Epidemic genotype of Coxiella burnetii among goats, sheep, and humans in the Netherlands.
In previous studies, genotypic investigations of human and animal samples in the Netherlands were performed by using a 3-locus multilocus variable-number tandem repeats analysis (MLVA) panel and single-nucleotide polymorphism genotyping, respectively (2,3). The first study, performed on relatively few samples from a minor part of the affected area, showed that farm animals and humans in the Netherlands were infected by different but apparently closely related genotypes. More recently, genotyping by using a 10-locus MLVA panel provided additional information about the genotypic diversity of Coxiella burnetii among ruminants in the Netherlands: 1 dominant MLVA genotype was identified among goats and sheep throughout the entire affected Q fever area (4). A different panel of MLVA markers was applied to human samples (5). Four markers that are shared by both panels showed identical alleles in human and animal samples, again implicating goats and sheep as possible sources of the outbreak.
MLVA, which is based on relatively unstable repetitive DNA elements, is sometimes criticized for producing results that are too discriminatory or difficult to reproduce in different settings (6). Because of their instability, use of tandem repeats as genotyping targets can lead to problems with data interpretation and to overestimation of genotypic diversity by showing small variations in MLVA genotypes in isolates of otherwise identical background.
We used a more stable, sequence-based typing method, multispacer sequence typing (MST), on samples from humans and a group of ruminant animals (goats, sheep, and cattle) to establish a firmer correlation between Q fever cases in humans and animals (7). We identified MST genotypes using a Web-based MST database (http://ifr48.timone.univmrs.fr/MST_Coxiella/mst) containing genotypes from several countries in Europe. Ultimately, this study could answer the question of whether the current outbreak situation could have been caused by a specific C. burnetii strain in the ruminant population in the Netherlands. Real-time PCR-positive specimens from 10 humans and 9 Q fever-positive specimens from goats and sheep collected from various locations throughout the affected area were used (8). We also included Q fever-positive specimens from cattle to rule out cattle as a possible source of Q fever infection. Five samples of cow's milk and 1 bovine vaginal swab sample were analyzed (online Appendix Table, wwwnc.cdc.gov/ EID/article/18/5/11-1907-TA1.htm). MST33 was identified in 9 of 10 tested human samples and in the remaining 8 of 9 clinical samples from goats and sheep (online Appendix Table). MST33 has been isolated incidentally in nonoutbreak situations in human clinical samples obtained in France during 1996, 1998, and 1999 and from a placenta of an asymptomatic ewe in Germany during 1992. All samples from cattle in the Netherlands, 1 goat, and cow's milk contained genotype MST20. Genotype MST20 has also been identified in human clinical samples from France, in a cow's placenta from Germany isolated in 1992 and in rodents from the United States isolated in 1958. In 1 human bronchoalveolar lavage sample, a novel (partial) MST genotype was found. This may be an incidental Q fever case unrelated to the outbreak situation. Because no historical genotyping data for the period before the outbreak of Q fever in the Netherlands are available, this explanation needs further research.
MST genotyping shows the presence of genotype MST33 in clinical samples from humans, goats and sheep. These results confirm that goats and sheep are the source of human Q fever in the Netherlands. Few worldwide genotyping studies have been conducted, and therefore information about a possible global persistence of this genotype is lacking. This study also indicates that the outbreak among humans is not linked to C. burnetii in cattle, although the infection is widespread among dairy herds in the Netherlands (10), exemplifying that most outbreaks are related to goats and sheep rather than to cattle. In conclusion, the increase in the number of Q fever cases in the Netherlands among humans most likely results from MST33 in the goat population in the Netherlands and could have been facilitated by intensive goat farming in the affected area and its proximity to the human population.
