- Research article
- Open Access
Infectious keratoconjunctivitis in wild Caprinae: merging field observations and molecular analyses sheds light on factors shaping outbreak dynamics
© The Author(s). 2017
- Received: 9 July 2016
- Accepted: 10 February 2017
- Published: 4 March 2017
Infectious keratoconjunctivitis (IKC) is an ocular infectious disease caused by Mycoplasma conjunctivae which affects small domestic and wild mountain ruminants. Domestic sheep maintain the pathogen but the detection of healthy carriers in wildlife has raised the question as to whether M. conjunctivae may also persist in the wild. Furthermore, the factors shaping the dynamics of IKC outbreaks in wildlife have remained largely unknown. The aims of this study were (1) to verify the etiological role of M. conjunctivae in IKC outbreaks recorded between 2002 and 2010 at four study sites in different regions of France (Pyrenees and Alps, samples from 159 Alpine ibex Capra ibex, Alpine chamois Rupicapra rupicapra and Pyrenean chamois Rupicapra pyrenaica); (2) to establish whether there existed any epidemiological links between the different regions through a cluster analysis of the detected strains (from 80 out of the 159 animals tested); (3) to explore selected pathogen, host and environmental factors potentially influencing the dynamics of IKC in wildlife, by joining results obtained by molecular analyses and by field observations (16,609 animal observations). All of the samples were tested for M. conjunctivae by qPCR, and cluster analysis was based on a highly variable part of the lppS gene.
We documented infections with M. conjunctivae in epidemic and endemic situations, both in symptomatic and asymptomatic animals. The identified M. conjunctivae strains were site-specific and persisted in the local wild population for at least 6 years. In epidemic situations, peaks of cases and disease resurgence were associated with the emergence of new similar strains in a given area. Social interactions, seasonal movements and the landscape structure such as natural and anthropogenic barriers influenced the spatio-temporal spread of IKC. Adults were more affected than young animals and host susceptibility differed depending on the involved strain.
Our study indicates that IKC is a multifactorial disease and that M. conjunctivae can persist in wildlife populations. The disease course in individual animals and populations is influenced by both host and mycoplasma characteristics, and the disease spread within and among populations is shaped by host behavior and landscape structure.
- Molecular epidemiology
- Mycoplasma conjunctivae
- Ocular disease
- Disease spread
Infectious keratoconjunctivitis (IKC) in Caprinae is a common disease characterized by varying ocular signs ranging from mild conjunctivitis with discrete lachrymation to severe keratitis with cornea perforation, resulting in irreversible blindness, associated behavioral changes and, eventually, death [1–5]. It affects both wild and domestic Caprinae but severe signs are more frequent in wildlife . In wild ruminants, the disease has been known for nearly a century and reported to occur in at least seven European countries (Switzerland, Italy, France, Austria, Slovenia , Spain , Norway ), in North America [10, 11] and in Oceania (New Zealand , Australia ).
IKC has been reported to be the cause of potentially important economic losses for farmers because of treatment costs, weight loss and mortality due to falls or drowning in affected animals . In wildlife, the disease can result in high mortality, reaching up to 30% of the estimated population size [2, 15], which is perceived as problematic due to the local significance of wild ungulates as game or as cultural symbol, for ecotourism and species conservation. In the Alps in particular, this disease has an emblematic character as it frequently occurs, is easily recognized by observers and is perceived to be a cause of suffering in animals, in particular when the cornea is perforated, animals are disoriented and numerous carcasses are found. There is therefore a strong interest among wildlife managers and farmers in collecting more knowledge on IKC dynamics in domestic and wild animal populations.
Mycoplasma conjunctivae has been isolated from domestic and wild animals with IKC signs in various parts of the world, including Europe , North America [10, 11], Africa , Asia  and Oceania [19, 20], and IKC was successfully induced by inoculation of M. conjunctivae under experimental conditions [3, 21]. Most recently, the existence of a strong association between M. conjunctivae infection and IKC signs has also been documented in epidemiological surveys [4, 22] and M. conjunctivae is now recognized as the major etiological agent of IKC in Caprinae species.
Transmission of M. conjunctivae occurs by direct contact  and possibly by eye-frequenting insects [24, 25], with subsequent rapid spread within a herd . Interspecific transmission of M. conjunctivae has been documented both experimentally and under field conditions [3, 26]. The disease is endemic in populations of small domestic ruminants, and healthy carriers have been implicated in IKC introduction into sheep herds [27, 28]. Sheep have therefore been proposed as reservoir for M. conjunctivae and as the main source of infection for wild ungulates on summer pastures, while wild ungulates have been considered to be spill-over hosts, i.e., as hosts susceptible to infection but unable to maintain the pathogen on their own [3, 6, 26, 29]. However, the presence of healthy carriers has recently been documented in free-ranging Alpine ibex (Capra ibex) and chamois (Rupicapra spp.) populations, both in the Alps and the Pyrenees [4, 22, 30] raising the question as to whether M. conjunctivae may also persist in wildlife [4, 15]. Furthermore, it has been discussed that IKC may be a multifactorial disease, with host, pathogen and environmental factors playing a role in disease occurrence and severity [4, 31].
In France, the first IKC cases were documented in 1935 and 1942 in the Ecrins National Park and in 1974 in the Vanoise National Park. The first important outbreak was documented in 1977 in the Bauge National Hunting Reserve, and in 1981 in the Pyrenees National Park . Several IKC outbreaks have been described [15, 29, 33] and some authors have proposed that the disease is endemic in wild populations, occasionally turning into epidemics with varying levels of mortality [15, 32]. However, so far M. conjunctivae has not been reported from affected chamois or ibex in that country. Furthermore, it has often been unclear whether an epidemiological link existed among affected subpopulations and by which mechanisms IKC spread occurred. Overall, the role of sheep in IKC re-emergence in wildlife remains controversial, and the potential role of intraspecific social interactions, landscape structure and varying virulence of M. conjunctivae strains in the dynamics of IKC outbreaks in wildlife has been poorly investigated.
The aims of this study were (1) to verify the implication of M. conjunctivae in IKC outbreaks in wild ruminants in France, (2) to establish whether there were epidemiological links between the different outbreaks that occurred in France over a period of 9 years, and (3) to explore selected pathogen, host and environmental factors potentially influencing the dynamics of IKC in wildlife. We hypothesized that M. conjunctivae strain characteristics, intraspecific social interactions and landscape structure may all influence the dynamics of IKC in wild populations. We analyzed documented field observations of IKC events in France between 2002 and 2010 and carried out molecular investigations on animal samples collected in the affected areas during the same time period.
