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Article

Exposure to Coxiella burnetii in Wild Lagomorphs in Spanish Mediterranean Ecosystems

by
Sabrina Castro-Scholten
1,
Javier Caballero-Gómez
1,2,3,*,
David Cano-Terriza
1,3,
Débora Jiménez-Martín
1,
Carlos Rouco
4,
Adrián Beato-Benítez
1,
Leonor Camacho-Sillero
5 and
Ignacio García-Bocanegra
1,3
1
Grupo de Investigación en Sanidad Animal y Zoonosis (GISAZ), Departamento de Sanidad Animal, UIC Zoonosis y Enfermedades Emergentes ENZOEM, Universidad de Córdoba, 14014 Córdoba, Spain
2
Grupo de Virología Clínica y Zoonosis, Unidad de Enfermedades Infecciosas, Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Hospital Universitario Reina Sofía, Universidad de Córdoba, 14004 Córdoba, Spain
3
CIBERINFEC, ISCIII—CIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III, 28029 Madrid, Spain
4
Departamento Biología Vegetal y Ecología, Área de Ecología, Universidad de Sevilla, 41012 Sevilla, Spain
5
Programa de Vigilancia Epidemiológica de la Fauna Silvestre en Andalucía (PVE), Consejería de Sostenibilidad, Medio Ambiente y Economía Azul, Junta de Andalucía, 29002 Málaga, Spain
*
Author to whom correspondence should be addressed.
Animals 2024, 14(5), 749; https://doi.org/10.3390/ani14050749
Submission received: 29 January 2024 / Revised: 24 February 2024 / Accepted: 26 February 2024 / Published: 28 February 2024
(This article belongs to the Special Issue Diagnosis, Evaluation, and Management of Wildlife, Exotic and Zoo Animals Disease)
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Abstract

:

Simple Summary

Coxiella burnetii, the causative agent of Q fever, is a multi-host zoonotic bacterium of public and animal health concern, with Spain being the European country with the highest number of Q fever cases in recent years. However, and despite that the European wild rabbit and the Iberian hare are two keystone species in the Iberian Peninsula and are considered important sources of food for humans, very little is known about the epidemiological role of these two species. To tackle this question, a cross-sectional study was carried out to determine the seroprevalence and risk factors associated with C. burnetii exposure in wild lagomorph populations of Southern Spain. Antibodies against this bacterium were found in 11.3% of 471 wild rabbits, and, for the first time, in 2.4% of 167 Iberian hares, which provides evidence of the moderate circulation of C. burnetii in wild lagomorph populations in Spanish Mediterranean ecosystems. Our results also demonstrated that wild lagomorphs from western Andalusia and those from hunting grounds in which sheep were present were at higher risk of exposure to C. burnetii. In this context, these risk factors should be prioritized in future risk-based surveillance programs for this zoonotic multi-host bacterium.

Abstract

Coxiella burnetii is an important zoonotic pathogen of worldwide distribution that can infect a wide range of wild and domestic species. The European wild rabbit (Oryctolagus cuniculus) can play a role as a reservoir for this bacterium in certain epidemiological scenarios, but, to date, a very limited numbers of large-scale serosurveys have been conducted for this species worldwide. Although exposure in hare species has also been described, C. burnetii in Iberian hare (Lepus granatensis) has never been assessed. Here, we aimed to determine the seroprevalence and risk factors associated with C. burnetii exposure in wild lagomorphs in the Mediterranean ecosystems of southern Spain. Between the 2018/2019 and 2021/2022 hunting seasons, blood samples from 638 wild lagomorphs, including 471 wild rabbits and 167 Iberian hares, were collected from 112 hunting grounds distributed across all eight provinces of Andalusia (southern Spain). The overall apparent individual seroprevalence was 8.9% (57/638; 95% CI: 6.8–11.4). Antibodies against C. burnetii were found in 11.3% (53/471; 95% CI: 8.4–14.1) of the wild rabbits and 2.4% (4/167; 95% CI: 0.1–4.7) of the Iberian hares. Seropositive animals were detected for 16 (14.3%; 95% CI: 7.8–20.8) of the 112 hunting grounds tested and in all the hunting seasons sampled. A generalized estimating equations model showed that the geographical area (western Andalusia) and presence of sheep were risk factors potentially associated with C. burnetii exposure in wild lagomorphs. A statistically significant spatial cluster (p < 0.001) was identified in the south-west of Andalusia. Our results provide evidence of moderate, endemic and heterogeneous circulation of C. burnetii in wild lagomorph populations in Spanish Mediterranean ecosystems. Risk-based strategies for integrative surveillance programs should be implemented in these species to reduce the risk of transmission of the bacterium to sympatric species, including humans.

