Effect of a Natural Trypanosome Infection in Trypanotolerant Cattle Reared in a Tsetse-Infested Area in Southern Gabon and Monitored Under Field Conditions
Gael
Darren Maganga1,2*, Gui Lov
Dibanganga1,3, Antoine Mitte Mbeang Beyeme2,
Brice Adjahoutonon3, Clency Sylde Mikala Okouyi2, Brice Kumulungui2,
Jacques-François Mavoungou2,4
1Centre International de Recherches Médicales de Franceville (CIRMF), Franceville, Gabon
2Institut National Supérieur
d'Agronomie et de Biotechnologies (INSAB), Franceville, Gabon
3SIAT-Gabon Group, Libreville, Gabon
4Institut de Recherche en Écologie Tropicale (IRET-CENAREST), Libreville, Gabon
*Corresponding author: Gael Darren Maganga, Centre International de Recherches Médicales de Franceville (CIRMF), BP 769, Franceville, Gabon. Tel : +24102521253 ; Fax: +24101677295 ; Email: gael.maganga@cirmf.ga; gael_maganga@yahoo.fr
Received Date: 06 July, 2018; Accepted Date: 05 September, 2018; Published Date: 10 September, 2018
Citation: Maganga GD, Dibanganga GL, Mbeang Beyeme AM, Adjahoutonon B, Mikala Okouyi CS, et al. (2018) Effect of a Natural Trypanosome Infection in Trypanotolerant Cattle Reared in a Tsetse-Infested Area in Southern Gabon and Monitored Under Field Conditions. J Agr Agri Aspect: JAAA-127. DOI: 10.29011/2574-2914. 000027
1. Abstract
1.1. Background: African trypanosomosis is a major constraint to agricultural production in Sub-Saharan Africa. N’Dama has the ability to survive and be productive in tsetse-infested areas without the aid of treatment where other breeds quickly succumb to the disease. Although trypanotolerant, N'Dama can become vulnerable as a result of frequent infections.
1.2. Results: A comparative study on the effect of trypanosome infection on body weight, chest circumference and Packed Cell Volume (PCV) between naturally infected N’Dama, reared in a tsetse-infested area, versus uninfected N’Dama has been undertaken over 13 weeks. The study was conducted on 29 N’Dama bull calves, 3-year-old, with an average live weight of 242.8±27.25 kg and reared at similar tsetse challenge levels. Fourteen animals infected with trypanosomes belonged to the infected group (n=14), and 15 bull calves randomly selected and having received curative and preventive treatments against trypanosomosis, composed the uninfected group (n=15). Trypanosomes have been detected using PCR. During the study, body weight, chest circumference and PCV of animals of both groups were monitored weekly. The body weight loss was much more pronounced in the infected animals (b = -1.0584) than in uninfected animals (b = -0.2609). The decrease of the average chest circumference was much more marked in the infected group (b = - 0.0052) compared with uninfected group (b = - 0.0025). However, trypanosome infection had no significant effect on PCV.
1.3. Conclusion: This study suggests that strict prophylactic programs should be conducted on N'Dama cattle to improve their production, in tsetse-infested areas.
2. Keywords: Body weight; Chest Circumference; N’Dama; PCV; Trypanosomes
1. Background
In sub-saharian Africa, African Animal Trypanosomosis (AAT), also known as nagana, is caused mainly by Trypanosoma congolense, Trypanosoma vivax and Trypanosoma brucei (the most widespread pathogenic trypanosomes in Africa). According to the Food and Agriculture Organization (FAO), animal trypanosomosis is responsible for the death of 3 million cattle per year, with an annual economic loss estimated at $1-1.2 billion [1,2]. These losses are due to stock mortality and depressed productivity, which may be of meat, milk, reproduction or traction [3]. The clinical signs of AAT in livestock include, anemia, intermittent fever, whimpering, lymphadenopathy, jaundice, edemas, progressive emaciation leading to cachexia, weakness and death, if not treated [4,5].
The prevalence of the AAT in tropical and equatorial Africa constitutes a major hurdle with the livestock productions. AAT control has mainly been directed towards eradicating or reducing the number of tsetse and towards the use of trypanocidal drugs. None of these two methods of control against this disease were fully satisfactory. As the attempts made against the parasite and the vector had not produced sustainable results, an alternative, potentially cost-effective and sustainable option to reduce the prevalence of trypanosomosis was the exploitation of the natural phenomenon known as trypanotolerance exhibited by certain livestock breeds, including the well-known N’Dama, that are indigenous to areas in which the disease is endemic [6].
