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Contagious agalactia (CA) of sheep and goats caused by Mycoplasma agalactiae is a widely occurring economically important disease that is difficult to control. The ELISA is commonly used for the serological detection of CA but it has some limitations and the performance of the available tests have not been properly evaluated.
Two commercial ELISA kits are widely used, one involving a fusion protein as target antigen and the other a total antigen. The objectives were to compare these tests by evaluating:
i. Their diagnostic sensitivity and specificity, the relevance of the recommended cut-off points, the correlation between the two tests, and, the correlation between serology data and the milk shedding of M. agalatiae;
ii. The influence of extrinsic factors such as the targeted animal species, geographical origin of the samples, intra-specific variability of M. agalactiae and concurrent mycoplasma infections.
A sample of 5900 animals from 211 farms with continuous CA monitoring for 20years and no prior vaccination history was used. The infection status was known from prior bacteriological, epidemiological and serological monitoring with a complementary immunoblotting test.
The average diagnostic sensitivity was 56% [51.8–59.8] for the fusion protein ELISA and 84% [81.3–87.2] for the total antigen ELISA, with noteworthy flock-related variations. The average diagnostic specificity for the fusion protein ELISA was 100% [99.9–100], and for the total antigen ELISA differed significantly between goats and sheep: 99.3% [97.4–99.9] and 95.7% [93.8–97.2] respectively.
Experimental inoculations with different M. agalactiae strains revealed that the ELISA kits poorly detected the antibody response to certain strains. Furthermore, test performances varied according to the host species or geographical origin of the samples.
Finally, the correlation between milk shedding of M. agalactiae and the presence of detectable antibodies in the blood was poor.
These serological tests are not interchangeable. The choice of a test will depend on the objectives (early detection of infection or disease control program), on the prevalence of infection and the control protocol used. Given the variety of factors that may influence performance, a preliminary assessment of the test in a given situation is recommended prior to widespread use.
Contagious agalactia (CA) is a disease of sheep and goats mainly characterized by mastitis with a subsequent drop in milk production. Mastitis is often associated with arthritis and/or kerato-conjunctivitis and sometimes with pneumonia and septicemia in young animals. Different species of mycoplasma (bacteria lacking a cell wall, in the class Mollicutes) cause CA. The main species in both sheep and goats is Mycoplasma agalactiae and three other species produce a clinically similar disease in goats: M. capricolum subsp. capricolum, M. putrefaciens and mainly M. mycoides subsp. capri. M. agalactiae CA is found worldwide and is common in high milk-producing regions including countries bordering the Mediterranean sea . The welfare and especially economic consequences of this disease justify its inclusion in the list of animal diseases of global concern established by the World Organization for Animal Health (OIE) (http://www.OIE.int).
Until recently, M. agalactiae CA was enzootic in two French regions: the northern Alps in goats (Savoie and Haute-Savoie departments) and the western Pyrénées (Pyrénées-Atlantiques (P.A.) department) in dairy sheep . Mandatory screening based on serological ELISA tests was introduced into these areas 20years ago. The disease appears to have been eradicated in the Alps as no M. agalactiae-infected herd has been identified for the last 10years. In the P.A., M. agalactiae CA regularly regressed from 1993 to 2005 but then re-emerged abruptly. The number of outbreaks increased from 0 to 200 between 2006 and 2010, underlining the inadequacy or misapplication of the applied control methods .
Two methods are generally used for detecting M. agalactiae-infected farms (with or without clinical expression): indirect serological detection when animals are not vaccinated and direct evidence of the organism in milk (individual or bulk tank milks) . The two methods are complementary: a direct search in tank milk is useful for early detection of newly infected herds while serological testing can be used on non-milk producers or to detect animals with chronic or latent infection where little or no mycoplasma are shed in the milk .
Several serological ELISA tests for M. agalactiae have been described and compared (Table (Table1)1) [4-8]. They use as target antigen, either the total antigens of M. agalactiae strain(s), or fusion proteins, copies of M. agalactiae specific immunogenic proteins. According to the literature, the diagnostic specificity (percentage of uninfected animals that test negative) is between 76 and 99% for tests using total antigens and between 97 and 100% for tests using fusion protein(s). The diagnostic sensitivity (percentage of infected animals that test positive) varies widely between tests (48 to 94%) and also according to the study for a given test (56 to 82%) [6-8]. Such differences may be partly explained by inadequate sampling, the different geographical locations of the studies (New Zealand, Brazil, Italy, France), the animal species targeted (goats or sheep) or the infection stage.
