Title: TB Genotyping in California 200405
1TB Genotyping in California 2004-05
CTCA Conference May 11, 2006
- Martin Cilnis, MS, MPH
- Tuberculosis Control Branch
- California Department of Health Services
2Objectives
- Status of the Universal Genotyping Project in
California 2004-05 - Epidemiology of genotype clusters
- Describe distribution and size of clusters
- Common clusters
- Characteristics of clustering
Genotype shared by at least 2 cases
3Del Norte
Genotyping Initiative Participation by County
Siskiyou
Modoc
Humboldt
Trinity
Shasta
Lassen
Tehama
Mendocino
Plumas
Glenn
Butte
Sierra
Colusa
Lake
Nevada
Yuba
Sutter
Placer
Yolo
Sonoma
Amador
Napa
El Dorado
Sacramento
Solano
Marin
Alpine
Berkeley
Calaveras
Contra Costa
San Joaquin
San Francisco
Tuolumne
Alameda
37 (61)
San Mateo
Mono
Stanislaus
Santa Clara
Mariposa
Merced
Santa Cruz
11 (18)
Madera
San Benito
Fresno
13 (21)
Monterey
Inyo
Tulare
Kings
San Luis Obispo
Kern
Santa Barbara
Ventura
San Bernardino
Los Angeles
Pasadena
Orange
Long Beach
Riverside
San Diego
Imperial
4Genotyping participation in CA 2004-05
4597 culture-positive TB cases reported in 2004-05
Universal 54
Selective 13
Not participating 33
1701 (37 of culturepositive) isolates submitted
for genotyping in 2004-05
Universal 62
Selective 14
Not participating 5
5Percentage of Culture-Positive Isolates Submitted
by Year
6CA Genotyping Results2004-05
7Description of Genotype Clusters in California
2004-05
- Frequency and distribution of clusters
- Common cluster types
8Frequency of Cluster SizeN190 clusters
9Distribution of Clusters N190 clusters
10Top 15 Cluster Names,CA 2004-05
11Top 15 Cluster Names,CA 2004-05
12Summary Description of Genotype Clusters
- The majority of clusters (54) contain 2 cases
- Most clusters (78) are found in more than one
jurisdiction - Local TB programs are unable to track clusters
outside of their jurisdiction because each
receives their own genotyping data - Solution Currently, 12 jurisdictions agreed to
share genotyping information
13Summary Description of Genotype Clusters
- The largest clusters (CA_021 and CA_006) are
widespread throughout the state/world - RFLP analysis can split clusters
- RFLP done for 12 CA_006 and 14 CA_021 isolates
- 13 (50) unique
- 13 (50) in 5 clusters
14Analysis of Clusters,CA 2004-05
- Is clustering associated with place of birth?
- U.S.-born and foreign-born?
Analysis includes data from universal
jurisdictions only and excludes clusters CA_021
and CA_006
15Place of Birth and Clustering
Significant pX2 lt 0.05
16Analysis of Clusters,CA 2004-05
- Is clustering associated with any TB case risk
factors? - Alcohol abuse
- Homelessness
- Injection and non-injection drug use
- Correctional facility resident/employee
- Health care worker
- HIV/AIDS
- Migratory agricultural worker
- Long-term care facility resident
- Multiple risk factrors
17Case Risk and Clustering
Significant pX2 lt 0.05
18Summary Place of Birth, Case Risk and Clustering
- U.S.-born cases are more likely to have clustered
genotypes than FB cases - Among the FB cases, there is no significance in
the time since arrival into the U.S. and
clustering - Higher proportions of clustering in alcohol
abuse, homelessness, IDU, and NIDU groups - Cases with multiple risk factors are more likely
to cluster than those with only one or none
19 - Multivariate Analysis
- Predictors include
- U.S.-born
- Age lt 45 years
- White or African-American race/ethnicity
- Case risk factors
- Homelessness
- Alcohol abuse
- Non-injection drug use
- Multiple risk factors
20 - Multivariate Analysis
- Having multiple risk factors is a significant
predictor of clustering regardless whether the
case is U.S.- or foreign-born - In U.S. cases, clustering is associated with
agelt45, African-American race/ethnicity, alcohol
abuse, and having multiple case risk factors
21Limitations
- Non-universal genotyping participation selection
bias resulting in under- or over-estimate of
clustering - Incomplete matching to RVCT selection bias
resulting in under- or over-estimate of
clustering - Limited discriminatory power of PCR genotyping
methods for Beijing and Manila strains results
in over-estimation of clustering
22Next Steps
- Increase participation in universal genotyping
- Sharing of genotyping data throughout the state
- Use of genotyping and epidemiologic data in TB
control
23Questions about genotyping?
- Contact
- Martin Cilnis
- Epidemiologist, TB Control Branch
- mcilnis_at_dhs.ca.gov
- (510) 620-3015