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A Q fever outbreak associated to courier transport of pets


Authors: Eva Alonso aff001;  Domingo Eizaguirre aff002;  Idoia Lopez-Etxaniz aff003;  José Ignacio Olaizola aff003;  Blanca Ocabo aff004;  Jesús Felix Barandika aff005;  Isabel Jado aff006;  Raquel Álvarez-Alonso aff005;  Ana Hurtado aff005;  Ana Luisa García-Pérez aff005
Authors place of work: Department of Epidemiology, Subdirección de Salud Pública de Bizkaia, Gobierno Vasco, Bilbao, Bizkaia, Spain aff001;  Department of Epidemiology, Subdirección de Salud Pública de Bizkaia, Gobierno Vasco, Vitoria-Gasteiz, Araba, Spain aff002;  Department of Epidemiology, OSALAN-Instituto Vasco de Seguridad y Salud Laborales, Barakaldo, Bizkaia, Spain aff003;  Department of Agriculture, Diputación Foral de Bizkaia, Bilbao, Bizkaia, Spain aff004;  Animal Health Department, NEIKER- Instituto Vasco de Investigación y Desarrollo Agrario, Derio, Bizkaia, Spain aff005;  National Microbiology Center, Instituto de Salud Carlos III, Majadahonda, Madrid, Spain aff006
Published in the journal: PLoS ONE 14(11)
Category: Research Article
doi: https://doi.org/10.1371/journal.pone.0225605

Summary

On August 3rd, 2017, a Q fever outbreak alert was issued at a courier company that in addition to urgent freight transport offered pet delivery services. The epidemiological investigation set the exposition period between June 1 and August 8. In this period, 180 workers from two operational platforms for parcel distribution located in two provinces of the Basque Country (Bizkaia and Araba) were exposed; 64 filled a questionnaire and provided blood samples for serological testing, resulting in 10 confirmed cases (15.6%) and six (9.4%) probable cases. Nine workers (8 confirmed and 1 probable) showed Q fever symptoms, including pneumonia (five cases), and required medical care services, including one hospital admission. The attack rate was 25% (16/64), being higher among workers that visited the Bizkaia platform. This suggested that the origin of the outbreak was in the Bizkaia platform, where animals in transit waited at a pet holding site until being moved to their destination. Environmental samples consisting on 19 surface dust and two aerosol samples were collected at the Bizkaia platform to investigate the presence of C. burnetti DNA. All dust samples were positive by real time PCR, the lowest Ct values being found in dust collected at the pet holding facilities, and therefore suggesting that contamination originated at the pet holding site. The genotype identified in dust was SNP1/MST13, one of the most commonly identified genotypes in goats and sheep in the Basque Country. During the exposure period, two deliveries of miniature goats were made, of which only one could be investigated and tested negative. Although the contamination source could not be unequivocally identified, transport of ruminants was banned at the company, and Q fever was included among the occupational-associated health risks.

Keywords:

Public and occupational health – Ruminants – Epidemiology – Serology – Goats – Veterinary epidemiology – Q fever – Coxiella burnetii

Introduction

The intracellular bacterium Coxiella burnetii is the causative agent of Q fever in people and animals. It has been reported that the inhalation of 1 to 10 bacteria can cause disease in people. The most important symptoms are fever, pneumonia and / or hepatitis, though about 60% of infected people are asymptomatic [1]. C. burnetii is worldwide distributed, the only exception being New Zealand [1], and numerous outbreaks of Q fever have been reported. EFSA [2] compiled 39 outbreaks of Q fever in Europe between 1982 and 2007, 32 of them being related to small ruminants. This is due to the fact that Q fever infected farm animals shed millions of bacteria during abortion and parturition through different routes of excretion such as feces, uterine fluids, milk, and placentas [3]. However, pets [1,2], as well as wild species [4], may also carry C. burnetii. In general, outbreaks of human Q fever are related to contact with the animal reservoirs, which maintain the infection active and shed C. burnetii by different routes to the environment. Therefore farmers, veterinarians, shearers or slaughterhouse workers, among others, are those most commonly affected. However, outbreaks occasionally occur in urban nuclei far from the source of infection when weather conditions favor wind transport of C. burnetii [58]. Moreover, C. burnetii can also contaminate materials and be transported from one place to another giving rise to unexpected outbreaks, and making the epidemiological investigation challenging. Environmental sampling proved very useful in tracing back recent outbreaks that occurred in our region at workplaces without apparent contact with animals [9,10]. In addition, the DNA obtained from dust allowed genotyping of the involved isolate and helped to identify the probable source of infection. In this study we present the investigation of an outbreak of Q fever in an express transport company authorized for the transport of pets.

