Διαβάστηκε το γονιδίωμα της πάπιας – Sequenced duck genome heralds breakthrough in fight against bird flu

mallardduck

Κινέζοι, Βρετανοί και άλλοι επιστήμονες αποκωδικοποίησαν για πρώτη φορά το γονιδίωμα της πάπιας, γεγονός που θα δώσει στους επιστήμονες νέες δυνατότητες στη μάχη κατά των διαφόρων στελεχών της γρίπης των πτηνών.
Οι ερευνητές, με επικεφαλής τον Γιανγουέν Λι του Αγροτικού Πανεπιστημίου της Κίνας και του Ινστιτούτου Γενωμικής του Πεκίνου, που έκαναν τη σχετική δημοσίευση στο περιοδικό γενετικής “Nature Genetics”, πέτυχαν την πλήρη αλληλούχιση του γενετικού υλικού της αγριόπαπιας (Anas platyrhynchos).

Μεταξύ των ζώων, η πάπια είναι ένα από τα κυριότερα είδη που αποτελούν φορείς των ιών Α της γρίπης των πτηνών, με πιο πρόσφατο επεισόδιο τη νέα επιδημία από το στέλεχος Η7Ν9, που ξέσπασε στην Κίνα φέτος τον Φεβρουάριο, έχοντας ήδη οδηγήσει στον θάνατο 36 ανθρώπους και προκαλώντας ζημιές ύψους 6,5 δισεκατομμυρίων δολαρίων στην κινεζική οικονομία.

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By  Wageningen University, Animal Breeding and Genetics – After having sequenced the genomes of several birds including the zebra finch, the chicken and the turkey, scientists have now succeeded in mapping the genome of the mallard (a.k.a. wild duck).

The total DNA sequence of this waterfowl shows the bird’s interaction with various bird flu viruses (influenza A) over extended periods of time. This provides good leads for further research into exactly how this virus affects birds, and in the long-term, also humans. Part of the infection mechanism and some of the physical reactions in birds are the same as in humans. This is written in an article by an international research team, including researchers from Wageningen University, which was published in Nature Genetics on 10 June.

Mallards (Anas platyrhynchos) constitute a natural reservoir for bird flu. Researchers have already discovered 25 strains of influenza A in this species of waterfowl. The birds themselves are rarely affected by the viruses, but since the emergence of the H5N1 strain, the virus has caused immense damage among poultry in some sixty countries. The fact that the virus can be transmitted to humans and has already claimed several hundred lives makes it even more of a concern. It is a continual threat, as the virus can change its genetic make-up in the mallard, thus creating a perpetual stream of new virus strains, any of which could be deadly to humans and animals.

The research team, which includes Wageningen researchers Martien Groenen, Richard Crooijmans and Robert Kraus, identified some 19,000 protein-coding genes in the genome of the mallard. This corresponds with the number in genomes of other birds sequenced previously, and is approximately 3,000 fewer than the average number found in mammals, including humans. The team used a 10-year-old Peking duck for the sequencing.

Infection

When the bird flu virus comes into contact with tissue (usually the lungs) of the mallard, it prompts a whole chain of reactions. After initial contact with the virus, signalling proteins (cytokines) sound a series of alarms around the bird’s body. Immune cells, such as white blood cells, migrate to the source of the infection via the blood and tissues. The body temperature rises in an attempt to increase its internal metabolism and disturbs the ideal temperature for the virus. Infected cells ‘commit suicide’ or are removed by the body’s own cells. The body needs a whole army of genes to mobilise this chain of reactions. “When a duck is infected with the flu virus, thousands of genes are activated. Many of them are also present and active in humans”, explains Martien Groenen. “However, studying the differences how ducks and humans fight an influenza infection will help us to find ways of controlling the infection process with medication in humans, and ultimately reduce the number of fatalities.”

Publication

The duck genome and transcriptome provide insight into an avian influenza virus reservoir species.

Yinhua Huang, Yingrui Li, David W Burt, Hualan Chen, Yong Zhang, Wubin Qian, Heebal Kim, Shangquan Gan, Yiqiang Zhao, Jianwen Li, Kang Yi, Huapeng Feng, Pengyang Zhu, Bo Li, Qiuyue Liu, Suan Fairley, Katharine E Magor, Zhenlin Du, Xiaoxiang Hu, Laurie Goodman, Hakim Tafer, Alain Vignal, Taeheon Lee, Kyu-Won Kim, Zheya Sheng, Yang An, Steve Searle, Javier Herrero, Martien A M Groenen, Richard P M A Crooijmans, Thomas Faraut, Qingle Cai, Robert G Webster, Jerry R Aldridge, Wesley C Warren, Sebastian Bartschat, Stephanie Kehr, Manja Marz, Peter F Stadler, Jacqueline Smith, Robert H S Kraus, Yaofeng Zhao, Liming Ren, Jing Fei, Mireille Morisson, Pete Kaiser, Darren K Griffin, Man Rao, Frederique Pitel, Jun Wang, & Ning Li. Nature Genetics online, 9 June 2013.

Source

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