Spatial heterogeneity of extensively drug resistant-tuberculosis in Western Cape Province, South Africa

被引:4
|
作者
Sy, Karla Therese L. [1 ]
Leavitt, Sarah, V [2 ]
de Vos, Margaretha [3 ]
Dolby, Tania [4 ]
Bor, Jacob [1 ,2 ]
Horsburgh, C. Robert [1 ,2 ,5 ,6 ]
Warren, Robin M. [3 ]
Streicher, Elizabeth M. [3 ]
Jenkins, Helen E. [2 ]
Jacobson, Karen R. [6 ]
机构
[1] Boston Univ, Dept Epidemiol, Sch Publ Hlth, Boston, MA USA
[2] Boston Univ, Dept Biostat, Sch Publ Hlth, Boston, MA USA
[3] Stellenbosch Univ, Fac Med & Hlth Sci, South African Med Res Council Ctr TB Res, Div Mol Biol & Human Genet,DSI NRF Ctr Excellence, Cape Town, South Africa
[4] Natl Hlth Lab Serv, Cape Town, South Africa
[5] Boston Univ, Dept Global Hlth, Sch Publ Hlth, Boston, MA USA
[6] Boston Univ, Sch Med & Boston Med Ctr, Sect Infect Dis, Boston, MA 02215 USA
基金
美国国家卫生研究院;
关键词
TRANSMISSION; HOTSPOTS;
D O I
10.1038/s41598-022-14581-4
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Tuberculosis (TB) remains a leading infectious disease killer globally. Treatment outcomes are especially poor among people with extensively drug-resistant (XDR) TB, until recently defined as rifampicin-resistant (RR) TB with resistance to an aminoglycoside (amikacin) and a fluoroquinolone (ofloxacin). We used laboratory TB test results from Western Cape province, South Africa between 2012 and 2015 to identify XDR-TB and pre-XDR-TB (RR-TB with resistance to one second-line drug) spatial hotspots. We mapped the percentage and count of individuals with RR-TB that had XDR-TB and pre-XDR-TB across the province and in Cape Town, as well as amikacin-resistant and ofloxacin-resistant TB. We found the percentage of pre-XDR-TB and the count of XDR-TB/pre-XDR-TB highly heterogeneous with geographic hotspots within RR-TB high burden areas, and found hotspots in both percentage and count of amikacin-resistant and ofloxacin-resistant TB. The spatial distribution of percentage ofloxacin-resistant TB hotspots was similar to XDR-TB hotspots, suggesting that fluoroquinolone-resistace is often the first step to additional resistance. Our work shows that interventions used to reduce XDR-TB incidence may need to be targeted within spatial locations of RR-TB, and further research is required to understand underlying drivers of XDR-TB transmission in these locations.
引用
收藏
页数:9
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