1. Introduction

The agent that causes Q fever disease, Coxiella burnetii (family Coxiellaceae), is an important and highly environmentally resistant zoonotic bacterium with a worldwide distribution [1]. In recent years, Europe has reported over 700 annual human cases of Q fever. Among European countries, Spain has recorded the highest number of Q fever cases in recent years [1], making it the most frequent reportable zoonosis in the country [2]. Different modes of transmission have been reported and although inhalation is considered the main mode, oral and tick-borne transmissions have also been evidenced [3]. In humans, Q fever causes fever, malaise, headache, muscle pain and endocarditis [4], whereas in animals, and particularly ruminants, this disease is characterized by abortions during late pregnancy or weak offspring, causing significant economic losses in the livestock industry [5].
Although domestic ruminants are the main reservoirs of the bacterium, a broad range of wild species can be infected with C. burnetii. The European wild rabbit (Oryctolagus cuniculus) has been denoted as a natural reservoir of C. burnetii in certain epidemiological contexts [6], and Q fever cases in humans have already been associated with indirect contact with wild rabbits [7]. Moreover, some studies have pointed out that hares may play a role in the maintenance and transmission of this zoonotic bacterium [8,9]. Nevertheless, information on the role of these lagomorph species in the epidemiology of Q fever is still very limited.
The European wild rabbit and the Iberian hare (Lepus granatensis) are two endemic and keystone species of the Iberian Peninsula [10,11], being a source of food for a large number of predators [12]. In Mediterranean ecosystems, both species have been shown to be natural reservoirs for a wide range of pathogens that can affect other species, including humans [13,14,15,16]. This, together with their wide distribution, gregarious behavior and close direct and indirect contact with other sympatric species, evidenced the potential role of wild lagomorphs in the maintenance and transmission of multi-host pathogens such is C. burnetii [17]. However, even though the European Food Safety Authority (EFSA) has included Q fever as a priority for the establishment of a coordinated surveillance system [18] and has highlighted the need for the epidemiological surveillance of C. burnetii in wild lagomorphs to assess the circulation of this zoonotic pathogen [17], no or only a very few serosurveys have been conducted to date for Iberian hares and European wild rabbits, respectively, worldwide. Here, we aimed to assess the seroprevalence and risk factors associated with C. burnetii exposure in European wild rabbit and Iberian hare populations in Mediterranean ecosystems of southern Spain.

