Surveillance : Workshop IIbamras.ddc.moph.go.th/userfiles/13_00-14_30 Surveillance Work...
Transcript of Surveillance : Workshop IIbamras.ddc.moph.go.th/userfiles/13_00-14_30 Surveillance Work...
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Chanwit Tribuddharat, M.D., Ph.D.
Siriraj Hospital, Mahidol University
ASM Ambassador to Thailand
www.asm.org
การเฝ้าระวังโรค : การปฏิบัติการ 2 Surveillance : Workshop II
mailto:[email protected]
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Patient’s history
A 37 years old Thai man
Acute Leukemia
Long-term hospitalization
Consumed food obtained from
street vendor before developing
bacteremia and diarrhea
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Methods
2 isolates of V. cholerae non-O1, non-
O139 have been recovered from
blood and stool culture
Antibiotic susceptibility test indicated
an ESBL production
Genetic confirmation was performed
by PCR amplification
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ESBL Screening in V. cholerae
non-O1, non-O139
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Horizontal Gene Transfer From
Enteric Bacteria?
Stool examination for other multidrug resistant bacteria was done
On 100 mg/L of ceftazidime MacConkey agar plate, Aeromonas sobria and 2 strains of Klebsiella pneumoniae were identified
PCR amplifications identified a blaVEB-1 and int genes in A. sobria
blaSHV and blaTEM were identified in K. pneumonia, but no blaVEB-1
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ESBL screening with A. sobria and K. pneumoniae
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Plasmid and conjugation assay
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Liquid phase conjugation
Laboratory strain of E. coli was used
as a recipient (TOP10, Invitrogen)
Donor : Recipient = 1 : 10
Selection of transconjugants on 100
mg/L of ceftazidime MacConkey agar
plate
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TOP10 E. coli Transconjugants
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Plasmid profiles of AmpC hyperproducers
M 108 T108 No.58 108 215 232 197
Single AmpC plasmid has been isolated
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Disk Diffusion of TOP10(p108)
15 mm
23 mm
25 mm
Cefotaxime
Cefotaxime/clavulanate
Cefoxitin
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Gene Orientation in pT108
•99% DNA sequence matched with plasmid from Taiwan
(Deposited in GenBank in Oct, 2006)
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The dot-blot hybridizations were performed on
247 strains of ESBL producing strains
(A) dhps probe (B) ColE1 ori probe
A B
dhps probe ColE1 probe
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86 kb Resistance Island Acinetobacter baumannii
Total of 45 resistance genes
PLoS Genetics: www.plosgenetics.org January 2006, Vol. 2, Issue 1 14
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Conventional PCR amplification of 5’ and 3’ junctions
PCR amplification Positive (No. of isolates/%)
5ʹand 3ʹ Junctions 23/63.8
5’ Junction 3/8.3
3’ Junction 7/19.44
Junction absent 3/8.3
OriC
AYE
5’ ATPase 3’ ATPase
AbaR1
AbaR2/ACICU
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PCR amplification Positive (No. of isolates/%)
intI1 13/36.11
blaVEB-1 7/19.44
arr-2 10/27.77
cmlA 5/13.8
blaOXA-10 9/25
blaIMP All negative
blaOXA-23 36/100
blaVIM All negative
blaTEM-1 14/38.8
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Amplification of variable region
and characterization of Integron
carrying isolates 32/36
5’CS 3’CS
intI1
Variable region
5ʹCS cmlA arr-2 aadB blaVEB-1 3ʹCS
5ʹCS-VEB-1R VEB-1F-
arr2R arr2F-cmlAR
cmlAF-3ʹCS
Ab03_168
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Headline in Hong Kong March 11, 2010
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Real Life Situation (1)
Long-term admission patient
– Unconscious
– Incontinence
– Catheterized
– Tracheostomy
– Bed sore
– History of MRSA and Pseudomonas
aeruginosa
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Real Life Situation (2)
Diaper change by one medical personnel
Soap and water
Baby powder (talcum) for odor masking
Patient was coated with feces containing
105 CFU/g of MRSA/Pseudomonas
IV injection introduces 1 bacteria into
blood stream
Bacteria divide every 30 minutes
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Real Life Situation (3)
Next day (24 hours later)
– There are 248 bacteria (THAT IS
281,474,976,710,656 cells!) in patient’s blood
The care team still didn’t wash their hands
The resistant organisms spread further
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Conclusions
There were evidences of horizontal gene
transfer of resistance genes from
nosocomial pathogens to virulent
pathogen of community origin
Prohibition of food consumption not
prepared by the hospital should be
enforced
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Conclusions Physicians should pay attention on whereabouts the reservoirs of multi-drug resistant bacteria
Awareness of unusual resistant phenotype also should be raised.
Reservoirs of multi-drug resistant bacteria exist
Decolonization of resistant bacteria may be needed in certain patients.
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