The study area “Ecrins” (Fig. 1b; 44° 33' N to 45° 28′ N and 5° 45′ E to 6° 58′ E) corresponds largely to the Ecrins National Park (272’000 ha). The area comprises a central mountain massif, with long and deep valleys characterized by large areas used as livestock pasture converging to the heart of the massif, made of rocky slopes and glaciers. Hunting is practiced everywhere except in the core area of the park (91,800 ha). The study area “Vanoise” (Fig. 1; 45° 12′ N to 45° 43′ N and 6° 19′ E to 7° 12′ E) corresponds to the Vanoise mountain massif, including the Vanoise National Park (200,000 ha, hunting prohibited in the core area, 52,900 ha) and the Encombres massif. The region is located in the heart of the northern Alps and is adjacent to the Italian National Park Gran Paradiso. In the Vanoise National Park, ibex have been caught and marked since 1981, with around 300 animals marked within the region where animals were sampled for this study (including 165 within the past 10 years).
Domestic sheep are found in all four study areas. Some live in the parks all year round; others are brought from different French departments (Additional file 2) each summer from June to October (transhumance) to graze on alpine pastures.
IKC epidemic events in wildlife have previously been reported in the Pyrenees, the Southern French Alps and the Vanoise [8, 15, 29] but never in the Ecrins, where to date only sporadic cases have occurred.
Targeted observations were performed on foot, using field glasses and telescopes. Observation protocols were standardized within each region and included fields to record at least the date of observation, geographical location of the observed animals and their species, age and sex. Observers were additionally asked to describe ocular signs for all observed IKC cases. Sex was determined based on morphological traits, i.e., body size and morphology, horn size and shape, penis and social behavior . Age was estimated based on horn length, hair color and behavior. Recorded eye lesions included ocular discharge, corneal opacity, perforation and neovascularization. Orphans were identified based on 1) behavioural differences compared to kids following their mother, 2) the number of kids and females within a social group, and 3) the known reproductive status of marked females.
In the Pyrenees, observations were carried out in the two zones of Cauterets during the entire period of the IKC outbreak that began in March 2007 and ended in November 2008. Observations were performed on given itineraries at varying times of day, approximately every 3 days, with a decrease in frequency as the epidemic wave vanished, i.e., when new cases were not observed any more. The area in the north-west of the Gaube valley of Cauterets was observed with particular intensity because it corresponded to the study area of other long-term investigations (e.g. [34–36]). All observations were recorded with the same data sheet by few well-trained gamekeepers.
In the Southern French Alps, itineraries were designed with the goal to observe at least 100 animals (Alpine ibex, Alpine chamois, mouflon) per observation day and per mountain massif (Queyras and Mercantour). This number of 100 was arbitrarily set to estimate the prevalence of symptomatic animals. Each itinerary was covered at dawn, with a frequency of observation varying from daily to every 2 weeks, the highest observation frequency corresponding to the outbreak peaks. Observations were carried out by a range of observers (hunters, gamekeepers, veterinarians, biologists and other trained people). Additionally, we considered data compiled in Italy in the region adjacent to our study area to describe the progression of the outbreak which spread over that region .
Overall, 4077 animal-observations were recorded in the Pyrenees, and 11,861 in the Southern French Alps, excluding mouflons because of the very low number of observations for this species.
Sampling and animals
Sampled animals and presence of signs of infectious keratoconjunctivitis (IKC)
Southern French Alps
No IKC signs
No IKC signs
No IKC signs
No IKC signs
Total per study area
Numbers of sampled animals are given per species and study area (Pyrenees, Vanoise, Ecrins, and Southern French Alps).
All frozen swabs, eyes, and heads were thawed, and swabs were taken from the organic material (98 swabs from defrosted eyes and 36 swabs from eyes of defrosted heads). Subsequently, DNA was extracted from the swabs using the method described by Vilei et al.  (n = 210). For swabs collected after October 2010 (n = 18) DNA was extracted with the Guanidium method , which includes a DNA-purification step after the DNA extraction, in contrast to the former method.
Primers used for this study
Belloy et al. 
Nested PCR, Sequencing
Mavrot et al. 
Mavrot et al. 
Mavrot et al. 
DNA sequence determination was performed using the BigDye termination cycle sequencing kit (Applied Biosystems, Forster City, CA, USA) with the sequencing primers Ser_start2, Ser_start0 and Ser_end0 (Table 2). The sequence analyzed is a highly variable region of the gene lppS, which is situated between positions 4013 and 4663 with reference to nucleotide sequence of lppS and lppT of M. conjunctivae type strain HRC/581T (GenBank accession number AJ318939). Belloy et al.  demonstrated that the use of this domain coding for serine repeats of lppS is a valuable approach for molecular epidemiology. To be able to compare the obtained fragments of this study with those from former investigations, we used the same method. In the present study, the term of “strain” refers to this specific sequence. All but six of the positive samples could be sequenced (n = 81). Sequencing products were analyzed on an ABI Prism 3100 genetic analyzer (Applied Biosystems) and edited using the DNA sequence analysis software Sequencher (GeneCodes, Ann Arbor, MI, USA).
Cluster relationships between strains were assessed first by alignment with the MAFFT-program (http://mafft.cbrc.jp/alignment/server) and then different phylogenetic programs were used from the websites http://mobyle.pasteur.fr and www.phylogeny.fr. The cluster analyses were compared with field observations and sequencing results in order to find the best associations between the strains. The final tree was represented with the program Bionumeric 6.6 (Applied Maths, Kortijk, Belgium) and cophenetic correlation was assessed to estimate the branch quality. Except for those identified in the present study, the strains used for the cluster analysis are a selection (one per cluster, all compared by using the method described above) of the 200 strains identified at the Institute of Veterinary Bacteriology of Bern since 1994, including the type strain HRC/581T and 31 strains from Europe, i.e. from Austria (n = 3 [3, 26]), Switzerland (n = 16 [4, 26]), Italy (n = 6 ), Croatia (n = 2 ), and Spain (n = 4 ). Only strains with low divergence (>87%), which were constant from one algorithm to another, were represented in the definitive tree as well as strains from Spain which were sampled at the same period but in another region of the Spanish Pyrenees. The reference strain HRC/581T was added for comparison among the different clusters.
Four age/sex categories were distinguished (kids: first year of life; yearling: second year of life; adult males and adult females: 2 years and older). Ocular signs were classified into four categories according to Mavrot et al. : (0) asymptomatic (no noticeable ocular change), (1) mild signs (subtle to marked ocular discharge in the absence of visible corneal lesions), (2) moderate signs (ocular discharge and corneal opacity) and (3) severe signs (ocular discharge and corneal lesions including neovascularization up to perforation).
Maps were drawn with the program quantum GIS (QGIS) version 2.4.0 . Maps showing the distribution of wild ungulates are based on documents from the Office national de la chasse et de la faune sauvage (ONCFS) . Maps of France were provided by the Institut national de l’Information géographique et forestière (IGN) . Distances were calculated drawing lines as the crow flies. Surfaces indicated as affected by an IKC outbreak refer to the surface of the affected epidemiological units.