2. Materials and Methods

2.1. Study Design and Sampling

A cross-sectional study was carried out on wild lagomorph populations in the region of Andalusia (south-western Europe) (87,268 km2; 36° N–38°60′ N, 1°75′ W–7°25′ W) between the 2018/2019 and 2021/2022 hunting seasons. The study area is characterized by a continental Mediterranean climate with mild wet winters and hot, dry summers. The western region presents higher mean humidity and less-extreme mean temperatures than the central and eastern regions [19].
The sample size was determined based on an assumed prevalence of 50%, which provides the maximum sample size in studies where the prevalence is unknown. The calculation was completed with a 95% confidence interval (95% CI) and a desired precision of ±5%. Whenever possible, 60 European wild rabbits were sampled in each of the eight provinces comprising the study area, in order to ensure a 95% probability of detecting at least one positive animal, assuming a minimum prevalence of 5% [20]. Sampling sites (hunting grounds) were randomly selected in each province. On each of these hunting grounds, hunters provided between 5 and 25 (mean: 12.1) European wild rabbits for sampling. A total of 471 wild rabbits from 38 hunting grounds distributed across all eight provinces were sampled during the study period. In addition, 167 Iberian hares from 82 hunting grounds were also sampled in the same study area and study period using a convenience sampling. In eight of these hunting grounds, both wild rabbit and Iberian hares were sampled.
Blood samples from all animals were obtained from the heart or thoracic cavity and centrifuged at 400× g for 10 min. The serum obtained was stored at −20 °C until serological analysis were performed. During sampling, an epidemiological questionnaire was also conducted through a direct interview with gamekeepers at each hunting grounds, wherever possible. The information obtained included the characteristics of the hunting ground, the presence of disease and control measures, management practices, and the presence of other sympatric species. Also, meteorological information for each sampling area [mean and maximum annual temperatures (°C), humidity (g/m3), and mean annual rainfall (mm)] was collected from the closest official meteorological station [19]. In addition, individual information, including species, location, year of sampling, age, kidney fat index and sex, was recorded for each animal. Bodyweight and body length were used as indicators of age [21].

2.2. Laboratory Analysis

Serum samples were tested for antibodies against C. burnetii using the commercial indirect and multispecies enzyme-linked immunosorbent assay (ELISA) ID Screen® Q Fever (IDvet, Grabels, France), according to the manufacturer’s instructions. This assay has previously been used in wild lagomorphs, being a satisfactory alternative to detect C. burnetii specific antibodies, compared to other commercial ELISA kits [22]. Results were expressed as an ELISA percentage (E%), calculated using the following formula: [E% = (sample Optical Density (OD)/mean OD of positive controls) × 100]. The positive threshold values were set as suggested by the manufacturers: sera with E% > 50 were considered positive.

2.3. Statistical Analysis

The individual apparent prevalence of antibodies against C. burnetii was estimated from the proportion of seropositive animals to the total number of individuals analyzed, using the two-sided exact binomial test, with 95% CI. To homogenize the scales of the explanatory variables, cut-off points for continuous variables were determined at the 33rd and 66th percentiles. Coefficients and standard error values generated using an intercept-only generalized estimating equation (GEE) binomial logistic regression model, with the hunting ground as the subject variable, were used to adjust the estimated seroprevalence and 95%CI for clustering at hunting ground level [23]. Pearson´s Chi-square or Fisher’s exact test was first used, as appropriate, to screen for associations between seroprevalence with explanatory variables. All variables with a p < 0.05 in the bivariate analysis were selected for further analyses. Collinearity between pairs of variables was then tested using Cramer’s V coefficient. When collinearity was detected (Cramer’s V coefficient ≥ 0.6), the variable with the strongest a priori biological association with C. burnetii was retained. Finally, a GEE analysis was carried out to study the effect of the variables selected from the bivariate analysis. The number of seropositive animals was assumed to follow a binomial distribution, and “hunting ground” was included as the subject variable. Forward selection was used for introduction of variables, starting with the variable with the lowest p-value in the bivariate analysis. At each step, the confounding effect of the included variable was assessed by calculating the change in odds ratio (OR). The model was re-run until all remaining variables showed statistically significant values (p < 0.05). For the choice of the best model, the quasi-likelihood under the independence model criterion (QIC) was considered. SPSS 25.0 software (Statistical Package for Social Sciences, Inc., Chicago, IL, USA) was used for all statistical analyses.

2.4. Spatial Cluster Analysis

A spatial scan statistical analysis was applied using a Bernoulli model [24] to detect areas with significant aggregations of high seroprevalence at hunting ground level, using SaTScanTM v10.1.2 software. The number of Monte Carlo simulations was set to 1000 for the cluster scan statistic. SaTScan was used to estimate relative risk (RR), representing the relative frequency of seropositive individuals compared to baseline, for each cluster. Clusters were considered significant at p < 0.05.

