-
Something wrong with this record ?
Haptoglobin is dispensable for haemoglobin uptake by Trypanosoma brucei
E. Horáková, M. Vrbacký, M. Tesařová, E. Stříbrná, J. Pilný, Z. Vavrušková, M. Vancová, R. Sobotka, J. Lukeš, J. Perner
Language English Country Switzerland
Document type Journal Article
NLK
Directory of Open Access Journals
from 2010
Free Medical Journals
from 2010
PubMed Central
from 2010
Europe PubMed Central
from 2010
Open Access Digital Library
from 2010-01-01
Open Access Digital Library
from 2010-01-01
ROAD: Directory of Open Access Scholarly Resources
from 2010
- MeSH
- Haptoglobins * genetics metabolism MeSH
- Hemoglobins * metabolism MeSH
- Disease Models, Animal MeSH
- Mice, Inbred C57BL MeSH
- Mice, Knockout * MeSH
- Mice MeSH
- Proteomics methods MeSH
- Trypanosoma brucei brucei * metabolism MeSH
- Trypanosomiasis, African * parasitology immunology MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
Haptoglobin is a plasma protein of mammals that plays a crucial role in vascular homeostasis by binding free haemoglobin released from ruptured red blood cells. Trypanosoma brucei can exploit this by internalising haptoglobin-haemoglobin complex to acquire host haem. Here, we investigated the impact of haptoglobin deficiency (Hp-/-) on T. brucei brucei infection and the parasite ́s capacity to internalise haemoglobin in a Hp-/- mouse model. The infected Hp-/- mice exhibited normal disease progression, with minimal weight loss and no apparent organ pathology, similarly to control mice. While the proteomic profile of mouse sera significantly changed in response to T. b. brucei, no differences in the infection response markers of blood plasma between Hp-/- and control Black mice were observed. Similarly, very few quantitative differences were observed between the proteomes of parasites harvested from Hp-/- and Black mice, including both endogenous proteins and internalised host proteins. While haptoglobin was indeed absent from parasites isolated from Hp-/-mice, haemoglobin peptides were unexpectedly detected in parasites from both Hp-/- and Black mice. Combined, the data support the dispensability of haptoglobin for haemoglobin internalisation by T. b. brucei during infection in mice. Since the trypanosomes knock-outs for their haptoglobin-haemoglobin receptor (HpHbR) internalised significantly less haemoglobin from Hp-/- mice compared to those isolated from Black mice, it suggests that T. b. brucei employs also an HpHbR-independent haptoglobin-mediated mode for haemoglobin internalisation. Our study reveals a so-far hidden flexibility of haemoglobin acquisition by T. b. brucei and offers novel insights into alternative haemoglobin uptake pathways.
Centre Algatech Institute of Microbiology Czech Academy of Sciences Třeboň Czechia
Faculty of Science University of South Bohemia České Budějovice Czechia
Institute of Parasitology Biology Centre Czech Academy of Sciences České Budějovice Czechia
Institute of Physiology Czech Academy of Sciences Prague Czechia
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc24019713
- 003
- CZ-PrNML
- 005
- 20241024110658.0
- 007
- ta
- 008
- 241015e20240718sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.3389/fimmu.2024.1441131 $2 doi
- 035 __
- $a (PubMed)39114668
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Horáková, Eva $u Institute of Parasitology, Biology Centre, Czech Academy of Sciences, České Budějovice, Czechia $u Centre Algatech, Institute of Microbiology, Czech Academy of Sciences, Třeboň, Czechia
- 245 10
- $a Haptoglobin is dispensable for haemoglobin uptake by Trypanosoma brucei / $c E. Horáková, M. Vrbacký, M. Tesařová, E. Stříbrná, J. Pilný, Z. Vavrušková, M. Vancová, R. Sobotka, J. Lukeš, J. Perner
- 520 9_