Trypanotolerance was defined as ‘the ability of some livestock breeds to survive, reproduce and produce in tsetse-trypanosome infested areas where others cannot, without recourse to use of chemical drug’ [7]. In AAT, the criteria to define trypanotolerance are Packed Cell Volume (PCV), which is an indicator of anemia, parasitemia, and body weight [8]. Indeed, it has been consistently noted that trypanotolerant cattle when they become infected develop less severe anaemia [9]. Moreover, trypanotolerant cattle as West African Shorthorn and N'Dama have the ability to resist the effects of infection, i.e. not only to survive, but to gain weight and reproduce [7]. In Gabon, as in other countries of Central Africa, the use of animals naturally less susceptible to the disease, such as N’Dama cattle, has produced encouraging results. It has long been recognised that some breeds of trypanotolerant cattle such as N’Dama, has the ability to survive and be productive in tsetse-infested areas without the aid of treatment where other breeds quickly succumb to the disease [10].
However, trypanotolerant animals tolerate infections, but this does not mean that the infection has no impact on their health. Indeed, study done in Senegal have shown that, even though it is trypanotolerant, N’Dama cattle sometimes becomes vulnerable, which affects its work performance (i.e. speed of work, distance covered) [11] because trypanotolerance is relative and its role in the immune defenses of the animal can be considerably reduced, in particular during frequent infections. Similarly, [12] showed that N'Dama cattle can suffer for trypanosomosis under high tsetse challenge. The objective of this study is to evaluate the effect of a trypanosome infection on N’Dama naturally infected, reared in a tsetse-infested area, by comparing the evolution of body weight, chest circumference and Packed Cell Volume (PCV) in infected and free from trypanosomes N’Dama.
2. Materials and Methods
2.1. Study Site
The study was conducted from june to september in the Nyanga ranch, located in the largest savannah zone of the country in the Mongo County, located about 65 km from Tchibanga (the main town of Nyanga province, southwest Gabon) and extended over 100,000 hectares. The Nyanga ranch includes three divisions (Nyanga, Bibora, and Voungou) divided into sections. The ranch represents a hilly landscape covered with herbaceous vegetation type and dotted with vegetation (Brachiaria, Hyparrhenia, Panicum, Andropogon and Digitaria species). Forest galleries are present along the gullies and rivers. Climate is equatorial with two dry seasons and two wet seasons. The presence of Glossina haningtoni, Glossina palpalis palpalis and Glossina tabaniformis has been confirmed in forests and forest galleries of the Nyanga valley [13,14]. In the Gala section of the Nyanga ranch, T. vivax and T. congolense have been detected in cattle.
2.2. Animals
Initially, a total of 57 N'Dama bulls calves, reared at similar tsetse challenge levels, were screened for trypanosomosis using PCR [15]. These animals live outdoors, feed through natural grazing, composed predominantly of Hyparrhenia diplandra and Panicum maximum, and drink from natural water courses or water troughs, for low irrigated areas. A mineral supplement based on a mixture of sodium chloride, copper sulfate, zinc carbonate and cobalt sulfate is provided ad libitum. Every two weeks, animals were dipped into a flumethrin bath to protect them from blood-sucking arthropods.
PCR assay was performed from DNA extracted from whole blood samples, collected by puncture of the caudal vein, using QIAamp DNA Blood Mini Kit (Qiagen, Germany). Blood samples from each animal was subjected to parasitological and hematological analyses, using the buffy coat method to estimate the parasitaemia according to the scoring system based on the darkground/phase contrast buffy coat technique [16,17], and the Packed Cell Volume (PCV), respectively. Animal was considered infected when PCR was found positive and at least one trypanosome was observed. Uninfected animals were those in which PCR was found negative and no parasite was observed.
Firstly, the animals of both groups (infected and uninfected) were subjected to different treatments: deworming using Levamisole (Alfamisol); every 2 weeks, animals were dipped into a Cypermethrin (Cypertop) bath to kill and repel ticks and tsetse flies (the transition to dipping tank was done every two weeks for all animals throughout the duration of the experiment); preventive antibiotic therapy based on oxytetracycline (Tenaline 20% L.A.); vaccinations against contagious bovine pleuropneumonia and bovine pasteurellosis. Moreover, uninfected animals received in addition to these treatments, a trypanocidal (Diminazene) (Veriben). Then, the animals were put to rest for one week before the start of the experiment. Two weeks after the start of the experiment, the uninfected animals received a second trypanocide based on Isometamidium chloride (Trypamidium-Samorin).