3. Results and Discussion

In the present study, we detected moderate and endemic circulation of C. burnetii in wild lagomorph populations of Spanish Mediterranean ecosystems. The overall apparent individual seroprevalence was 8.9% (57/638; 95% CI: 6.8–11.4) (Table 1). By species, antibodies against C. burnetii were found in 11.3% (53/471; 95% CI: 8.4–14.1) of European wild rabbits and 2.4% (4/167; 95% CI: 0.1–4.7) of Iberian hares. After adjustment for clustering, the estimated individual seroprevalences were 12.9% (95% CI: 7.2–22.3) in wild rabbit and 2.5% (95% CI: 0.9–6.5) in Iberian hare, which denote different exposure level to C. burnetii between these two lagomorph species. This finding could be related to differences in behavior. While Iberian hares are generally solitary [25], wild rabbits live in social groups in burrows [26], which might favor the transmission and maintenance of the bacterium.
The prevalence of anti-C. burnetii antibodies detected in wild rabbits in the present study is lower than those reported in the only two previous serosurveys conducted on this species so far. A seroprevalence of 37.9% (176/464) was found in wild rabbit populations in a survey carried out in different regions of Spain, including Andalusia, where certain areas exhibited seroprevalence values ranging between 45.0% and 62.5% [27]. Higher seroprevalence (65.5%; 394/602) was also found in wild rabbits from central areas of this country [28]. The differences may be due to the presence of sympatric wild ungulates, particularly of red deer (Cervus elaphus) [28,29], which is considered an important node in the epidemiological cycle of this pathogen in Mediterranean ecosystems [27]. While both studies found higher seroprevalences in areas with a high density of this wild ruminant species, in our study, red deer were only present in 10 of the 112 (8.9%) hunting grounds analyzed. Nevertheless, a further large-scale serosurvey is warranted to assess differences among regions.
To the best of the authors’ knowledge, this is the first report of C. burnetii exposure in Iberian hare, increasing the range of susceptible species to this zoonotic pathogen. The low seroprevalence detected in this species is consistent with the absence of antibodies against C. burnetii reported in European hare (Lepus europaeus) in Germany (0/78) [30], the Czech Republic (0/48) [31] and Greece (0/105) [32]. In contrast, higher seropositivity values were observed in other hare species, including the black-tailed jack rabbit (Lepus californicus) in the USA (39.4%; 99/251) [33] and in snowshoe hares (Lepus americanus) in Canada (45.5%; 10/22) [7]. The seroprevalence detected in Iberian hare suggests that this species may be considered spillover hosts rather than true reservoirs for C. burnetii in the study area, although additional studies, including a high number of tested animals, are needed to support this hypothesis.
Temporally, anti-C. burnetii antibodies were detected in all the hunting season samples and an increasing trend in seroprevalence was found over the years. The lowest seroprevalence (3.3%) was detected during the 2018–2019 hunting season, rising to 20.9% during 2021/2022. Geographically, seropositive animals were detected in all provinces with frequencies of antibodies ranging between 0.9% (1/107; 95% CI: 0.0–2.8) in Córdoba and 46.5% (33/71; 95% CI: 34.9–58.1) in Cádiz, indicating a wide but heterogeneous spatial distribution of C. burnetii in wild lagomorphs in the Mediterranean ecosystems of southern Spain. Indeed, the GEE model revealed that the prevalence of anti-C. burnetii antibodies was significantly higher (p = 0.006) in western (20.7%) compared to central (1.5%) Andalusia. Consistently, spatial analysis identified one statistically significant cluster of hunting grounds positive for anti-C. burnetii antibodies in southwestern Andalusia (RR: 13.6; p < 0.001) (Figure 1). Previous studies have suggested that host density could be associated with a higher risk of C. burnetii exposure in mammal species, including wild lagomorphs [27,28,34]. In this respect, a higher mean of hunted wild lagomorphs, which is a reliable index of relative animal abundance [35], was reported in the western region of Andalusia compared with central and eastern regions [36]. In addition, the western region presents higher mean humidity and less-extreme mean temperatures than those observed in central and eastern regions [19]. In fact, the area identified in the spatial cluster includes the Spanish area with the highest average annual rainfall [19]. These climatic features may favor not only the persistence of the bacterium in pastures but also the presence and abundance of competent tick species in the environment. All these findings indicate that western Andalusia could be a hotspot area for C. burnetii circulation.
The presence of sheep (Ovis aries) in the sampled hunting grounds was also identified as a risk factor potentially associated with C. burnetii exposure (Table 2), which is consistent with previous studies carried out on domestic ruminants [37]. Hunting grounds where sheep were present had 4.6 times more risk of C. burnetii exposure than those without sheep. Domestic ruminants are recognized as the main reservoirs of C. burnetii and sheep are frequently raised under extensive production systems in the study region [38]. In this respect, pastures contaminated with feces from C. burnetii positive livestock have been described as an important source for infection in wildlife [33], including wild rabbit and hare species [8,33,39]. This hypothesis is supported by the high seroprevalence of C. burnetii detected by our research group in sheep farms of Andalusia, where 100.0% of the farms had at least one positive sheep and 40.0% of the tested sheep were confirmed to be exposed to C. burnetii (unpublished data).