Material and methods

Case presentation

The outbreak occurred in the Basque Country (northern Spain), a region divided into three provinces: Araba, Bizkaia and Gipuzkoa. On August 3, 2017, the Microbiology Laboratory of Hospital Universitario de Cruces (Bizkaia) informed the Epidemiology Surveillance Unit of the province of a possible Q fever outbreak at a courier company located in Bizkaia. The company confirmed that in July several workers of the company branch in Bizkaia were on sick leave. Also in July, another two possible cases of Q fever were reported by the Health Service from a nearby Spanish region (Castilla-León) in two workers of the Araba branch of the same company (60 km away from the Bizkaia platform) who lived in Castilla-León. Since the company was a licensed pet transporter, transported animals were suspected as a possible source of the Q fever outbreak. Under these circumstances, by August 3 the facility where animals were kept had already been cleaned and disinfected, and transport of animals had been suspended.

Courier company description

The outbreak occurred in a courier company that in addition to urgent freight transport of parcels offered pet delivery services. The company is organized in several sections: reception and delivery offices where clients place the parcels; operational platforms for parcel distribution; and, transport services. Only workers at operational platforms are employees of the courier company, whereas reception and delivery offices are franchises and drivers are self-employed.

Pet delivery services offered by the company included transport and delivery of all type of animals, the only restriction being the maximum weight allowed. Pet delivery needs to comply with certain requirements of animal health and welfare. Notably, animals ought to be healthy and health status be accredited by an official health certificate that complies with regulations at origin and destination. Besides, animals cannot be pregnant or not having recently given birth when travelling. Transport routes include delivery to the local platform by the collection site, transfer to the central platform in Madrid, where a veterinarian visually examines the animal, and transport to the local platform at destination. In each platform animals are located in specific pet holding facilities while waiting (less than 1 hour) to be transported. Maximum transit times are 24 hours. About 6–7 animals are delivered each day. Transported animals are mostly dogs and cats, while other animals like miniature sheep and goats, birds or rabbits are delivered once per month on average.

Epidemiological investigation

Once the Epidemiology Surveillance Unit was informed of the suspected Q fever outbreak, a multidisciplinary group that included microbiologists, veterinarians, occupational health technicians and epidemiologists was gathered to investigate the infection source, monitor the exposed workers and design control measures.

On August 9, the Epidemiology Surveillance Unit and the Occupational Health Authority (OSALAN) met with the company management, the doctor and the occupational health technicians to collect information on the outbreak circumstances. The company informed that on July 16 they became aware of several workers from the Bizkaia and Araba branches reporting health problems compatible with Q fever starting on July 4. The following day, July 17, transport of ruminants was suspended at affected branches. That same day, pet holding facilities at the Bizkaia platform were cleaned with soap and bleach by the platform workers, who did not use the necessary protection equipment (eg. respiratory protection masks). Later, on July 22, a specialized cleaning company was subcontracted to clean and disinfect the pet holding facilities at the Bizkaia and Araba platforms, as well as the van used to transport animals. On July 24, transport of ruminants was banned for all transport routes.

Taking into account the incubation period of Q fever infection (2–3 weeks) and the onset date of the clinical signs in the affected patients, the exposure period was defined as that extended between June 1 and August 8. All workers that had any contact with either of the two affected platforms during that period, independently of their contractual relationship with the company, were considered exposed. Two meetings were held, one on each platform, to inform the workers, and conduct an epidemiological questionnaire and a serological study among workers who volunteered to participate. Workers unable attend to the meetings were approached by the Epidemiological Surveillance Unit by phone and asked to complete the questionnaire (S1 Appendix) and those who agreed to also provide blood samples. The workers’ general practitioners (GP) and local hospitals were informed of the outbreak.