3. Monitoring of Animals and Data Collection
Once a week, the animals were brought back to the health center for blood sampling, weighing and taking chest circumference. So, during this weekly passage, for each animal approximately 5 mL of whole blood was collected in EDTA vacuum tubes VENOJECTR, by puncture of the caudal vein. The buffy coat zone, prepared in a micro-hematocrit capillary tube heparinized (DrummondR, USA) filled with 75 µL of blood and centrifuged for 6 min was examined for trypanosomes and packed cell volume value was determined. Animals were weighed using weighing bars (Avery-Weigh Tronix PC 820, UK), chest circumference were taken using a ribbon. At the end of the experiment, blood samples from uninfected animals were again screened by PCR to exclude any possibility of infection during the experiment.
3.1. Statistical Analysis
The data obtained was previously analyzed as recommended by [18]. The effect of trypanosome infection on body weight, chest circumference and PCV was studied in two ways. First, by analyzing the weekly average gain of the parameter considered. A "gain" is a positive variation (or increase) of the parameter over a given period. The weekly gain (GP) was calculated as the ratio of the variation of the parameter on the time variation:
Pit is the measured value of the parameter P on the individual i at time t; is the value of the same parameter, measured on the same individual at time t + k, where k is the number of weeks between the two measurements.
This variation was studied using a linear mixed effects model. Indeed, with data from multiple measurements on the same
individuals, these observations are dependent and correlated. An
appropriate procedure for analyzing this type of data is the use of mixed
models, which allow the inclusion of random effects, to account for individual [18-20] and temporal variability.
A logarithmic transformation has been applied to reduce the large disparity
between observations [20]. This transformation
concerns only the body weight and chest circumference variables; the added constant allows small values to be
taken into account (Equation 1). Regarding the PCV, it is an arcsinus
transformation (,P is in proportion) that was performed (Equation 2 and Equation 4), as recommended by [21] for the analysis of
percentage data.
Ln = logarithm base "e";gain or increase in body weight or
chest circumference of animal i of status s in period t;
gain or increase in hematocrit or
PCV of animal i of status s in period t; S = infectious status of the animal with respect to trypanosomosis (S is 0 if the animal is uninfected and 1 if it is infected); α, β = fixed parameters to be estimated;
random parameters related to the
period and the subject, respectively. The individual random effect is fitted
into the effect period;
Then, by analyzing the temporal evolution of the average of the parameter in each
group. The average body weight and the average chest circumference were
analyzed as a simple linear function of time (Equation 3). However, the average
PCV was adjusted as a quadratic function of time (Equation 4).
average body weight
or chest circumference calculated for individuals of the same infectious
status;
average hematocrit or PCV calculated
for individuals of the same infectious status;
time (in weeks);
fixed parameters to estimate varying
according to infectious status;
All statistical analyzes were performed using the R
software version 3.4.1.
4. Results
4.1. Experimental Animals
From the 57 N’Dama bull calves, 29 animals, 3-year-old, with an average live weight of 242.8±27.25 kg, were selected and divided into 2 groups: 14 bull calves composing the group of infected animals, among which 5 were infected by Trypanosoma vivax et 9 by Trypanosoma congolense, and 15 bull calves randomly selected (random sampling double raw) among the 43 non-infected animals, which were the uninfected group. PCV values and parasitemia of all the infected animals are shown in (Table 1). The average PCV of the infected animals was 23.8% before the start of the experiment. All animals of both groups appeared healthy.
4.2. Effect of Trypanosome Infection on Body Weight and Chest Circumference
The study of the correlation between variables using principal component analysis, showed a strong association between body weight and chest circumference (Figure 1). A possible link between the infectious status of animals and changes in their weight and chest circumference was observed in (Figure 1).
Analysis of weight gain in both groups of animals showed that over the same period, the average body weight of infected N’Dama bull calves would increase more slowly (1.501 ± 0.268 kg per week) than that of uninfected animals (1.769±0.259 kg per week). This weekly difference of 0.238±0.251 kg would be significant at 10% threshold (Table 2). Thus, considering two individuals, one infected and the other uninfected, and of the same body weight at time t0, if their mass increases steadily during the period t0+k (k number of weeks passed), the body weight of the uninfected is expected to be k x 0.238±0.251 higher than that of the infected animal. The results of the regression of the average body weight according to time in both groups of animal are summarized in Figure 2 and (Table 2).