4. Conclusions

In summary, the results obtained in the present study revealed widespread, but not homogeneous exposure to C. burnetii in wild lagomorph populations of Spanish Mediterranean ecosystems. The risk factors identified (western Andalusia and hunting grounds with presence of sheep) should be prioritized in future risk-based surveillance programs for C. burnetii. Additional molecular and serological studies are required to elucidate differences between wild rabbits and Iberian hares and to assess the risk of zoonotic transmission of C. burnetii from these wild lagomorph species in Iberian Mediterranean ecosystems.

Author Contributions

Conceptualisation, J.C.-G., C.R. and I.G.-B.; methodology, S.C.-S., J.C.-G., D.C.-T., D.J.-M., A.B.-B. and L.C.-S.; software, S.C.-S., J.C.-G., D.C.-T. and D.J.-M.; validation, J.C.-G. and I.G.-B.; formal analysis, S.C.-S., J.C.-G. and I.G.-B.; investigation, S.C.-S., J.C.-G., D.C.-T., D.J.-M. and A.B.-B.; resources, C.R., L.C.-S. and I.G.-B.; data curation S.C.-S. and J.C.-G.; writing—original draft preparation, S.C.-S., J.C.-G. and I.G.-B.; writing—review and editing, S.C.-S., J.C.-G., D.C.-T., D.J.-M., C.R., A.B.-B., L.C.-S. and I.G.-B.; visualisation, I.G.-B.; supervision, J.C.-G. and I.G.-B.; project administration, C.R. and I.G.-B.; funding acquisition, C.R. and I.G.-B. All authors have read and agreed to the published version of the manuscript.

Funding

This work has benefited from the financial aid of research grants funded by the Spanish Ministry of Science and Innovation (project LagoHealth; REF: PID2019-111080RB-C21 and LAGOMED project REF: PRIMAS2-11-PCI2019-103698) and by the University of Córdoba (REF: UCO-FEDER-1264967). This research was also partially supported by TED2021-132599B-C22 project, funded by MCIN/AEI/10.13039/501100011033 and by the European Union “NextGenerationEU”/PRTR Recovery, Transformation and Resilience Plan–Funded by the European Union –NextGenerationEU, the research project LifeWATCH INDALO–Scientific Infrastructures for Global Change Monitoring and Adaptation in Andalusia (LIFEWATCH-2019-04-AMA-01), financed with FEDER funds (POPE 2014-2020), the Sub-modality 2.4. “UCOLIDERA” of the “Enrique Aguilar Benítez de Lugo” Research Plan of the University of Cordoba and CIBER-Consorcio Centro de Investigación Biomédica en Red (CB 2021), Instituto de Salud Carlos III, Ministerio de Ciencia e Innovación and Unión Europea-Next Generation EU.