Laboratory methods

Serological analyses were carried out at different hospitals and health prevention services. Two blood samples were obtained 3 to 4 weeks apart for serological determination of C. burnetii phase II IgM and IgG antibodies to evaluate seroconversion in exposed workers. Laboratory results were considered positive when seroconversion was observed; laboratory results were considered doubtful when only one blood sample was available and an indirect immunofluorescence antibody test (IFAT) titers for phase II IgG were >1/128 and for phase II IgM of >1/256.

Since ruminants are considered the main source of human Q fever infection in the study area, the investigation of potential infection sources focused on small ruminants that had travelled through either of the affected platforms (Bizkaia and/or Araba) during the exposure period (June 1—August 8). Blood samples (4 mL) were collected from animals to investigate the presence of antibodies against C. burnetii in their blood using a commercial indirect ELISA test (LSIVET Ruminant Milk/Serum Q Fever kit; Thermo Fisher Scientific).

Environmental samples (air and dust) were collected at different locations of the Bizkaia platform on September 15. Two aerosol samples were taken with an air sampler (Airport MD8, Sartorius) inside the platform of Bizkaia. Nineteen surface dust samples were collected using cotton swabs in areas with accumulated dust that included the pet holding facilities and other sites in the company premises. After DNA extraction, samples were analyzed by Real Time PCR (RTi-PCR) [11]. Samples with a positive RTi-PCR result and a Ct value below 31 were genotyped by multispacer sequence typing (MST) and a 10-loci single-nucleotide polymorphism (SNP) discrimination using RTi-PCR as described elsewhere [12,13].

Case definition

A confirmed human case was defined as a worker who had any contact with the Bizkaia and/or Araba platforms of the courier company between June 1 and August 8, 2017, independently of their contractual relationship with the company, and showed seroconversion in laboratory analyses, with or without clinical symptoms (fever, pneumonia and/or hepatitis). Probable cases included those exposed workers with mild clinical symptoms who tested serology positive without seroconversion or produced doubtful laboratory results (see Laboratory methods).

Statistical analyses

Associations between personnel risk factors and data collected in the epidemiological investigation were analyzed by Chi squared test (categorical variables) or by Student's t–test (numerical and dichotomous variables) using SPSS Statistic 21. Attack rates were assessed by Mantel-Haenszel Chi squared test using Epi Info 7 and Odds Ratios were assessed by exact test using Stata 12.1.

Ethical considerations

Since outbreaks are routinely investigated according to the Public Health services’ ethical guidelines to ensure patients safety, this study did not require additional ethical approval. Written informed consent was obtained from the workers for blood sample collection and for filling a questionnaire, which included personal data collection following legal regulations (Ley Orgánica 15/1995). Data analysis was performed on an anonymized dataset.

Blood samples were taken directly from the jugular vein of the goats following Spanish ethical guidelines and animal welfare regulations (Real Decreto 53/2013) after obtaining informed consent from the flock owner. According to this regulation, extraction of blood samples from livestock in this type of studies is considered routine veterinary clinical practice and does not require ethical approval. Samples were collected by the highest authority in animal research, welfare and ethics in the regions, i.e., veterinarians of the local Animal Health and Welfare Authorities (Servicio de Ganadería, Diputación Foral de Bizkaia and Servicio de Sanidad y Producción Animal de Lugo, Xunta de Galicia), responsible of livestock sanitation and studies of zoonotic outbreaks.

Results

Epidemiological investigation

A total of 180 workers from 29 different organizations (including self-employees) were considered to be exposed to the infection and were informed of the outbreak. Of them, 36 lived in other regions and their cases were referred to their local Health Services. Sixty-four of the remaining 144 workers agreed to fill a questionnaire to investigate risk factors of exposure and to provide blood samples for serological testing. Ten of them (15.6%) were identified as confirmed cases and another six (9.4%) met the definition of probable case; the remaining 48 were regarded as non-cases. Nine workers (8 confirmed and 1 probable) showed symptoms compatible with Q fever, including five cases with pneumonia (Table 1). They all required medical care services, including one who needed hospital admission. Another 7 workers had compatible symptoms (including one case of pneumonia) in the outbreak period but none of them met the laboratory criteria of Q fever, and they were thus considered as non-case. The attack rate among the investigated workers was 25% (16/64). Although it was difficult to precisely know if workers visited just one or both of the affected platforms, attack rate at the Bizkaia platform was estimated to be 28.3% (13/46) and 16.7% (3/18) at the Araba platform, all of the latter being asymptomatic. Serological results compiled from workers are shown in S1 Table.

