Presentation on theme: "Case Study Pathogenic Bacteriology 2009"— Presentation transcript:
1Case Study Pathogenic Bacteriology 2009 Luu, HelenChiu, AllenNavarrete, Maria
2Case SummaryA 2-year-old male child experienced upper respiratory infection.Anorexia and lethargy was seen.At the emergency room, he had a fever of 39.9°C.Physical examination showed a clear chest, exudative pharyngitis, and bilaterally enlarged cervical lymph nodes.Throat culture was taken and indicated no group A streptococci.Penicillin was given, but worsened and he became increasingly lethargic.He developed respiratory distress when admitted to the hospital.Examination revealed patient was febrile to 38.9°C and had an exudate in the posteriour pharynx that was yellowish, thick membrane which bled when scraped and removed.Patient’s medical history indicated no immunizations received.
3Key Information Pointing to Diagnosis Site of infection was the upper respiratory, pharynx.Symptoms were anorexia, drowsiness, mild fever, and respiratory distress.Examination showed exudate in posterior pharynx which bled when scraped.Figure 1 was a special isolation medium used to isolate the throat culture specimen.Figure 2 showed a Gram stain of the throat swab.No immunizations received.
4Diagnosis Pathogen causing infection : Corynebacterium diphtheriae C. diphtheriae is normal inhabitant of the nasopharynx that causes upper respiratory tract illness.Stages of infection in respiratory disease:Initial stage: sore throat, low-grade fever; followed by adherent pseudomembrane on the pharynx and tonsils.Later stage: localized damage, bleeding, difficulty in breathing, and mocarditis and peripheral neuritis.Figure 1 shows black colonies on tellurite agar.Tellurite selects and differentiate amongst Corynebacterium.Figure 2 shows small Gram-positive bacilli that are pleomorphic.Arrangement is palisade or Chinese letters.Figure 1Figure 2
5Classification,Gram Stain Results, and Microscopic Appearance of Corynebacterium diphtheriae Family: CorynebacteriaceaeGenus: CorynebacteriumSpecies: diphtheriaeSmall Gram-positive bacilli that are club-shaped.Arrangement = palisade or Chinese lettersClassification based on colony morphology.Subspecies:C. diptheriae mitischodis : black colonies with a gray peripheryC. diptheriae intermedius: large, gray coloniesC. diptheriae gravis; small, dull gray to blackAll produce an immunologically identical toxin with gravis being associated with the most severe disease.Gravis grows faster and depletes the local iron supply which allows earlier and greater toxin production.
6Diagnosis/Isolation/Identification/ of Corynebacterium diphtheriae Gram stain showing gram-positive bacillus with arrangement of Chinese lettersLoeffler’s agar slant:An enrichment medium that contains serum and egg to enhance the formation of metachromatic granules in C. diphtheriae.Stained with methylene blue for better visualization.Requires selective media containing tellurite to isolate the organism. Tellurite selects for Corynebacterium and other Gram-positive organisms and inhibits Gram-negative organismsCystine tellurite: longer shelf lifeTinsdale: differentiate amongst Corynebacterium; helps to distinguish other Corynebacterium species (diptheroids) that normally inhabit the nasopharynx.Colonies appear black or gray due to tellurite reduction.C. diphtheria would form brown halos around the colonies due to formation of ferric sulfide on tinsdale agar.
7Diagnosis/Isolation/Identification/ of Corynebacterium diphtheriae To prove that it can cause diphtheria, toxigenicity of C. diphtheriae strains is demonstrated.Most common in vitro assay is the Elek immunodiffusion test.-Based on double diffusion of diphtheria toxin and antitoxin in an agar medium.- Organism is streaked on the plate.Low concentration of iron is required in the medium which triggers toxin production.- A filter paper strip with diphtheria antitoxin is placed perpendicular to he streak of the organism.- Formation of a toxin- antitoxin precipitin band at the zone of equivalence indicates production of diphtheria toxin.
8Diseases and Pathogenesis of Disease Caused by Corynebacterium diphtheriae Normally found in the throats of healthy carriers.Organism can cause:Diphtheria which starts as a local infection of the mucous membrane causing a membranous pharyngitisCutaneous diphtheria which necrotic lesionswith occasional formation of a localpseudomembrane occur.More common in tropical and subtropical areas.Toxigenic strains cause severe disease.Secretes a potent heat-labilepolypeptide exotoxin that cause diphtheria.Exotoxin causes diphtheria, not the organism.In order for toxin production to occur:Bacterium must be lysogenized by abacteriophage that carries the tox gene.Aerobic conditions, alkaline pH of ,and a low iron level.
9Diseases and Pathogenesis of Disease Caused by Corynebacterium diphtheriae C. diphtheria toxin:Toxin binds to its cell surface receptor and enters through receptor mediated endocytosis.Acidification of endocytic vesicle allows A to dissociate from B.A enters the cytoplasm and catalyzes the transfer of ADP-ribose from NAD to the eukaryotic elongation factor-2.This results in inhibition of protein synthesis and cell death.