Data handling was done in MS Excel© spread sheets. Prevalences were calculated assuming test sensitivity and specificity of 100%. Monthly prevalence was only estimated for selected sectors (one sector in the Pyrenees and 19 sectors in the Mercantour, Fig. 4) and time periods with high observation pressure, i.e. when at least 50 ibex or chamois per month had been observed. The two-tailed Fisher’s exact test (FET) was used to determine differences in prevalence of infection among age/sex categories, study areas and time periods, as well as differences in diagnostic success obtained with different sample materials or DNA extraction techniques. Level of significance was set at p < 0.05.
Presence of M. conjunctivae
Animals positive to M. conjunctivae were found in all study areas. At individual level, 72 out of 87 (82.8%) symptomatic chamois and ibex were positive, including 13 ibex from the Vanoise and six chamois from the Ecrins. Furthermore, four out of 37 asymptomatic ibex captured from two adjacent population nuclei in the Vanoise (Modane and Champagny) were positive (two from each subpopulation). These animals were marked 2 years after the IKC epidemic and followed up for several years within the framework of another study ; they were never observed with IKC signs. The other eight asymptomatic individuals tested in this study were negative for M. conjunctivae.
Disease spread and cluster analysis
The IKC outbreak in Pyrenean chamois lasted 4 years. It began in 2005 in Larboust (Fig. 2a), reached the France-Spain border in 2006 (12 km as the crow flies), followed the main mountain range and spread both in Spain and France through the perpendicular valleys. It covered 46 km as the crow flies in 2006 and an additional 30 km in 2007. Cases were regularly observed during the 4 years. Disease signs were typical, i.e., ocular discharge with or without corneal opacity, perforation and/or neovascularization , and often severe (blind animals with perforated cornea) during the entire outbreak, with marked associated mortality .
The first peak (up to 76 cases within a month and 7.3% prevalence) corresponded to the disease spread within the chamois herds of the eastern part of the Gaube valley, and to cases in the south-western part of this valley (near the French-Spanish boundary). These cases in the south-west were the consequence of contacts with herds of the eastern side of the valley through the main mountain range of the boundary, which is the only known possibility of interactions between herds from the east and the west . The cases in the south-west were observed in migrating herds coming from the north-west of the valley to graze in the south-west during summer (Fig. 2b–d).
The second peak reached up to 70 cases within a month and 23.3% prevalence, and was due to the disease spread in the north-western part of the valley. The first evidence of IKC in this zone corresponded to the return of the migrating chamois herds from their summer to their winter territory (Fig. 2b–d) .
A total of 383 Pyrenean chamois were observed with IKC in Cauterets. The estimated prevalence was significantly higher in adults (10.5%, 95% CI 9.4–11.6) than in younger animals (4.2%, 95% CI 3.2–5.3; P = 0.0000). Prevalence did not differ between sexes among the diseased adults (P = 0.1417).
Mortality due to IKC was not recorded in kids and yearlings (except for two 1-year-old females) but in adults two peaks of mortality were observed, corresponding to the two peaks of morbidity: 29 carcasses were found in June-September 2007 (i.e. 55.8% of the total IKC-related adult mortality), and 14 carcasses (26.9%) were retrieved from December 2007 to January 2008 (Fig. 7c). The presence of orphans was recorded in 39 of 176 (22.2%) observed family groups, which was significantly more (P = 0.0000) than during the previous 13 years of observations in this region (71/2757, 2.6%) [J.-P. Crampe, unpubl. data].
Prevalence was significantly higher in the spring (calendar season and biological period; P ≤ 0.0011). It reached 20.4% (95% CI: 17.1–24.7) during the gestation period, dropped to 5.8% (4.8–7.0) during the birth period, remained stable during the lactation period (5.1%, 4.1–6.1) and increased again during the rut (12.7%, 10.3–15.4). The pattern for calendar seasons was similar.
Concerning the cluster analysis in Pyrenean chamois, three very similar strains were detected (Figs. 2d and 6, Additional file 3) in 36 animals, all with IKC signs. This cluster of strains was very different from the strains isolated in another region of the Spanish Pyrenees during the same period (Fig. 6) . The first strain (PYR_07-08a; GenBank accession number KR052478) was detected in the whole area of Cauterets (Fig. 2d) in 27 animals and during the whole period of the outbreak. It was detected mostly in animals with severe ocular signs. The second strain (PYR_07b, GenBank accession number KR052472) differed in the lppS gene from the first by a deletion of 36 nucleotids (deletion of 12 amino acids) out of 767 and was only found in three animals, including two with severe IKC signs, from migrating herds sampled in the south-west of the Gaube valley (Fig. 2d). The third strain (PYR_07-08c, GenBank accession number KR052473) differed from the first by a deletion of 51 nucleotides (17 amino acids). It was identified in six animals in the north-west of the Gaube valley (Fig. 2d), which was the latest part of Cauterets affected by the outbreak. The appearence of this strain corresponded to the second peak of cases noticed in autumn/winter 2007–2008 (Fig. 6) but it was found mostly in animals with mild signs.
Southern French Alps
Like in the Pyrenees, the prevalence significantly differed between adults (12.7%, 95% CI 11.8–13.7) and younger chamois (9.5%, 95% CI 8.5–10.6; P = 0.0000), and there was no significant difference of prevalence between adult males and females (P = 0.1430) despite the higher percentage of females (62.1%) among the recorded cases (672 cases in all).
A weak epidemic wave was observed in 2006 in ibex, with associated mortality, but the local IKC situation is considered to be endemic with a few cases reported every year in chamois and ibex. The cluster analysis revealed two very different strains detected in ten ibex (Figs. 6 and 11). Both strains were found in symptomatic as well as in asymptomatic ibex, but the strain VAN_08 (GenBank accession number KR052475) was detected only in 2008 whereas the strain VAN_07-08 (GenBank accession number KR052476) was found both in 2007 and 2008. Furthermore, both strains were present in three different ibex colonies suspected to have contact with each other (Encombres, Maurienne, Peisey-Champagny; Fig. 11).
Overall, the Vanoise and Ecrins were characterized by an endemic situation, with a low number of cases and mild disease signs, and different clusters of strains. Furthermore, asymptomatic carriers were detected. By contrast, severe epidemics were observed in the Pyrenees and Southern French Alps, with a high morbidity, severe disease signs and associated mortality. In these two areas, few similar strains of M. conjunctivae were identified.
Comparison of the French strains identified with over 200 strains detected in former studies (database of the Institute of Veterinary Bacteriology, University of Bern) revealed that the French strains represented clusters that are different from those detected in the Swiss Alps and in the Spanish Pyrenees (Fig. 6).
Many IKC outbreaks have been observed in France since 1935  but unlike in other European countries an etiological agent had not yet been identified in ibex and chamois. Here, we confirmed the etiological role of M. conjunctivae in IKC outbreaks affecting ibex and chamois populations both in the French Pyrenees and in the French Alps. Furthermore, we documented asymptomatic carriers in free-ranging wild Caprinae in France, corroborating observations in other European countries [4, 22, 30].