Tab. 1. Summary of the results obtained in the epidemiological questionnaire according to variables and case definition.
Summary of the results obtained in the epidemiological questionnaire according to variables and case definition.

Median and mean age in confirmed cases did not significantly differ from non-affected workers. Percentage of smokers was higher in confirmed and probable cases than in non-cases (p = 0.043). Proportion of workers that had contact with animals at work was higher among confirmed cases, but differences were non-significant (p>0.05). Likewise, attack rate among the personnel involved in cleaning operations was non-significantly higher. No significant differences in incidence were observed between workers living in a rural or urban setting.

The epidemic curve representing the progression of illnesses onset in confirmed and probable cases is shown in Fig 1. First symptoms were recorded on July 5, and extended until August 2, with most cases concentrating during the first two weeks of July; only two cases delayed to August 1 and 2, after cleaning operations at the Bizkaia platform and the ban on animal transport was implemented.

Schematic representation of the main events associated to the outbreak.
Fig. 1. Schematic representation of the main events associated to the outbreak.

Outbreak source investigation: Animal and environmental study findings

Among all animal delivery services carried out between June 1 and August 8, two were considered the most probable sources of the infection. Delivery 1 involved two miniature goats travelling on June 28 from Bizkaia to Orense. Travelling route was as follows: reception at the Bizkaia platform–Araba platform (animals did not leave the van)–central headquarters at Madrid (360 km from Araba platform), where a veterinarian inspected the animals and they were then transferred to a different van–reception office and delivery at Orense. The farm where these miniature goats originated from was inspected by Animal Authority Services. Blood samples were collected from five miniature goats and seven sheep for C. burnetii ELISA test (August 23), all of them being negative. The two suspected miniature goats also tested negative in the ELISA test when investigated at destination (August 25). Delivery 2 took place three weeks before the onset of the outbreak. It also involved the transport of miniature goats but animals only passed through the Bizkaia platform while travelling from Cantabria to Valencia. Since animals did not travel through the Araba platform, and considering the time elapsed since the outbreak and the difficulties associated to the several regions involved, these animals were not investigated.

Being the suspected animal source negative, an environmental study was set up to investigate the presence of C. burnetii at the company premises surrounding the pet holding facilities of the Bizkaia platform, where the higher number of cases occurred. Although by this time the Bizkaia platform had been cleaned and disinfected twice, on September 15, environmental samples (19 surface dust and two aerosols) were collected at different sites of the Bizkaia platform premises. Special attention was paid in collecting samples from sites with accumulated dust and dirt, both inside and outside the pet holding facilities as well as at different surfaces within the company premises (see Fig 2). Real time PCR results were weak positive (Ct>35) for the aerosol samples but all dust samples were positive (Ct≤35), with the lowest Ct values for samples collected at the pet holding facilities (Ct 23.9 and 27.9) (Fig 2). Specifically, the lowest Ct value (23.9) was found for a dust sample collected from the rails of the sliding doors of the pet holding site, where cleaning operations did not reach. These results suggested that contamination had originated there and then spread through the platform premises. The two samples collected at the pet holding site were subjected to genotyping but only one (Ct = 23.9) could be completely genotyped as SNP1 and MST13.

Schematic representation of the Bizkaia platform (2,500 m<sup>2</sup>) along with the sampling sites and their corresponding <i>C</i>. <i>burnetii</i> Real Time PCR results (Ct values).
Fig. 2. Schematic representation of the Bizkaia platform (2,500 m2) along with the sampling sites and their corresponding C. burnetii Real Time PCR results (Ct values).