The objective of this study was to compare two ELISA tests that are widely used in Europe for the serological detection of M. agalactiae antibodies by evaluating: i) the performances per se : namely diagnostic sensitivity and specificity, the relevance of the recommended cut-off points, the correlation between the tests, and, the correlation between the presence of detectable antibodies and M. agalactiae shedding in milk; ii) the influence of extrinsic factors such as targeted animal species, geographical origin of samples, the intra-specific variability of M. agalactiae and mycoplasma co-infections.
The«POURQUIER-ELISA M. agalactiae»kit (IDEXX-Institut Pourquier, 326 rue de la Galera, F-36097 Montpellier cedex 5, France) is an indirect ELISA test. It targets antibodies against a fusion protein equivalent to M. agalactiae P48 protein  (P48-ELISA kit) and uses an anti-immunoglobulin G (IgG) conjugate. Normalised values (NV) based on optical density (OD) are given by the following formula: NV=(sample OD - negative control OD)×100/(average OD of the positive control - average OD of the negative control). Results are interpreted as follows: negative when NV≤50%, doubtful when NV is between [50-60%] and positive when NV≥60%.
The«LSIVET M. agalactiae»kit (Laboratoire Service International, 6 allée des Ecureuils Parc Tertiaire Bois-Dieu, F-69380 Lissieu, France) is an indirect ELISA test that targets antibodies against the total antigens (TA-ELISA kit) of a M. agalactiae strain isolated from a goat in Spain. It uses an anti-IgG conjugate. Normalised values (NV) are given by the following formula: NV=sample OD/(2 x negative control OD). Results are interpreted as follows: negative when NV<0.8, doubtful when NV is between [0.8-1] and positive when NV>1.
The confidence interval for a single measurement was established from repeated measurements of a positive serum (PAL97) and three 2 by 2 dilutions of this serum on each test plate : 80 test plates of four different batches (20 plates by batch) for TA-ELISA kits and 60 test plates of two different batches (30 plates by batch) for P48-ELISA kits. The confidence interval on a single measurement was defined as +/− twice the standard deviation of the mean of the replicates . PAL97 serum was used as the positive reference serum for an European serological inter-laboratory testing (http://www.OIE.int). It originated from an outbreak of M. agalactiae CA in P.A. and was obtained from a ewe eight months after clinical recovery.
M. agalactiae detection in milk was performed in two steps. First, samples were enriched with mycoplasmas by two successive incubations at 37°C and 5%C02 for four days into appropriate broth media (Oxoid), secondly the presence of M. agalactiae was fast screened by a sensitive real time PCR test that targeted a M. agalactiae/M. bovis specific sequence located on the gene coding for 16S RNA . Finally all cultures found positive or doubtful were tested again by a different PCR test that targeted the M. agalactiae specific P30 protein . Only positive samples with both PCR tests were considered as positive in the study.
Three hundred cultures that were positive with the above-described method were also tested by a dot-immunobinding technique .
Experimental infections were conducted with three different M. agalactiae strains: the PG2 reference strain, the 5632 strain isolated in Spain from a goat joint prior to 1991  and the 14628 strain isolated in France from bronchopneumonia lesions in a wild Capra ibex in 2006 . The Lyon Veterinary School Ethical Committee gave approval under agreement number #0730.
Test animals came from a goat herd that was certified free of pathogenic mycoplasma. Certification was based on regular bacteriological monitoring for the last five years (ear swabs, bulk tank and individual milk samples). All three experiments were performed under identical conditions: 2 to 3 adult goats were inoculated subcutaneously with 2ml of culture containing 108–109CFU/ml twice at a 16-day interval for strains 5632 and 14628 or at a 23-day interval for strain PG2.
Blood samples were taken every 3days after the first inoculation until slaughter, 20 to 35days later. The serological response was monitored by immunoblotting test and with both P48- and TA- ELISA kits.
