Transcript

Technical Note

Field study of a homologous vaccine against peste

des petits ruminants in northern Cameroon

A. Martrenchara,*, N. Zoyema, A. Njoyab, A.-C. Ngo Tamab, D. Bouchelb, A. Dialloc

a Laboratoire National VeÂteÂrinaire de BokleÂ, BP 503, Garoua, Cameroonb Institut de Recherche Agricole pour le deÂveloppement, Station polyvalente, BP 1073, Garoua, Cameroon

c CIRAD-EMVT, Campus International de Baillarguet, BP 5035, Montpellier Cedex 01, France

Accepted 20 April 1998

Abstract

A homologous vaccine against peste des petits ruminants (PPR) was investigated in northern Cameroon. The vaccine strain

was the attenuated PPRV 75/1 strain. The cost-effectiveness of the vaccine was studied by vaccinating ¯ocks of small

ruminants kept in their traditional environment. After 1 year, the mortality rates of the ¯ocks were compared with those of a

control group. The results demonstrated that the mortality rates were signi®cantly decreased in the vaccinated ¯ocks. The

annual bene®t for the herder was estimated to be about 13 400 FCFA (about US$ 22) for a ¯ock of 45 animals. # 1999

Elsevier Science B.V. All rights reserved.

Keywords: Peste des petits ruminants; Homologous vaccine; Field study; Sheep; Goats

1. Introduction

Peste des petits ruminants (PPR) is a highly con-

tagious disease which is endemic in northern Came-

roon. The prevalence rate of PPR was assessed to be

about 64% in the Far North Province and 14% in the

North Province (Martrenchar et al., 1995). Earlier

studies demonstrated that PPR, associated with capri-

pox infections, could explain partly the loss of pro-

ductivity in the ¯ocks (Martrenchar et al., 1997a). A

homologous vaccine against PPR has been developed

but a ®eld evaluation still needed to be carried out

(Diallo et al., 1989). The present study was conducted

in order to assess the in¯uence of a ®eld vaccination

with the PPR homologous vaccine on the mortality

rates of small ruminants ¯ocks.

2. Material and methods

2.1. Animals

Local ¯ocks, consisting of both sheep and goats,

were used. Overall, 1562 animals were involved in the

study (438 sheep and 1124 goats). The mean age of the

animals at the beginning of the study was 20 months

(min.� 1 week, max.� 9.5 years). The sheep were of

the local Fulbe and Oudah breeds. The goats were of

the local Kirdi breed.

Small Ruminant Research 31 (1999) 277±280

*Corresponding author. Fax: +33-2-96-01-62-23; e-mail:

[email protected]

0921-4488/99/$ ± see front matter # 1999 Elsevier Science B.V. All rights reserved.

P I I : S 0 9 2 1 - 4 4 8 8 ( 9 8 ) 0 0 1 3 8 - 2

2.2. Virus

2.2.1. Vaccine strains

Homologous PPR vaccine strain (Diallo et al.,

1989) was used. The strain was cultured on Vero cells

at the Bokle Veterinary National Laboratory and then

stored in freeze-dried form at �48C until use. Freeze-

dried vaccines were titrated on Vero cells using a

microtitre system as described elsewhere (OIE,

1992). The titre was calculated with the Reed and

Muench method after 10 days of culture. The vaccine

was used at the 103 tissue culture infective dose 50

(TCID 50). The RM 65 strain used for the control of

sheep pox (Ramyar and Hessami, 1968) was also

included in the vaccine at the 103 TCID 50 dose.

2.3. Field experiment

Two groups of ten ¯ocks, each of which were

concurrently part of a zootechnic trial in the traditional

environment of northern Cameroon, distributed in

eight localities were constituted in July 1993 (see

Fig. 1). One group (792 small ruminants) was vacci-

nated with the homologous PPR vaccine. Having

regard to herders' willingness, animals � 3 months

of age were not vaccinated. The second group (770

small ruminants) was used as control. There was at

least one test and one control ¯ock in each of the eight

localities to minimize the geographical effect. Within

each locality, the ¯ocks were randomly assigned to

one treatment. The causes of mortality during the trial

were established through herder's and ®eld agent's

observations. All the animals were identi®ed by ear

tags and a ®eld agent visited each ¯ock at least every

two weeks to record the dead animals. After 1 year the

mortality rates were calculated using the PIKBEU

software programmes (Planchenault and Sahut,

1989). The in¯uence of vaccination on mortality

was tested in creating different dichotomous variables.

The dependent variable was the mortality which took

the value 1 if the animal had died during the observa-

tion period and 0 if it had not. The independent

variables were the vaccination status of the animals

(value 1 if the animal had been vaccinated and 0 if it

had not) and the localities (8ÿ1�7 variables); the

latter variables were created to account for clustering

effect (each of the 7 variables took the value 1 if the

animal was in this locality and 0 it he was not) and

were forced into the model (McDermott et al., 1994).

The variables were entered in a multiple logistic

regression (Norusis, 1992). Two analyses were con-

ducted according to the age class (less or more than 1

year old).