Undertaken control measures

As mentioned above, on July 24, transport of ruminants was banned for all transport routes. After the initial cleaning operations at the Araba platform in July, new cleaning and disinfection were performed on August 5 and August 19 using 1% Virkon® S (Bayer Hispania S.L., Barcelona, Spain). At the Bizkaia platform, a third and more stringent cleaning and disinfection procedure was implemented in September 15 upon receipt of the results from the environmental study that confirmed C. burnetii contamination. It involved exhaustive cleaning and disinfection of the pet holding facilities (inside and outside) using wet methods (avoiding any procedures that involved dust formation such as sweeping or aspiration), as well as cleaning and disinfection with water and Virkon® S (Bayer Hispania S.L., Barcelona, Spain) of floors, banisters and any other dust accumulating sites. Differently to the operations in July, now the necessary protection equipment, i.e. respiratory protection masks (filtering face pieces class 3-FFP3), gloves and goggles, were used during cleaning and disinfection.

Prevention Services of the affected companies were asked to follow-up confirmed and probable cases in order to assess possible evolution to chronic Q fever. For self-employees monitoring would be carried out by their GPs.

Discussion

A Q fever outbreak was declared in August 2017 at a courier company. The epidemiological investigation of the outbreak was hampered by the structure of the service that included not only personnel directly employed by the courier company but also workers from franchises and self-employed drivers. This situation hindered the identification of the personnel outside the platforms exposed to the infection source. In addition, workers had their residence in different regions and therefore the collaboration of different Health Services was required. Consequently, not all workers were included in the epidemiological survey. Despite these difficulties, the epidemiological and laboratory studies identified Q fever in 25% of the investigated workers. Pneumonia was the most relevant clinical sign and the cause of hospitalization of one patient. These results support previous studies which also identified pneumonia as the main clinical manifestation associated to other Q fever outbreaks recently reported in the Basque Country [9,10,14], unlike other Spanish regions where hepatitis is the most common clinical presentation [15]. In this sense, the Basque Country has been reported to have the highest rate of Q fever-associated pneumonia in Spain [15,16] and Europe as reviewed elsewhere [17].

Two deliveries of small ruminants (miniature goats) that took place within three weeks prior to the onset of the outbreak were considered as the most probable source of the outbreak. The first one, which took place three weeks before the outbreak (June 15), unfortunately could not be investigated. The second delivery, on June 28, involved the transport of two miniature goats from Bizkaia to Orense passing through both affected platforms. After serological investigation these animals did not show antibodies against C. burnetii, and neither did other animals from their flock of origin. It is nevertheless known that serology is not a good indicator of infection status since a percentage of C. burnetii infected ruminants do not seroconvert [18]. The high values of C. burnetii DNA detected by Real Time PCR on dust samples collected at the pet holding facilities of the Bizkaia platform clearly indicated that contamination originated there. The hypothesis that small ruminants were the infection source was supported by the C. burnetii genotype identified from dust samples (SNP1 / MST13), which corresponds to a type already detected from sheep [19] and goats [14] in the region. Although other pets like cats and dogs can also carry C. burnetii [20], genotype SNP1 / MST13 points at small ruminants as the source. In the study region cats and dogs have never been associated to Q fever outbreaks, but outbreaks were reported elsewhere after cats or dogs gave birth [21,22]. Although cats and dogs cannot be fully ruled out as a possible source of the outbreak, transport of parturient animals is not allowed. Considering all these, the contamination source could not be unequivocally identified. In the case of small ruminants, infected animals are known to shed C. burnetii through feces for several weeks after parturition or abortion [14,23]. Fecal contamination could have been the origin of the spread of high level of bacteria to the environment. Before transport, animals are kept for a while (less than 1h, according to the information provided by the company) in pet holding facilities, a place that workers frequently visited. In fact, about 72.6% of the interviewed workers confirmed direct or indirect contact with the animals at the platforms. Moreover, the air ventilation system of the pet holding facilities expelled air towards the platform. This might have been the main contamination route since C. burnetii DNA was detected all over the platform premises, the lowest PCR Ct values being found at the pet holding facilities. Although detection of C. burnetii DNA in dust samples collected far after the onset of the clinical cases and even after cleaning and disinfection does not prove that the bacteria were viable, it does suggest that contamination originated there. From there, travel containers, transport vans or workers travelling from Bizkaia to Araba could have acted as vehicles for C. burnetii contamination of the Araba platform, where three workers seroconverted but did not show clinical signs of infection. This would explain why attack rate was higher among workers that visited the Bizkaia platform, and those in closer contact with the transported animals.

