Can we say goodbye to unreliable food diaries and diet recall in exchange for a urine test that will better aid researchers in figuring out what foods might help prevent cancer?
Georgetown researchers have developed a method that can quickly evaluate specific food compounds in human urine.
The new urine test looks for specific members of the isothiocyanates (ITCs) family (among other compounds), found in cruciferous vegetables. Animal and cell studies have shown that different types of ITCs have varying anticancer properties and potency, suggesting they are not equal
in protecting against cancer, Dyba says. “We developed our test because there has been no way to find out which specific ITCs works best,” he says.
For their study, the researchers focused on cruciferous vegetables, which showed a protective benefit against lung cancer in a study of more than 63,000 people who participated in the National Institutes of Health’s Singapore Chinese Health Study. Cruciferous vegetables, a major food in the Asian diet, include cabbage, Brussels sprouts, broccoli, cauliflower, bok choy and watercress, among others.
Read more:
Urine Test Can Measure Specific Compounds from Food Consumed
Source: News wice
Art and Science of Laboratory Medicine. Clinical laboratory and biomedical science related news, abstracts and images for medical laboratory professionals, students and other laboratory geeks.
Thursday, March 17, 2016
Monday, March 14, 2016
Quality Improvement in the Coagulation Laboratory
Reducing the Number of Insufficient Blood Draw Specimens for Coagulation Testing
To report the efforts of our laboratory to reduce quantity-not-sufficient (QNS) specimens via several methods and to directly measure the effect of expired collection tubes on the amount of blood that can be drawn.
A study tracked the number of QNS venous-blood specimens per month received by our coagulation laboratory from March 2008 to December 2012. Interventions involved communications that informed nurses and phlebotomists how to avoid drawing QNS specimens and floor sweeps, in which laboratory staff searched for and removed expired vacuum-based blood-collection tubes (VBCTs) from inpatient hospital floors. Also, we assessed 11 healthy donors to determine the amount of blood that could be drawn into expired VBCTs.
During the study period, the rate of QNS specimens dropped from a mean of 0.7% to 0.3%. In expired VBCTs collected from healthy donors, we observed a statistically significant difference in the amount of blood drawn into nonexpired vs expired VBCTs (P <.001). Also, there was a negative relationship between the number of months that the VBCT had been expired and the amount of blood that could be drawn into the VBCTs (P <.001). For every month that VBCTs were expired, the amount of blood drawn decreased by approximately 1.8 mm (0.1 mL), using linear regression analysis.
This study strongly suggests that expired VBCTs consistently and progressively yield QNS specimens. Methods to reduce blood draws from expired VBCTs may include communications promoting proper blood draw technique, floor sweeps to remove expired VBCTs, and improved inventory management.
Read more:
Quality Improvement in the Coagulation Laboratory
Source: Medscape
To report the efforts of our laboratory to reduce quantity-not-sufficient (QNS) specimens via several methods and to directly measure the effect of expired collection tubes on the amount of blood that can be drawn.
A study tracked the number of QNS venous-blood specimens per month received by our coagulation laboratory from March 2008 to December 2012. Interventions involved communications that informed nurses and phlebotomists how to avoid drawing QNS specimens and floor sweeps, in which laboratory staff searched for and removed expired vacuum-based blood-collection tubes (VBCTs) from inpatient hospital floors. Also, we assessed 11 healthy donors to determine the amount of blood that could be drawn into expired VBCTs.
During the study period, the rate of QNS specimens dropped from a mean of 0.7% to 0.3%. In expired VBCTs collected from healthy donors, we observed a statistically significant difference in the amount of blood drawn into nonexpired vs expired VBCTs (P <.001). Also, there was a negative relationship between the number of months that the VBCT had been expired and the amount of blood that could be drawn into the VBCTs (P <.001). For every month that VBCTs were expired, the amount of blood drawn decreased by approximately 1.8 mm (0.1 mL), using linear regression analysis.