We noted a decrease of the average body weight over the experimentation period regardless of the group (Figure 2). While this decrease was not statistically different between the both groups (p = 0.2463) (Table 3), it does not occur nevertheless at the same pace. However, the average body weight of the infected animals was significantly higher in early experimentation (p = 0.0222) (Table 3) and the body weight loss was much more pronounced in the infected animals (b = -1.0584) than in uninfected animals (b = -0.2609). In addition, in the infected group, the average body weight decreased so much throughout the observation period that it was almost equal to the average weight, which fell slightly, in the uninfected group, at the end of the study (Figure 2).
The observation of the evolution of the chest circumference in both groups during the same period showed that the average thoracic perimeter of the infected animals would increase significantly less rapidly (p = 0.0422) than the uninfected animals; with a difference of about 0.013 ± 0.012 m per week (Table 4). For a trypanosome-infected animal a weekly chest circumference increase would be approximately 0.026 ± 0.010 m, whereas it would be around 0.039 ± 0.007 m for an uninfected animal.
The results of the regression of the average chest circumference according to time in both groups of animal are summarized in (Figure 3 and Table 5). We noted a decrease of the average chest circumference over the experimentation period regardless of the group (Figure 3). Although the gradients of the two regressions are not statistically different (p = 0.1472), that of the infected group is nevertheless more accentuated. The decrease is much more marked in the infected group (b = - 0.0052) compared with uninfected group (b = - 0.00256). Moreover, the average chest circumference of the infected group was significantly higher (p = 0.0101) at the start of the study (Table 5), and the regression coefficient of the infected group was significant (p = 0.000864). The Figure 3 showed that the average chest circumference of the trypanosome-infected animals was significantly higher at the start of the experimentation, before decreasing and getting closer to the value of uninfected group, which weakly regressed, at the end of the experiment.
4.3. Effect of Trypanosome Infection on Packed Cell Volume
The increase of PCV in trypanotolerant N’Dama bull’s calves would appear to be more attenuated (α = 0.22 > 0 and β = -0.03 < 0) in individuals infected with trypanosomes (Table 6). We would expect a weekly increase of approximately 3.58% in an affected animal against 4.78% for a trypanosome free animal. However, we found that the average PCV did not differ significantly between the two groups, from the start (p = 0.2481) to the end of the experiment (p = 0.9761) (Figure 4 and Table 7). The figure 1 already showed a lack of association between PCV and infectious status of animals. In addition, the difference observed at the start of the study between the two groups is maintained throughout the experiment period (see regression curve in Figure 4).
5. Discussion
One of the most important factors which influences the level of trypanotolerance is the severity of the tsetse challenge to which the animals are exposed. In fact, as the level of challenge rises, productivity falls, and in high-risk situations even N'Dama cattle can be severely affected by trypanosomiasis [10]. Very little studies [22] have been conducted on the effect of trypanosome infection on N'Dama trypanotolerant cattle by comparing naturally infected N'Damas with a control group of uninfected N'Dama under field conditions.
Our study was conducted on N'Dama bulls aged 3 years; they are growing animals which allows to appreciate the evolution of the morphological parameters. Indeed, the complete development of N'Dama is reached at 7 years for males and 6 years for females [23]. Previous study carried out in one section of the Nyanga ranch showed that the prevalence of trypanosomosis was high (57.3%), with the co-circulation of two pathogenic species of trypanosomes, T. congolense (47.3%) and T. vivax (10%) [24]. The study animals were found naturally infected either by T. vivax or T. congolense [25,22], major pathogenic trypanosome species in Africa. Thus, the 14 animals in the infected group were predominantly found infected with T. congolense (9 individuals). The 5 T. vivax-infected individuals were included in the study because of the virulent nature of this species in cattle and to increase the number of animals infected with trypanosomes. Although T. congolense is often considered to be the most virulent of the trypanosomes in cattle, T. vivax is often found to be responsible for the first infections in cattle [26].
