Immunodiagnostic usefulness of monoclonal antibodies specific to conformational epitopes of Taenia solium oncosphere protein TSOL18.

Taenia solium oncosphere protein TSOL18 is the host-protective antigen against porcine cysticercosis. Little attention has been given to use it as target molecule in immunodiagnostic tests. The objective of this paper is to describe the immunodiagnostic potential of monoclonal antibodies (MoAbs) raised against conformational epitopes of TSOL18. Three murine IgG1 MoAbs (25D12C1, 21C2D2, 10H1F2) against three different conformational epitopes of TSOL18 were produced and evaluated with an inhibition enzyme-linked immunosorbent assay (i-ELISA) for the detection of anti-TSOL18 and anti-oncosphere antibodies. Serum samples from pigs immunized with TSOL18 inhibited the binding of the three MoAbs to TSOL18 antigen in i-ELISA. The highest inhibition of anti-TSOL18 antibodies in immunized pigs was observed with MoAb 25D12C1. Ten field sera (12.19%) from 82 non-vaccinated and non-infected pigs showed anti-oncosphere antibodies inhibiting the binding of MoAb 25D12C1. Anti-oncosphere antibodies in pigs experimentally infected with T. solium eggs inhibited the binding of MoAb 25D12C1 from 2 to 8 week-post infection. It is concluded that MoAb 25D12C1 has excellent immunodiagnostic potentials to detect anti-oncosphere antibodies in the intermediate hosts at early exposure to T. solium eggs. Further investigations on potential use of MoAb 25D12C1 in a capture antigen ELISA for the detection of post-oncospheral antigens in infected pigs cannot be overemphasized.

Epidemiology of African Swine Fever in Piggeries in the Center, South and South-West of Cameroon.

African Swine Fever (ASF) is enzootic in Cameroon. A cross-sectional study was conducted in the center, south and south-west regions of Cameroon in order to determine: the knowledge, skills and practices at risk of pig breeders; the prevalence of the disease in piggeries; the genome of the circulating virus. A total of 684 blood samples were collected in 209 farms for RT-PCR and ELISA analyses at the National Veterinary Laboratory (LANAVET) annex in Yaoundé. Prevalences of 15.2% (95CI: 12.5-17.9%) by ELISA, 23.8% (95CI: 20.6-27.0%) by RT-PCR, and 15.2% (95CI: 12.5-17.9%) by ELISA-PCR, were recorded. Of the farmers surveyed, 90% knew about the ASF and 55.3% have already experienced it. The 47.4% of them would not be able to recognize ASF if it occurred and, according to them, the risk of the disease introduction in farms would be 32% linked to the animal health personnel who work on farms. Molecular characterization revealed that only ASF genotype-I variable 19T-RSs is circulating. ASF is still hovering at a risky rate over the pig sector of Cameroon. The control of ASF needs an epidemiological surveillance, a better involvement of all stakeholders, sensitization of breeders and an effective State support for producers.

Prevalence of porcine Taenia solium and Taenia hydatigena cysticercosis in Cameroon.

Taenia solium, a zoonotic tapeworm species of human and pigs, has been targeted by the World Health Organisation (WHO) for elimination in endemic areas of Africa, Latin America and some parts of Asia. Unfortunately, the assessment of control measures against T. solium is complicated by the lack of specificity of current immunodiagnostic techniques for diagnosis of porcine cysticercosis. Many authors have concluded that the prevalence of T. hydatigena in pigs in Africa is low and extensive epidemiological studies on T. solium cysticercosis in pigs have been carried out using serological tests that cannot differentiate the taeniid species. To estimate and compare the prevalence of T. solium and T. hydatigena in pigs in Cameroon, we examined 416 slaughtered pigs at a pig abattoir in Yaoundé city with the animals originating from several parts of the country. At post-mortem inspection, 35 pigs (8.4%; 95% Confidence Interval (CI), 5.9-11.5 %) were found infected exclusively with T. solium and 27 (6.5%; 95% CI, 4.3-9.3 %) infected exclusively with T. hydatigena metacestodes. One animal was infected with T. solium and T. hydatigena. A stochastic simulation model which took into account the sensitivity of dissection of the tongue, external masseters and heart for diagnosis of T. solium porcine cysticercosis (TMH dissection test) and examination of mesentery, surfaces of the intestines and liver to identify T. hydatigena cysticerci in slaughtered pigs was developed to estimate the prevalence of these taeniid species. The results revealed that the actual prevalence of T. solium and T. hydatigena in Cameroon were 24.8% (95% CI, 20.1-30.5%) and 19.2% (95% CI, 15.1-24.1%), respectively. This study reports the highest porcine T. hydatigena prevalence ever in Africa and adjusted the prevalence of porcine T. solium infection obtained with genus-specific Ag-ELISA (Dorny et al., 2000) in Cameroon due to the presence of T. hydatigena.