This study strongly suggests that expired VBCTs consistently and progressively yield QNS specimens. Methods to reduce blood draws from expired VBCTs may include communications promoting proper blood draw technique, floor sweeps to remove expired VBCTs, and improved inventory management.
Read more:
Quality Improvement in the Coagulation Laboratory
Source: Medscape
Sunday, March 13, 2016
Scientists identify a virus and two bacteria that could be causing Alzheimer's
An international group of 31 Alzheimer's researchers has published an
editorial urging the science world to change its focus when it comes to
Alzheimer's disease. The message is clear - after a decade of failed
attempts to treat and prevent the disease, it's time to reassess the
evidence that Alzheimer's could be spread by microbes.
Study says that the first microbes we should investigate are the herpes simplex virus type 1 (HSV1), the chlamydia bacteria, and spirochaetes.
So how could viruses and bacteria trigger Alzheimer's disease? Well, we still don't really know, which is one of the reasons research has stalled in this area, but the herpes virus is already known to damage the nervous system, and microbial infections are known to inflammation around the body, which is a characteristic of Alzheimer's disease.
Of course, the issue is not as clear-cut as the editorial makes it out to be - if it was, we'd already know how to fix the disease. And most importantly, experts are urging people not to freak out about the implication that Alzheimer's could be 'caught'.
Read more:
Scientists identify a virus and two bacteria that could be causing Alzheimer's
Source: ScienceAlert
Study says that the first microbes we should investigate are the herpes simplex virus type 1 (HSV1), the chlamydia bacteria, and spirochaetes.
So how could viruses and bacteria trigger Alzheimer's disease? Well, we still don't really know, which is one of the reasons research has stalled in this area, but the herpes virus is already known to damage the nervous system, and microbial infections are known to inflammation around the body, which is a characteristic of Alzheimer's disease.
Of course, the issue is not as clear-cut as the editorial makes it out to be - if it was, we'd already know how to fix the disease. And most importantly, experts are urging people not to freak out about the implication that Alzheimer's could be 'caught'.
Read more:
Scientists identify a virus and two bacteria that could be causing Alzheimer's
Source: ScienceAlert
List of culture media used in microbiology
Many types of bacterial growth media are used to culture (grow) microbes in the laboratory. Here's a summary of defined, complex, selective and differential media.
Read more:
Microbiology notes
Source:Microbiology notes
Read more:
Microbiology notes
Media
|
Uses
|
· Alkaline Peptone Water
|
Enrichment media for Vibrio cholerae
|
· Alkaline Salt Transport Medium
·
Taurocholate Peptone Transport Medium
|
Transport media for diarrheal diseases suspected of
being caused by V. cholerae
|
· Anaerobic Media
|
Liquid media by addition of
·
Glucose (0.5 % to 1 %)
·
Ascorbic Acid (0.1 %)
·
Cysteine (0.1 %)
·
Sodium Merceptoacetate (0.1 %)
·
Thioglycollate (0.1 %)
·
Particles of cooked meat broth
|
· Bile Salt Agar
·
Thiosulphate Citrate Bile Salts-Sucrose Agar (TCBS)
·
Monsur’s Tellurite Taurocholate Gelatin Agar
|
Selective media for V. cholerae
|
· Bile Esculin Agar (Contains 40% Bile)
|
Selective media for Enterococcus species (Black
coloration of the medium)
|