Until recently, Q fever was considered an occupational disease linked only to the livestock sector. This outbreak highlights the risk of Q fever infection in other working settings where contact with potential animal reservoirs also occurs. Although animal delivery was included among the services offered by the company, Q fever was not considered among the occupational-associated health risks. In fact, even though animals need an official health certificate to travel, the analysis of C. burnetii antibodies is not legally requested, not even for domestic ruminants as occurs for example for Brucella spp. or tuberculosis in sheep and goats. This study highlighted the need to revise policies associated to animal health requirements for transport and consider the inclusion of laboratory tests (serology and PCR) to rule out C. burnetii infection.

This outbreak adds up to other cases and outbreaks where C. burnetii has been accidentally transported to environments far from livestock [5,8,24]. In such cases, outbreak investigations are even greater challenges that need rapid and coordinated One Health approaches. Here, expertise in human, animal and environmental health gathered together to collect epidemiological data and produce laboratory results to investigate the infection source and implement control and prevention measures. Exhaustive cleaning and disinfection procedures were implemented at both affected platforms after the epidemiological outbreak investigation. Transport of ruminants was banned for all transport routes at the company, and Q fever was included among the company occupational-associated health risks.

Supporting information

S1 Appendix [docx]
Questionnaire used in the epidemiological investigation.

S1 Table [xlsx]
Serological data compiled from workers.


Zdroje

1. Eldin C, Melenotte C, Mediannikov O, Ghigo E, Million M, Edouard S et al. From Q fever to Coxiella burnetii infection: a paradigm change. Clin Microbiol Rev. 2017; 30(1): 115–190. doi: 10.1128/CMR.00045-16 27856520

2. EFSA. Scientific Opinion on Q fever. EFSA J. 2010; 8(5): 1595.

3. Rodolakis A, Berri M, Hechard C, Caudron C, Souriau A, Bodier CC et al. Comparison of Coxiella burnetii shedding in milk of dairy bovine, caprine, and ovine herds. J Dairy Sci. 2007; 90(12): 5352–5360. doi: 10.3168/jds.2006-815 18024725

4. Gonzalez-Barrio D, Ruiz-Fons F. Coxiella burnetii in wild mammals: A systematic review. Transbound Emerg Dis. 2019; 66(2): 662–671. doi: 10.1111/tbed.13085 30506629

5. Clark NJ, Soares Magalhaes RJ. Airborne geographical dispersal of Q fever from livestock holdings to human communities: a systematic review and critical appraisal of evidence. BMC Infect Dis. 2018; 18(1): 218. doi: 10.1186/s12879-018-3135-4 29764368

6. Tissot-Dupont H, Torres S, Nezri M, Raoult D. Hyperendemic focus of Q fever related to sheep and wind. Am J Epidemiol. 1999; 150(1): 67–74. doi: 10.1093/oxfordjournals.aje.a009920 10400556

7. Tissot-Dupont H, Amadei MA, Nezri M, Raoult D. Wind in November, Q fever in December. Emerg Infect Dis. 2004; 10(7): 1264–1269. doi: 10.3201/eid1007.030724 15324547

8. van den Brom R, van EE, Roest HI, van der Hoek W, Vellema P. Coxiella burnetii infections in sheep or goats: an opinionated review. Vet Microbiol. 2015; 181(1–2): 119–129. doi: 10.1016/j.vetmic.2015.07.011 26315774

9. Alonso E, Lopez-Etxaniz I, Hurtado A, Liendo P, Urbaneja F, Aspiritxaga I et al. Q Fever outbreak among workers at a waste-sorting plant. PLoS One. 2015; 10(9): e0138817. doi: 10.1371/journal.pone.0138817 26398249

10. Hurtado A, Alonso E, Aspiritxaga I, Lopez E, I, Ocabo B, Barandika JF et al. Environmental sampling coupled with real-time PCR and genotyping to investigate the source of a Q fever outbreak in a work setting. Epidemiol Infect. 2017; 145(9): 1834–1842. doi: 10.1017/S0950268817000796 28434420