Six sheep flocks infected by M. agalactiae (Table (Table2)2) were selected from the P.A. department, where CA has re-emerged recently. The bacteriological, serological and clinical statuses of the P.A. flocks were well known after 20years of continuous CA monitoring without any vaccination scheme. The infected reference flocks were approximately the same size, and contained only one breed of sheep (Manech) reared under similar animal husbandry conditions. In particular, breeding was synchronized, so that milk production started at approximately the same time for all sheep and lasted 8 to 9months. However the anteriority of M. agalactiae infection in each flock ranged from one to eight years after the first M. agalactiae detection in bulk tank milk. The prevalence of mastitis, arthritis and kerato-conjonctivitis during the study period was low in all flocks, less than 6%, but acute CA clinical signs reappeared during the following two years in 5 out of the 6 flocks. No animal purchase or grouping with another flock (mountain pasture, winter pension) occurred during the study.
Infected reference animals were chosen from the six infected reference flocks described above. These flocks were monitored regularly during the 2009 milking campaign. For each lactating animal: i) milk samples (composite milk) were collected monthly from the second month after weaning and tested for the presence of M. agalactiae and ii) one blood sample was taken after six months of milk production.
Animals shedding M. agalactiae in milk at least once in the samples taken 150, 120, 90 or 45days before blood sampling were classified as infected.
Four separate and independent animal populations were used in this study: two goat, one sheep and one mixed sheep/goat populations (Table (Table33).
Poitou-Charentes is the major area of goat milk production in France. The health status of the goat population is monitored regularly. Goats in this region are known to be frequently infected with M. mycoides subsp. capri but M. agalactiae is rare [15,16]. Sixteen herds that had experienced an episode of clinical CA caused by M. mycoides subsp. capri (confirmed after isolation in tank and individual milk samples) were selected: 10 in 2003 and 6 in 2007. Approximately 10 individual serum samples were collected from each herd selected in 2003 and 30 samples in 2007. A total of 276 goat sera were analyzed.
The Haute-Savoie goat population has been under serological and bacteriological surveillance for M. agalactiae CA for over 15years, and M. agalactiae infected herds have been systematically stamped out. No clinical outbreak of M. agalactiae CA has been detected since 2000. Sera collected during the 2007–2009 monitoring campaigns were used. 116 herds were selected at random: 87 contained fewer than 30 animals and 29 were large herds. All animals in the small herds were analyzed whereas only 20 randomly selected samples were analyzed in the large herds. In total, 1381 individual sera were analyzed.
The Tarn department is a major French producer of ewe’s milk with no history of CA. Sera from 21 flocks averaging 400 heads were collected in 2007 during a Maedi-Visna surveillance campaign. Sera from 50 to 60 adult animals from each flock were analyzed, providing a total of 1195 sera.
Only the western part of the P.A. department (Basque country) is infected with M. agalactiae. The eastern part (Béarn region) has been disease-free for 10years following an eradication program with stamping out of M. agalactiae infected flocks. Samples were analyzed from: i) 604 sheep from 43 randomly selected flocks, at a rate of about 15 adults from each flock (average flock size 300 sheep) and ii) all 275 adult goats from 9 herds.
M. agalactiae PG2 strain clone 55–5  was cultivated in liquid medium at 37°C for 48 hours. Cells were harvested by centrifugation at 12000g for 20min at 4°C followed by three washes in phosphate-buffered saline solution (PBS, 0.1M Na2HPO4, 0.1M Na2H2PO4, 0.15M NaCl, pH 7.2). Washed cells were resuspended and stored at −20°C in the same buffer. The protein content of the cellular extract was determined as described by Lowry et al. . Samples were mixed with lysis buffer (0.5M Tris/HCl pH 6.8, 4.6% (w/v) SDS, 20% (v/v) glycerol, 10% (v/v) 2-mercaptoethanol and 0.004% bromophenol blue) and boiled for 5min. Proteins were separated on a 4-12% gradient Bis-Tris polyacrylamide gel (Invitrogen). An electrophoresis was run on the Invitrogen Xcell surelock system following the manufacturer’s instructions. The separated proteins were transferred to a nitrocellulose membrane (Biorad) at 20V constant voltage for 45min in Tris glycine buffer (Tris 3.03g/l, glycine 14.4g/l) using the Biorad semi-dry transfer system. The membranes were blocked with a milk buffer (1M glycine, 1% ovalbumin, 5% dry skim milk in PBS buffer) at room temperature and shaken for 2 hours then washed for 15min at room temperature three times with PBS buffer 0.1% (v/v) tween 20 and finally with PBS alone. Each lane corresponding to a single well was cut, dried and immediately used or stored at −20°C. For immunoblotting, membranes were incubated for 2 hours at room temperature with 200μl of serum diluted with 1ml of dilution buffer (PBS containing 0.1% dry skim milk, 0.1% ovalbumin). After three washes in PBS 0.1% tween 20 and PBS buffer for 15min at room temperature, the membranes were incubated for 2 hours at room temperature with an appropriate dilution of peroxidase-conjugated anti-sheep- or goat-IgG in dilution buffer then washed as described above. The peroxidase substrate containing 30mg 4-chloro-1-naphthol dissolved in 10ml methanol and 50ml PBS and then 30μl H2O2 was added and left in the dark for 5–15min at room temperature.