· Blood Agar
|
· Enriched media (Supports
the growth of fastidious organisms, e.g. Streptococcus)
·
Indicator media to show hemolytic properties of certain organisms (Staphylococcus
aureus: β-Hemolytic; Streptococcus pneumonia and S
viridans: α-Hemolytic; Enterococcus: Non-Hemolytic)
|
· Bordet-Gengou Agar
·
Charcoal Blood Agar
·
Regan-Lowe Medium (Charcoal Agar with blood, cephalexin and Amphotericin B)
|
Isolation of Bordetella pertussis
|
· Brain Heart Infusion Broth
|
Used in blood culture bottles (both adult and
pediatric patients)
|
· Buffered Charcoal Yeast Agar (BCYA)
· Feeley Gorman Agar
|
Specialized media for isolation of Legionella
|
· Campylobacter Thioglycollate Broth
|
Selective holding media for recovery of Campylobacter
species
|
· Castaneda Medium
|
Biphasic medium for the isolation of Brucella
|
· Cefoxitin Cycloserine Fructose Agar
(CCFA)
·
Cefoxitin Cycloserine Egg-Yolk Agar (CCEY)
|
Selective media for isolation of Clostridium
difficile form suspected cases of pseudomembranous
colitis/antibiotic-associated diaeehea
|
· Cefsulodin-Irgasan-Novobiocin medium (CIN Medium)
|
Selective media for Yersinia (and may be used
for Aeromonas also)
|
· Columbia-Colistin Nalidixic Acid agar
(CNA Agar)
|
Selective media for the isolation of Gram-positive
cocci
|
· Cooked meat broth
·
Nutrient agar slopes
·
Semisolid nutrient agar stabs
·
Heated blood agar slopes
|
In general, used for preservation and storage of
bacterial cultures
|
· Crystal violet blood agar
|
Selective media for Streptococcus pyogenes
|
· Cysteine Lactose Electrolyte Deficient Media (CLED Media)
|
Most commonly used media for culturing urine samples
|
· Egg Saline Medium
|
Preservation of cultures of Gram-negative bacilli
|
· Egg Yolk Agar
|
Detection of lipase and lecithinase activity of Clostridium
species
|
· Ellner’s Medium
·
Medium of Duncan and Strong
·
Medium of Phillips
·
Alkaline Egg Medium
|
Specialized media to induce sporulation in Clostridium
|
· Fildes Blood-Digest Agar and Broth
· Levinthal’s Agar
|
Enriched media for recovery of Haemophilus influenzae
|
· Firm Agar (4% to 6% Agar)
|
Prevents swarming of Proteus mirabilis, P.
vulgaris and Clostridium tetani
|
· Fletcher’s Agar
·
Ellinghausen and McCullough Medium
· Ellinghausen-McCullough-Johnson-Harris (EMJH) Media
|
Solid media for isolation of Leptospira
|
· Glycerol Saline Transport Medium
|
Transport stool specimen for typhoid bacilli
|
· Heated Blood Agar/Chocolate Agar
|
Growth of fastidious organisms (E.g. Hemophilus
influenzae, Neisseria
gonorrhoeae and S. pneumoniae
|
· Hoyle’s Tellurite Lysed Blood Agar
·
Tinsdale Medium
|
Selective media for isolation of Corynebacterium
from throat swabs
|
· Loeffler Serum Slope
|
Stimulation of metachromatic granules in Corynebacterium
diphtheriae
|
· Lowenstein-Jensen Medium
·
Middlebrook Media
|
Selective media for isolation of Mycobacterium
tuberculosis from sputum and other samples
|
· MacConkey Agar
|
Differential media for Enterobacteriacaeae (i.e.,
lactose fermenting and non-lactose fermenting)
|
· MacConkey Bile Salt Lactose Agar
·
Brilliant MacConkey Agar
·
Leifson’s Deoxycholate-Citrate Agar (DCA)
·
Wilson and Blair’s Brilliant Green Bismuth- Sulphite Agar (BBSA)
·
Taylor’s Xylose Lysine Deoxycholate Agar (XLD)
· Hektoen Enteric Agar
· Salmonella–Shigella Agar
|
Differential and media for isolation of Salmonella
and Shigella from stool specimens
|
· Mannitol Salt Agar
|
Selective and indicator media for S. aureus
|
· Modified Barbour Stoenner Kelly medium (BSK)
|
