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내부자에 의한 위장 공격을 방지하는 개선된 ID 기반 그룹 인증 및 키 합의 프로토콜
박혜원(Hyewon Park),Asano Tomoyuki,김광조(Kwangjo Kim) 한국정보보호학회 2009 정보보호학회논문지 Vol.19 No.5
인터넷에 존재하는 많은 그룹 기반 시스템들은 안전한 통신을 위해 그룹 인증 및 키 합의 (AGKA)를 필요로 한다. 1984년에 Shamir가 ID 기반 암호시스템을 제안한 이후 이 시스템의 공개키 관리 연산 감소를 이용한 ID 기반 AGKA 프로토콜이 지속적으로 연구되고 있다. 이와 관련해서 2006년에 Zhou 등은 두 번의 라운드를 가지면서 통신 및 연산에서 매우 효율적인 ID 기반 AGKA 프로토콜을 제안하였다. 본 논문에서는 이 프로토콜이 임시 그룹 비밀 정보를 소유하고 있는 악성 내부자에 의한 위장 공격에 취약하다는 것을 보이고 이를 개선한 ID 기반 AGKA 프로토콜을 제안한다. 제안된 프로토콜은 악성 공격자가 임시 그룹 비밀 정보를 알고 있더라도 각 구성원의 개인 키를 포함하는 서명을 사용하여 위장 공격이 불가능하도록 설계되었다. 또한 Zhou 등의 프로토콜에서 수행되었던 불필요한 연산을 감소하여 성능 또한 향상시켰다. Many conference systems over the Internet require authenticated group key agreement (AGKA) for secure and reliable communication. After Shamir [1] proposed the ID-based cryptosystem in 1984, ID-based AGKA protocols have been actively studied because of the simple public key management. In 2006, Zhou et al. [12] proposed two-round ID-based AGKA protocol which is very efficient in communication and computation complexity. However, their protocol does not provide user identification and suffers from the impersonation attack by malicious participants. In this paper, we propose improved ID-based AGKA protocol to prevent impersonation attack from Zhou et al.’s protocol. In our protocol, the malicious insider cannot impersonate another participants even if he knows the ephemeral group secret value. Moreover, our protocol reduces the computation cost from Zhou et al.’s protocol.
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Insect’s intestinal organ for symbiont sorting
Ohbayashi, Tsubasa,Takeshita, Kazutaka,Kitagawa, Wataru,Nikoh, Naruo,Koga, Ryuichi,Meng, Xian-Ying,Tago, Kanako,Hori, Tomoyuki,Hayatsu, Masahito,Asano, Kozo,Kamagata, Yoichi,Lee, Bok Luel,Fukatsu, Tak National Academy of Sciences 2015 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF Vol.112 No.37
<P><B>Significance</B></P><P>In general, animals have a mouth for feeding, an anus for defecation, and a gut connecting them for digestion and absorption. However, we discovered that the stinkbug’s gut is functionally disconnected in the middle by a previously unrecognized organ for symbiont sorting, which blocks food fluid and nonsymbiotic bacteria but selectively allows passing of a specific bacterial symbiont. Though very tiny and inconspicuous, the organ governs the configuration and specificity of stinkbug gut symbiosis, wherein the posterior gut region is devoid of food flow, populated by a specific bacterial symbiont, and transformed into an isolated organ for symbiosis. Mutant analyses showed that the symbiont’s flagellar motility is needed for passing the host organ, highlighting intricate host–symbiont interactions underpinning the symbiont sorting process.</P><P>Symbiosis has significantly contributed to organismal adaptation and diversification. For establishment and maintenance of such host–symbiont associations, host organisms must have evolved mechanisms for selective incorporation, accommodation, and maintenance of their specific microbial partners. Here we report the discovery of a previously unrecognized type of animal organ for symbiont sorting. In the bean bug <I>Riptortus pedestris</I>, the posterior midgut is morphologically differentiated for harboring specific symbiotic bacteria of a beneficial nature. The sorting organ lies in the middle of the intestine as a constricted region, which partitions the midgut into an anterior nonsymbiotic region and a posterior symbiotic region. Oral administration of GFP-labeled <I>Burkholderia</I> symbionts to nymphal stinkbugs showed that the symbionts pass through the constricted region and colonize the posterior midgut. However, administration of food colorings revealed that food fluid enters neither the constricted region nor the posterior midgut, indicating selective symbiont passage at the constricted region and functional isolation of the posterior midgut for symbiosis. Coadministration of the GFP-labeled symbiont and red fluorescent protein-labeled <I>Escherichia coli</I> unveiled selective passage of the symbiont and blockage of <I>E. coli</I> at the constricted region, demonstrating the organ’s ability to discriminate the specific bacterial symbiont from nonsymbiotic bacteria. Transposon mutagenesis and screening revealed that symbiont mutants in flagella-related genes fail to pass through the constricted region, highlighting that both host’s control and symbiont’s motility are involved in the sorting process. The blocking of food flow at the constricted region is conserved among diverse stinkbug groups, suggesting the evolutionary origin of the intestinal organ in their common ancestor.</P>
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