A serum was considered positive if its profile contained four bands at 80, 48, 40 and 30kDa simultaneously.
Three types of serum samples were used to validate the immunoblotting technique:
22 sera from infected reference ewes collected from the six infected reference flocks (Table (Table2).2). These animals shed M. agalactiae in milk and were positive with both P48 and TA-ELISA kits.
20 sera from ewes collected from flocks in disease-free areas and with no positive or doubtful ELISA result.
31 “doubtful” samples. These sera tested positive with the TA-ELISA kit. Animals originated from presumed M. agalactiae-free flocks that were thought to be free from M. agalactiae, based on bacteriological tank milk monitoring, but bordered the contaminated area of the Basque country.
When at least two animals from flocks located in CA-free areas tested positive with an ELISA test (2 to 12 per farm), the positive sera were re-assessed using IBT. A total of 20 sera from 5 flocks in the Béarn and 37 sera from 7 flocks in the Tarn were re-assessed.
Data management was conducted with Excel. The correlation between results from different tests was calculated using the Kendall rank correlation coefficient (or Kendall’s tau coefficient) computed with R software (R Development Core Team, 2010, R Foundation for Statistical Computing, Vienna, Austria. http://www.R-project.org/). The other statistical analyses were conducted using the EpiInfo® software. Confidence intervals of proportions were calculated using an exact binomial distribution. Comparisons between proportions were based on chi-square tests with an alpha level of significance of 5%.
All 22 sera from infected reference animals had an identical IBT profile characterized by simultaneous presence of four bands at 80, 48, 40 and 30kDa and in most cases an additional band at 27kDa (Figure (Figure1-A).1-A). This profile was identical to the IBT profile obtained with sera from animals experimentally infected with the reference strain PG2 (Figure (Figure22-A-a).
Several of the 20 sera from uninfected animals revealed IBT bands. However, the profiles were highly variable and never presented the 80-48-40-30kDa bands simultaneously (Figure (Figure11-B).
In general, the 31 doubtful samples had diverse profiles, all dissimilar to those of the infected reference animals. Only three samples (out of five) from one flock had profiles with bands at 80, 48, 40, 30 and 27kDa (Figure (Figure1-C).1-C). This farm experienced a clinical outbreak of CA in the following months.
The apparent prevalence of infection in the population of 2165 lactating ewes was calculated from the six infected reference flocks in the P.A. (Table (Table2).2). On average, 61% of the animals were positive with the TA-ELISA kit and 36% with the P48-ELISA kit. However, these averages masked differences between flocks. Major differences between the two tests were apparent in the two flocks that had been recently infected (one year ago). The correlation coefficient (Kendall’s tau coefficient) between the two tests was 0.41 which is considered moderate.
Kit diagnostic sensitivity was estimated using sera collected from 609 infected reference ewes after six months of milk production (Table (Table2).2). The average diagnostic sensitivity of the TA-ELISA kit was 84% [81.3–87.2] and that of the P48-ELISA kit was 56% [51.8–59.8] (Table (Table2).2). The difference was significant (chi-square test, p<10-6) indicating that the TA-ELISA kit was more sensitive. However, this average sensitivity masked major differences between flocks for both tests, ranging from 52% to 100% for the TA-ELISA kit and from 34 to 96% for the P48-ELISA kit. For the latter kit, the lowest values were obtained in recently infected herds.