Specialized media for Borrelia burgdorferi
|
· Modified Korthoff’s Medium
|
Liquid media for isolation of Leptospira
|
· Modified New York City Medium (contains colistin, lincomycin, trimethoprim,
amphotericin B)
|
Selective media for Neisseria gonorrhoeae
|
· Mueller-Hinton Agar
|
Performing antimicrobial susceptibility for bacteria
|
· Nutrient Agar (1% to 2% Agar)
|
Basal media in microbiology
Supports the
growth of all non-fastidious organisms
|
· Non-Nutrient Agar
|
Cultivation of parasites (e.g., Acanthamoeba)
|
· Peptone Water
|
· Basal media for
preparation for carbohydrate fermentation media
·
To ascertain whether a bacteria is motile or non-motile
· Basis for Indole test
|
· Phenol-Red Egg Yolk Polymyxin Agar
|
Selective media for isolation of Bacillus cereus
from food, feces, and vomitus
|
· Pike’s Media
|
Preservation of S. pyogenes, pneumococci, and
Hemophilus influenzae in nose and
throat swabs
|
· Polymyxin B-lysozyme-EDTA-Thallous
Acetate (PLET)
|
Selective media for isolation of Bacillus
anthracis from soil and other medium materials containing numerous spore
formers of other species
|
· Polymyxin B, Neomycin, Fusidic Acid
Media (PNF)
|
Selective media for S. pyogenes (or β-hemolytic Streptococcus)
|
· PPLO Medium (Contains Sterol)
|
Specialized media for Mycoplasma pneumoniae
|
· Pre-Reduced Anaerobically Sterilized
(PRAS) Media
|
Commercially available media for anaerobic organisms
|
· Proteose Peptone-Yeast Extraction
Broth
|
Media for carrying out biochemical tests for
anaerobes
|
· Requirements of X and V Factors
|
Isolation of Haemophilus influenzae
|
· Roswell Park Memorial Institute (RPMI)
1640 Medium
|
Cultivation of malarial parasites (i.e., Plasmodium)
|
· Robertson Cooked Meat Broth (RCMB)
|
· Growth of anaerobes
(e.g., Clostridium)
·
Maintaining stock cultures of anaerobic organisms
|
· Salt-Cooked Meat Broth (Cooked Meat
Broth with 10% NaCl)
|
Enrichment media for isolation of S. aureus
from heavily contaminated materials
|
· Semisolid Agar (0.05% to 0.1% Agar)
|
Prevents convection current and allows the growth of
anaerobic and micro-aerophilic organisms
|
· Skirrow’s Campylobacter Medium
(contains polymixin B, trimethoprim, vancomycin)
·
Preston Campylobacter Medium (contains polymixin B, rifampicin, trimethoprim)
·
Campy Blood Agar
·
CVA Medium (contains cefoperazone, vancomycin, amphotericin)
|
Selective media for Campylobacter jejuni
|
· Smith-Noguchi Medium
|
Cultivation of nonpathogenic treponemes (e.g.,
Reiter strain of Treponema phagedenis)
|
· Sorbitol MacConkey Agar
|
Isolation of verocytotoxin-producing
(enterohemorrhagic) E. coli of 0157 type (as it fails to ferment
D-sorbitol)
|
· Stuart Transport Media
·
Amies Transport Media
|
Maintaining the viability of gonococci on swabs
during transportation
|
· Tetrathionate Broth
·
Gram-Negative Broth
·
Selenite-F Broth
|
Enrichment media for isolation of Shigella
and Salmonella from stool samples
|
· Thayer-Martin Medium (contains
vancomycin, colistin, nystatin)
|
Selective media for Neisseria gonorrhoeae
|
· Thioglycollate Broth
·
Trypticase Soy Broth
|
All purpose enrichment broth for anaerobes, aerobes,
micro-aerophilic, and fastidious organisms
|
· Todd Hewitt Broth with Antibiotics
|
Selective and enrichment for Streptococccus
agalactiae in female genital specimens
|
· Triple Sugar Iron Agar (TSI) Medium
|
Differentiation of various members of
Enterobacteriaceae
|
· Wilkins-Chalgren Agar
|
Performing antimicrobial susceptibility of anaerobic
bacteria
|
Source:Microbiology notes