A number of ibex and chamois with typical severe IKC signs were tested negative, as previously observed [4, 22, 40]. It may be that secondary microbial agents compete with the mycoplasmas in late disease stages [5, 8, 22] or that part of the observed IKC-like signs are due to another etiology . In addition, false negative results may be due to a reduced sensitivity of the test in highly contaminated samples.
We documented marked differences in the qPCR diagnostic success depending on both sample quality and the DNA extraction method. Based on our results, we recommend collecting eye swabs on the animals immediately rather than freezing heads and eyes before swab collection. Furthermore, we advise to directly extract DNA or at least conserve the samples in Guanidium buffer  rather than freezing the swabs and subsequently extracting the DNA .
Disease course and host factors
According to our data, only ibex were affected during the mild outbreak of 2007 in the Vanoise, although chamois shared the same home ranges (ONCFS, Additional file 1). By contrast, during the Southern French Alps epidemics both ibex and chamois were observed to have typical ocular signs. It has been previously described that chamois which belong to a distinct taxonomic group (Rupicapra spp.)  are generally more often and more severely affected than ibex [4, 15, 29, 30], domestic goats (Capra spp.) and domestic sheep (Ovis spp.) , which are phylogenetically closely related to each other . For the same degree of ocular signs, mycoplasma load in affected eyes has been shown to be higher in Alpine ibex than in Alpine chamois , claiming that chamois are particularly sensitive to M. conjunctivae infections. However, depending on the involved M. conjunctivae strain it also happens that only ibex are affected [4, 30] indicating some degree of strain-related host specificity.
In the Southern French Alps, both in this study and in former outbreaks [15, 29], ibex were affected at a later time point than chamois. Although there are exceptions, this suggests that IKC outbreaks tend to begin in chamois. Since ibex apparently need a higher mycoplasma load to develop disease signs , they may require more time to develop disease signs after an infection. Furthermore, when an epidemic starts in chamois, close interspecific interactions and a sufficient infection pressure are likely needed for ibex to become infected, which may contribute to the delay of the onset of the epidemics wave in this species.
Although mortality was high during epidemic outbreaks, our prevalence estimations put the impact of the disease on the population in perspective. We documented a significantly higher morbidity and higher mortality in adult animals compared to younger age classes in both sites with an epidemic pattern, in concordance with an unusually high occurrence of orphans. Although anecdotal, it is also interesting that the three asymptomatic carriers detected in the Ecrins were young animals. The lower susceptibility to IKC of the young age classes, characterized by a low morbidity and mortality and a higher proportion of healthy carriers, concurs with data from previous studies [4, 22] although a comparison was not always possible because either age classes were defined differently  or only the mortality was considered . Based on similar observations in domestic sheep, Janovsky et al.  proposed that lambs play an important role in the persistence of M. conjunctivae. The weaker immune reactivity characterizing young individuals may reduce their susceptibility to mycoplasmoses because these are diseases resulting from adverse effects of the host’s immune reaction and inflammatory processes rather than from the direct toxicity of mycoplasma compounds [49–51].
Nevertheless, genetic differences among individuals may also influence susceptibility to infection and disease development, as already reported for a wide variety of mycoplasma diseases .
Epidemic spread: role of social factors
In both study areas with an IKC epidemic (Pyrenees and Southern French Alps), prevalence was highest during the winter and spring rather than in summer, which contradicts former observations [6, 48]. This increased seasonal prevalence may be explained at least in part by the increase of animal movements and intraspecific contacts during the rut (from November to December ) and the resulting increased transmission of M. conjunctivae among social groups. The fact that in a former epidemic in Switzerland males were affected after females, with a peak of males affected during the rut , supports this suggestion. Furthermore, our data from the Pyrenees show the role of sexual segregation and movement of social groups in the pattern of spread of the disease. This was also observed in the Southern French Alps after the main IKC epidemic wave in summer 2005 in the Queyras, where spatial movements of affected young males during the rutting period contributed to disease spread (D. Gauthier, unpubl. obs.).
IKC spread twice as fast in the Mercantour National Park than in other parts of the Southern French Alps. As the estimated chamois density is higher in the Mercantour than in the rest of the Southern French Alps (Réseau Ongulés Sauvages, ONCFS/FNC/FDC, Additional file 1), population density may have additionally influenced IKC spread.
Regional differences and strain virulence
We observed very different epidemiological scenarios depending on the study area. Beside host factors such as previous exposure to M. conjunctivae, environmental and population factors may contribute to regional differences [30, 31]. However, regions as different as the Pyrenees and the Southern Alps presented a similar disease pattern (severe epidemics), whereas the situation in the Southern French Alps was the opposite of that in both the Vanoise and Ecrins located close by (few mild cases).
The strains of M. conjunctivae detected in this study were site-specific: The same strains were identified within an epidemiological unit but strains differed among units. Our definition of an “epidemiological unit” was already supported by genetic data on Alpine ibex in Switzerland  and by telemetry studies in the Vanoise . Here, our cluster analysis demonstrated that this definition is appropriate for the study of disease dynamics in mountain ungulates.
Our molecular data revealed the occurrence of few similar strains in areas with epidemics and of several very different strains in areas without epidemics, an observation already reported in the case of other mycoplasmoses in ruminants (M. mycoides subsp. capri  and M. bovis ) and of chytridiomycosis in amphibians (Batrachochytrium dendrobatidis ). Mycoplasmas are characterized by a high diversity of surface antigens, generated by random combinatorial expression and high frequency variation of multiple membrane surface lipoproteins. These major coat proteins determine their ability to adhere to host cells and are the major targets of the host humoral immune response . Since our cluster analysis was based on the lipoprotein S (LppS ), the different M. conjunctivae strains we detected may potentially differ in antigenicity and possibly also in virulence. Overall, these results suggest a role of pathogen factors (strain diversity and virulence) in the observed regional differences.
Epidemic peaks and strain emergence
We documented that IKC can spread over mountain ranges and causes a peak of cases once it reaches a new sector, subsequently decreasing in prevalence or even vanishing at a local level. Considering the landscape and host population characteristics used to define a sector in this study, and the general stability of the detected strains in time and space, it is obvious that this outbreak dynamic was due to temporary pathogen “confinement” within a sector and subsequent pathogen introduction into naïve adjacent chamois groups via animal movements. However, we could show in the Pyrenees and in one Alpine sector that resurgence sometimes occurs within a sector and corresponds to the detection of new strains slightly different from the strain found during the first peak of cases. This suggests a clonal spread of M. conjunctivae, as was previously reported for other mycoplasmas such as M. mycoides subsp. capri in domestic goats  and M. bovis in cattle .