Diagnostic specificity was estimated using 3711 sera from five distinct populations (Table (Table3).3). The specificity of the P48-ELISA kit was almost 100%, regardless of which M. agalactiae uninfected reference population was used. The specificity of the TA-ELISA kit varied from 95% to 100% according to the population and the animal species. Thus, 87 sheep in M. agalactiae-free populations (26 sheep from 14 flocks in the Béarn region and 61 sheep from 19 flocks in the Tarn department) gave positive results with the TA-ELISA kit. They were considered to be false positives as none of these sera had the IBT profile characteristic of M. agalactiae infection.
The confidence interval for a single measurement was approximately +/−20% regardless of the test, dilution of the reference serum or plate batch.
For both the TA- and P48-ELISA kits, the distribution of serum titers in four distinct sheep populations was expressed as the percentage of animals from a given population which fell into each titer category (Figures (Figures33 and and4).4). For each kit, the titer distributions for two “M. agalactiae infected” and two “M. agalactiae uninfected” populations were plotted on the same graph. These were the two uninfected sheep populations from the Tarn department and Béarn region, the 609 infected reference sheep and finally a “probably infected” population consisting respectively of: i) 783 positive animals with the P48-ELISA kit for the titer distribution of the TA-ELISA kit and ii) 1090 positive animals with the TA-ELISA kit for the titer distribution of the P48-ELISA kit.
The positive cut-off point suggested by the TA-ELISA kit manufacturer (Figure (Figure3)3) showed a good fit with the intersection of the infected and uninfected population distributions (with a confidence interval for a single measurement about 20%).
The cut-off point of 60% suggested by the P48-ELISA kit manufacturer (Figure (Figure4)4) appeared excessive, given the distribution of the titers in both uninfected populations where no titer exceeded 25%. For a given 100% specificity and 20% confidence interval, lowering the threshold to 50% or 40% or 35% would increase the sensitivity of the test from 56% to 61%, 66% and 70% respectively (with a confidence interval for a single measurement about 20%).
The correlation between the presence of detectable antibodies in the blood and M. agalactiae milk shedding was poor for both tests with a Kendall correlation coefficient of 0.31 for the TA-ELISA kit and 0.26 for the P48-ELISA kit. Respectively 31% and 15% of the ewes that were known to have shed M. agalactiae between 45 and 150days prior to blood collection tested negative with the P48-ELISA and TA-ELISA kits. This result was not attributed to false positive PCR reactions. The M. agalactiae detection was specific, the first positive PCR were confirmed by a second independent PCR. In addition 299 (99.7%) of the 300 cultures that tested M. agalactiae positive with PCR were also M. agalactiae positive when further tested by dot-immunobinding.
The serological responses to experimental infections with three M. agalactiae strains (PG2, 5632 and 14628) were monitored by IBT, and with the TA-ELISA and P48-ELISA kits (Figure (Figure22).
IBT showed that all goats developed a significant humoral immune response following inoculation regardless of the strain used. No band was identified by IBT on the inoculation day, and multiple bands appeared from the 16th day after inoculation (Figure (Figure22A).
Animals inoculated with strains 5632 and PG2 tested positive nine days later with the TA-ELISA kit and 16days later with the P48-ELISA kit (Figures (Figures2B2B and and2C).2C). However the increase in antibodies of animals inoculated with strain 14628 was only weakly detected by the TA-ELISA kit and not at all with the P48-ELISA kit, despite a booster shot 16days after the initial inoculation (Figures (Figures2B2B and and22C).
In this study, the specificity of the TA-ELISA kit appeared to be lower in sheep (on average 95%) than in goats (99%). Specificity differed significantly between sheep and goats from the same geographic region (Béarn) (p=0.005).
The specificity of the TA-ELISA kit differed significantly between three goat populations from three different geographical locations: Haute-Savoie, Poitou-Charentes and Béarn (p=0.008). However, the specificity did not differ significantly between the two sheep populations from the Tarn department and Béarn region (p=0.45).
In the 256 animals in the 16 herds currently infected with M. mycoides subsp. capri, only five in three herds were positive with the TA-ELISA kit, corresponding in 98% of specificity that was similar to that of other goat populations (Table (Table33).
This study compared two commercial ELISA kits widely used in Europe to detect antibodies against M. agalactiae, the primary agent of CA. Kits were tested on a large number of sera collected from 5900 animals from 211 farms. The constitution of representative samples of farms with well known infection status was possible for several reasons: first, the epidemiological situation of CA in France is well surveyed , second, a large number of farms and animals had been monitored for many years as part of several distinct eradication campaigns and third, animals had not been vaccinated against this agent. This large sample size guaranteed the statistical reliability and accuracy of the study. Nevertheless, the average performance values should be regarded with caution because a sampling bias may still have occurred, and furthermore, the values varied according to the region, host species or M. agalactiae strain.
