High Streptococcus pneumoniae colonization prevalence among HIV-infected Kenyan parents in the year before pneumococcal conjugate vaccine introduction

被引:21
作者
Conklin, Laura M. [1 ,4 ]
Bigogo, Godfrey [2 ,5 ]
Jagero, Geofrey [2 ]
Hampton, Lee [1 ]
Junghae, Muthoni [2 ]
Carvalho, Maria da Gloria [1 ]
Pimenta, Fabiana [1 ]
Beall, Bernard [1 ]
Taylor, Thomas [1 ]
Plikaytis, Brian [1 ]
Laserson, Kayla F. [2 ]
Vulule, John [3 ]
Van Beneden, Chris [1 ]
Whitney, Cynthia G. [1 ]
Breiman, Robert F. [2 ]
Feikin, Daniel R. [2 ]
机构
[1] Ctr Dis Control & Prevent, Div Bacterial Dis, Atlanta, GA 30329 USA
[2] Ctr Dis Control & Prevent, Kenya Med Res Inst, Kisumu, Kenya
[3] Kenya Govt Med Res Ctr, Ctr Global Hlth Res, Kisumu, Kenya
[4] Ctr Dis Control & Prevent, Resp Dis Branch, Atlanta, GA 30333 USA
[5] CDC Res Collaborat, KEMRI, Kisumu 40100, Kenya
关键词
Streptococcus pneumoniae; Pneumococcus; Nasopharyngeal colonization; HIV; Kenya; Africa; PCV; IMMUNODEFICIENCY-VIRUS-INFECTION; NASOPHARYNGEAL CARRIAGE; SEROTYPE; 19A; ANTIBIOTIC-RESISTANCE; GENETIC-STRUCTURE; RISK-FACTORS; HIGH-RATES; ADULTS; CHILDREN; DISEASE;
D O I
10.1186/s12879-015-1312-2
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Streptococcus pneumoniae is a leading cause of pneumonia, meningitis and sepsis in developing countries, particularly among children and HIV-infected persons. Pneumococcal oropharyngeal (OP) or nasopharyngeal (NP) colonization is a precursor to development of invasive disease. New conjugate vaccines hold promise for reducing colonization and disease. Methods: Prior to introduction of 10-valent pneumococcal conjugate vaccine (PCV10), we conducted a cross-sectional survey among HIV-infected parents of children < 5 years old in rural Kenya. Other parents living with an HIV-infected adult were also enrolled. After broth enrichment, NP and OP swabs were cultured for pneumococcus. Serotypes were identified by Quellung. Antimicrobial susceptibility was performed using broth microdilution. Results: We enrolled 973 parents; 549 (56.4 %) were HIV-infected, 153 (15.7 %) were HIV-uninfected and 271 (27.9 %) had unknown HIV status. Among HIV-infected parents, the median age was 32 years (range 15-74) and 374/549 (68 %) were mothers. Pneumococci were isolated from 237/549 (43.2 %) HIV-infected parents and 41/153 (26.8 %) HIV-non-infected parents (p = 0.0003). Colonization with PCV10 serotypes was not significantly more frequent in HIV-infected (12.9 %) than HIV-uninfected parents (11.8 %; p = 0.70). Among HIV-infected parents, cooking site separate from sleeping area and CD4 count > 250 were protective (OR = 0.6; 95 % CI 0.4, 0.9 and OR = 0.5; 95 % CI 0.2, 0.9, respectively); other associations were not identified. Among 309 isolates tested from all parents, 255 (80.4 %) were penicillin non-susceptible (MIC = 0.12 mu g/ml). Conclusions: Prevalence of pneumococcal colonization is high among HIV-infected parents in rural Kenya. If young children are the pneumococcal reservoir for this population, PCV10 introduction may reduce vaccine-type colonization and disease among HIV-infected parents through indirect protection.
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