11. Schets FM, de Heer L, de Roda Husman AM. Coxiella burnetii in sewage water at sewage water treatment plants in a Q fever epidemic area. Int J Hyg Environ Health. 2013; 216(6): 698–702. doi: 10.1016/j.ijheh.2012.12.010 23347968

12. Glazunova O, Roux V, Freylikman O, Sekeyova Z, Fournous G, Tyczka J et al. Coxiella burnetii genotyping. Emerg Infect Dis. 2005; 11(8): 1211–1217. doi: 10.3201/eid1108.041354 16102309

13. Huijsmans CJ, Schellekens JJ, Wever PC, Toman R, Savelkoul PH, Janse I et al. Single-Nucleotide-Polymorphism genotyping of a Coxiella burnetii during a Q Fever outbreak in The Netherlands. Appl Environ Microbiol. 2011; 77(6): 2051–2057. doi: 10.1128/AEM.02293-10 21257816

14. Alvarez-Alonso R, Basterretxea M, Barandika JF, Hurtado A, Idiazabal J, Jado I et al. A Q fever outbreak with a high rate of abortions at a dairy goat farm: Coxiella burnetii shedding, environmental contamination, and viability. Appl Environ Microbiol. 2018; 84(20): e01650–18. doi: 10.1128/AEM.01650-18 30076194

15. Alende-Castro V, Macia-Rodriguez C, Novo-Veleiro I, Garcia-Fernandez X, Trevino-Castellano M, Rodriguez-Fernandez S et al. Q fever in Spain: Description of a new series, and systematic review. PLoS Negl Trop Dis. 2018; 12(3): e0006338. doi: 10.1371/journal.pntd.0006338 29543806

16. Perez-Arellano JL, Carranza-Rodriguez C, Gutierrez C, Bolaños M. Epidemiología de la fiebre Q en España (2018). Rev Esp Quimioter. 2018; 31(5): 386–405. 30027720

17. Maurin M, Raoult D. Q fever. Clin Microbiol Rev. 1999; 12(4): 518–553. 10515901

18. de Cremoux R, Rousset E, Touratier A, Audusseau G, Nicollet P, Ribaud D et al. Coxiella burnetii vaginal shedding and antibody responses in dairy goat herds in a context of clinical Q fever outbreaks. FEMS Immunol Med Microbiol. 2012; 64(1): 120–122. doi: 10.1111/j.1574-695X.2011.00893.x 22066517

19. Alvarez-Alonso R, Barandika JF, Ruiz-Fons F, Ortega-Araiztegi I, Jado I, Hurtado A et al. Stable levels of Coxiella burnetii prevalence in dairy sheep flocks but changes in genotype distribution after a 10-year period in northern Spain. Acta Vet Scand. 2018; 60(1): 75. doi: 10.1186/s13028-018-0429-x 30454011

20. Angelakis E, Raoult D. Q fever. Vet Microbiol. 2010; 140(3–4): 297–309. doi: 10.1016/j.vetmic.2009.07.016 19875249

21. Buhariwalla F, Cann B, Marrie TJ. A dog-related outbreak of Q fever. Clin Infect Dis. 1996; 23(4): 753–755. doi: 10.1093/clinids/23.4.753 8909839

22. Malo JA, Colbran C, Young M, Vasant B, Jarvinen K, Viney K et al. An outbreak of Q fever associated with parturient cat exposure at an animal refuge and veterinary clinic in southeast Queensland. Aust N Z J Public Health. 2018; 42(5): 451–455. doi: 10.1111/1753-6405.12784 29644762

23. Astobiza I, Barandika JF, Hurtado A, Juste RA, García-Pérez AL. Kinetics of Coxiella burnetii excretion in a commercial dairy sheep flock after treatment with oxytetracycline. Vet J. 2010; 184(2): 172–175. doi: 10.1016/j.tvjl.2009.01.017 19269867

24. Georgiev M, Afonso A, Neubauer H, Needham H, Thiery R, Rodolakis A et al. Q fever in humans and farm animals in four European countries, 1982 to 2010. Euro Surveill. 2013; 18(8): pii = 20407. 23449232


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