Accurate determination of the infection status of individual animals regarding M. agalactiae is difficult in the absence of a gold standard diagnostic technique. Thus, the criteria used to define animals as “infected reference” differ from one study to another and may be clinical, bacteriological or serological [5-8]. The OIE recommends that in the absence of a gold standard for classifying an animal as infected, isolation of the disease agent can legitimately be considered the method of choice . Classification of an animal as infected may be biased because animals may shed the organism early in the course of infection even if the humoral immune response is still low. Furthermore, animals with latent infection that have developed an immune response may intermittently or no longer shed the organism and are therefore difficult to detect.
Here, the “infected reference” status of an animal was based on bacteriological identification of M. agalactiae in individual milk samples. The M. agalactiae detection protocol used in this study is highly sensitive and specific. Sensitivity was provided by the first step of culture: an inter-laboratory assay including 32 French diagnosis laboratories demonstrated that 70% of them detected M. agalactiae by culture when test aliquots contained only 2 to 25CFU and 100% when test aliquots contained 25 to 250CFU [unpublished data]. Specificity was provided by using two sets of PCR primers for the identification of M. agalactiae, and was confirmed by dot-immunobinding. Finally, bias associated with intermittent shedding and with early infection were limited by i) repeating bacteriological examinations of individual milk samples at regular intervals and ii) not taking into account milk samples performed during the period of 45days prior to blood sampling.
The uninfected reference animals were recruited from geographical areas where M. agalactiae-related CA had never been reported or where routine monitoring had been in place for over 20years and where no case had occurred in the last 10years. Different independent populations and animal species (goats, sheep) were included to ensure diversity. Nevertheless, a number of animals, sometimes from the same farm, gave positive results with the TA-ELISA kit at the threshold recommended by the manufacturer. These positive results could have resulted from insufficient test specificity or from individual infections that escaped prior detection. A further technique was needed to unequivocally determine the status of these animals.
IBT is used for the serological diagnosis of contagious bovine pleuropneumonia (CBPP), another mycoplasma disease of ruminants, when routine tests are insufficiently accurate or ambiguous . Sera from infected animals give five specific IBT antigenic bands at 110, 98, 95, 60 and 48kDa simultaneously (http://www.oie.int). IBT has been used in several studies to identify M. agalactiae infection in cases of CA [6,7,19,20]. These authors described five stable immunogenic proteins with specific molecular masses of 80, 55, 48, 40, and 30kDa, which presumably could be used as a specific signature of M. agalactiae infection much like with CBPP. However, three proteins (55, 30 and 40kDa) are not expressed by all strains [6,12,21]. Thus an M. agalactiae-IBT should only be interpreted in the light of the antigenic profile of local strains.
A thorough analysis of 63 isolates collected between 1977 and 2007 in the P.A. showed that a single strain, very similar to the reference strain PG2, had been present for 30years in the P.A . This strain expressed the 80, 48, 40, and 30kDa proteins but not the 55kDa one identified in Sardinian strains . A posteriori, the 55kDa protein appeared to be antigenically similar to a variable protein of M. agalactiae known as Vpma U . On the PG2 antigenical phenotype used in IBT, Vpma U is apparent at 27kDa. Understandably, if a single M. agalactiae strain, similar to PG2 reference strain, was circulating in the P.A., it seems reasonable to suspect that all serum samples from infected animals would express the same IBT profile with four major bands corresponding to stable proteins and a 27kDa band, as confirmed by analysis of the 22 sera from infected reference animals. In contrast, the profiles of uninfected animals were heterogeneous and bands at 80, 48, 40, 30kDa never occurred simultaneously. One recently infected flock that had escaped monitoring was detected by IBT. So IBT proved to be useful in determining the status of P.A. flocks with regard to M. agalactiae when the ELISA test results were ambiguous.
Several sera from the uninfected population gave positive results with the TA-ELISA kit. Even in the most doubtful cases (several positives in one farm), the IBT profiles were never similar to those of infected animals. Presumably, these were false positives and the wide distribution of non-negative responses to the TA-ELISA kit on several farms would support this hypothesis.