3. Results

Mortality was signi®cantly lower in the vaccinated

¯ocks than in the control ¯ocks: 13% against 19% (P

<0.01) for the age class <1 year old and 18% against

28% (P<0.003) in the age class >1 year old (see

Table 1). Mortality in the control group was mainly

caused by pulmonary diseases. Unfortunately, due to

communication problems, a laboratory diagnosis of

these diseases could not be established. Clinical signs

Table 1

Comparison of mortality rates (%) in control (C) and vaccinated

(V) flocks according to the age class

<1 year old �1 year oldLocation

C(n) V(n) C(n) V(n)

1 18.0 4.0 18.6 4.9

(50) (50) (59) (41)

2 2.9 4.9 24.0 0.0

(35) (41) (25) (37)

3 15.4 20.0 26.7 12.5

(26) (25) (15) (8)

14.3 31.6

(28) (19)

4 21.1 10.0 23.4 23.5

(109) (100) (94) (85)

5 25.5 23.6 35.3 25.0

(55) (72) (34) (32)

6 18.2 10.5 0.0 9.8

(22) (57) (6) (41)

7 17.8 21.9 47.5 40.0

(45) (32) (59) (40)

29.2 15.0 21.4 18.9

(24) (20) (14) (16)

8 27.3 12.9 33.3 16.0

(33) (70) (18) (25)

There were one control and one vaccinated flock per location

except in location 3 where there were two control flocks and one

vaccinated flock and in locality 7 where there were two control and

two vaccinated flocks. Overall, mortality rates were significantly

higher in C flocks compared with V flocks (P<0.01 for the age

class <1 year old, P<0.003 for the age class � 1 year old, logistic

regression)

278 A. Martrenchar et al. / Small Ruminant Research 31 (1999) 277±280

characteristic of sheep and goat pox were not seen in

either the vaccinated or control groups.

4. Discussion

As no signs of capripox were observed during the

study and as another experiment carried out after the

beginning of our ®eld vaccination trial has shown

(Martrenchar et al., 1997b) that the capripox valence

was not effective against goat pox, it can be supposed

that the main effect of the vaccine was due to the PPR

valence.

Prior infection status of the ¯ocks was not deter-

mined and this may appear as a cause of concern.

Nevertheless, due to the study design, this drawback

should be minimized. As a matter of fact, PPR is a

highly contagious disease and it has been previously

shown (Martrenchar et al., 1997a) that during a sero-

conversion outbreak, all the animals of the ¯ocks

seroconverted at the same time. It can be assumed

that within the small area of a locality, where ¯ocks

Fig. 1. Location of the survey sites (* denotes localities).

A. Martrenchar et al. / Small Ruminant Research 31 (1999) 277±280 279

mixed frequently during daily grazing, all the ¯ocks

have the same PPR serologic prevalence; hence, the

prior PPR status should have been the same between

control and treatment groups. Furthermore, Diallo

et al. (1989) have shown that the PPR vaccination

strain did not diffuse from vaccinated animals to

unvaccinated animals.

Conventional good practise does not allow to treat

individuals as the statistical unit when the allocation

has been on the basis of ¯ocks (Elbers and Schukken,

1995). In the case of such a serious disease as PPR, it

was interesting to assess the effect of vaccination on

the mortality rates of the ¯ocks and not on the

occurrence of the disease within a ¯ock; this could

provide a direct economic consequence of vaccina-

tion. In this way, a comparison of means of mortality

rates between ¯ocks (comparison of two samples of

ten and nine units, respectively) would have not

accounted for the number of animals used to calculate

these mortality rates. Hence, the statistical unit was

chosen to be the animal.

Economic analyses based on a theoretical 5-year

dynamic herd model in Niger (Stem, 1993) have

outlined the high cost effectiveness of a PPR vaccina-

tion campaign using rinderpest vaccine. Our ®eld

experiment allows an other estimate of the economic

bene®ts of PPR vaccination using homologous vac-

cine. If we consider a ¯ock of 15 young animals and 30

adults, the annual productivity of the ¯ock will be

increased by approximately one young animal

(0.06�15) and three adults (0.1�30); this corresponds

to a bene®t of (2000�1)�(5000 � 3) �17 000 FCFA

per year (FCFA comes from the French: Franc Com-

munaute FinancieÁre Africaine [Franc African Finan-

cial Community]; 600 FCFA being roughly equal to

US$ 1). The cost of the vaccine is 20 FCFA per dose.

At the present time in northern Cameroon, the PPR

vaccine is sold 80 FCFA per dose, including 60 FCFA

to cover the cost of the ®elds agents needed to carry

out the vaccination. The annual cost of the vaccination

will be: 80�45�3600 FCFA while the annual bene®t

to the herder will be 13 400 FCFA (about US$ 22).

Furthermore, in case of severe outbreaks of PPR this

bene®t would certainly strongly increase. However, as

other zootechnical parameters have not been taken

into account, this result may not be an absolutely exact

estimate.

Acknowledgements

This work was supported by grants from the

research regional project on small ruminants (Coop-

eration Aid Fund, Ministry of French Cooperation).

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