Seroprevalence and risk factors of brucellosis among slaughtered indigenous cattle, abattoir personnel and pregnant women in Ngaoundéré, Cameroon.

BACKGROUND: Brucellosis is a neglected debilitating zoonosis with a high prevalence in many developing countries. Bovine brucellosis is widespread in Cameroon but the epidemiological situation of human brucellosis is not known. A cross sectional study was carried to determine the seroprevalence and factors associated with bovine and human Brucellosis among abattoir personnel and pregnant women in Ngaoundéré, Cameroon. METHODS: Serum sample from 590 abattoir cattle and 816 plausible occupational risk and vulnerable humans to brucellosis (107 abattoir personnel and 709 pregnant women) were collected and screened for anti-brucella antibodies using Rose Bengal Plate Test (RBPT) and ELISA tests. Structured questionnaires were used to collect data on socio-demographics and risk-factors. The differences in proportions between seropositive and seronegative reactors were tested using odds-ratio and χ2tests. RESULTS: Bovine brucellosis seroprevalence was at 3.40% (n = 590; 3.4% for RBPT, 5.93% for i-ELISA). Human Brucella seroprevalence was at 5.6% among abattoir personnel (n = 107; 5.6% for RBPT, 12.15% for Brucella IgG ELISA) and 0.28% in pregnant women (n = 709; both tests). Breed (P < 0.00001) was associated with increased risk of brucellosis in cattle and the seroprevalence was highest among the Djafoun (OR = 16.67, 95%CI: 4.49-28.85) and Akou (OR = 16.96, 95% CI: 0.10-23.91) cattle compared to the other breeds. There was a moderate positive correlation (R2 = 0.5025) of Brucella IgG concentrations (> 200 U/ml) and clinical data for Brucella IgG ELISA seropositive humans. Several potential factors were associated (P > 0.05) with increased risk of human brucellosis seroprevalence among the abattoir personnel. The abattoir personnel were essentially males; the seropositive respondents were male and did not use protective equipment at work. Handling of foetus and uterine contents (OR = 13.00, 95%CI: 1.51-111.88) was associated with increased risk of human brucellosis. CONCLUSIONS: Antibrucella antibodies are prevalent in cattle (3.40%), among abattoir personnel (5.60%) and in pregnant women (0.28%) in Ngaoundéré, Cameroon. The study reports the first evidence of human brucellosis in Cameroon and therefore, an indication of a real public health problem. Public awareness campaigns and health education especially among livestock professional and in agropastoral communities should be highlighted to disseminate knowledge, associated risk factors and control measures of brucellosis.

Effect of nutritional status on the ovarian follicular population, yield and quality of oocytes in the Ngaoundere Gudali zebu (Bos indicus).

AIM: The aim of this study was to investigate the effect of nutritional status of the Gudali cows slaughtered at the Ngaoundere abattoir on follicular population, quality, and oocytes yield. MATERIALS AND METHODS: Blood and ovaries were collected from 81 cows aged 6.35±0.24 years (3-12 years old), with a body condition score (BCS) of 2.93±0.09 (1-5). In each ovary, the follicle were counted and classified as small (<3 mm), medium (3-8 mm) and large (>8 mm) using an electronic caliper. Oocytes were collected by slicing technique and classified according to the homogeneity of the cytoplasm and layers of granulosa into four groups: I, II, III, and IV. The nutritional status of the animals was determined by quantification of serum glucose, total cholesterol, total protein, albumin, globulins, urea, and phosphorus level. RESULTS: Of the total 162 ovaries harvested, 2916 follicles were counted on the ovarian surface with an average population of 36.00±2.17 follicles/cow. According to a size distribution, 16.67±1.54 (46.3%), 18.83±1.27 (52.3%), and 0.51±0.07 (1.4%), respectively for small (<3 mm), medium (3-8 mm), and large (>8 mm) were recorded. About 1,929 oocytes were obtained, with an average recovered of 23.81±1.53 oocytes/cow. Depending on the quality, 7.79±0.55 (32.7%), 6.04±0.41 (25.3%), 4.89±0.44 (20.6%), and 5.10±0.54 (21.4%) oocytes qualities I, II, III, and IV were obtained respectively; with an average cultivable oocyte recovered of 13.83±0.89 (58%). Cows with BCS > 3 and a high albumin and phosphorus level showed a highest number of follicles and oocytes able for in vitro maturation. CONCLUSION: These results indicated that nutrition remains an important factor for the in vitro production of the good embryo and the BCS is a useful tool for the selection of females' oocytes donors.