Variability within M. agalactiae strains can affect test performances, and test sensitivity may be improved by using a local strain as antigen . In the present study, the kinetics of antibody response were followed after experimental inoculations of goats with three different M. agalactiae strains. Detection of the immune response to one strain was poor with both ELISA kits. The variability of M. agalactiae is expressed in two ways. First, not all strains express certain specific immunogenic stable proteins [12-21]. Second, the expression and size of several surface proteins, such as the Vpma family, can show rapid and random fluctuations, thereby generating multiple antigenic surface configurations and broad intra-clonal variability . These two concomitant phenomena may alter the host’s immune response, thereby affecting the sensitivity of diagnostic tests based on the degree of proximity between the phenotype of the test antigen and the phenotypes of the infecting strain. The consequences of antigenic variability on test performance are difficult to predict from strain characteristics. For example, both ELISA kits detect an immune response to strain 5632 even though this strain is genetically very different from the reference strain PG2 .
Test performance is also modified by geographic region and host species (sheep or goats). Regional differences may be due to antigenic variations between locally circulating strains. The TA-ELISA kit is less specific when used to detect M. agalactiae antibodies in sheep than in goats. This may be because it was developed with a goat strain that is possibly “adapted” to this species. Test specificity is not affected when goats are infected concurrently with other mycoplasma(s), even though these organisms may have many genes in common with M. agalactiae. However, given the genetic and antigenic variability of M. mycoides subsp. capri[15,26], certain strains may well express atypical cross antigens, as is the case with CBPP .
The main source of CA contagion is by M. agalactiae shedding in milk [1,2]. This study showed that the correlation between milk shedding and a detectable serological IgG response in blood was poor, implying that serology should not be used as an indicator of infectiousness. The percentage of animals that shed and tested negative with the TA-ELISA kit varied from 0 to 48% (average 16%) between farms, and from 4 to 62% (average 31%) with the P48-ELISA kit. Reports in the literature concerning the duration of the humoral response to mammary infection show considerable divergence, ranging from a rapid, systematic and persistent sero-conversion of at least 320days  to a highly transient sero-conversion of less than 32days . Further studies with reliable tests will be required to see whether the negativity in some infected animals results from the absence of serological response or from the rapid decrease of antibodies.
Two commercially available ELISA kits are widely used in several European countries to detect IgG antibodies against M. agalactiae.
The P48-ELISA kit is highly specific but not very sensitive. Its analytical performance characteristics may retard the detection of newly infected flocks especially when an insufficient number of animals are sampled. It is best used at the flock level.
The TA-ELISA kit is more sensitive, especially early in infection. On the other hand, it lacks specificity, especially with regard to sheep. When infection prevalence is low, false positive reactions hamper the monitoring and have to be tested again with expert serological test such as IBT. But no universal and standardized IBT test has been published for M. agalactiae yet.
In practice, the choice of kit should depend on: the user’s objective (early detection of infection or ongoing control program), the epidemiological situation (prevalence) and the type of disease control program. The present ELISA kits because they do not detect all animals that are shedding M. agalactiae, are not well appropriate to estimate the infectious risk of a herd.
The analytical performance of both ELISA kits is highly subject to variations depending on the characteristics of the infecting strains. A preliminary assessment of their performance in a new situation is recommended prior to widespread use.
Future serological tests should involve several fusion proteins which reproduce antigens that are complementary, specific, stable and widely representative of M. agalactiae strains and furthermore are able to differentiate between responses to natural and vaccine antibodies.
The authors have declared no conflict of interest.
FP conceived, coordinated and drafted the manuscript, DB coordinated all epidemiological and bacteriological studies in the P.A. and provided sera from the Tarn, MC and EG performed the statistical analysis, PG developed the immunoblotting test, YG coordinated serological monitoring in Haute-Savoie, DLG was in charge of experimental infections. All authors helped to improve the manuscript and approved the final version.
The authors are grateful to 1) A. Paoli (Anses Lyon Laboratory) who carried out the immunoassays and was responsible for sera collection management, 2) The “Groupement de Défense Sanitaire” of P.A. in charge of the CA control plan, for providing us with sera and access to the flock sanitary status 3) P. Mercier (Anses Niort Laboratory) for providing us with goat sera.