Successive epidemic waves have previously been reported in IKC outbreaks (e.g. [22, 29]) and two peaks were typically separated by 4 to 5 months. This time lapse may correspond to the time needed for the local population to recover from clinical signs and to clear the infection [3, 15, 30, 48]. The resurgence of IKC cases suggests that M. conjunctivae is able to escape host immunity. If the immune pressure gives rise to new strains, a recrudescence of cases may subsequently occur. In accordance with this hypothesis, in the Pyrenees the second IKC wave not only corresponded to the detection of a M. conjunctivae strain slightly different from the original one, it was also characterized by less severe disease signs than the initial case peak.
Furthermore, two marked individuals developed the disease a second time. The recovery period separating the clinical episodes in these chamois suggests that they underwent two consecutive infections. Trotter et al.  observed that antibodies produced against M. conjunctivae do not protect from re-infection. Similarly, vaccination attempts against mycoplasmoses did not protect from disease but even resulted in a worse disease course due to the artificially induced immune reaction [58–60]. By contrast, Baas et al.  documented that sheep infected twice showed milder ocular signs the second than the first time, and overall, the protective role of an acquired immunity against M. conjunctivae remains controversial. However, the virulence of the strain apparently influences the strength of the immune response, i.e., depending on the strain causing the first infection, the immune reaction and associated clinical outcome in case of a re-infection may greatly differ [54, 55, 61].
Maintenance of M. conjunctivae in wild populations
Based on serological investigations, it had been previously proposed that M. conjunctivae does not persist in wildlife populations . However, an IKC event may last from 2 to 9 years in wildlife ; M. conjunctivae is able to persist after recovery from clinical disease in both domestic and wild hosts [3, 21, 28] and the occurrence of healthy carriers in wild Caprinae is now established ([4, 22, 30], this study).
In agreement with a non-persistence of M. conjunctivae in the wild, domestic sheep have been proposed as a main infection source for wildlife [6, 26]. Every summer each of our study area hosts a mixture of sheep from various geographical origins. Considering that sheep are commonly infected with M. conjunctivae , we expected this diversity of sheep to be associated with numerous different M. conjunctivae strains. However, only two to three different strains were identified in each area, with a persistence of 3 to 6 years of the same strain independently of the epidemiological pattern. This is not in agreement with a yearly reintroduction of strains, and rather suggests that endemic M. conjunctivae strains circulate within wild ungulate populations. This hypothesis is also supported by the fact that IKC prevalence in wildlife is highest in the spring, i.e. before sheep occupy alpine pastures, and by the detection of infected asymptomatic ibex before the arrival of sheep .
Overall, there is increasing evidence in favor of a persistence of M. conjunctivae in the wild. Healthy carriers are often reported for mycoplasma species [54, 57, 62] and the ability of mycoplasmas to persist in a population is well-known and increasingly demonstrated by molecular evidence. For example, it had been assumed that new strains of M. agalactiae were recurrently introduced in the Pyrenees by imported sheep and responsible for the re-emergence of contagious agalactiae but it was recently demonstrated that a single cluster of M. agalactiae had been responsible for all known re-emergences and that it had persisted within the local sheep herds for 30 years .
Mycoplasmas are able to persist within a host by escaping the immune response of the host [50, 57, 62, 64] by various processes. Almost all of these processes induce changes in expression and/or structure of surface lipoproteins anchored in the mycoplasma membrane [57, 62, 64], and non-cytadhering mutants have been shown to be avirulent . These mechanisms are crucial for the adaptation of mycoplasmas to their hosts and for the chronic colonization within a host . In other words, immune pressure can induce antigenic modifications of surface proteins  and the immune system of the host represents an important selection factor for mycoplasmas . Therefore, the severity of clinical signs in animals infected with M. conjunctivae is likely to result from both the ability of the host to develop an immune reaction towards a specific strain, and the ability of the strain to escape the immune response of a given host. Based on this knowledge, three scenarios have been proposed when a mycoplasma strain enters a host population able to develop an immune response [57, 62, 63, 68]: 1) the strain is efficiently combatted by the immune system of the hosts and vanishes from the population , likely after having caused severe disease signs in infected animals; 2) the strain undergoes mutations and an “equilibrium” between strain and host is achieved (mild signs, healthy carriers; [54, 55, 62] and particularities in Vanoise , Switzerland  and Ecrins [this study]); 3) the strain undergoes mutations and causes new epidemic waves until the situation evolves into scenario 1 or 2 (Pyrenees and Southern French Alps [this study]). In other words, a new outbreak could be due either to a mutation of a strain maintained in the population or to the introduction of new strains by other hosts such as domestic sheep. Nevertheless, our data suggest that this last scenario may be far less frequent than formerly assumed.
With this study we confirmed the implication of M. conjunctivae in IKC in wild Caprinae in France, showed that the different outbreaks were not linked to each other, and demonstrated the persistence for at least 6 years of site-specific strains within local wild populations. Furthermore, we documented that strain characteristics, social interactions and landscape structure shape the dynamics of IKC outbreaks. Together with previous studies [4, 15, 31], this shows that IKC has a pronounced multifactorial character and that host, pathogen as well as environmental factors all play an important role in disease occurrence, spread and severity. Importantly, IKC presents features inherent in the biology of other mycoplasmas. From a technical point of view, this work demonstrates the usefulness of performing long-term studies, joining field observations and molecular analyses, and harmonizing data collection in different study sites to track factors influencing the dynamic of infectious disease outbreaks in free-ranging wildlife . It also illustrates the necessity to define epidemiological units to document and possibly predict the spread of infectious agents transmitted mainly by direct contact. IKC, which is a visible disease, may well represent an interesting model to study the epidemiology of diseases with similar transmission routes in wildlife populations.
We thank the numerous people who contributed to field data and sample collection: for the French Pyrenees, the team of the gamekeepers of the Pyrenees National Park in Cauterets; for the French Alps, the Fédération départementale des Chasseurs des Hautes Alpes (Jacques Chevallier, president; Nicolas Jean, director; and the hunting society of the Massif du Queyras), the gamekeepers of the Queyras regional Natural Park, the VNP, the ENP and the National Forest Office (Thierry Anel), the scientific team and the gamekeepers of the MNP; the departemental laboratories of the Savoie and the Hautes Alpes. Data from Italy were provided by Andrea Dematteis (CERIGEFAS, Sampeyre), Omar Giordano and Giogio Ficetto (Comprensorio Alpino CACN2, Val Varaita). We acknowledge Paola Pilo for excellent advices in the laboratory, and Fabien Mavrot for laboratory work introduction and QGIS technical support. Many thanks go to the Office National de la Chasse et de la Faune Sauvage (France) for providing maps of the geographic distribution of wild Caprinae.
The study was funded by the contributing institutions.
Availability of data and materials
All relevant data supporting the conclusions of this study are presented in the article. Strain accession numbers in GenBank are given in Additional file 3. Raw data could be obtained from the first author upon request.
