DOI: https://doi.org/10.21203/rs.3.rs-62998/v1
Background: It is generally recognized that there is a risk for humans to acquire toxoplasmosis through consumption of raw milk from infected animals. Although several studies have been conducted to detect the seroprevalence of T. gondii in cattle in China, no study has been conducted to detect T. gondii DNA in milk of cattle in China. Thus, the present study was firstly conducted to explore the prevalence of T. gondii DNA in fresh milk of cattle in China.
Results: A total of 2092 blood samples and fresh bovine milk were collected from six provinces between January 2018 and June 2019, respectively, and examined by ELISA and semi-nested PCR, respectively. In total, 123/2092 (5.88%) of the blood samples and 22/2092 (1.05%) of the milk samples were positive for T. gondii, respectively. Fifteen of these 22 positive milk samples (68.18%) were animals who also recorded serologically positive. Moreover, cattle and milk from family farming have significantly higher T. gondii prevalence than those from commercial farm.
Conclusions: To our knowledge, this is the first report of T. gondii DNA was found in the fresh milk of cattle in China, suggesting that the consumption of raw milk from seropositive cattle could be a potential source of human infection.
Toxoplasmosis is a global zoonotic parasitic diseases, caused by Toxoplasma gondii, an important opportunistic protozoa, which can cause great financial losses, especially for the animal production industries, and is of great importance for public health [1-3]. All kinds of hosts may be infected through ingestion of T. gondii oocysts or cysts containing bradyzoites, via ingestion of tachyzoites in non-pasteurized milk products or through the transplacental transmission [4].
Tachyzoites of T. gondii have been detected and isolated from the milk of numerous species and milk has been considered as a significant source of T. gondii infection in humans [4-8]. Experimental studies on animal models have indicated that tachyzoites existed in the milk of infected animals and could transmit to their offspring [5]. Moreover, some studies has shown that humans can be infected with T. gondii through consuming non-pasteurized goat milk [9,10]. Several studies have been conducted to detect the seroprevalence of T. gondii in cattle in China [11-15], but, until now, no study has been conducted to detect T. gondii DNA in milk of cattle in China. Thus, in view of this information is scarce, the present study was firstly carried out to explore the prevalence of T. gondii DNA in fresh milk of cattle in China.
Sample collection
A total of 2092 blood samples and fresh bovine milk were collected from six provinces (Heilongjiang, Jilin, Shandong, Hebei, Shanxi, Inner Mongolia and Xinjiang) (Figure 1) between January 2018 and June 2019, respectively. Cattle were handled with good ethical animal practices required by the Animal Ethics Procedures and Guidelines of the People’s Republic of China. Permission has been obtained from the owners of cattle to collect the serum samples. In the present study, clinically healthy animals were sampled and sick animals were excluded. For blood sampling, 10 ml blood sampling of each cattle were collected from the tail vessel by sterile tubes sans/without anticoagulant. The blood samples were transferred to the lab by the ice box and stored at 4°C for 2 hour and then centrifuged at 1500×g for 10 min. After this, the serum was obtained and stored at -20°C for serology. For the milk sampling, teats was firstly been cleaned and disinfected with iodine solution (0.5%), then milk was manually collected. The first few squirts were excluded. Then, approximately 5 ml of milk was collected in sterile glass tubes and frozen for molecular examination.
Serology
IgG antibodies against T. gondii was detected by a commercially available ELISA kit (ID Screen® Toxoplasmosis Indirect, Montpellier, France) following the instructions of the manufacturer.
Molecular examination to detect the T. gondii DNA
The commercial QIAamp DNA mini kit (Qiagen, GmbH, Hilden, Germany) was employed to extract the genomic DNA from milk samples following the instructions of the manufacturer. After extraction, the DNA samples were stored at -20◦C until used.
To detect the presence of T. gondii DNA in fresh milk of cattle, a semi-nested PCR targeting the T. gondii B1 gene was employed as previously described elsewhere [16]. Positive controls of DNA from parasite-infected mice and negative control from non-infected mice (PBS) were included throughout the whole examination.
In the serum samples, 123/2092 (5.88%) of the animals were positive for T. gondii (Table 1). Among the age category, the highest seroprevalence was detected in cattle of 2-3 year old category (6.26%), followed by > 5 year old category (5.95%) and 4-5 year old category (5.63%). In view of the geographical origin, T. gondii seroprevalence varied in cattle from different regions, ranging from 4.14% in Shandong province to 6.59% in Inner Mongolia Autonomous Region (Table 1). Moreover, cattle from family farming (9.48%) have a significantly higher T. gondii seroprevalence than those from commercial farm (5.26%) (P<0.01). The samples collected in 2018 (5.78%) have a similar seroprevalence with those collected in 2019 (5.97%).
In the milk samples, the T. gondii DNA was detected in 22/2092 (1.05%) of the milk samples. Fifteen of these 22 positive milk samples (68.18%) were animals who also recorded positive samples in the serology. The T. gondii DNA prevalence in >5 year old category (0.05%) was lower than that in other categories. Moreover, milk from family farming (3.27%) have a significantly higher T. gondii prevalence than those from commercial farm (0.07%) (P<0.01).