The results of this study showed a link between the infectious status of N’Dama naturally infected in field and changes in their body weight and chest circumference. The principal component analysis already showed a strong association between body weight and chest circumference as previously reported by [27]. The effect of trypanosome infection on the body weight of N’Dama bulls was significant. The body weight loss was much more pronounced in the infected animals than in uninfected animals, as shown by [22] who studied N’Dama from Mushie Ranch, in Democratic Republic of Congo. However, this finding was contrary to the result obtained by [11] who, working over a period of 4 weeks on N’Dama experimentally infected with T. congolense, had not observed a significant effect of the infection on weight probably due to the relatively short period of his study. Moreover, authors argue that if the experiment had been prolonged for a few more weeks, a significant difference in weight gain would probably have been observed in the event that the animals did not feed well. These conditions could correspond to those of our study, insofar as this one was carried out over a period 3 times longer than that of their study and in the dry season, where the food in the pastures of the ranch was scarce. In general, compared to other cattle breeds such as Boran, trypanosome infection does not affect liveweight gains in the N'Dama [7].
The chest circumference of infected animals was significantly influenced by trypanosome infection. Indeed, the average chest circumference of infected animals decreased significantly faster than that of uninfected animals, with a difference of about 0.013±0.012 m per week (p = 0.0422). The uninfected animals have a more significant weight gain than the infected animals, and therefore would grow larger, resulting in widening of the chest circumference. The very significant regression coefficient of the infected group reflects a proven effect of the infection on the chest circumference, i.e. the trypanosome infection has a negative effect on the evolution of the chest circumference of the animals. Besides we noted a decrease of the average chest circumference over the experimentation period regardless of the group which would result of the scarcity of forage on pastures linked to the dry season. Our results contrast with the results obtained by [28], who could not conclude from the significant effects of trypanosome infection on the chest circumference. According to them, in their study, this parameter was influenced by the feeding problem and by the effects of gastrointestinal parasitism. In our study, the animals of both groups (infected and uninfected) have been de-wormed. The feeding pattern of animals was the same for all of them. They fed in the park based on natural forage.
We found that the average PCV did not differ significantly between the two groups, from the start to the end of the experiment, although the increase of PCV in trypanotolerant N’Dama bull’s calves would appear to be more attenuated in individuals infected with trypanosomes, as shown by [22], suggesting the existence of a weak possible effect of the infectious status on the PCV level, but it would be difficult to better quantify in the field conditions. In their studies, [29] and [11] found that the PCV of infected N’Dama was lower than that of healthy N’Dama. A lower PCV is synonymous with anemia, and the latter is one of the hallmarks of trypanosomosis [11]. The N’Dama's ability to control parasitaemia, a capacity conferred by trypanotolerance [23,30], was confirmed by the low parasitaemias observed in infected animals. In addition, the detection of trypanosomes in infected animals, despite the very low parasitaemia noted, confirms the very good sensitivity provided by PCR of the order of 1 to 50 trypanosomes/ml of blood [31,32].
6. Conclusion
This is a recent study that describes the effect of trypanosomose infection
on naturally infected trypanotolerant cattle and monitored under field
conditions, raised in a country where cattle breeding is struggling to develop.
Bovine trypanosomiasis is a limiting factor in cattle rearing. The disease
affects the growth and reproduction performance of these animals. The breeding
of trypanotolerant cattle is one of the main solutions to this problem. This
study showed that N'Dama cattle would therefore not be simply reservoirs of
trypanosomes but could be affected by these parasites in the absence of
prophylactic programs. This study, however, would need to be carried out over a
longer period of time and in the rainy season when pastures are rich in fodder,
in order to better appreciate the real impact of this disease on
trypanotolerant cattle breeds reared in their natural environment, which
according to some authors, would not suffer from this infection. In parallel,
this study could also be reproduced under experimental conditions, in order to
better control some parameters which could interfere with the observed effects;
such as the level of infection of the animals, trypanosome species involved and
availability of food resources.
7. Declarations
7.1. Acknowledgements
The authors thank SIAT-Gabon, especially Bruno Besnard and Ernest Agossou as well as the drovers for the technical assistance. We acknowledge Elsa Assengone for the english revision. The CIRMF is supported by the Government of Gabon, Total-Fina-Elf Gabon, and the Ministère de la Coopération Française.
7.2. Authors’ Contribution
Maganga GD has initiated the study and drafted the manuscript. Dibanganga GL performed analyses and drafted the manuscript. Mbeang Beyeme AM, Mikala Okouyi CS and Adjahoutonon B performed analyses. All authors read and approved the final.
