González-Andrade Baltazar, Santos-Lartigue Ramiro, Flores-Treviño Samantha, Ramirez-Ochoa Natalie Sofia, Bocanegra-Ibarias Paola, Huerta-Torres Francisco J, Mendoza-Olazarán Soraya, Villarreal-Treviño Licet, Camacho-Ortiz Adrián, Villarreal-Vázquez Hipólito, Garza-González Elvira
Servicio de Otorrinolaringología, Hospital Universitario "Dr. José Eleuterio González", Universidad Autónoma de Nuevo León, Monterrey, Nuevo Leon, Mexico.
Servicio de Gastroenterología, Hospital Universitario "Dr. José Eleuterio González", Universidad Autónoma de Nuevo León, Monterrey, Nuevo Leon, Mexico.
PLoS One. 2017 May 24;12(5):e0178115. doi: 10.1371/journal.pone.0178115. eCollection 2017.
The aim of the present study was to estimate the relative contribution of immunogenetic and microbiological factors in the development of recurrent tonsillitis in a Mexican population. Patients (n = 138) with recurrent tonsillitis and an indication of tonsillectomy (mean age: 6.05 years ± 3.00; median age: 5 years, female: 58; age range: 1-15 years) and 195 non-related controls older than 18 years and a medical history free of recurrent tonsillitis were included. To evaluate the microbial contribution, tonsil swab samples from both groups and extracted tonsil samples from cases were cultured. Biofilm production of isolated bacteria was measured. To assess the immunogenetic component, DNA from peripheral blood was genotyped for the TNFA-308G/A single-nucleotide polymorphism (SNP) and for the IL1B -31C/T SNP. Normal microbiota, but no pathogens or potential pathogens, were identified from all control sample cultures. The most frequent pathogenic species detected in tonsils from cases were Staphylococcus aureus (48.6%, 67/138) and Haemophilus influenzae (31.9%, 44/138), which were found more frequently in patient samples than in samples from healthy volunteers (P < 0.0001). Importantly, 41/54 (75.9%) S. aureus isolates were biofilm producers (18 weak and 23 strong), whereas 17/25 (68%) H. influenzae isolates were biofilm producers (10 weak, and 7 strong biofilm producers). Patients with at least one copy of the IL1B-31C allele had a higher risk of recurrent tonsillitis (OR = 4.03; 95% CI = 1.27-14.27; P = 0.013). TNFA-308 G/A alleles were not preferentially distributed among the groups. When considering the presence of IL1B-31C plus S. aureus, IL1B-31C plus S. aureus biofilm producer, IL1B-31C plus H. influenzae or IL1B-31C plus H. influenzae biofilm producer, the OR tended to infinite. Thus, the presence of IL1B-31C allele plus the presence of S. aureus and/or H. influenzae could be related to the development of tonsillitis in this particular Mexican population.
本研究的目的是评估免疫遗传学和微生物学因素在墨西哥人群复发性扁桃体炎发病中的相对作用。纳入了138例有复发性扁桃体炎且有扁桃体切除指征的患者(平均年龄:6.05岁±3.00;中位数年龄:5岁,女性58例;年龄范围:1 - 15岁)以及195名年龄超过18岁且无复发性扁桃体炎病史的非亲属对照。为评估微生物学因素的作用,对两组的扁桃体拭子样本以及病例组的扁桃体提取物样本进行培养。检测分离出细菌的生物膜形成情况。为评估免疫遗传学因素,对来自外周血的DNA进行基因分型,检测肿瘤坏死因子α(TNFA)-308G/A单核苷酸多态性(SNP)以及白细胞介素1β(IL1B)-31C/T SNP。在所有对照样本培养物中均鉴定出正常微生物群,但未发现病原体或潜在病原体。在病例组扁桃体中检测到的最常见致病菌种为金黄色葡萄球菌(48.6%,67/138)和流感嗜血杆菌(31.9%,44/138),在患者样本中发现这些菌种的频率高于健康志愿者样本(P < 0.0001)。重要的是,54株金黄色葡萄球菌分离株中有41株(75.9%)是生物膜形成菌(18株弱生物膜形成菌和23株强生物膜形成菌),而25株流感嗜血杆菌分离株中有17株(68%)是生物膜形成菌(10株弱生物膜形成菌和7株强生物膜形成菌)。携带至少一个IL1B - 31C等位基因拷贝的患者患复发性扁桃体炎的风险更高(比值比[OR]=4.03;95%置信区间[CI]=1.27 - 14.27;P = 0.013)。TNFA - 308 G/A等位基因在各组间无优先分布。当考虑IL1B - 31C与金黄色葡萄球菌同时存在、IL1B - 31C与金黄色葡萄球菌生物膜形成菌同时存在、IL1B - 31C与流感嗜血杆菌同时存在或IL1B - 31C与流感嗜血杆菌生物膜形成菌同时存在时,OR值趋于无穷大。因此,在这一特定的墨西哥人群中,IL1B - 31C等位基因的存在以及金黄色葡萄球菌和/或流感嗜血杆菌的存在可能与扁桃体炎的发病有关。