J 2011

"Mycobacterium avium subsp. hominissuis" in Neck Lymph Nodes of Children and their Environment Examined by Culture and Triplex Quantitative Real-Time PCR

KAEVSKA, Marija, Iva SLANÁ, Petr KRALIK, Udo REISCHL, Jaroslava OROSOVA et. al.

Basic information

Original name

"Mycobacterium avium subsp. hominissuis" in Neck Lymph Nodes of Children and their Environment Examined by Culture and Triplex Quantitative Real-Time PCR

Authors

KAEVSKA, Marija (807 North Macedonia), Iva SLANÁ (203 Czech Republic, belonging to the institution), Petr KRALIK (203 Czech Republic), Udo REISCHL (276 Germany), Jaroslava OROSOVA (203 Czech Republic), Alena HOLČÍKOVÁ (203 Czech Republic, guarantor, belonging to the institution) and Ivo PAVLÍK (203 Czech Republic)

Edition

Journal of Clinical Microbiology, Washington, American Society for Microbiology, 2011, 0095-1137

Other information

Language

English

Type of outcome

Článek v odborném periodiku

Field of Study

30300 3.3 Health sciences

Country of publisher

United States of America

Confidentiality degree

není předmětem státního či obchodního tajemství

Impact factor

Impact factor: 4.153

RIV identification code

RIV/00216224:14110/11:00051667

Organization unit

Faculty of Medicine

UT WoS

000285787100022

Keywords in English

Mycobacterium avium

Tags

International impact
Změněno: 12/4/2012 09:25, Mgr. Michal Petr

Abstract

V originále

“Mycobacterium avium subsp. hominissuis” often causes cervical lymphadenitis in children; its prompt and accurate identification enables adequate therapy, tracing, and prevention. The aims of this study were to determine the causative agent of lymphadenitis using culture, PCR, and triplex quantitative real-time PCR (qPCR) methods with DNA directly isolated from tissue, as well as to identify possible sources of infection from the environment. We confirmed the diagnoses by detecting M. avium subsp. hominissuis using qPCR with DNA directly isolated from lymph node biopsy specimens of two patients. In order to trace the source of infection from the environment, a method of DNA isolation from soil and other environmental samples, such as dust, cobwebs, and compost, was developed. The triplex qPCR examination revealed the presence of M. avium subsp. hominissuis in a high proportion of the environmental samples (42.8% in the first patient’s house and 47.6% in the second patient’s house). Both patients were also exposed to M. avium subsp. avium, which was present due to the breeding of infected domestic hens. The high infectious dose of M. avium subsp. hominissuis or the increased susceptibility of humans to M. avium subsp. hominissuis compared to M. avium subsp. avium could be the reason why the children were infected with M. avium subsp. hominissuis.