7.3. Competing Interests
The authors declare that they have no competing interests.
7.4. Consent for Publication
Not applicable.
Figure 1: Correlation between
the infectious status of animals and the body weight, chest circumference and packed
cell volume (PCV).
Figure 2: Regression of
average body weight in both groups of animals. Blue square and black triangle
represent the average for animals of each group.
Figure 3: Regression of
average chest circumference in both groups of animals. Blue square and black
triangle represent the average for animals of each group.
Figure 4: Regression of average PCV in both groups of
animals. Blue square and black triangle represent the average for animals of
each group.
Animal ID |
PCV (%) |
Trypanosome/field |
Trypanosome identified by PCR |
265 |
30.5 |
1 |
T. vivax |
1402 |
23,5 |
1 |
T. congolense |
1618 |
22 |
2 |
T. congolense |
1709 |
30.5 |
1 |
T. vivax |
2606 |
24 |
1 |
T. vivax |
2656 |
25 |
1 |
T. congolense |
2662 |
29 |
1 |
T. vivax |
2896 |
20 |
1 |
T. congolense |
2881 |
26 |
2 |
T. congolense |
2884 |
20 |
1 |
T. congolense |
1146 |
20 |
3 |
T. congolense |
2852 |
21 |
1 |
T. vivax |
2878 |
21 |
2 |
T. congolense |
2895 |
22 |
2 |
T. congolense |
Table 1: Characteristics of the infected animals selected for the study before different treatments applied.
Parameters |
Values |
p values |
|
1.739 (± 0.259) |
<0.0001 |
|
- 0.238 (± 0.251) |
0.0617 |
Standard deviation of time-related random effects |
0.399 |
|
Standard deviation of the random effects related to animal |
0.549 |
|
Residual standard deviation |
0.222 |
|
α, β: fixed parameters to be estimated |
Table 2: Summary of the weight gain model.
Parameters |
Average body weight |
p value of equality test parameters between the two groups |
|
|
Uninfected |
Infected |
|
|
234.5612 (± 7.3330) ***
|
247.631 (± 9.1123) ***
|
0.0222 |
|
- 0.2609 (± 0.9238)
|
- 1.0584 (± 1.1480) a
|
0.2463 |
Residual standard deviation |
5.663 |
7.037 |
|
|
Table 3: Summary of the model of evolution of the average body weight over the study period for both groups.
Parameters |
Values |
p values |
|
0.0386 (± 0.0074)*** |
<0.001 |
|
- 0.0125 (± 0.0120)* |
0.0422 |
Standard deviation of time-related random effects |
0.0014 |
|
Standard deviation of the random effects related to animal |
0.0283 |
|
Residual standard deviation |
0.0047 |
|
*: significant at the 5% significance level. |
Table 4: Summary of the chest circumference variation model.
Parameters |
Average chest circumference |
p value of equality test parameters between the two groups |
|
|
Uninfected |
Infected |
|
|
1.4959 (± 0.0231) ***
|
1.535 (± 0.02007) ***
|
0.0101 |
|
- 0.00256 (± 0.0029) a
|
- 0.0052 (± 0.00253) ***
|
0.1472 |
Residual standard deviation |
0.01782 |
0.0155 |
|
|
Table 5: Summary of the model of evolution of the average chest circumference over the study period for both groups.
Parameters |
Values |
p values |
|
0.2204 (± 0.0316)*** |
<0.0001 |
|
- 0.0300 (± 0.0355)a |
0.0972 |
Standard deviation of time-related random effects |
0.0403 |
|
Standard deviation of the random effects related to animal |
0.0863 |
|
Residual standard deviation |
0.0327 |
|
***: Highly significant at the 5% significance level; a : significant at the 10% significance level. |
Table 6: Summary of the PCV variation model.
Parameters |
Average PCV |
p value of equality test parameters between the two groups |
|
|
Uninfected |
Infected |
|
|
0.608 (± 0.055)*** |
0.569 (± 0,047)*** |
0.248 |
|
0.0187 (± 0.018)* |
0.019 (± 0,015) *
|
0.977 |
c (± CI) |
- 0.0014 (± 0.0013)* |
- 0.0015 (± 0.0011)* |
0.976 |
Residual standard deviation |
0.0254 |
0.0216 |
|
|
Table 7: Summary of the model of evolution of the average PCV over the study period for both groups.
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