10Therapy, Prevention and Prognosis of Patient Infected with diphtheria For a patient infected with C. diphtheria, therapy treatment with antitoxin and antibiotics.Goal for both is to kill the organism and stop toxin production.Antitoxin is only effective before toxin enters the cell.The antitoxin neutralizes circulating (unbound) toxin that prevents progression of the disease.Sensitivity testing needs to be done prior to using antitoxin.Antibiotics such as penicillin, erythromycin to eliminate the organism.Usually given for 14 days.Individuals that recover from diphtheria may become asymptomatic carriers of the organism.Transmission is from person-to-person viarespiratory droplets.Rarely from skin to skin contact.Disease can keep spreading and become epidemic.Historically, diphtheria has been a deadly disease mainly for children.Patients infected with diphtheria should be isolated for a couple of days to prevent other individuals catching this contagious disease.
11Therapy, Prevention and Prognosis of Patient Infected with diphtheria Prognosis depends on the size and location of the membrane.Early detection and treatment will eliminate the organism and toxin.The longer the delay, the higher the death rate.If untreated, it is fatal due to airway obstruction, kidney and heart problems.VaccinationChildhood vaccination with diphtheria/pertussis/tetanus (DPT).Primary 3 doses given within half a year with anotherdose given later more than a year after that.Tetanus-diphtheria toxoid (Td) is also available and recommended as a booster every 10 years.Due to waning antitoxin titers, most individuals have antitoxin levels below the optimal level 10 years after the last dose.Schick SkinTest:Used to test for an individual’s immunity to diphtheria toxin.Done by injecting a small amount of diphtheria toxin intradermallyObservance for a local erythematous and necrotic reaction.An erythematous reaction with or without necrosis indicates that there is no antitoxin antiboides to neutralize the toxin and therefore, the individual is susceptible to diphtheria.
12Primary Research Article Van Damme, P., Burgess, M., “Immunogenicity of a combined diphtheria-tetanus-acellular pertussis vaccine in adults.” VaccineTwo clinical studies were set-up (1 in Belgium and 1 in Australia) to evaluate the immunogenicity of a booster vaccination, using either a dTpa vacine (Boostrix) or a licensed bivalent tetanus and diphtheria (Td) vaccine.METHODS:Randomly, chose 824 people that are over 18 years of age to receive either one dose of Boostrix or a licensed bivalent Td vaccine.No history of diphtheria or tetanus vaccination.No previous exposure to disease, for at least 5 years.Two blood samples, 1 prior to the vaccination and 1 one month after vaccination, were taken to evaluate the serostatus and imunnogenicity of the adults.Used ELISA test to measure antibody concentrations for diptheria, tetanus, and pertussis.Seroprotection for each antibody concentration were as followed:Anti-diphtheria antibody concentrations > 0.1 IU/mLAnti-tetanus antibody concentrations > 0.1 IU/mLCutt off for pertussis was 5 E1.u/mL
13Primary Research Article RESULTS:From the blood sample collected prior to vaccination, about a quarter or more of the test subjects were seronegative for antibodies against diphtheria, tetanus, and pertussis.From the blood sample collected 1 month post-vaccination, almost all individuals had seroprotection for both diphtheria and tetanus.Individuals vaccinated with Boostrix were also seropositive for the pertussis antigens PT, FHA, and PRN.
14Primary Research Article CONCLUSIONS:Even with childhood vaccination programs available in these countries, this shows that a portion of the adults in both Belgium and Australia is seronegative for antibodies against diphtheria and tetanus antitoxin.After one vaccination, individuals had antibody concentrations for the diseases that were above seroprotection limits.Despite the recommendation of getting vaccinated for the infectious diseases, this study comes to show that many individuals are either not up-to-date with getting a booster shot or have never been vaccinated before.Individuals are susceptible to the diseases and can become an epidemic problem once again.Vaccination for DPT wears off over timeand in order to prevent the spread of thisinfection or get infected, booster shotsmust be taken at least every 10 years.
15Take Home MessagesDisease includes diphtheria that starts as a local infection of the mucous membrane involving an exotoxin.High yields of toxin are synthesized only by lysogenic bacteria under iron deficiency conditions.Cutaneous diphtheria also seen but mainly in tropical areas.Typical symptoms are symptom low-grade fever,malaise, inflammation, edema, and exudatepharyngitis.Pathogen is the diphtheria toxin that the organism produces which can disseminate in the bloodstream and lymph nodes.Diagnostics include looking at site of infection, followed with culture swab to perform Gram stain, isolation on selective agar containing tellurite, and followed with in vitro or in vivo tests (ie. ELEK plate) to show presence of toxigenicity.Therapy is based on sensitivity testings followed by treatment with antitoxin and antibiotics.Prognosis depends on the size and location of the membrane.Early detection and treatment is crucial.Delayed treatment or no treatment can lead to more severe, fatal infections and even death.Prevention is DPT vaccination followed with a booster Td vaccine every 10 years.Transmission is spread by respiratory droplets from person-to-person.Threat is severe in children, unimmunized individuals, low levels of immunity individuals and frequent travelers.
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