Institutional Review Board Statement

This study did not involve purposeful killing of animals. All samples were collected from legally hunted animals during the hunting seasons or using passive surveillance under Spanish and Andalusian legislation. Thus, no ethical approval was necessary.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available on request from the corresponding author. The data are not publicly available due to privacy restrictions and long extension of datasets.

Acknowledgments

We gratefully acknowledge the help of the personnel of the Epidemiological Surveillance Program in Wildlife (Regional Government of Andalusia) and all the members of the GISAZ research group in the collection of samples and epidemiological information. S. Castro-Scholten and D. Jiménez-Martín are supported by an FPU grant from the Spanish Ministry of Universities (FPU19/06026 and FPU22/03649, respectively). A. Beato-Benítez holds a PhD contract supported by Agents of the Andalusian System of Knowledge of the Regional Government of Andalusia.

Conflicts of Interest

None of the authors of this study has a financial or personal relationship with other people or organizations that could inappropriately influence or bias the content of this paper.

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Animals 14 00749 g001
Figure 1. Spatial distribution of C. burnetii seroprevalence in wild lagomorphs in the study region (Andalusia, southern Spain). The discontinuous circle represents a significant cluster of seropositivity identified using spatial analysis.
Figure 1. Spatial distribution of C. burnetii seroprevalence in wild lagomorphs in the study region (Andalusia, southern Spain). The discontinuous circle represents a significant cluster of seropositivity identified using spatial analysis.
Animals 14 00749 g001
Table 1. Distribution of the seroprevalence against Coxiella burnetii in wild lagomorphs in Andalusia (southern Spain) by animal and hunting ground categories and results of the bivariate analysis.
Table 1. Distribution of the seroprevalence against Coxiella burnetii in wild lagomorphs in Andalusia (southern Spain) by animal and hunting ground categories and results of the bivariate analysis.
VariableCategoriesNo. Positives/
Overall 1		Seroprevalence (%)p
Data recorded from the sampled animals
SpeciesWild rabbit53/47111.3<0.001
Iberian hare4/1672.4
AgeAdult53/46011.50.001
Subadult3/1352.2
Young0/360.0
SexMale28/3079.10.516
Female29/3268.9
Kidney fat index019/15412.30.541
116/14810.8
210/1148.8
37/997.1
Bodyweight (kg)0.4–0.913/1667.80.420
1.0–1.27/1444.9
1.3–3.17/1474.8
Body length (cm)19–376/1613.70.075
38–4014/1439.8
41–597/1365.1
Hunting season2018/20192/603.3<0.001
2019/20202/484.2
2020/202124/3916.1
2021/202229/13920.9
Hunting ground’s characteristics
Geographical areaWestern45/21720.7<0.001
Central3/1961.5
Eastern9/2254.0
Burrow densityHigh43/41810.3<0.001
Medium10/3727.0
Low0/760.0
High abundance of ticks in the hunting groundYes24/2978.10.001
No1/1420.7
High abundance of fleas in the hunting groundYes16/2735.90.514
No9/1665.4
Fenced hunting groundYes5/3713.50.305
No48/4949.7
Presence of rabbit feedersYes26/3108.40.097
No27/22112.2
Feed supplementation in rabbitsYes32/21714.70.002
No21/3146.7
Presence of swampsYes18/8521.20.001
No35/4467.8
Presence of troughsYes50/44211.30.012
