knowledge. This would include the ability to recognise the indicators of genetic disorders and the confidence to manage these patients.

This is why dentists need a sound understanding of genetics. And its why genetics and genomics should be included in the undergraduate and postgraduate curriculum. Investing in structured dental genetics programmes in dental schools in Africa would ensure an increase in the dental genetics workforce. This would ultimately improve the management of patients with inherited conditions with oral and dental manifestations.

To evaluate the need for human genetics in the dentistry curriculum my colleagues and I conducted a survey at the dental school at a South African university. Academic staff, 4th and 5th-year undergraduate dental students as well as postgraduate dental students participated in the survey.

The results indicated that students and clinicians had limited training and experience pertaining to the diagnosis and management of individuals with genetic disorders.

Currently, there are no plans in place to train dentists with a sound understanding of genetics. There are also no programmes in place to allow trained African dentists to choose such a career pathway.

As a result, there is an over-dependence of African clinical practice on research findings from technologically advanced Western countries. Secondly, it means that clinical research capacity building isnt happening. And finally, it means that patients arent being offered the best possible diagnosis and treatment.

There are several factors responsible for the lack of dental genetics in Africa. Among a few challenges are poor biomedical research infrastructure, minimal funding and an absence of a structured dentist genetics career pathways.

To address these challenges, African universities and dental schools need to develop and include dental genetics courses in undergraduate and postgraduate programmes. These should be designed to ensure they help members of the dental fraternity to treat patients with hereditary conditions.

The dental genetics workforce would, in turn, increase trained dentists some of whom could have the option of following a research career. This would enhance networking among African dental researchers and lead to better dental research output across the continent.

Several first world universities, such as the universities of Pittsburg, Manchester and Oslo have included dental genetics into their curricula. Their vast research capacity has resulted in evidence-based dentistry being offered to patients in those countries.

Another way to foster an interest and understanding of genetics in the dental community is by developing collaborative relationships. One already exists in South Africa between the division of human genetics at the University of Cape Town and the dental faculty at the University of the Western Cape. This partnership runs a dental genetics clinic which serves patients with genetic disorders from across the Western Cape province. Postgraduate students also rotate through the clinic and are mentored in the dental management of children with genetic disorders and congenital abnormalities.

Adding courses on human genetics in the curriculum at dental schools would be a first step to ensuring that more dentists have an understanding of the field.

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Dentists in South Africa aren't being taught genetics. Why they should - The Conversation Africa

Genetics (B.S.) | Degree Programs | Clemson University …

The first major-specific course required of freshman genetics majors is Careers in Genetics and Biochemistry. This introductory course brings in professionals to aid students in discovering the diversity of career opportunities available from this degree. This course also helps you become aware of professional organizations, ethical issues and the requirements for advanced studies.

In the first two years at Clemson, youll take various science courses such as general and organic chemistry, biology, physics and mathematics. These will prepare you for upper-level course work that includes molecular biochemistry, molecular and general genetics, comparative genetics and population genetics. Additionally, youll be able to tailor your degree to your specific interests by selecting from approved scientific courses such as microbiology, immunology, and human anatomy and physiology.

Genetics students spend quite a bit of time in Clemsons laboratories with our nationally recognized faculty. Our faculty have diverse research interests from alternative fuel to molecular parasitology. You also have a chance to participate in internships and study abroad, as well as join any of Clemsons hundreds of student organizations.

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Genetics (B.S.) | Degree Programs | Clemson University ...

Welcome to the Department of Genetics | Department of Genetics

Genetics is the future and the past. The history and the promise of every organism is written in its DNA.

Geneticists are leading one of the major scientific revolutions of humankind, delving into the distant past and providing an unprecedented understanding of the biological world.

Our department offers a supportive and unique training environment across the full spectrum of genetics, bridging the disciplines of molecular genetics, development, genomics, and evolutionary biology.

The Department of Genetics is in UGA'sFranklin College of Arts and Sciences.

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Welcome to the Department of Genetics | Department of Genetics

Genetics Are Just One Part of How Children Develop

What determines how a child develops? While it is impossible to account for each and every influence that contributes to who a child eventually becomes, what researchers can do is look at some of the most apparent factors. These include things such as genetics, parenting, experiences, friends, family, education, and relationships. By understanding the role that these factors play, researchers are better able to identify how such influences contribute to development.

Think of these influences as building blocks. While most people tend to have the same basic building blocks, these components can be put together in an infinite number of ways. Consider your own overall personality. How much of who you are today was shaped by your genetic background, and how much is a result of your lifetime of experiences?

This question has puzzled philosophers, psychologists, and educators for hundreds of years and is frequently referred to as the nature versus nurture debate. Are we the result of nature (our genetic background) or nurture (our environment)? Today, most researchers agree that child development involves a complex interaction of both nature and nurture.

While some aspects of development may be strongly influenced by biology, environmental influences may also play a role. For example, the timing of when the onset of puberty occurs is largely the results of heredity, but environmental factors such as nutrition can also have an effect.