(1.) Roest HIJ, Tilburg JJHC, van der Hoek W, Vellema P, van Zijderveld FG, Klaassen CHW, et al. The Q fever epidemic in the Netherlands: history, onset, response and reflection. Epidemiol Infect. 2011;139:1-12. http://dx.doi.org/10.1017/ S0950268810002268
(2.) Huijsmans CJJ, Schellekens JJA, Wever PC, Toman R, Savelkoul PHM, Janse I, et al. Single-nucleotide-polymorphism-genotyping of Coxiella burnetii during a Q fever outbreak in the Netherlands. Appl Environ Microbiol. 2011;77:2051-7. http://dx.doi.org/10.1128/AEM.02293-10
(3.) Klaassen CHW, Nabuurs-Franssen MH, Tilburg JJHC, Hamans MAWM, Hor revorts AM. Multigenotype Q fever outbreaks, the Netherlands. Emerg Infect Dis. 2009;15:613-4. http://dx.doi.org/10.3201/ eid1504.081612
(4.) Roest HIJ, Ruuls RC, Tilburg JJHC, Nabuurs-Franssen MH, Klaassen CHW, Vellema P, et al. Molecular epidemiology of Coxiella burnetii from ruminants in Q fever outbreak, the Netherlands. Emerg Infect Dis. 2011;17:668-75.
(5.) Tilburg JJHC, Rossen JWA, van Hannen EJ, Melchers WJG, Hermans MHA, van de Bovenkamp J, et al. Genotypic diversity of Coxiella burnetii in the 2007-2010 Q fever outbreak episodes in the Netherlands. J Clin Microbiol. 2012;50:1076-8. http://dx.doi.org/10.1128/JCM.05497-11
(6.) van Belkum A. Tracing isolates of bacterial species by multilocus variable number of tandem repeat analysis (MLVA). FEMS Immunol Med Microbiol. 2007;49:22-7. http://dx.doi.org/10.1111/j.1574-695X. 2006.00173.x
(7.) Glazunova O, Roux V, Freylikman O, Sekeyova Z, Fournous G, Tyczka J, et al. Coxiella burnetii genotyping. Emerg Infect Dis. 2005;11:1211-7.
(8.) Tilburg JJHC, Melchers WJG, Pettersson AM, Rossen JWA, Hermans MHA, van Hannen EJ, et al. Interlaboratory evaluation of different extraction and real-time PCR methods for detection of Coxiella burnetii DNA in serum. J Clin Microbiol. 2010;48:3923-7. http://dx.doi. org/10.1128/JCM.01006-10
(9.) Bleichert P, Hanczaruk M, Stasun L, Fran goulidis D. MST vs. IS1111 distribution: a comparison of two genotyping systems for Coxiella burnetii. In: Proceedings of the 6th International Meeting on Rickettsiae and Rickettsial Diseases; Heraklion, Crete, Greece; 2011 Jun 5-7. p. 187.
(10.) Muskens J, van Engelen E, van Maanen C, Bartels C, Lam TJGM. Prevalence of Coxiella burnetii infection in Dutch dairy herds based on testing bulk tank milk and individual samples by PCR and ELISA. Vet Rec. 2011;168:79-82. http://dx.doi. org/10.1136/vr.c6106
Jeroen J.H.C. Tilburg, Hendrik-Jan I.J. Roest, Sylvain Buffet, Marrigje H. Nabuurs-Franssen, Alphons M. Horrevorts, Didier Raoult, and Corne H.W. Klaassen
Author affiliations: Canisius Wilhelmina Hospital, Nijmegen, the Netherlands (J.J.H.C. Tilburg, M.H. Nabuurs-Franssen, A.M. Horrevorts, C.H.W. Klaassen); Central Veterinary Institute part of Wageningen UR, Lelystad, the Netherlands (H.I.J. Roest); and Universite de la Mediterranee, Marseille, France (S. Buffet, D. Raoult)
Address for correspondence: Corne H.W. Klaassen, Department of Medical Microbiology and Infectious Diseases, Canisius Wilhelmina Hospital, Weg door Jonkerbos 100, 6532 SZ Nijmegen, the Netherlands; email: c.klaassen@ cwz.nl
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|Author:||Tilburg, Jeroen J.H.C.; Roest, Hendrik-Jan I.J.; Buffet, Sylvain; Nabuurs-Franssen, Marrigje H.; Hor|
|Publication:||Emerging Infectious Diseases|
|Article Type:||Letter to the editor|
|Date:||May 1, 2012|
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