Haddad Maryam B, Diem Lois A, Cowan Lauren S, Cave M Donald, Bettridge Juli, Yun Lourdes, Winkler Carolyn S, Ingman Denise D, Oemig Tanya V, Lynch Allen, Montero Jose T, McCombs Scott B, Ijaz Kashef
Division of Tuberculosis Elimination, Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA.
Am J Prev Med. 2007 Mar;32(3):239-43. doi: 10.1016/j.amepre.2006.10.013. Epub 2007 Jan 22.
As tuberculosis incidence declines in the United States, a new tool for TB control efforts is Mycobacterium tuberculosis genotyping. Colorado, Iowa, Montana, New Hampshire, West Virginia, and Wisconsin began routine genotyping of all culture-confirmed TB cases in October 2000.
M. tuberculosis isolates from cases reported October 2000 through December 2003 were genotyped by spoligotyping, mycobacterial interspersed repetitive units, and IS6110-based restriction fragment length polymorphism methods. Genotyping results were linked to demographic variables from national surveillance records. Patients who were in genotype clusters were interviewed and their records reviewed to determine possible transmission links among clustered patients. Final analysis was completed during April 2004 through June 2005.
Of 971 reported TB cases, 774 (80%) were culture-confirmed, of which 728 (94%) were genotyped. Most genotyped isolates (634 [87%]) were unique. Within 36 clusters linking 94 individuals, four clusters involved both U.S.- and foreign-born individuals. For eight clusters, genotyping results led to the discovery of previously unsuspected transmission. Transmission links between individuals were established in 21 (58%) of the 36 clusters.
In these six low-incidence states, most isolates had unique genotypes, suggesting that most cases arose from activation of latent infection. Few TB clusters involved the foreign-born. For 58% of genotype clusters, epidemiologic investigation ascertained that clustering represented recent M. tuberculosis transmission.
随着美国结核病发病率的下降,结核分枝杆菌基因分型成为结核病防控工作的一项新工具。科罗拉多州、爱荷华州、蒙大拿州、新罕布什尔州、西弗吉尼亚州和威斯康星州于2000年10月开始对所有培养确诊的结核病病例进行常规基因分型。
对2000年10月至2003年12月报告病例的结核分枝杆菌分离株采用间隔寡核苷酸分型、分枝杆菌插入重复单位和基于IS6110的限制性片段长度多态性方法进行基因分型。基因分型结果与国家监测记录中的人口统计学变量相关联。对基因分型聚类中的患者进行访谈并审查其记录,以确定聚类患者之间可能的传播联系。最终分析于2004年4月至2005年6月完成。
在报告的971例结核病病例中,774例(80%)培养确诊,其中728例(94%)进行了基因分型。大多数基因分型分离株(634株[87%])是独特的。在连接94人的36个聚类中,有4个聚类涉及美国出生和外国出生的个体。对于8个聚类,基因分型结果导致发现了先前未被怀疑的传播情况。在36个聚类中的21个(58%)中建立了个体之间的传播联系。
在这六个低发病率州,大多数分离株具有独特的基因型,这表明大多数病例是由潜伏感染激活引起的。很少有结核病聚类涉及外国出生者。对于58%的基因分型聚类,流行病学调查确定聚类代表了近期结核分枝杆菌的传播。