From the earliest moments of life, the interaction of heredity and the environment works to shape who children are and who they will become. While the genetic instructions a child inherits from his parents may set out a road map for development, the environment can impact how these directions are expressed, shaped or event silenced. The complex interaction of nature and nurture does not just occur at certain moments or at certain periods of time; it is persistent and lifelong.

In this article, we'll take a closer look at how biological influences help shape child development. We'll learn more about how our experiences interact with genetics and learn about some of the genetic disorders that can have an impact on child psychology and development.

At its very beginning, the development of a child starts when the male reproductive cell, or sperm, penetrates the protective outer membrane of the female reproductive cell, or ovum. The sperm and ovum each contain chromosomes that act as a blueprint for human life.

The genes contained in these chromosomes are made up of a chemical structure known as DNA (deoxyribonucleic acid) that contains the genetic code, or instructions, that make up all life. Except for the sperm and ova, all cells in the body contain 46 chromosomes. As you might guess, the sperm and ova each contain only contain 23 chromosomes. This ensures that when the two cells meet, the resulting new organism has the correct 46 chromosomes.

So how exactly do the genetic instructions passed down from both parents influence how a child develops and the traits they will have? In order to fully understand this, it is important to first distinguish between a child's genetic inheritance and the actual expression of those genes.

A genotype refers to all of the genes that a person has inherited. A phenotype is how these genes are actually expressed. The phenotype can include physical traits, such as height and color or the eyes, as well as nonphysical traits such as shyness and extroversion.

While your genotype may represent a blueprint for how children grow up, the way that these building blocks are put together determines how these genes will be expressed. Think of it as a bit like building a house. The same blueprint can result in a range of different homes that look quite similar but have important differences based on the material and color choices used during construction.

Whether or not a gene is expressed depends on two different things: the interaction of the gene with other genes and the continual interaction between the genotype and the environment.

Genetic instructions are not infallible and can go off track at times. Sometimes when a sperm or ovum is formed, the number of chromosomes may divide unevenly, causing the organism to have more or less than the normal 23 chromosomes. When one of these abnormal cells joins with a normal cell, the resulting zygote will have an uneven number of chromosomes.

Researchers suggest that as many as half of all zygotes that form have more or less than 23 chromosomes, but most of these are spontaneously aborted and never develop into a full-term baby.

In some cases, babies are born with an abnormal number of chromosomes. In every case, the result is some type of syndrome with a set of distinguishing characteristics.

The vast majority of newborns, both boys and girls, have at least one X chromosome. In some cases, about 1 in every 500 births, children are born with either a missing X chromosome or an additional sex chromosome. Klinefelter syndrome, Fragile X syndrome,and Turner syndrome are all examples of abnormalities involving the sex chromosomes.

Kleinfelter's syndrome is caused by an extra X chromosome and is characterized by a lack of development of the secondary sex characteristics and as well as learning disabilities.

Fragile X syndrome is caused when part of the X chromosome is attached to the other chromosomes by such a thin string of molecules that it seems in danger of breaking off. It can affect both males and females, but the impact can vary. Some with Fragile X show few if any signs, while others develop mild to severe mental retardation.

Turner syndrome occurs when only one sex chromosome (the X chromosome) is present. It affects only females and can result in short stature, a "webbed" neck and a lack of secondary sex characteristics. Psychological impairments associated with Turner syndrome include learning disabilities and difficulty recognizing emotions conveyed through facial expressions.

The most common type of chromosomal disorder is known as trisomy 21, or Down syndrome. In this case, the child has three chromosomes at the site of the 21st chromosomes instead of the normal two.

Down syndrome is characterized by facial characteristics including a round face, slanted eyes, and a thick tongue. Individuals with Down syndrome may also face other physical problems including heart defects and hearing problems. Nearly all individuals with Down syndrome experience some type of intellectual impairment, but the exact severity can vary dramatically.

Clearly, genetics have an enormous influence on how a child develops. However, it is important to remember that genetics is just one piece of the intricate puzzle that makes up a child's life. Environmental variables including parenting, culture, education, and social relationships also play a vital role.

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Genetics Are Just One Part of How Children Develop

Consumer DNA testing is a bust: Here’s how companies like Ancestry and 23andMe can survive – CNBC

A reporter examines a 23andMe DNA genetic testing kit in Oakland, California.

Cayce Clifford | Bloomberg | Getty Images

It has not been a good year for consumer DNA testing companies.

In January, Silicon Valley-based 23andMe laid off 100 employees, about 14% of its workforce. A month later, Ancestry, which has offices in Utah and San Francisco, also cut 100 jobs, representing about 6% of its staff.

The major reason for the downsizing? Simply put, consumers aren't buying as many at-home DNA tests as they used to.

The first sign came in the summer, when Illumina, maker of the DNA sequencing machines that are used by Ancestry and 23andMe, acknowledged in an earnings call to investors that the category had hit a lull. CEO Francis DeSouza didn't share an explanation for that, but noted that Illumina was taking a "cautious view" of the opportunity in the near term. Orasure, maker of the spit tubes used by consumer DNA testing companies, has also seen its stock take a hit.