No3/893.4
Presence of streamsYes23/2778.30.115
No30/25411.8
The hunting ground is weededYes17/11814.40.054
No36/4138.7
Presence of artificial burrowsYes4/3710.80.517
No49/4949.9
Detection of clinical cases of other infectious diseases
Outbreaks of myxomatosis in the last yearYes53/50810.40.084
No0/230.0
Outbreaks of RHD 2 in the last yearYes47/43510.80.120
No6/966.3
Outbreaks of myxomatosis in the last monthYes51/43411.80.001
No2/972.1
Outbreaks of RHD 2 in the last monthYes18/12114.90.034
No35/4108.5
Presence of other sympatric species in the hunting ground
Presence of wild boar (Sus scrofa)Yes18/3335.40.003
No34/28611.9
Presence of red deer (Cervus elaphus)Yes3/634.80.199
No49/5568.8
Presence of wildcat (Felis silvestris)Yes14/1708.20.224
No39/36110.8
Presence of Iberian lynx (Lynx pardinus)Yes14/8616.30.032
No39/4458.8
Presence of domestic cat (Felis silvestris catus)Yes45/4769.50.168
No8/5514.5
Presence of dog (Canis familiaris)Yes34/3968.60.051
No19/13514.1
Presence of cattle (Bos taurus)Yes5/2520.00.012
No19/3725.1
Presence of goat (Capra aegagrus hircus)Yes5/1493.40.060
No19/2487.7
Presence of sheep (Ovis aries)Yes21/19210.9<0.001
No3/2051.5
Presence of farmed rabbit (Oryctolagus cuniculus)Yes7/6011.70.390
No46/4719.8
Presence of domestic pig (Sus scrofa domesticus)Yes5/4012.50.081
No19/3575.3
Climate characteristics of the hunting ground
Mean temperature (°C)12.3–16.82/2300.9<0.001
16.9–17.47/1066.6
17.5–18.517/16310.4
Max temperature (°C)18.9–23.010/1845.40.060
23.1–24.28/2183.7
24.3–27.48/7311.0
Mean annual rainfall (mm)273.3–563.83/1691.80.002
563.9–597.99/1994.5
598.0–1134.614/13110.7
Humidity (g/m3)33–560/260.00.346
57–659/1326.8
66–1006/758.0
1 Missing values omitted, 2 RHD: rabbit hemorrhagic disease.
Table 2. Generalized estimating equations analysis of risk factors associated with exposure to Coxiella burnetii in wild lagomorphs in Andalusia (southern Spain).
Table 2. Generalized estimating equations analysis of risk factors associated with exposure to Coxiella burnetii in wild lagomorphs in Andalusia (southern Spain).
VariableCategoriesp-ValueOR 95% CI
Presence of sheepYes0.0234.6 (1.2–17.0)
Noaa
Geographical areaWestern0.00619.9 (2.3–170.4)
Eastern0.1335.2 (0.6–43.8)
Centralaa
a: Reference Category.
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Castro-Scholten, S.; Caballero-Gómez, J.; Cano-Terriza, D.; Jiménez-Martín, D.; Rouco, C.; Beato-Benítez, A.; Camacho-Sillero, L.; García-Bocanegra, I. Exposure to Coxiella burnetii in Wild Lagomorphs in Spanish Mediterranean Ecosystems. Animals 2024, 14, 749. https://doi.org/10.3390/ani14050749

AMA Style

Castro-Scholten S, Caballero-Gómez J, Cano-Terriza D, Jiménez-Martín D, Rouco C, Beato-Benítez A, Camacho-Sillero L, García-Bocanegra I. Exposure to Coxiella burnetii in Wild Lagomorphs in Spanish Mediterranean Ecosystems. Animals. 2024; 14(5):749. https://doi.org/10.3390/ani14050749

Chicago/Turabian Style

Castro-Scholten, Sabrina, Javier Caballero-Gómez, David Cano-Terriza, Débora Jiménez-Martín, Carlos Rouco, Adrián Beato-Benítez, Leonor Camacho-Sillero, and Ignacio García-Bocanegra. 2024. "Exposure to Coxiella burnetii in Wild Lagomorphs in Spanish Mediterranean Ecosystems" Animals 14, no. 5: 749. https://doi.org/10.3390/ani14050749

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