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Chemokine, cytokine and haematological profiles in Sprague-Dawley rats co-infected with Plasmodium berghei ANKA and Trichinella zimbabwensis-A laboratory animal model for malaria and tissue-dwelling nematodes co-infection

Identifieur interne : 000193 ( Main/Exploration ); précédent : 000192; suivant : 000194

Chemokine, cytokine and haematological profiles in Sprague-Dawley rats co-infected with Plasmodium berghei ANKA and Trichinella zimbabwensis-A laboratory animal model for malaria and tissue-dwelling nematodes co-infection

Auteurs : Pretty Murambiwa [Afrique du Sud] ; Ekuyikeno Silas [Afrique du Sud] ; Yanga Mdleleni [Afrique du Sud] ; Samson Mukaratirwa [Afrique du Sud, Saint-Christophe-et-Niévès]

Source :

RBID : PMC:7044667

Abstract

Malaria remains a major cause of mortality and morbidity in sub-Saharan Africa (SSA) and tissue-dwelling helminth parasites (TDHPs) are also prevalent in this region presenting a geographical overlap in endemicity. There is paucity of information on the specific host immune responses elicited at different phases of the life cycle by the co-infecting helminth parasites. This study aimed at using a laboratory animal model to determine selected chemokine, cytokine and hematological profiles in Sprague-Dawley rats co-infected with Plasmodium berghei ANKA (Pb) and a tissue-dwelling nematode, Trichinella zimbabwensis (Tz). One-hundred-and-sixty-eight male Sprague-Dawley rats (90–150g) were randomly divided into four experimental groups; Control (n = 42), Pb-infected (n = 42), Tz-infected (n = 42) and Pb + Tz-infected group (n = 42). Trichinella zimbabwensis infection (3 muscle larvae/g body weight per os) was done on day 0 while intra-peritoneal Pb infection (105 parasitised RBCs) was done at day 28 of the 42-day experimental study for the co-infection group which corresponded with day 0 of the Pb group on the protocol. Haematological parameters, cytokines (TNF-α, IL-10, IL-4, IL-6), chemokines (CXCL10, CCL5, CCL11) and burden of Tz adult worms and muscle larvae burden were determined as per need for each group. Results showed that Tz infection predisposed the co-infected animals towards rapid development of Pb parasitaemia during co-infection, reaching a higher peak percentage parasitaemia at day 7 post-infection than the Pb mono-infected group at day 6 post-infection. Animals in the co-infected group also exhibited severe anaemia, basophilia, neutrophilia, eosinophilia and lymphopenia at day 7 post Pb infection compared to the control groups. Significant elevation of Pb parasitaemia coincided with elevated pro-inflammatory cytokine TNF-α (P < 0.001), regulatory anti-inflammatory IL-10 (P < 0.001), and pro-inflammatory chemokines CXCL10 (P < 0.001) concentration in comparison to control group, at day 7 post Pb infection. Our results confirm that co-infection of Pb with Tz resulted in increased Pb parasitaemia compared to the control group in the early stages of infection and this might translate to severe malaria.


Url:
DOI: 10.1016/j.heliyon.2020.e03475
PubMed: 32140591
PubMed Central: 7044667


Affiliations:


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Le document en format XML

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ANKA and
<italic>Trichinella zimbabwensis</italic>
-A laboratory animal model for malaria and tissue-dwelling nematodes co-infection</title>
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<p>Malaria remains a major cause of mortality and morbidity in sub-Saharan Africa (SSA) and tissue-dwelling helminth parasites (TDHPs) are also prevalent in this region presenting a geographical overlap in endemicity. There is paucity of information on the specific host immune responses elicited at different phases of the life cycle by the co-infecting helminth parasites. This study aimed at using a laboratory animal model to determine selected chemokine, cytokine and hematological profiles in Sprague-Dawley rats co-infected with
<italic>Plasmodium berghei</italic>
ANKA (Pb) and a tissue-dwelling nematode,
<italic>Trichinella zimbabwensis</italic>
(Tz). One-hundred-and-sixty-eight male Sprague-Dawley rats (90–150g) were randomly divided into four experimental groups; Control (n = 42), Pb-infected (n = 42), Tz-infected (n = 42) and Pb
<italic>+</italic>
Tz-infected group (n = 42).
<italic>Trichinella zimbabwensis</italic>
infection (3 muscle larvae/g body weight
<italic>per os</italic>
) was done on day 0 while intra-peritoneal Pb infection (10
<sup>5</sup>
parasitised RBCs) was done at day 28 of the 42-day experimental study for the co-infection group which corresponded with day 0 of the Pb group on the protocol. Haematological parameters, cytokines (TNF-α, IL-10, IL-4, IL-6), chemokines (CXCL10, CCL5, CCL11) and burden of Tz adult worms and muscle larvae burden were determined as per need for each group. Results showed that Tz infection predisposed the co-infected animals towards rapid development of Pb parasitaemia during co-infection, reaching a higher peak percentage parasitaemia at day 7 post-infection than the Pb mono-infected group at day 6 post-infection. Animals in the co-infected group also exhibited severe anaemia, basophilia, neutrophilia, eosinophilia and lymphopenia at day 7 post Pb infection compared to the control groups. Significant elevation of Pb parasitaemia coincided with elevated pro-inflammatory cytokine TNF-α (
<italic>P <</italic>
0.001), regulatory anti-inflammatory IL-10 (
<italic>P <</italic>
0.001), and pro-inflammatory chemokines CXCL10 (
<italic>P <</italic>
0.001) concentration in comparison to control group, at day 7 post Pb infection. Our results confirm that co-infection of Pb with Tz resulted in increased Pb parasitaemia compared to the control group in the early stages of infection and this might translate to severe malaria.</p>
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<name sortKey="Murambiwa, Pretty" sort="Murambiwa, Pretty" uniqKey="Murambiwa P" first="Pretty" last="Murambiwa">Pretty Murambiwa</name>
</noRegion>
<name sortKey="Mdleleni, Yanga" sort="Mdleleni, Yanga" uniqKey="Mdleleni Y" first="Yanga" last="Mdleleni">Yanga Mdleleni</name>
<name sortKey="Mukaratirwa, Samson" sort="Mukaratirwa, Samson" uniqKey="Mukaratirwa S" first="Samson" last="Mukaratirwa">Samson Mukaratirwa</name>
<name sortKey="Silas, Ekuyikeno" sort="Silas, Ekuyikeno" uniqKey="Silas E" first="Ekuyikeno" last="Silas">Ekuyikeno Silas</name>
</country>
<country name="Saint-Christophe-et-Niévès">
<noRegion>
<name sortKey="Mukaratirwa, Samson" sort="Mukaratirwa, Samson" uniqKey="Mukaratirwa S" first="Samson" last="Mukaratirwa">Samson Mukaratirwa</name>
</noRegion>
</country>
</tree>
</affiliations>
</record>

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EXPLOR_STEP=$WICRI_ROOT/Sante/explor/ChloroquineV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000193 | SxmlIndent | more

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Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Sante
   |area=    ChloroquineV1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     PMC:7044667
   |texte=   Chemokine, cytokine and haematological profiles in Sprague-Dawley rats co-infected with Plasmodium berghei ANKA and Trichinella zimbabwensis-A laboratory animal model for malaria and tissue-dwelling nematodes co-infection
}}

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Data generation: Wed Mar 25 22:43:59 2020. Site generation: Sun Jan 31 12:44:45 2021