At that time, some smaller companies were already feeling the impact. Helix, a start-up that spun out of Illumina to build an "app store" model for DNA tests, cut staff in May. The company revealed to Bloomberg that it was shifting its focus away from consumers to population health, meaning it would work with health industry partners. A few months later, Veritas Genetics another company focused on consumers that sold more expensive but more detailed whole genome sequencing tests shuttered its U.S. operations.

So what happened? There hasn't yet been a detailed study to understand the shift in consumer thinking around these tests. But CNBC spoke with some of the leading genetics experts and doctors, who shared a few theories.

Dawn Barry, a former Illumina executive with a start-up in the space called LunaDNA, blames a few factors, especially privacy concerns.

Consumers have seen a slew of reports in the past few years about how companies are using their personal data for targeted advertising, without their knowledge, and might be feeling particularly sensitive about their health information.

Anne Wojcicki, CEO of 23andMe, has previously referred to these concerns as the "Facebook effect." In her view, consumers are increasingly freaked out about stories they're reading in the media about privacy, mostly about Facebook and other technology companies, and are reacting by feeling anxious about getting DNA tests.

Companies like 23andMe do make money off this information. Her company does ask for consent from users and it has publicly explained its revenue model, but a big part of its business involves its relationships with pharmaceutical companies like GlaxoSmithKline. 23andMe also has a therapeutics arm, where it is hoping to leverage its database of millions of people's DNA to develop new drugs.

Making matters worse for these companies, suggests Barry, is the Golden State Killer case. Law enforcement honed in on a suspect after running DNA from a decades-old crime scene through a free online database, where anyone can upload their genetic information.

A suspect was found through a distant relative who might have paid for a test via Ancestry or 23andMe, and then uploaded it into the database.

The case raised all sorts of complicated questions about whether genetic information is fundamentally different than other types of data because it implicates family members and not just individuals.

Other experts suspect that consumer DNA testing companies might have run out of early adopters. The theory goes that there's about 20 million or 30 million consumers who are naturally interested in learning more about their family background, and it's not that challenging or expensive to sell tests to them. At this point, many of these people have already been sold to, and there's no reason for them to buy a second test. Ancestry has sold about 14 million tests, and 23andMe has sold some 9 million.

But many people are wary about learning information they might not want to know like the father who raised them isn't their biological father or that they have a risk for a genetic disease that they can't take a pill to prevent.

There's likely a larger consumer segment that's interested, but still wary about these tests. They might not believe that the information is valuable enough to warrant the price tag. The cheapest tests sell for $99, and they'll cover ancestry and some health risks but lack truly actionable health information, like whether an individual might respond poorly to a drug based on their genetic makeup.

"The ancestry market is a finite market," said David Mittelman, CEO of Othram, a genomics start-up and a molecular physicist. A decade or so in, "these companies are beginning to tap out the market."

Mittelman notes that customer acquisition costs, including ad dollars these companies need to spend on sites like Facebook, will increase over time.

"I think the companies know this," he said. "The investment in health shows that they are working to appeal to a broader market."

What's noteworthy about the recent round of layoffs is that Ancestry kept all of its employees at its Ancestry Health business. And 23andMe is still highly focused on its drug development business. That suggests that both companies are indeed hinging their future on developing powerful health applications.

In light of that, some geneticists are optimistic about their future.

"First of all, a slowdown isn't a stoppage," said Dr. Robert Green, a professor of genetics at Harvard Medical School. "Our research is finding that genetics is about to take its rightful place in medical care for the world."

As Green explains, it's been a challenge for doctors to understand how genetics can inform their patient care. Many haven't had the education about genetics to understand how to talk about it with their patients or recommend tests that might be beneficial. But that's starting to change.

For instance, 23andMe is starting to roll out new tests that can identify people's risk for chronic diseases like diabetes, called polygenic risk scores. These results could be used by doctors to help steer their patients toward making healthier lifestyle choices to help them avoid getting the disease.

And for these companies, which already have genetic databases of millions of people, they might not need to keep spending ample marketing dollars to acquire new customers. Instead, they could focus on developing new insights from their existing databases. if they succeed at that, they can forge partnerships to the medical industry.

As Mittelman puts it, there's no need to "force people down an ancestry funnel."

Green agrees, saying companies like 23andMe and Ancestry might double down on more expensive but more detailed sequencing tests that provide a lot more relevant health information. 23andMe has dabbled with those kinds of tests but has been reluctant to roll out higher-priced tests while its main focus has been growth.

"The direct-to-consumer phenomenon will give way to a more of a proper integration of genomics into the day-to-day care of patients," said Green. "What we're seeing is a course correction, and consumers are waking up to the potential limitations of a $99 test."

CNBC Evolve will return, this time to Los Angeles, on June 8. Visit cnbcevents.com/evolve to apply to attend.

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Consumer DNA testing is a bust: Here's how companies like Ancestry and 23andMe can survive - CNBC