Conception and design of the experiment: DG, EV. The experiments were performed by: GG, JC, DG, EV. The data were analyzed by: GG, MR, JC. Contributed to reagents, materials and analysis tools: DG, JC, JF, EV. The paper was written by: GG, MR. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
None of the animals concerned by this study was killed for research purposes. All of the samples originated either from free-ranging wildlife which was found dead in the fields or legally shot for hunting purposes, or else from live animals captured within the framework of other wildlife projects. Collection and sampling of dead animals respected France’s legislation (hunting law: legal sections L425-6 to L425-13 of the French Environment Code; and animal protection law: legal sections L411-1 to L411-6 of the French Environment Code). Sampling was carried out by public wardens appointed by the French legislation (under oath) or by hunters involved in health surveillance. The animals coming from hunting activity were killed by persons owning the hunting permit and were harvested outside protected areas. No Alpine ibex was killed, as hunting this protected species is strictly prohibited in France. No culling program provided samples for this study. Sampling and transport of the specimens of protected wild species were carried out according to the National Order of 5th of June 2009 established for epidemiological surveys. Capture and sampling of live animals were carried out by national park wardens appointed by the French legislation (under oath). In the Vanoise National Park the capture of Alpine ibex benefited from a specific authorization relative to species submitted to the 1st title of the chapter IV of the French Environment Code: Order Nr. 2008-16 of the Préfet de Savoie.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Baas EJ, Trotter SL, Franklin RM, Barile MF. Epidemic caprine keratoconjunctivitis: recovery of Mycoplasma conjunctivae and its possible role in pathogenesis. Infect Immun. 1977;18:806–15.PubMedPubMed CentralGoogle Scholar
- Degiorgis MP, Frey J, Nicolet J, Abdo EM, Fatzer R, Schlatter Y, et al. An outbreak of infectious keratoconjunctivitis in Alpine chamois (Rupicapra r. rupicapra) in Simmental-Gruyères, Switzerland. SAT Schweiz. Arch Für Tierheilkd. 2000;142:520–7.Google Scholar
- Giacometti M, Nicolet J, Frey J, Krawinkler M, Meier W, Welle M, et al. Susceptibility of alpine ibex to conjunctivitis caused by inoculation of a sheep-strain of Mycoplasma conjunctivae. Vet Microbiol. 1998;61:279–88.View ArticlePubMedGoogle Scholar
- Mavrot F, Vilei EM, Marreros N, Signer C, Frey J, Ryser-Degiorgis M-P. Occurrence, quantification, and genotyping of Mycoplasma conjunctivae in wild Caprinae with and without infectious keratoconjunctivitis. J Wildl Dis. 2012;48:619–31.View ArticlePubMedGoogle Scholar
- Mayer D, Degiorgis MP, Meier W, Nicolet J, Giacometti M. Lesions associated with infectious keratoconjunctivitis in alpine ibex. J Wildl Dis. 1997;33:413–9.View ArticlePubMedGoogle Scholar
- Giacometti M, Janovsky M, Jenny H, Nicolet J, Belloy L, Goldschmidt-Clermont E, et al. Mycoplasma conjunctivae infection is not maintained in alpine chamois in eastern Switzerland. J Wildl Dis. 2002;38:297–304.View ArticlePubMedGoogle Scholar
- Giacometti M. Infectious keratoconjunctivitis of ibex, chamois and other Caprinae. Rev Sci Tech OIE. 2002;21(2):335–45.View ArticleGoogle Scholar
- Marco I, Mentaberre G, Ballesteros C, Bischof DF, Lavín S, Vilei EM. First report of Mycoplasma conjunctivae from wild Caprinae with infectious keratoconjunctivitis in the Pyrenees (NE Spain). J Wildl Dis. 2009;45:238–41.View ArticlePubMedGoogle Scholar
- Akerstedt J, Hofshagen M. Bacteriological investigation of infectious keratoconjunctivitis in Norwegian sheep. Acta Vet Scand. 2004;45:19–26.View ArticlePubMedPubMed CentralGoogle Scholar
- Jansen BD, Heffelfinger JR, Noon TH, Krausman PR, Devos JC. Infectious keratoconjunctivitis in bighorn sheep, Silver Bell Mountains, Arizona, USA. J Wildl Dis. 2006;42:407–11.View ArticlePubMedGoogle Scholar
- Langford EV. Mycoplasma and associated bacteria isolated from ovine pink-eye. Can J Comp Med. 1971;35:18–21.PubMedPubMed CentralGoogle Scholar
- Christie AHC, Andrews JRH. Introduced ungulates in New Zealand — (c) Chamois | NZETC. Tuatara J Biol Soc. 1965;13:105–10.Google Scholar
- Surman PG. Cytology of “pink-eye” of sheep, including a reference to trachoma of man, by employing acridine orange and iodine stains, and isolation of Mycoplasma agents from infected sheep eyes. Aust J Biol Sci. 1968;21:447–67.View ArticlePubMedGoogle Scholar
- Jones GE. Infectious keratoconjunctivitis. Dis. Sheep. 2nd ed. London: Blackwell Scientific Publications; 1991. p. 280–3.Google Scholar
- Gauthier D. La kérato-conjonctivite infectieuse du chamois; étude épidémiologique dans le département de la Savoie 1983-1990. Veterinary thesis. Lyon: Claude Bernard; 1991.Google Scholar
- Mayer D, Nicolet J, Giacometti M, Schmitt M, Wahli T, Meier W. Isolation of Mycoplasma conjunctivae from conjunctival swabs of Alpine ibex (Capra ibex ibex) affected with infectious keratoconjunctivitis. Zentralblatt Für Veterinärmedizin Reihe B J. Vet Med Ser B. 1996;43:155–61.View ArticleGoogle Scholar
- Van Halderen A, Van Rensburg WJ, Geyer A, Vorster JH. The identification of Mycoplasma conjunctivae as an aetiological agent of infectious keratoconjunctivitis of sheep in South Africa. Onderstepoort J Vet Res. 1994;61:231–7.PubMedGoogle Scholar
- Shahzad W, Munir R, Rana MY, Ahmad R, Khan MS, Akbar G, et al. Prevalence, molecular diagnosis and treatment of Mycoplasma conjunctivae isolated from infectious keratoconjunctivitis affected Lohi sheep maintained at Livestock Experiment Station, Bahadurnagar, Okara, Pakistan. Trop Anim Health Prod. 2013;45:737–42.View ArticlePubMedGoogle Scholar