It is believed that almost a third of human worldwide has been infected with T. gondii [2,17]. Regions with hot, humid climates and lower altitudes are considered to contribute to the infection of T. gondii [1]. Although T. gondii can infect all kinds of warm-blooded animal, cattle with a more effective immune response to T. gondii infection are considered as poor hosts for T. gondii compared with other animals, such as sheep or goat [18-20]. However, cattle tissues and unpasteurized milk has been proved to contain virulent T. gondii [20], suggesting that human may get infection through consuming the meat and milk.
In the present study, T. gondii DNA was detected in 22/2092 (1.05%) fresh milk samples of cattle, suggesting that natural infection has been occurred in these farms. This information is very important because some families in those farms consume milk very day, indicating that they are at a risk of exposure for T. gondii. Moreover, cattle and milk from family farming have significantly higher T. gondii prevalence than those from commercial farm, suggesting that cattle and milk from family farming have more chance to connect with T. gondii, thus, more preventive measure should be recommended in family farming. More disease awareness efforts should be carried out among individual farmers.
It is generally believed that tachyzoites, the stage most likely present in milk, could be immediately destroyed by the gastric juice when we consumed the unpasteurized milk or its products [21]. To our disappointment, ingested tachyzoites have been verified to can cause infection [22]. T. gondii exists in unpasteurized or unseemly processed milk or fresh cheese, can be a significant risk for the people lived in the rural regions because they are their major food source [23].
Positive results of the PCR showed that T. gondii DNA exist in the milk, but this result is still not enough to verdict the possible transmission of toxoplasmosis by directly ingesting the fresh milk because no living parasites have been isolated from the fresh milk in the present study. However, the present results have already indicated that chronic infection of T. gondii has been occurring in these positive cattle, especially for those of T. gondii DNA detection in milk who also recorded positive samples in the serology, providing useful information for future studies.
Although low prevalence of T. gondii DNA has been detected in the fresh milk of cattle by molecular analysis, it is still possible that toxoplasmosis transmission may occur in some rural regions because milk is used for subsistence without pasteurization or boiling prior to consumption. However, more studies should be carried out to explore the possible transmission of toxoplasmosis by directly ingesting the fresh milk or its products.
ELISA: Enzyme-linked Immunosorbent Assay; PCR: Polymerase Chain Reaction
Acknowledgements
The authors would like to thank the owners of cattle for their involvement in the study. We are grateful to the veterinary staff for their help with the collection of blood samples.
Authors’ contributions
QFM conceived and designed the study and critically revised the manuscript. YLW collected the samples, performed the experiments, analysed the data and drafted the manuscript. All authors read and approved the final manuscript.
Funding
Project support was provided by the Science and Technology Development Plan of Jilin Province (Grant No. 20180520034JH). The founder had no role in the study design, sample collection, detection, sequencing, analysis and interpretation, or the manuscript preparation.
Availability of data and materials
The datasets used and analyzed during the study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
The present study was approved by the Animal Ethics Committee of Jilin Agricultural University (Approval No. JLAU 2018-006). The samples were collected and handled in accordance with the good animal practices required by the Animal Ethics Procedures and Guidelines of the People’s Republic of China.
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
Author details
1College of Animal Science and Technology, Jilin Agricultural University, Changchun, Jilin Province, The People’s Republic of China. 2Technology center of Changchun Customs, Jilin Province, PR China.
Table 1. Seroprevalence of T. gondii infection in blood samples of cattle in China
Variable |
Category |
No. tested |
No. positive |
Prevalence (%) |
P-value |
Age |
2-3 year |
607 |
38 |
6.26 |
0.870 |
4-5 year |
1065 |
60 |
5.63 |
||
>5 year |
420 |
25 |
5.95 |
||
Region |
Heilongjiang |
263 |
16 |
6.08 |
0.931 |
Jilin |
344 |
19 |
5.52 |
||
Inner Mongolia |
440 |
29 |
6.59 |
||
Shandong |
241 |
10 |
4.14 |
||
Xinjiang |
279 |
17 |
6.09 |
||
Shanxi |
281 |
17 |
6.05 |
||
Hebei |
244 |
15 |
6.15 |
||
Feeding model |
Commercial farm |
1786 |
94 |
5.26 |
0.004 |
Family farming |
306 |
29 |
9.48 |
||
Sampling time |
2018 year |
969 |
56 |
5.78 |
0.856 |
2019 year |
1123 |
67 |
5.97 |
||
Total |
2092 |
123 |
5.88 |
Table 2. Prevalence of T. gondii DNA in fresh milk of cattle in China. Prevalence of T. gondii DNA in fresh milk of cattle in China
Variable |
Category |
No. tested |
No. positive |
Prevalence (%) |
P-value |
Age |
2-3 year |
607 |
9 |
1.48 |
0.298 |
4-5 year |
1065 |
11 |
1.03 |
||
>5 year |
420 |
2 |
0.05 |
||
Region |
Heilongjiang |
263 |
3 |
1.14 |
0.992 |
Jilin |
344 |
3 |
0.09 |
||
Inner Mongolia |
440 |
4 |
0.09 |
||
Shandong |
241 |
2 |
0.08 |
||
Xinjiang |
279 |
4 |
1.43 |
||
Shanxi |
281 |
3 |
1.07 |
||
Hebei |
244 |
3 |
1.22 |
||
Feeding model |
Commercial farm |
1786 |
12 |
0.07 |
<0.001 |
Family farming |
306 |
10 |
3.27 |
||
Sampling time |
2018 year |
969 |
10 |
1.03 |
0.941 |
2019 year |
1123 |
12 |
1.07 |
||
Total |
2092 |
22 |
1.05 |