- $a Haptoglobin is a plasma protein of mammals that plays a crucial role in vascular homeostasis by binding free haemoglobin released from ruptured red blood cells. Trypanosoma brucei can exploit this by internalising haptoglobin-haemoglobin complex to acquire host haem. Here, we investigated the impact of haptoglobin deficiency (Hp-/-) on T. brucei brucei infection and the parasite ́s capacity to internalise haemoglobin in a Hp-/- mouse model. The infected Hp-/- mice exhibited normal disease progression, with minimal weight loss and no apparent organ pathology, similarly to control mice. While the proteomic profile of mouse sera significantly changed in response to T. b. brucei, no differences in the infection response markers of blood plasma between Hp-/- and control Black mice were observed. Similarly, very few quantitative differences were observed between the proteomes of parasites harvested from Hp-/- and Black mice, including both endogenous proteins and internalised host proteins. While haptoglobin was indeed absent from parasites isolated from Hp-/-mice, haemoglobin peptides were unexpectedly detected in parasites from both Hp-/- and Black mice. Combined, the data support the dispensability of haptoglobin for haemoglobin internalisation by T. b. brucei during infection in mice. Since the trypanosomes knock-outs for their haptoglobin-haemoglobin receptor (HpHbR) internalised significantly less haemoglobin from Hp-/- mice compared to those isolated from Black mice, it suggests that T. b. brucei employs also an HpHbR-independent haptoglobin-mediated mode for haemoglobin internalisation. Our study reveals a so-far hidden flexibility of haemoglobin acquisition by T. b. brucei and offers novel insights into alternative haemoglobin uptake pathways.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a myši $7 D051379
- 650 _2
- $a modely nemocí na zvířatech $7 D004195
- 650 12
- $a haptoglobiny $x genetika $x metabolismus $7 D006242
- 650 12
- $a hemoglobiny $x metabolismus $7 D006454
- 650 _2
- $a myši inbrední C57BL $7 D008810
- 650 12
- $a myši knockoutované $7 D018345
- 650 _2
- $a proteomika $x metody $7 D040901
- 650 12
- $a Trypanosoma brucei brucei $x metabolismus $7 D014346
- 650 12
- $a trypanozomóza africká $x parazitologie $x imunologie $7 D014353
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a ženské pohlaví $7 D005260
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Vrbacký, Marek $u Institute of Physiology, Czech Academy of Sciences, Prague, Czechia
- 700 1_
- $a Tesařová, Martina $u Institute of Parasitology, Biology Centre, Czech Academy of Sciences, České Budějovice, Czechia
- 700 1_
- $a Stříbrná, Eva $u Institute of Parasitology, Biology Centre, Czech Academy of Sciences, České Budějovice, Czechia
- 700 1_
- $a Pilný, Jan $u Centre Algatech, Institute of Microbiology, Czech Academy of Sciences, Třeboň, Czechia
- 700 1_
- $a Vavrušková, Zuzana $u Institute of Parasitology, Biology Centre, Czech Academy of Sciences, České Budějovice, Czechia
- 700 1_
- $a Vancová, Marie $u Institute of Parasitology, Biology Centre, Czech Academy of Sciences, České Budějovice, Czechia $u Faculty of Science, University of South Bohemia, České Budějovice, Czechia
- 700 1_
- $a Sobotka, Roman $u Centre Algatech, Institute of Microbiology, Czech Academy of Sciences, Třeboň, Czechia $u Faculty of Science, University of South Bohemia, České Budějovice, Czechia
- 700 1_
- $a Lukeš, Julius $u Institute of Parasitology, Biology Centre, Czech Academy of Sciences, České Budějovice, Czechia $u Faculty of Science, University of South Bohemia, České Budějovice, Czechia
- 700 1_
- $a Perner, Jan $u Institute of Parasitology, Biology Centre, Czech Academy of Sciences, České Budějovice, Czechia
- 773 0_
- $w MED00181405 $t Frontiers in immunology $x 1664-3224 $g Roč. 15 (20240718), s. 1441131
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/39114668 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20241015 $b ABA008
- 991 __
- $a 20241024110652 $b ABA008
- 999 __
- $a ok $b bmc $g 2202130 $s 1231686
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2024 $b 15 $c - $d 1441131 $e 20240718 $i 1664-3224 $m Frontiers in immunology $n Front Immunol $x MED00181405
- LZP __
- $a Pubmed-20241015