- Motha MXJ, Frey J, Hansen MF, Jamaludin R, Tham KM. Detection of Mycoplasma conjunctivae in sheep affected with conjunctivitis and infectious keratoconjunctivitis. N Z Vet J. 2003;51:186–90.View ArticlePubMedGoogle Scholar
- Surman PG. Mycoplasma aetiology of keratoconjunctivitis (“pink-eye”) in domestic ruminants. Aust J Exp Biol Med Sci. 1973;51:589–607.View ArticlePubMedGoogle Scholar
- Trotter SL, Franklin RM, Baas EJ, Barile MF. Epidemic caprine keratoconjunctivitis: experimentally induced disease with a pure culture of Mycoplasma conjunctivae. Infect Immun. 1977;18:816–22.PubMedPubMed CentralGoogle Scholar
- Arnal M, Herrero J, de la Fe C, Revilla M, Prada C, Martínez-Durán D, et al. Dynamics of an infectious keratoconjunctivitis outbreak by Mycoplasma conjunctivae on Pyrenean chamois Rupicapra p. pyrenaica. PLoS One. 2013;8:e61887.View ArticlePubMedPubMed CentralGoogle Scholar
- Hosie BD. Keratoconjunctivitis in a hill sheep flock. Vet Rec. 1988;122:40–3.View ArticlePubMedGoogle Scholar
- Degiorgis M-P, Obrecht E, Ryser A, Giacometti M. The possible role of eye-frequenting flies in the transmission of Mycoplasma conjunctivae. Mitteilungen Schweiz Entomol Ges. 1999;72:189–94.Google Scholar
- Ter Laak EA, Schreuder BE, Smith-Buys CM. The occurrence of Mycoplasma conjunctivae in The Netherlands and its association with infectious keratoconjunctivitis in sheep and goats. Vet Q. 1988;10:73–83.View ArticlePubMedGoogle Scholar
- Belloy L, Janovsky M, Vilei EM, Pilo P, Giacometti M, Frey J. Molecular epidemiology of Mycoplasma conjunctivae in Caprinae: Transmission across species in natural outbreaks. Appl Environ Microbiol. 2003;69:1913–9.View ArticlePubMedPubMed CentralGoogle Scholar
- Fernández-Aguilar X, Cabezón O, Marco I, Mentaberre G, Frey J, Lavín S, et al. Mycoplasma conjunctivae in domestic small ruminants from high mountain habitats in Northern Spain. BMC Vet Res. 2013;9:253.View ArticlePubMedPubMed CentralGoogle Scholar
- Janovsky M, Frey J, Nicolet J, Belloy L, Goldschmidt-Clermont E, Giacometti M. Mycoplasma conjunctivae infection is self-maintained in the Swiss domestic sheep population. Vet Microbiol. 2001;83:11–22.View ArticlePubMedGoogle Scholar
- Hars J, Gauthier D. Suivi de l’évolution de la kérato-conjonctivite sur le peuplement d’ongulés sauvages du Parc national de la Vanoise en 1983. Trav Sci Parc Natl Vanoise. 1984;XIV:157–210.Google Scholar
- Ryser-Degiorgis M-P, Bischof DF, Marreros N, Willisch C, Signer C, Filli F, et al. Detection of Mycoplasma conjunctivae in the eyes of healthy, free-ranging Alpine ibex: possible involvement of Alpine ibex as carriers for the main causing agent of infectious keratoconjunctivitis in wild Caprinae. Vet Microbiol. 2009;134:368–74.View ArticlePubMedGoogle Scholar
- Mavrot F, Zimmermann F, Vilei EM, Ryser-Degiorgis M-P. Is the development of infectious keratoconjunctivitis in Alpine ibex and Alpine chamois influenced by topographic features? Eur J Wildl Res. 2012;58:869–74.View ArticleGoogle Scholar
- Terrier M-E. La kérato-conjonctivite des ongulés sauvages de montagne: reproduction expérimentale chez le mouflon (Ovis gmelini musimon) Veterinary thesis. Lyon: Claude Bernard; 1998.Google Scholar
- Gibert P. La réserve nationale de chasse des bauges (Savoie): contribution à l’étude de l’étiologie de la kérato-conjonctivite du chamois. Lyon: Ecole Nationale Vétérinaire; 1979.Google Scholar
- Crampe J-P. Kératoconjonctivite de l’isard. L’épizootie de 2007-2008 en Vallée de Cauterets : modalités et conséquences démographiques, sur la base des données récoltées par les agents du PNP à Cauterets. Cauterets: Parc National des Pyrénées; 2008. Report No.: 08/01/IP.Google Scholar
- Crampe J-P, Gaillard J-M, Loison A. L’enneigement hivernal : un facteur de variation du recrutement chez l’isard (Rupicapra pyrenaica pyrenaica). Can J Zool. 2002;80:1306–12.View ArticleGoogle Scholar
- Crampe J-P, Loison A, Gaillard J-M, Florence É, Caens P, Appolinaire J. Patrons de reproduction des femelles d’isard (Rupicapra pyrenaica pyrenaica) dans une population non chassée et conséquences démographiques. Can J Zool. 2006;84:1263–8.View ArticleGoogle Scholar
- Schröder W, Von Elsner-Schack I. Correct age determination in “The biology and management of mountain ungulates”. Croom Helm. London: S.Lovari; 1985.Google Scholar
- CE.RI.GE.FA.S. Resoconto Monitoraggio 2004 sulla cheratocongiuntivite dei bovidi selvatici alpini in valle po e in valle varaita [Internet]. Italy: Ce.Ri.Ge.Fa.S; 2004. p. 6. http://www.provincia.cuneo.gov.it/allegati/node/1321/resoconto_monitoraggio_2004_28413.pdf.Google Scholar
- Michallet J, Loison A, Gaillard J-M, Gauthier D. Valeur de critères biométriques externes pour la détermination de l’âge du bouquetin des Alpes (Capra ibex ibex) : Rôle du sexe et de l’habitat. Gibier Faune Sauvage. 1994;11:99–118.Google Scholar
- Vilei EM, Bonvin-Klotz L, Zimmermann L, Ryser-Degiorgis M-P, Giacometti M, Frey J. Validation and diagnostic efficacy of a TaqMan real-time PCR for the detection of Mycoplasma conjunctivae in the eyes of infected Caprinae. J Microbiol Methods. 2007;70:384–6.View ArticlePubMedGoogle Scholar
- Bürki S, Vilei EM, Frey J, Wittenbrink MM. Allelic variations of the nox gene of Brachyspira pilosicoli impair its detection by qPCR. Vet Microbiol. 2011;149:291–2.View ArticlePubMedGoogle Scholar
- Belloy L, Vilei EM, Giacometti M, Frey J. Characterization of LppS, an adhesin of Mycoplasma conjunctivae. Microbiol Read Engl. 2003;149:185–93.View ArticleGoogle Scholar
- QGIS Development Team. QGIS Geographic Information System [Internet]. Open Source Geospatial Foundation Project; 2014. Available from: http://qgis.osgeo.org. Accessed 15 June 2015.
- Réseau Ongulés Sauvages, ONCFS/FNC/FDC. Répartition des ongulés de montagne [Internet]. France: ONCFS; 2010 [cited 2014 Oct 2]. Available from: http://carmen.carmencarto.fr/38/ongules_montagne.map
- IGN-Institut National de l’Information Géographique et Forestière [Internet]. 2014. Available from: http://professionnels.ign.fr/
- Garnier A. Conséquence des pathologies sur la dynamique des populations d’ongulés sauvages: exemple du bouquetin des Alpes dans le parc national de la Vanoise [Mémoire]. [Montpellier]: Centre d’écologie fonctionelle et évolutive, science de la vie et de la terre; 2013.Google Scholar
- Fernández MH, Vrba ES. A complete estimate of the phylogenetic relationships in Ruminantia: A dated species-level supertree of the extant ruminants. Biol Rev. 2005;80:269–302.View ArticleGoogle Scholar
- Tschopp R, Frey J, Zimmermann L, Giacometti M. Outbreaks of infectious keratoconjunctivitis in alpine chamois and ibex in Switzerland between 2001 and 2003. Vet Rec. 2005;157:13–8.View ArticlePubMedGoogle Scholar
- Rosengarten R, Citti C, Glew M, Lischewski A, Droesse M, Much P, et al. Host-pathogen interactions in mycoplasma pathogenesis: Virulence and survival strategies of minimalist prokaryotes. Int J Med Microbiol IJMM. 2000;290:15–25.View ArticlePubMedGoogle Scholar
- Rottem S, Naot Y. Subversion and exploitation of host cells by mycoplasmas. Trends Microbiol. 1998;6:436–40.View ArticlePubMedGoogle Scholar
- Sarradell J, Andrada M, Ramírez AS, Fernández A, Gómez-Villamandos JC, Jover A, et al. A morphologic and immunohistochemical study of the bronchus-associated lymphoid tissue of pigs naturally infected with Mycoplasma hyopneumoniae. Vet Pathol. 2003;40:395–404.View ArticlePubMedGoogle Scholar
- Simecka JW. Immune responses following Mycoplasma infection. Mycoplasmas Mol. Biol. Pathog. Strateg. Control. Norfolk: CRC Press; 2005. p. 485–534.Google Scholar
- Marreros N, Hüssy D, Albini S, Frey CF, Abril C, Vogt H-R, et al. Epizootiologic investigations of selected abortive agents in free-ranging Alpine ibex (Capra ibex ibex) in Switzerland. J Wildl Dis. 2011;47:530–43.View ArticlePubMedGoogle Scholar
- Tardy F, Mercier P, Solsona M, Saras E, Poumarat F. Mycoplasma mycoides subsp. mycoides biotype large colony isolates from healthy and diseased goats: prevalence and typing. Vet Microbiol. 2007;121:268–77.View ArticlePubMedGoogle Scholar
- Arcangioli M-A, Aslan H, Tardy F, Poumarat F, Grand DL. The use of pulsed-field gel electrophoresis to investigate the epidemiology of Mycoplasma bovis in French calf feedlots. Vet J. 2012;192:96–100.View ArticlePubMedGoogle Scholar
- Dejean T, Miaud C, Ouellet M. La chytridiomycose: une maladie émergente des amphibiens. Bull. Société Herpétologique Fr. 2010;134:27–46.Google Scholar
- Citti C, Nouvel L-X, Baranowski E. Phase and antigenic variation in mycoplasmas. Future Microbiol. 2010;5:1073–85.View ArticlePubMedGoogle Scholar
- Hamsten C, Tjipura-Zaire G, McAuliffe L, Huebschle OJB, Scacchia M, Ayling RD, et al. Protein-specific analysis of humoral immune responses in a clinical trial for vaccines against contagious bovine pleuropneumonia. Clin Vaccine Immunol CVI. 2010;17:853–61.View ArticlePubMedGoogle Scholar
- Mulongo M, Prysliak T, Perez-Casal J. Vaccination of feedlot cattle with extracts and membrane fractions from two Mycoplasma bovis isolates results in strong humoral immune responses but does not protect against an experimental challenge. Vaccine. 2013;31:1406–12.View ArticlePubMedGoogle Scholar
- Prysliak T, van der Merwe J, Perez-Casal J. Vaccination with recombinant Mycoplasma bovis GAPDH results in a strong humoral immune response but does not protect feedlot cattle from an experimental challenge with M. bovis. Microb. Pathog. 2013;55:1–8.Google Scholar
- Pirofski L, Casadevall A. Q and A: What is a pathogen? A question that begs the point. BMC Biol. 2012;10:6.View ArticlePubMedPubMed CentralGoogle Scholar
- Citti C, Blanchard A. Mycoplasmas and their host: Emerging and re-emerging minimal pathogens. Trends Microbiol. 2013;21:196–203.View ArticlePubMedGoogle Scholar
- Nouvel L-X, Marenda MS, Glew MD, Sagné E, Giammarinaro P, Tardy F, et al. Molecular typing of Mycoplasma agalactiae: Tracing European-wide genetic diversity and an endemic clonal population. Comp Immunol Microbiol Infect Dis. 2012;35:487–96.View ArticlePubMedGoogle Scholar
- Rocha E, Sirand-Pugnet P, Blanchard A. Genome analysis: Recombination, repair and Recombinatorial Hotspots. Mycoplasmas Mol. Biol. Pathog. Strateg. Control. Norfolk: CRC Press; 2005. p. 31–74.Google Scholar
- Le Grand D, Solsona M, Rosengarten R, Poumarat F. Adaptive surface antigen variation in Mycoplasma bovis to the host immune response. FEMS Microbiol Lett. 1996;144:267–75.View ArticlePubMedGoogle Scholar
- Baseman JB, Tully JG. Mycoplasmas: Sophisticated, reemerging, and burdened by their notoriety. Emerg Infect Dis. 1997;3:21–32.View ArticlePubMedPubMed CentralGoogle Scholar
- Citti C, Browning G, Rosengarten R. Phenotypic diversity and cell invasion in host subversion by pathogenic mycoplasmas. Mycoplasmas Mol. Biol. Pathog. Strateg. CONTROL. Norfolk: CRC Press; 2005. p. 439.Google Scholar
- De la Fe C, Amores J, Tardy F, Sagne E, Nouvel L-X, Citti C. Unexpected genetic diversity of Mycoplasma agalactiae caprine isolates from an endemic geographically restricted area of Spain. BMC Vet Res. 2012;8:146.View ArticlePubMedPubMed CentralGoogle Scholar
- Ryser-Degiorgis M-P. Wildlife health investigations: needs, challenges and recommendations. BMC Vet Res. 2013;9:223.View ArticlePubMedPubMed CentralGoogle Scholar
- Zimmermann L, Jambresic S, Giacometti M, Frey J. Specificity of Mycoplasma conjunctivae strains for alpine chamois Rupicapra r. rupicapra. Wildl. Biol. 2008;14:118–24.Google Scholar
- Parcs nationaux de France. Alpages et estives dans les parcs nationaux métropolitains de montagne. Montpellier: Parcs nationaux de France; 2011.Google Scholar